Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 90141 |
| ensemblid | ENSG00000140025.16 |
| hgncid | 20357 |
| symbol | EFCAB11 |
| name | EF-hand calcium binding domain 11 |
| refseq_nuc | NM_145231.4 |
| refseq_prot | NP_660274.1 |
| ensembl_nuc | ENST00000316738.12 |
| ensembl_prot | ENSP00000326267.7 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 89794669 |
| end | 89954730 |
| strand | - |
| ver | v1.2 |
| region | chr14:89794669-89954730 |
| region5000 | chr14:89789669-89959730 |
| regionname0 | EFCAB11_chr14_89794669_89954730 |
| regionname5000 | EFCAB11_chr14_89789669_89959730 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 163 | 265 | 68 | 49 | 102 | 8 | 36 | 78 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | MFFSE others(158): Show |
chr14 | 89789669 | 89959730 |
| a0002 | 0/0 | 163 | 13 | 10 | 3 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | MFFSE others(158): Show |
chr14 | 89789669 | 89959730 |
| a0003 | 0/0 | 163 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | MFFSE others(158): Show |
chr14 | 89789669 | 89959730 |
| a0004 | 0/0 | 163 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | MFFSE others(158): Show |
chr14 | 89789669 | 89959730 |
| a0005 | 0/0 | 163 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | MFFSE others(158): Show |
chr14 | 89789669 | 89959730 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 489 | 158 | 30 | 33 | 66 | 6 | 22 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | ATGTT others(484): Show |
chr14 | 89789669 | 89959730 | ||
| a0001c0002 | 0/1 | 489 | 64 | 9 | 13 | 29 | 1 | 11 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | ATGTT others(484): Show |
chr14 | 89789669 | 89959730 | ||
| a0001c0003 | 0/0 | 489 | 23 | 9 | 3 | 7 | 1 | 3 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | ATGTT others(484): Show |
chr14 | 89789669 | 89959730 | ||
| a0001c0004 | 0/0 | 489 | 13 | 13 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | ATGTT others(484): Show |
chr14 | 89789669 | 89959730 | ||
| a0001c0006 | 0/0 | 489 | 4 | 4 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | ATGTT others(484): Show |
chr14 | 89789669 | 89959730 | ||
| a0001c0009 | 0/0 | 489 | 3 | 3 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | ATGTT others(484): Show |
chr14 | 89789669 | 89959730 | ||
| a0002c0005 | 0/0 | 489 | 10 | 8 | 2 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | ATGTT others(484): Show |
chr14 | 89789669 | 89959730 | ||
| a0002c0007 | 0/0 | 489 | 3 | 2 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | ATGTT others(484): Show |
chr14 | 89789669 | 89959730 | ||
| a0003c0008 | 0/0 | 489 | 3 | 3 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | ATGTT others(484): Show |
chr14 | 89789669 | 89959730 | ||
| a0004c0010 | 0/0 | 489 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | ATGTT others(484): Show |
chr14 | 89789669 | 89959730 | ||
| a0005c0011 | 0/0 | 489 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | ATGTT others(484): Show |
chr14 | 89789669 | 89959730 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3134 | 34 | 5 | 1 | 26 | 0 | 2 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3129): Show |
chr14 | 89789669 | 89959730 |
| a0001c0001t0002 | 0/0 | 3137 | 25 | 4 | 8 | 0 | 4 | 9 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3132): Show |
chr14 | 89789669 | 89959730 |
| a0001c0001t0003 | 0/0 | 3133 | 15 | 0 | 4 | 10 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3128): Show |
chr14 | 89789669 | 89959730 |
| a0001c0001t0004 | 0/0 | 3135 | 16 | 5 | 3 | 3 | 0 | 5 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3130): Show |
chr14 | 89789669 | 89959730 |
| a0001c0001t0005 | 0/0 | 3138 | 19 | 1 | 2 | 14 | 2 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3133): Show |
chr14 | 89789669 | 89959730 |
| a0001c0001t0006 | 0/0 | 3138 | 4 | 1 | 3 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3133): Show |
chr14 | 89789669 | 89959730 |
| a0001c0001t0007 | 0/0 | 3135 | 7 | 1 | 4 | 2 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3130): Show |
chr14 | 89789669 | 89959730 |
| a0001c0001t0008 | 0/0 | 3133 | 6 | 5 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3128): Show |
chr14 | 89789669 | 89959730 |
| a0001c0001t0010 | 0/0 | 3135 | 6 | 4 | 0 | 0 | 0 | 2 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3130): Show |
chr14 | 89789669 | 89959730 |
| a0001c0001t0011 | 0/0 | 3137 | 5 | 0 | 0 | 5 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3132): Show |
chr14 | 89789669 | 89959730 |
| a0001c0001t0012 | 1/0 | 3136 | 3 | 1 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3131): Show |
chr14 | 89789669 | 89959730 |
| a0001c0001t0013 | 0/0 | 3135 | 4 | 0 | 3 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3130): Show |
chr14 | 89789669 | 89959730 |
| a0001c0001t0014 | 0/0 | 3134 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3129): Show |
chr14 | 89789669 | 89959730 |
| a0001c0001t0015 | 0/0 | 3134 | 3 | 0 | 0 | 3 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3129): Show |
chr14 | 89789669 | 89959730 |
| a0001c0001t0018 | 0/0 | 3136 | 2 | 0 | 1 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3131): Show |
chr14 | 89789669 | 89959730 |
| a0001c0001t0022 | 0/0 | 3134 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3129): Show |
chr14 | 89789669 | 89959730 |
| a0001c0001t0028 | 0/0 | 3135 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3130): Show |
chr14 | 89789669 | 89959730 |
| a0001c0001t0030 | 0/0 | 3136 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3131): Show |
chr14 | 89789669 | 89959730 |
| a0001c0001t0032 | 0/0 | 3137 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3132): Show |
chr14 | 89789669 | 89959730 |
| a0001c0001t0033 | 0/0 | 3135 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3130): Show |
chr14 | 89789669 | 89959730 |
| a0001c0001t0034 | 0/0 | 3137 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3132): Show |
chr14 | 89789669 | 89959730 |
| a0001c0001t0038 | 0/0 | 3134 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3129): Show |
chr14 | 89789669 | 89959730 |
| a0001c0001t0039 | 0/0 | 3138 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3133): Show |
chr14 | 89789669 | 89959730 |
| a0001c0002t0001 | 0/0 | 3134 | 7 | 2 | 0 | 4 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3129): Show |
chr14 | 89789669 | 89959730 |
| a0001c0002t0002 | 0/1 | 3137 | 13 | 3 | 6 | 0 | 0 | 3 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3132): Show |
chr14 | 89789669 | 89959730 |
| a0001c0002t0003 | 0/0 | 3133 | 18 | 0 | 1 | 14 | 0 | 3 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3128): Show |
chr14 | 89789669 | 89959730 |
| a0001c0002t0004 | 0/0 | 3135 | 10 | 1 | 2 | 7 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3130): Show |
chr14 | 89789669 | 89959730 |
| a0001c0002t0005 | 0/0 | 3138 | 2 | 0 | 1 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3133): Show |
chr14 | 89789669 | 89959730 |
| a0001c0002t0006 | 0/0 | 3138 | 2 | 0 | 2 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3133): Show |
chr14 | 89789669 | 89959730 |
| a0001c0002t0010 | 0/0 | 3135 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3130): Show |
chr14 | 89789669 | 89959730 |
| a0001c0002t0019 | 0/0 | 3136 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3131): Show |
chr14 | 89789669 | 89959730 |
| a0001c0002t0020 | 0/0 | 3135 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3130): Show |
chr14 | 89789669 | 89959730 |
| a0001c0002t0024 | 0/0 | 3136 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3131): Show |
chr14 | 89789669 | 89959730 |
| a0001c0002t0027 | 0/0 | 3133 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3128): Show |
chr14 | 89789669 | 89959730 |
| a0001c0002t0031 | 0/0 | 3133 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3128): Show |
chr14 | 89789669 | 89959730 |
| a0001c0002t0035 | 0/0 | 3133 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3128): Show |
chr14 | 89789669 | 89959730 |
| a0001c0002t0040 | 0/0 | 3136 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3131): Show |
chr14 | 89789669 | 89959730 |
| a0001c0002t0041 | 0/0 | 3133 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3128): Show |
chr14 | 89789669 | 89959730 |
| a0001c0002t0042 | 0/0 | 3137 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3132): Show |
chr14 | 89789669 | 89959730 |
| a0001c0002t0043 | 0/0 | 3133 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | GGGCC others(3128): Show |
chr14 | 89789669 | 89959730 |
| a0001c0003t0001 | 0/0 | 3134 | 4 | 0 | 1 | 3 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3129): Show |
chr14 | 89789669 | 89959730 |
| a0001c0003t0002 | 0/0 | 3137 | 3 | 1 | 1 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3132): Show |
chr14 | 89789669 | 89959730 |
| a0001c0003t0003 | 0/0 | 3133 | 3 | 0 | 0 | 0 | 0 | 3 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3128): Show |
chr14 | 89789669 | 89959730 |
| a0001c0003t0004 | 0/0 | 3135 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3130): Show |
chr14 | 89789669 | 89959730 |
| a0001c0003t0008 | 0/0 | 3133 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3128): Show |
chr14 | 89789669 | 89959730 |
| a0001c0003t0009 | 0/0 | 3135 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3130): Show |
chr14 | 89789669 | 89959730 |
| a0001c0003t0012 | 0/0 | 3136 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3131): Show |
chr14 | 89789669 | 89959730 |
| a0001c0003t0016 | 0/0 | 3137 | 3 | 0 | 0 | 3 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3132): Show |
chr14 | 89789669 | 89959730 |
| a0001c0003t0021 | 0/0 | 3137 | 2 | 0 | 1 | 0 | 1 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3132): Show |
chr14 | 89789669 | 89959730 |
| a0001c0003t0025 | 0/0 | 3133 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3128): Show |
chr14 | 89789669 | 89959730 |
| a0001c0003t0037 | 0/0 | 3134 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3129): Show |
chr14 | 89789669 | 89959730 |
| a0001c0004t0001 | 0/0 | 3134 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3129): Show |
chr14 | 89789669 | 89959730 |
| a0001c0004t0002 | 0/0 | 3137 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3132): Show |
chr14 | 89789669 | 89959730 |
| a0001c0004t0006 | 0/0 | 3138 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3133): Show |
chr14 | 89789669 | 89959730 |
| a0001c0004t0009 | 0/0 | 3135 | 3 | 3 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3130): Show |
chr14 | 89789669 | 89959730 |
| a0001c0004t0017 | 0/0 | 3133 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3128): Show |
chr14 | 89789669 | 89959730 |
| a0001c0004t0020 | 0/0 | 3135 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3130): Show |
chr14 | 89789669 | 89959730 |
| a0001c0004t0023 | 0/0 | 3137 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3132): Show |
chr14 | 89789669 | 89959730 |
| a0001c0004t0036 | 0/0 | 3136 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3131): Show |
chr14 | 89789669 | 89959730 |
| a0001c0006t0004 | 0/0 | 3135 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3130): Show |
chr14 | 89789669 | 89959730 |
| a0001c0006t0006 | 0/0 | 3138 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3133): Show |
chr14 | 89789669 | 89959730 |
| a0001c0006t0009 | 0/0 | 3135 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3130): Show |
chr14 | 89789669 | 89959730 |
| a0001c0006t0014 | 0/0 | 3134 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3129): Show |
chr14 | 89789669 | 89959730 |
| a0001c0009t0001 | 0/0 | 3134 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3129): Show |
chr14 | 89789669 | 89959730 |
| a0001c0009t0002 | 0/0 | 3137 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3132): Show |
chr14 | 89789669 | 89959730 |
| a0001c0009t0014 | 0/0 | 3134 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3129): Show |
chr14 | 89789669 | 89959730 |
| a0002c0005t0002 | 0/0 | 3137 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3132): Show |
chr14 | 89789669 | 89959730 |
| a0002c0005t0003 | 0/0 | 3133 | 2 | 1 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3128): Show |
chr14 | 89789669 | 89959730 |
| a0002c0005t0004 | 0/0 | 3135 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3130): Show |
chr14 | 89789669 | 89959730 |
| a0002c0005t0006 | 0/0 | 3138 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3133): Show |
chr14 | 89789669 | 89959730 |
| a0002c0005t0007 | 0/0 | 3135 | 2 | 1 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3130): Show |
chr14 | 89789669 | 89959730 |
| a0002c0005t0009 | 0/0 | 3135 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3130): Show |
chr14 | 89789669 | 89959730 |
| a0002c0005t0029 | 0/0 | 3098 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3093): Show |
chr14 | 89789669 | 89959730 |
| a0002c0007t0004 | 0/0 | 3135 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3130): Show |
chr14 | 89789669 | 89959730 |
| a0002c0007t0009 | 0/0 | 3135 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3130): Show |
chr14 | 89789669 | 89959730 |
| a0002c0007t0017 | 0/0 | 3133 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3128): Show |
chr14 | 89789669 | 89959730 |
| a0003c0008t0001 | 0/0 | 3134 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3129): Show |
chr14 | 89789669 | 89959730 |
| a0003c0008t0026 | 0/0 | 3134 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3129): Show |
chr14 | 89789669 | 89959730 |
| a0004c0010t0004 | 0/0 | 3135 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3130): Show |
chr14 | 89789669 | 89959730 |
| a0005c0011t0009 | 0/0 | 3135 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | AGGCT others(3130): Show |
chr14 | 89789669 | 89959730 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0004g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0004g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0004g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0004g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0004g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0005g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0005g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0005g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0005g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0005g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0005g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0005g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0005g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0005g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0006g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0006g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0006g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0007g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0007g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0007g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0007g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0007g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0007g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0007g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0008g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0008g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0008g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0008g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0008g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0008g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0010g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0010g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0010g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0010g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0010g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0010g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0011g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0011g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0011g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0011g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0011g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0012g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0012g0111 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0012g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0013g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0013g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0013g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0013g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0014g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0015g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0015g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0015g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0018g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0018g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0022g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0028g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0030g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0032g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0033g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0034g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0038g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0001t0039g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0002g0184 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0003g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0003g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0004g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0004g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0004g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0005g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0006g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0006g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0010g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0019g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0019g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0020g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0024g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0027g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0031g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0035g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0040g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0041g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0042g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0002t0043g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0003t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0003t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0003t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0003t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0003t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0003t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0003t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0003t0003g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0003t0003g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0003t0003g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0003t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0003t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0003t0008g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0003t0008g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0003t0009g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0003t0012g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0003t0016g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0003t0016g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0003t0016g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0003t0021g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0003t0021g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0003t0025g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0003t0037g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0004t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0004t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0004t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0004t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0004t0006g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0004t0006g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0004t0009g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0004t0009g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0004t0009g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0004t0017g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0004t0020g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0004t0023g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0004t0036g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0006t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0006t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0006t0009g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0006t0014g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0009t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0009t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0001c0009t0014g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0002c0005t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0002c0005t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0002c0005t0003g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0002c0005t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0002c0005t0004g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0002c0005t0006g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0002c0005t0007g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0002c0005t0007g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0002c0005t0009g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0002c0005t0029g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0002c0007t0004g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0002c0007t0009g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0002c0007t0017g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0003c0008t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0003c0008t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0003c0008t0026g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0004c0010t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0004c0010t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| a0005c0011t0009g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0005 | g0086 | EUR | GBR | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0033 | EUR | GBR | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0156 | EUR | FIN | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG00323 | hp2 | a0001 | c0003 | t0021 | g0003 | EUR | FIN | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG00408 | hp1 | a0001 | c0002 | t0004 | g0204 | EAS | CHS | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG00408 | hp2 | a0001 | c0001 | t0005 | g0113 | EAS | CHS | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG00438 | hp2 | a0001 | c0001 | t0005 | g0128 | EAS | CHS | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | CHS | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG00621 | hp2 | a0001 | c0001 | t0012 | g0089 | EAS | CHS | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG00673 | hp1 | a0001 | c0002 | t0003 | g0065 | EAS | CHS | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG00673 | hp2 | a0001 | c0001 | t0011 | g0056 | EAS | CHS | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG00735 | hp2 | a0002 | c0005 | t0007 | g0252 | AMR | PUR | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01070 | hp1 | a0001 | c0001 | t0032 | g0235 | AMR | PUR | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01071 | hp1 | a0001 | c0001 | t0007 | g0126 | AMR | PUR | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0207 | AMR | PUR | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01074 | hp2 | a0001 | c0001 | t0007 | g0036 | AMR | PUR | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0244 | AMR | PUR | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01081 | hp2 | a0002 | c0007 | t0004 | g0261 | AMR | PUR | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01099 | hp1 | a0001 | c0001 | t0013 | g0108 | AMR | PUR | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | PUR | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01109 | hp1 | a0002 | c0005 | t0003 | g0253 | AMR | PUR | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01109 | hp2 | a0001 | c0001 | t0018 | g0048 | AMR | PUR | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01168 | hp1 | a0001 | c0003 | t0021 | g0002 | AMR | PUR | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01168 | hp2 | a0001 | c0001 | t0013 | g0028 | AMR | PUR | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01175 | hp2 | a0001 | c0001 | t0007 | g0161 | AMR | PUR | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01192 | hp1 | a0001 | c0001 | t0008 | g0178 | AMR | PUR | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01192 | hp2 | a0001 | c0001 | t0007 | g0123 | AMR | PUR | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01243 | hp1 | a0001 | c0001 | t0006 | g0063 | AMR | PUR | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01243 | hp2 | a0001 | c0001 | t0005 | g0135 | AMR | PUR | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0208 | AMR | CLM | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01255 | hp2 | a0001 | c0001 | t0033 | g0050 | AMR | CLM | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01256 | hp1 | a0001 | c0003 | t0002 | g0021 | AMR | CLM | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01256 | hp2 | a0001 | c0002 | t0004 | g0223 | AMR | CLM | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | CLM | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01261 | hp2 | a0001 | c0001 | t0006 | g0037 | AMR | CLM | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | CLM | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0105 | AMR | CLM | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01358 | hp1 | a0001 | c0001 | t0013 | g0106 | AMR | CLM | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0117 | AMR | CLM | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0017 | AMR | CLM | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01433 | hp2 | a0001 | c0002 | t0006 | g0225 | AMR | CLM | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01496 | hp1 | a0001 | c0001 | t0004 | g0160 | AMR | CLM | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01496 | hp2 | a0001 | c0001 | t0005 | g0119 | AMR | CLM | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0162 | EUR | IBS | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0071 | EUR | IBS | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01884 | hp1 | a0004 | c0010 | t0004 | g0041 | AFR | ACB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01884 | hp2 | a0001 | c0001 | t0004 | g0171 | AFR | ACB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01891 | hp1 | a0001 | c0002 | t0027 | g0172 | AFR | ACB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01891 | hp2 | a0003 | c0008 | t0001 | g0268 | AFR | ACB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0220 | AMR | PEL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0073 | AMR | PEL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PEL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01934 | hp2 | a0001 | c0002 | t0003 | g0194 | AMR | PEL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01943 | hp1 | a0001 | c0002 | t0006 | g0224 | AMR | PEL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01981 | hp1 | a0001 | c0001 | t0038 | g0069 | AMR | PEL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG01981 | hp2 | a0001 | c0002 | t0041 | g0226 | AMR | PEL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02004 | hp1 | a0001 | c0002 | t0004 | g0201 | AMR | PEL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02004 | hp2 | a0001 | c0001 | t0006 | g0133 | AMR | PEL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02015 | hp1 | a0001 | c0001 | t0004 | g0085 | EAS | KHV | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02015 | hp2 | a0001 | c0001 | t0005 | g0034 | EAS | KHV | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02027 | hp1 | a0001 | c0001 | t0005 | g0241 | EAS | KHV | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02027 | hp2 | a0001 | c0002 | t0019 | g0221 | EAS | KHV | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02055 | hp1 | a0001 | c0001 | t0007 | g0231 | AFR | ACB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02055 | hp2 | a0002 | c0005 | t0002 | g0250 | AFR | ACB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02056 | hp1 | a0001 | c0001 | t0028 | g0084 | EAS | KHV | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02056 | hp2 | a0001 | c0001 | t0005 | g0035 | EAS | KHV | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02071 | hp1 | a0001 | c0001 | t0015 | g0099 | EAS | KHV | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02071 | hp2 | a0001 | c0001 | t0011 | g0153 | EAS | KHV | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02132 | hp2 | a0001 | c0002 | t0003 | g0197 | EAS | KHV | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02148 | hp1 | a0001 | c0001 | t0003 | g0052 | AMR | PEL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02148 | hp2 | a0001 | c0002 | t0002 | g0243 | AMR | PEL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02155 | hp1 | a0001 | c0001 | t0005 | g0055 | EAS | CDX | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0101 | EAS | CDX | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02165 | hp1 | a0001 | c0002 | t0004 | g0205 | EAS | CDX | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02165 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | CDX | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02257 | hp1 | a0001 | c0009 | t0014 | g0270 | AFR | ACB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ACB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02258 | hp1 | a0001 | c0003 | t0012 | g0016 | AFR | ACB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02258 | hp2 | a0001 | c0004 | t0001 | g0278 | AFR | ACB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0091 | AMR | PEL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0222 | AMR | PEL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02280 | hp2 | a0001 | c0001 | t0008 | g0176 | AFR | ACB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02293 | hp1 | a0001 | c0002 | t0005 | g0206 | AMR | PEL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0104 | AMR | PEL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02451 | hp1 | a0001 | c0003 | t0009 | g0022 | AFR | ACB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0228 | AFR | ACB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02572 | hp1 | a0001 | c0003 | t0004 | g0019 | AFR | GWD | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02572 | hp2 | a0001 | c0001 | t0006 | g0149 | AFR | GWD | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0154 | SAS | PJL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02602 | hp2 | a0001 | c0002 | t0003 | g0248 | SAS | PJL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02622 | hp1 | a0001 | c0003 | t0008 | g0020 | AFR | GWD | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02622 | hp2 | a0001 | c0004 | t0002 | g0276 | AFR | GWD | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02630 | hp1 | a0002 | c0005 | t0002 | g0259 | AFR | GWD | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02630 | hp2 | a0001 | c0006 | t0009 | g0262 | AFR | GWD | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02647 | hp1 | a0001 | c0002 | t0031 | g0026 | AFR | GWD | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0148 | SAS | PJL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02717 | hp1 | a0001 | c0004 | t0002 | g0279 | AFR | GWD | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02717 | hp2 | a0001 | c0001 | t0008 | g0177 | AFR | GWD | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02723 | hp1 | a0001 | c0001 | t0014 | g0240 | AFR | GWD | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | GWD | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02735 | hp1 | a0001 | c0001 | t0004 | g0151 | SAS | PJL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02738 | hp1 | a0001 | c0002 | t0003 | g0183 | SAS | PJL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02738 | hp2 | a0001 | c0002 | t0002 | g0247 | SAS | PJL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02809 | hp1 | a0002 | c0007 | t0009 | g0256 | AFR | GWD | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02809 | hp2 | a0005 | c0011 | t0009 | g0245 | AFR | GWD | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0179 | AFR | GWD | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02896 | hp1 | a0001 | c0002 | t0001 | g0168 | AFR | GWD | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02896 | hp2 | a0001 | c0003 | t0002 | g0007 | AFR | GWD | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02897 | hp1 | a0001 | c0003 | t0025 | g0006 | AFR | GWD | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0169 | AFR | GWD | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02922 | hp1 | a0001 | c0004 | t0017 | g0281 | AFR | ESN | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | ESN | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02965 | hp1 | a0001 | c0006 | t0004 | g0265 | AFR | ESN | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02965 | hp2 | a0001 | c0003 | t0037 | g0018 | AFR | ESN | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02970 | hp1 | a0002 | c0005 | t0003 | g0258 | AFR | ESN | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02970 | hp2 | a0001 | c0002 | t0020 | g0025 | AFR | ESN | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0173 | AFR | ESN | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02976 | hp2 | a0002 | c0007 | t0017 | g0257 | AFR | ESN | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0116 | SAS | PJL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03017 | hp2 | a0001 | c0002 | t0042 | g0227 | SAS | PJL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03098 | hp1 | a0001 | c0001 | t0030 | g0043 | AFR | MSL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03098 | hp2 | a0001 | c0004 | t0006 | g0280 | AFR | MSL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03130 | hp1 | a0001 | c0003 | t0008 | g0008 | AFR | ESN | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03130 | hp2 | a0002 | c0005 | t0004 | g0249 | AFR | ESN | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03139 | hp1 | a0001 | c0001 | t0008 | g0175 | AFR | ESN | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03139 | hp2 | a0003 | c0008 | t0026 | g0267 | AFR | ESN | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03195 | hp1 | a0001 | c0004 | t0020 | g0283 | AFR | ESN | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03195 | hp2 | a0001 | c0001 | t0010 | g0237 | AFR | ESN | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03209 | hp1 | a0003 | c0008 | t0001 | g0266 | AFR | MSL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03209 | hp2 | a0001 | c0001 | t0008 | g0239 | AFR | MSL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03225 | hp1 | a0001 | c0004 | t0009 | g0275 | AFR | MSL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03225 | hp2 | a0001 | c0002 | t0002 | g0230 | AFR | MSL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03239 | hp1 | a0001 | c0001 | t0018 | g0100 | SAS | PJL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03453 | hp1 | a0001 | c0009 | t0001 | g0269 | AFR | MSL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03453 | hp2 | a0002 | c0005 | t0006 | g0255 | AFR | MSL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03486 | hp1 | a0004 | c0010 | t0004 | g0040 | AFR | MSL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03486 | hp2 | a0001 | c0004 | t0023 | g0274 | AFR | MSL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03491 | hp1 | a0001 | c0002 | t0010 | g0209 | SAS | PJL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0158 | SAS | PJL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0157 | SAS | PJL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03492 | hp2 | a0001 | c0001 | t0022 | g0064 | SAS | PJL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03540 | hp2 | a0001 | c0003 | t0004 | g0005 | AFR | GWD | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03654 | hp1 | a0001 | c0002 | t0035 | g0186 | SAS | PJL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0246 | SAS | PJL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03669 | hp1 | a0001 | c0002 | t0024 | g0192 | SAS | PJL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03669 | hp2 | a0001 | c0001 | t0010 | g0122 | SAS | PJL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03710 | hp1 | a0001 | c0001 | t0013 | g0112 | SAS | PJL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03710 | hp2 | a0001 | c0003 | t0003 | g0013 | SAS | PJL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0075 | SAS | BEB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0166 | SAS | BEB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03834 | hp1 | a0001 | c0003 | t0003 | g0015 | SAS | BEB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0190 | SAS | BEB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | BEB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03927 | hp2 | a0001 | c0001 | t0004 | g0107 | SAS | BEB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0159 | SAS | BEB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0109 | SAS | BEB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG04204 | hp1 | a0001 | c0002 | t0003 | g0191 | SAS | STU | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0145 | SAS | STU | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG04228 | hp1 | a0001 | c0003 | t0003 | g0014 | SAS | STU | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG04228 | hp2 | a0001 | c0001 | t0010 | g0072 | SAS | STU | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18522 | hp1 | a0001 | c0004 | t0009 | g0272 | AFR | YRI | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18522 | hp2 | a0001 | c0001 | t0012 | g0238 | AFR | YRI | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18747 | hp1 | a0001 | c0002 | t0004 | g0203 | EAS | CHB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | CHB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18906 | hp1 | a0002 | c0005 | t0029 | g0260 | AFR | YRI | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0097 | AFR | YRI | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18943 | hp1 | a0001 | c0002 | t0003 | g0198 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18943 | hp2 | a0001 | c0001 | t0011 | g0130 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18945 | hp1 | a0001 | c0002 | t0003 | g0210 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18947 | hp1 | a0001 | c0001 | t0011 | g0094 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18947 | hp2 | a0001 | c0002 | t0004 | g0193 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18949 | hp1 | a0001 | c0001 | t0015 | g0103 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18949 | hp2 | a0001 | c0002 | t0001 | g0188 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18952 | hp1 | a0001 | c0002 | t0003 | g0189 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18954 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18959 | hp1 | a0001 | c0003 | t0016 | g0009 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18959 | hp2 | a0001 | c0002 | t0003 | g0199 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18970 | hp2 | a0001 | c0002 | t0043 | g0001 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18971 | hp2 | a0001 | c0002 | t0004 | g0195 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18973 | hp1 | a0001 | c0002 | t0003 | g0213 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18973 | hp2 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18974 | hp1 | a0001 | c0002 | t0003 | g0181 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18982 | hp2 | a0001 | c0002 | t0003 | g0219 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18983 | hp1 | a0001 | c0002 | t0003 | g0214 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18983 | hp2 | a0001 | c0001 | t0005 | g0053 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18984 | hp1 | a0001 | c0002 | t0003 | g0217 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18986 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18989 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18989 | hp2 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18990 | hp1 | a0001 | c0001 | t0005 | g0146 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18991 | hp1 | a0001 | c0002 | t0003 | g0182 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18994 | hp1 | a0001 | c0002 | t0005 | g0187 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19001 | hp1 | a0001 | c0001 | t0005 | g0124 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19003 | hp2 | a0001 | c0002 | t0004 | g0185 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19004 | hp2 | a0001 | c0002 | t0004 | g0200 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19007 | hp1 | a0001 | c0001 | t0005 | g0138 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19009 | hp1 | a0001 | c0001 | t0007 | g0234 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0059 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19010 | hp2 | a0001 | c0001 | t0011 | g0131 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19030 | hp1 | a0001 | c0001 | t0010 | g0047 | AFR | LWK | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19030 | hp2 | a0002 | c0005 | t0007 | g0251 | AFR | LWK | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19043 | hp1 | a0001 | c0002 | t0002 | g0229 | AFR | LWK | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19043 | hp2 | a0001 | c0009 | t0002 | g0273 | AFR | LWK | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19054 | hp1 | a0001 | c0001 | t0005 | g0092 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19056 | hp1 | a0001 | c0003 | t0016 | g0010 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19060 | hp1 | a0001 | c0002 | t0003 | g0212 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19060 | hp2 | a0001 | c0001 | t0005 | g0121 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19068 | hp1 | a0001 | c0001 | t0004 | g0054 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19068 | hp2 | a0001 | c0001 | t0034 | g0066 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19077 | hp1 | a0001 | c0001 | t0005 | g0134 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19077 | hp2 | a0001 | c0001 | t0007 | g0079 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19083 | hp1 | a0001 | c0003 | t0001 | g0023 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19083 | hp2 | a0001 | c0002 | t0003 | g0211 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19084 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19086 | hp2 | a0001 | c0002 | t0019 | g0218 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19089 | hp1 | a0001 | c0003 | t0016 | g0024 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19089 | hp2 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19240 | hp1 | a0001 | c0001 | t0004 | g0174 | AFR | YRI | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA19240 | hp2 | a0001 | c0004 | t0001 | g0277 | AFR | YRI | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0170 | AFR | ASW | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0115 | AFR | ASW | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA20805 | hp1 | a0001 | c0001 | t0005 | g0087 | EUR | TSI | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA20805 | hp2 | a0001 | c0002 | t0040 | g0118 | EUR | TSI | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA20905 | hp1 | a0001 | c0001 | t0004 | g0110 | SAS | GIH | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0152 | SAS | GIH | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02109 | hp1 | a0001 | c0001 | t0039 | g0132 | AFR | ACB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02109 | hp2 | a0001 | c0004 | t0036 | g0282 | AFR | ACB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02486 | hp1 | a0001 | c0004 | t0009 | g0271 | AFR | ACB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02486 | hp2 | a0001 | c0006 | t0006 | g0263 | AFR | ACB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02559 | hp1 | a0001 | c0001 | t0010 | g0236 | AFR | ACB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG02559 | hp2 | a0001 | c0004 | t0006 | g0284 | AFR | ACB | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03471 | hp1 | a0002 | c0005 | t0009 | g0254 | AFR | MSL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| HG03471 | hp2 | a0001 | c0001 | t0010 | g0180 | AFR | MSL | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18955 | hp1 | a0001 | c0001 | t0005 | g0080 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA18955 | hp2 | a0001 | c0001 | t0015 | g0027 | EAS | JPT | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA20300 | hp1 | a0001 | c0006 | t0014 | g0264 | AFR | USA | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| NA20300 | hp2 | a0001 | c0002 | t0004 | g0202 | AFR | USA | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0184 | REF | REF | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0012 | g0111 | REF | REF | EFCAB11_chr14_89789669_89959730 | EFCAB11 | chr14 | 89789669 | 89959730 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:89797278 | C | G | 1 | a0004 | 2 | HG01884.hp1 HG03486.hp1 |
missense_variant | MODERATE | c.457G>C | p.Glu153Gln | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 527/3136 | 457/492 | 153/163 | chr14 | 89797278 | |||
| chr14:89953944 | T | C | 1 | a0005 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.133A>G | p.Thr45Ala | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/6 | 203/3136 | 133/492 | 45/163 | chr14 | 89953944 | |||
| chr14:89953985 | T | C | 1 | a0003 | 3 | HG01891.hp2 HG03139.hp2 HG03209.hp1 |
missense_variant | MODERATE | c.92A>G | p.Asp31Gly | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/6 | 162/3136 | 92/492 | 31/163 | chr14 | 89953985 | |||
| chr14:89954617 | G | A | 1 | a0002 | 13 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(10): Show |
missense_variant | MODERATE | c.44C>T | p.Ala15Val | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | 114/3136 | 44/492 | 15/163 | chr14 | 89954617 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:89932563 | G | A | 5 | a0001c0002 a0001c0003 a0001c0009 others(2): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
synonymous_variant | LOW | c.282C>T | p.Asn94Asn | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 4/6 | 352/3136 | 282/492 | 94/163 | chr14 | 89932563 | |||
| chr14:89953954 | C | T | 1 | a0001c0003 | 23 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(20): Show |
synonymous_variant | LOW | c.123G>A | p.Glu41Glu | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/6 | 193/3136 | 123/492 | 41/163 | chr14 | 89953954 | |||
| chr14:89954625 | C | A | 2 | a0001c0006 a0003c0008 |
7 | HG01891.hp2 HG02486.hp2 HG02630.hp2 others(4): Show |
synonymous_variant | LOW | c.36G>T | p.Thr12Thr | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | 106/3136 | 36/492 | 12/163 | chr14 | 89954625 | |||
| chr14:89954637 | G | A | 2 | a0001c0004 a0001c0009 |
16 | HG02109.hp2 HG02257.hp1 HG02258.hp2 others(13): Show |
synonymous_variant | LOW | c.24C>T | p.Ala8Ala | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | 94/3136 | 24/492 | 8/163 | chr14 | 89954637 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:89794739 | T | G | 1 | a0001c0002t0035 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2504A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 2504 | chr14 | 89794739 | ||||||
| chr14:89794916 | T | G | 15 | a0001c0001t0008 a0001c0001t0014 a0001c0001t0032 others(12): Show |
23 | HG01070.hp1 HG01192.hp1 HG02109.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2327A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 2327 | chr14 | 89794916 | ||||||
| chr14:89794921 | C | T | 15 | a0001c0001t0008 a0001c0001t0014 a0001c0001t0032 others(12): Show |
23 | HG01070.hp1 HG01192.hp1 HG02109.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2322G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 2322 | chr14 | 89794921 | ||||||
| chr14:89794968 | C | CT | 9 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0039 others(6): Show |
33 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*2274dupA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 2274 | chr14 | 89794968 | ||||||
| chr14:89794968 | CT | C | 9 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0018 others(6): Show |
23 | HG00735.hp2 HG01071.hp1 HG01074.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2274delA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 2274 | chr14 | 89794968 | ||||||
| chr14:89794968 | CTT | C | 27 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0013 others(24): Show |
104 | HG00408.hp1 HG00438.hp1 HG01070.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*2273_*2274delAA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 2273 | chr14 | 89794968 | ||||||
| chr14:89794968 | CTTT | C | 13 | a0001c0001t0003 a0001c0001t0014 a0001c0002t0003 others(10): Show |
47 | HG00621.hp1 HG00673.hp1 HG01081.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*2272_*2274delAAA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 2272 | chr14 | 89794968 | ||||||
| chr14:89794968 | CTTTT | C | 6 | a0001c0001t0008 a0001c0002t0031 a0001c0002t0041 others(3): Show |
12 | HG01192.hp1 HG01981.hp2 HG02280.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2271_*2274delAAAA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 2271 | chr14 | 89794968 | ||||||
| chr14:89795189 | G | A | 1 | a0001c0002t0031 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2054C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 2054 | chr14 | 89795189 | ||||||
| chr14:89795233 | C | T | 2 | a0001c0001t0018 a0001c0001t0033 |
3 | HG01109.hp2 HG01255.hp2 HG03239.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2010G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 2010 | chr14 | 89795233 | ||||||
| chr14:89795266 | C | CG | 37 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(34): Show |
138 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*1976_*1977insC | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 1976 | chr14 | 89795266 | ||||||
| chr14:89795279 | T | C | 75 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(72): Show |
271 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*1964A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 1964 | chr14 | 89795279 | ||||||
| chr14:89795364 | A | AT | 15 | a0001c0001t0008 a0001c0001t0014 a0001c0001t0032 others(12): Show |
23 | HG01070.hp1 HG01192.hp1 HG02109.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1878dupA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 1878 | chr14 | 89795364 | ||||||
| chr14:89795440 | C | T | 1 | a0001c0001t0013 | 4 | HG01099.hp1 HG01168.hp2 HG01358.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1803G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 1803 | chr14 | 89795440 | ||||||
| chr14:89795623 | C | T | 11 | a0001c0001t0003 a0001c0001t0015 a0001c0001t0030 others(8): Show |
47 | HG00621.hp1 HG00673.hp1 HG01081.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1620G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 1620 | chr14 | 89795623 | ||||||
| chr14:89795677 | G | A | 1 | a0001c0002t0042 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1566C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 1566 | chr14 | 89795677 | ||||||
| chr14:89795969 | T | G | 11 | a0001c0001t0003 a0001c0001t0015 a0001c0001t0030 others(8): Show |
47 | HG00621.hp1 HG00673.hp1 HG01081.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1274A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 1274 | chr14 | 89795969 | ||||||
| chr14:89795976 | C | T | 1 | a0001c0002t0031 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1267G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 1267 | chr14 | 89795976 | ||||||
| chr14:89796077 | A | G | 61 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(58): Show |
206 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*1166T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 1166 | chr14 | 89796077 | ||||||
| chr14:89796133 | C | T | 1 | a0001c0001t0030 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1110G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 1110 | chr14 | 89796133 | ||||||
| chr14:89796191 | A | G | 62 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(59): Show |
207 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(204): Show |
3_prime_UTR_variant | MODIFIER | c.*1052T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 1052 | chr14 | 89796191 | ||||||
| chr14:89796233 | C | G | 1 | a0001c0001t0039 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1010G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 1010 | chr14 | 89796233 | ||||||
| chr14:89796510 | C | T | 1 | a0001c0003t0016 | 3 | NA18959.hp1 NA19056.hp1 NA19089.hp1 |
3_prime_UTR_variant | MODIFIER | c.*733G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 733 | chr14 | 89796510 | ||||||
| chr14:89796511 | G | A | 2 | a0001c0004t0017 a0002c0007t0017 |
2 | HG02922.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*732C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 732 | chr14 | 89796511 | ||||||
| chr14:89796595 | T | C | 61 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(58): Show |
206 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*648A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 648 | chr14 | 89796595 | ||||||
| chr14:89796658 | T | C | 1 | a0001c0001t0028 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*585A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 585 | chr14 | 89796658 | ||||||
| chr14:89796726 | G | A | 2 | a0001c0002t0020 a0001c0004t0020 |
2 | HG02970.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*517C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 517 | chr14 | 89796726 | ||||||
| chr14:89796732 | T | C | 2 | a0001c0004t0017 a0002c0007t0017 |
2 | HG02922.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*511A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 511 | chr14 | 89796732 | ||||||
| chr14:89796797 | G | C | 3 | a0001c0001t0005 a0001c0001t0011 a0001c0002t0005 |
26 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*446C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 446 | chr14 | 89796797 | ||||||
| chr14:89796838 | T | C | 8 | a0001c0003t0009 a0001c0003t0037 a0001c0004t0009 others(5): Show |
10 | HG02109.hp2 HG02451.hp1 HG02486.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*405A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 405 | chr14 | 89796838 | ||||||
| chr14:89796915 | C | T | 2 | a0001c0004t0017 a0002c0007t0017 |
2 | HG02922.hp1 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*328G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 328 | chr14 | 89796915 | ||||||
| chr14:89797012 | T | C | 1 | a0001c0003t0021 | 2 | HG00323.hp2 HG01168.hp1 |
3_prime_UTR_variant | MODIFIER | c.*231A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 231 | chr14 | 89797012 | ||||||
| chr14:89797050 | T | C | 1 | a0001c0001t0038 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*193A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 193 | chr14 | 89797050 | ||||||
| chr14:89797109 | TATGTACC others(29): Show |
T | 1 | a0002c0005t0029 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*98_*133delTAAACAT others(29): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 98 | chr14 | 89797109 | ||||||
| chr14:89797156 | T | A | 17 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0039 others(14): Show |
64 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*87A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 87 | chr14 | 89797156 | ||||||
| chr14:89797181 | C | A | 61 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(58): Show |
206 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(203): Show |
3_prime_UTR_variant | MODIFIER | c.*62G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 6/6 | 62 | chr14 | 89797181 | ||||||
| chr14:89954686 | C | G | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-26G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | 26 | chr14 | 89954686 | ||||||
| chr14:89954687 | A | G | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-27T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | 27 | chr14 | 89954687 | ||||||
| chr14:89954688 | A | G | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-28T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | chr14 | 89954688 | |||||||
| chr14:89954691 | C | T | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-31G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | 31 | chr14 | 89954691 | ||||||
| chr14:89954692 | A | C | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-32T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | 32 | chr14 | 89954692 | ||||||
| chr14:89954693 | A | G | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-33T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | chr14 | 89954693 | |||||||
| chr14:89954694 | C | G | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-34G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | 34 | chr14 | 89954694 | ||||||
| chr14:89954695 | C | T | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-35G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | 35 | chr14 | 89954695 | ||||||
| chr14:89954696 | A | T | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-36T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | 36 | chr14 | 89954696 | ||||||
| chr14:89954698 | C | T | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-38G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | 38 | chr14 | 89954698 | ||||||
| chr14:89954700 | A | G | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-40T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | 40 | chr14 | 89954700 | ||||||
| chr14:89954701 | C | T | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-41G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | 41 | chr14 | 89954701 | ||||||
| chr14:89954702 | C | A | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-42G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | chr14 | 89954702 | |||||||
| chr14:89954703 | A | G | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-43T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | 43 | chr14 | 89954703 | ||||||
| chr14:89954704 | C | T | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-44G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | chr14 | 89954704 | |||||||
| chr14:89954708 | T | G | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-48A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | 48 | chr14 | 89954708 | ||||||
| chr14:89954709 | T | A | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-49A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | 49 | chr14 | 89954709 | ||||||
| chr14:89954711 | C | G | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-51G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | 51 | chr14 | 89954711 | ||||||
| chr14:89954715 | G | T | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-55C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | chr14 | 89954715 | |||||||
| chr14:89954716 | C | T | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-56G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | 56 | chr14 | 89954716 | ||||||
| chr14:89954719 | G | T | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-59C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | 59 | chr14 | 89954719 | ||||||
| chr14:89954720 | G | C | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-60C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | 60 | chr14 | 89954720 | ||||||
| chr14:89954721 | C | T | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-61G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | 61 | chr14 | 89954721 | ||||||
| chr14:89954722 | T | C | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-62A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | 62 | chr14 | 89954722 | ||||||
| chr14:89954723 | G | C | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-63C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | 63 | chr14 | 89954723 | ||||||
| chr14:89954725 | C | A | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-65G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | 65 | chr14 | 89954725 | ||||||
| chr14:89954726 | A | G | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-66T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | 66 | chr14 | 89954726 | ||||||
| chr14:89954730 | T | C | 1 | a0001c0002t0043 | 1 | NA18970.hp2 | 5_prime_UTR_variant | MODIFIER | c.-70A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/6 | 70 | chr14 | 89954730 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:89797371 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.411-47G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89797371 | |||||||
| chr14:89797464 | C | T | 1 | a0001c0001t0030g0043 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.411-140G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89797464 | |||||||
| chr14:89797577 | A | G | 5 | a0001c0001t0002g0114 a0001c0001t0039g0132 a0001c0002t0002g0229 others(2): Show |
5 | HG02109.hp1 HG02723.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.411-253T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89797577 | |||||||
| chr14:89797931 | T | G | 67 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(64): Show |
67 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.411-607A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89797931 | |||||||
| chr14:89798089 | T | A | 1 | a0001c0001t0002g0166 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.411-765A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89798089 | |||||||
| chr14:89798144 | T | C | 1 | a0001c0002t0002g0208 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.411-820A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89798144 | |||||||
| chr14:89798456 | G | A | 42 | a0001c0001t0003g0042 a0001c0001t0003g0052 a0001c0001t0003g0057 others(39): Show |
42 | HG00621.hp1 HG00673.hp1 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.411-1132C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89798456 | |||||||
| chr14:89798463 | G | A | 1 | a0001c0002t0003g0183 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.411-1139C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89798463 | |||||||
| chr14:89798533 | A | C | 1 | a0001c0001t0038g0069 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.411-1209T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89798533 | |||||||
| chr14:89798569 | C | T | 1 | a0001c0001t0005g0128 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.411-1245G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89798569 | |||||||
| chr14:89798718 | T | C | 2 | a0001c0004t0017g0281 a0002c0007t0017g0257 |
2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.411-1394A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89798718 | |||||||
| chr14:89798836 | G | C | 1 | a0001c0001t0010g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.411-1512C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89798836 | |||||||
| chr14:89798961 | A | AT | 9 | a0001c0003t0009g0022 a0001c0003t0037g0018 a0001c0004t0009g0271 others(6): Show |
9 | HG02109.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.411-1638dupA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89798961 | |||||||
| chr14:89798975 | G | C | 63 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(60): Show |
63 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.411-1651C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89798975 | |||||||
| chr14:89798975 | G | T | 1 | a0002c0005t0029g0260 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.411-1651C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89798975 | |||||||
| chr14:89798997 | G | C | 206 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(203): Show |
206 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(203): Show |
intron_variant | MODIFIER | c.411-1673C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89798997 | |||||||
| chr14:89799040 | C | T | 5 | a0001c0001t0001g0046 a0001c0002t0001g0168 a0001c0003t0025g0006 others(2): Show |
5 | HG00735.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.411-1716G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89799040 | |||||||
| chr14:89799080 | T | A | 1 | a0001c0002t0003g0213 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.411-1756A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89799080 | |||||||
| chr14:89799087 | C | T | 1 | a0002c0007t0017g0257 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.411-1763G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89799087 | |||||||
| chr14:89799256 | A | G | 2 | a0001c0001t0003g0042 a0001c0001t0015g0027 |
2 | NA18955.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.411-1932T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89799256 | |||||||
| chr14:89799304 | G | A | 1 | a0001c0006t0014g0264 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.411-1980C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89799304 | |||||||
| chr14:89799493 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.411-2169C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89799493 | |||||||
| chr14:89799571 | C | A | 27 | a0001c0001t0001g0045 a0001c0001t0001g0150 a0001c0001t0007g0231 others(24): Show |
27 | HG01070.hp1 HG01192.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.411-2247G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89799571 | |||||||
| chr14:89799680 | G | A | 54 | a0001c0001t0001g0046 a0001c0001t0001g0058 a0001c0001t0001g0060 others(51): Show |
54 | HG00438.hp1 HG00735.hp2 HG01070.hp2 others(51): Show |
intron_variant | MODIFIER | c.411-2356C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89799680 | |||||||
| chr14:89799749 | A | G | 2 | a0001c0002t0027g0172 a0003c0008t0026g0267 |
2 | HG01891.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.411-2425T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89799749 | |||||||
| chr14:89799752 | G | A | 1 | a0001c0001t0015g0099 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.411-2428C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89799752 | |||||||
| chr14:89799825 | T | G | 1 | a0001c0002t0001g0228 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.411-2501A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89799825 | |||||||
| chr14:89800006 | T | G | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-2682A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89800006 | |||||||
| chr14:89800073 | C | A | 45 | a0001c0001t0001g0096 a0001c0001t0004g0054 a0001c0001t0004g0073 others(42): Show |
45 | HG00408.hp1 HG01099.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.411-2749G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89800073 | |||||||
| chr14:89800101 | G | T | 3 | a0001c0001t0001g0144 a0001c0001t0001g0242 a0001c0003t0001g0011 |
3 | NA18942.hp2 NA18989.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.411-2777C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89800101 | |||||||
| chr14:89800132 | G | A | 1 | a0001c0002t0006g0225 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.411-2808C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89800132 | |||||||
| chr14:89800165 | G | A | 26 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0053 others(23): Show |
26 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.411-2841C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89800165 | |||||||
| chr14:89800188 | T | TAAAC | 70 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0038 others(67): Show |
70 | HG00323.hp2 HG00673.hp1 HG00735.hp1 others(67): Show |
intron_variant | MODIFIER | c.411-2868_411-2865d others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89800188 | |||||||
| chr14:89800188 | T | TAAACAAA others(1): Show |
12 | a0001c0002t0002g0243 a0001c0002t0003g0181 a0001c0002t0003g0183 others(9): Show |
12 | HG02148.hp2 HG02738.hp1 HG03710.hp2 others(9): Show |
intron_variant | MODIFIER | c.411-2872_411-2865d others(10): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89800188 | |||||||
| chr14:89800188 | TAAAC | T | 108 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(105): Show |
108 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.411-2868_411-2865d others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89800188 | |||||||
| chr14:89800188 | TAAACAAA others(1): Show |
T | 40 | a0001c0001t0001g0096 a0001c0001t0004g0054 a0001c0001t0004g0073 others(37): Show |
40 | HG00408.hp1 HG01109.hp2 HG01255.hp2 others(37): Show |
intron_variant | MODIFIER | c.411-2872_411-2865d others(10): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89800188 | |||||||
| chr14:89800228 | C | T | 2 | a0002c0005t0003g0253 a0002c0005t0003g0258 |
2 | HG01109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.411-2904G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89800228 | |||||||
| chr14:89800257 | C | G | 13 | a0001c0001t0004g0107 a0001c0001t0004g0110 a0001c0001t0004g0151 others(10): Show |
13 | HG01099.hp1 HG01109.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.411-2933G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89800257 | |||||||
| chr14:89800498 | C | T | 5 | a0001c0001t0002g0154 a0001c0003t0002g0004 a0001c0003t0016g0009 others(2): Show |
5 | HG02602.hp1 NA18959.hp1 NA19056.hp1 others(2): Show |
intron_variant | MODIFIER | c.411-3174G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89800498 | |||||||
| chr14:89800620 | G | C | 4 | a0001c0001t0002g0030 a0001c0001t0002g0038 a0001c0001t0002g0136 others(1): Show |
4 | HG01175.hp1 HG01243.hp1 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-3296C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89800620 | |||||||
| chr14:89800770 | T | C | 227 | a0001c0001t0001g0045 a0001c0001t0001g0096 a0001c0001t0001g0150 others(224): Show |
227 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(224): Show |
intron_variant | MODIFIER | c.411-3446A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89800770 | |||||||
| chr14:89800903 | C | T | 1 | a0001c0002t0031g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.411-3579G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89800903 | |||||||
| chr14:89800935 | C | T | 3 | a0001c0001t0004g0097 a0001c0004t0006g0284 a0002c0007t0004g0261 |
3 | HG01081.hp2 HG02559.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.411-3611G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89800935 | |||||||
| chr14:89801030 | A | G | 1 | a0001c0002t0031g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.411-3706T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89801030 | |||||||
| chr14:89801041 | GA | G | 16 | a0001c0001t0001g0074 a0001c0001t0001g0082 a0001c0001t0010g0180 others(13): Show |
16 | HG00621.hp2 HG02109.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.411-3718delT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89801041 | |||||||
| chr14:89801059 | A | AAAG | 6 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(3): Show |
6 | HG01884.hp2 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.411-3736_411-3735i others(5): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89801059 | |||||||
| chr14:89801059 | A | AAG | 43 | a0001c0001t0001g0096 a0001c0001t0004g0054 a0001c0001t0004g0073 others(40): Show |
43 | HG00408.hp1 HG00438.hp2 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.411-3737_411-3736d others(4): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89801059 | |||||||
| chr14:89801059 | A | AG | 92 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(89): Show |
92 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.411-3736_411-3735i others(3): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89801059 | |||||||
| chr14:89801059 | A | G | 86 | a0001c0001t0001g0045 a0001c0001t0001g0150 a0001c0001t0003g0042 others(83): Show |
86 | HG00621.hp1 HG00621.hp2 HG00673.hp1 others(83): Show |
intron_variant | MODIFIER | c.411-3735T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89801059 | |||||||
| chr14:89801177 | A | C | 1 | a0001c0001t0008g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.411-3853T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89801177 | |||||||
| chr14:89801467 | GA | G | 43 | a0001c0001t0001g0096 a0001c0001t0004g0054 a0001c0001t0004g0073 others(40): Show |
43 | HG00408.hp1 HG01099.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.411-4144delT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89801467 | |||||||
| chr14:89801487 | G | C | 10 | a0001c0001t0010g0180 a0001c0003t0009g0022 a0001c0003t0037g0018 others(7): Show |
10 | HG02109.hp2 HG02451.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.411-4163C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89801487 | |||||||
| chr14:89801508 | T | C | 1 | a0002c0005t0004g0249 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.411-4184A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89801508 | |||||||
| chr14:89801669 | A | T | 225 | a0001c0001t0001g0045 a0001c0001t0001g0096 a0001c0001t0001g0150 others(222): Show |
225 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.411-4345T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89801669 | |||||||
| chr14:89801676 | A | C | 225 | a0001c0001t0001g0045 a0001c0001t0001g0096 a0001c0001t0001g0150 others(222): Show |
225 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(222): Show |
intron_variant | MODIFIER | c.411-4352T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89801676 | |||||||
| chr14:89801723 | A | G | 157 | a0001c0001t0001g0045 a0001c0001t0001g0150 a0001c0001t0002g0029 others(154): Show |
157 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.411-4399T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89801723 | |||||||
| chr14:89801759 | C | T | 2 | a0004c0010t0004g0040 a0004c0010t0004g0041 |
2 | HG01884.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.411-4435G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89801759 | |||||||
| chr14:89801761 | C | T | 1 | a0001c0002t0004g0223 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.411-4437G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89801761 | |||||||
| chr14:89801955 | C | T | 1 | a0002c0005t0004g0249 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.411-4631G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89801955 | |||||||
| chr14:89801980 | C | T | 14 | a0001c0001t0004g0097 a0001c0001t0010g0047 a0001c0001t0010g0072 others(11): Show |
14 | HG00621.hp2 HG01081.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.411-4656G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89801980 | |||||||
| chr14:89801984 | ACT | A | 45 | a0001c0001t0001g0096 a0001c0001t0004g0054 a0001c0001t0004g0073 others(42): Show |
45 | HG00408.hp1 HG01099.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.411-4662_411-4661d others(4): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89801984 | |||||||
| chr14:89802104 | T | C | 1 | a0001c0002t0031g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.411-4780A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89802104 | |||||||
| chr14:89802207 | TA | T | 223 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0070 others(220): Show |
223 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.411-4884delT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89802207 | |||||||
| chr14:89802207 | TAA | T | 17 | a0001c0001t0001g0140 a0001c0001t0003g0059 a0001c0001t0003g0061 others(14): Show |
17 | HG02109.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.411-4885_411-4884d others(4): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89802207 | |||||||
| chr14:89802377 | A | G | 14 | a0001c0001t0004g0097 a0001c0001t0010g0047 a0001c0001t0010g0072 others(11): Show |
14 | HG00621.hp2 HG01081.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.411-5053T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89802377 | |||||||
| chr14:89802400 | A | T | 17 | a0001c0001t0003g0088 a0001c0001t0004g0097 a0001c0001t0008g0178 others(14): Show |
17 | HG00621.hp2 HG01081.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.411-5076T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89802400 | |||||||
| chr14:89802418 | G | A | 1 | a0001c0002t0002g0247 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.411-5094C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89802418 | |||||||
| chr14:89802447 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.411-5123T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89802447 | |||||||
| chr14:89802517 | G | A | 1 | a0001c0002t0031g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.411-5193C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89802517 | |||||||
| chr14:89802520 | T | C | 10 | a0001c0001t0010g0180 a0001c0003t0009g0022 a0001c0003t0037g0018 others(7): Show |
10 | HG02109.hp2 HG02451.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.411-5196A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89802520 | |||||||
| chr14:89802668 | T | C | 2 | a0001c0004t0017g0281 a0002c0007t0017g0257 |
2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.411-5344A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89802668 | |||||||
| chr14:89802688 | C | T | 1 | a0001c0002t0002g0246 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.411-5364G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89802688 | |||||||
| chr14:89802689 | G | A | 2 | a0001c0004t0017g0281 a0002c0007t0017g0257 |
2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.411-5365C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89802689 | |||||||
| chr14:89802790 | G | T | 1 | a0002c0005t0004g0249 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.411-5466C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89802790 | |||||||
| chr14:89802816 | T | G | 2 | a0001c0001t0004g0097 a0002c0007t0004g0261 |
2 | HG01081.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.411-5492A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89802816 | |||||||
| chr14:89803318 | A | G | 1 | a0001c0002t0004g0195 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.411-5994T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89803318 | |||||||
| chr14:89803400 | G | C | 1 | a0002c0005t0004g0249 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.411-6076C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89803400 | |||||||
| chr14:89803471 | G | A | 2 | a0001c0004t0017g0281 a0002c0007t0017g0257 |
2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.411-6147C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89803471 | |||||||
| chr14:89803535 | C | G | 153 | a0001c0001t0001g0045 a0001c0001t0001g0150 a0001c0001t0002g0029 others(150): Show |
153 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.411-6211G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89803535 | |||||||
| chr14:89803745 | C | T | 1 | a0001c0001t0002g0162 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.411-6421G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89803745 | |||||||
| chr14:89803759 | G | T | 11 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0086 others(8): Show |
11 | HG00140.hp1 HG00408.hp2 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.411-6435C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89803759 | |||||||
| chr14:89804027 | C | T | 9 | a0001c0001t0008g0175 a0001c0001t0008g0176 a0001c0001t0008g0177 others(6): Show |
9 | HG01070.hp1 HG01192.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.411-6703G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89804027 | |||||||
| chr14:89804074 | C | T | 224 | a0001c0001t0001g0045 a0001c0001t0001g0096 a0001c0001t0001g0150 others(221): Show |
224 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.411-6750G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89804074 | |||||||
| chr14:89804132 | C | A | 1 | a0001c0002t0001g0228 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.411-6808G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89804132 | |||||||
| chr14:89804213 | C | A | 43 | a0001c0001t0003g0042 a0001c0001t0003g0052 a0001c0001t0003g0057 others(40): Show |
43 | HG00621.hp1 HG00673.hp1 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.411-6889G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89804213 | |||||||
| chr14:89804296 | G | A | 1 | a0001c0001t0008g0178 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.411-6972C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89804296 | |||||||
| chr14:89804322 | C | T | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.411-6998G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89804322 | |||||||
| chr14:89804477 | G | T | 2 | a0001c0001t0002g0032 a0001c0001t0002g0033 |
2 | HG00140.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.411-7153C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89804477 | |||||||
| chr14:89804549 | A | G | 2 | a0001c0002t0020g0025 a0001c0004t0020g0283 |
2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.411-7225T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89804549 | |||||||
| chr14:89804558 | C | T | 1 | a0001c0001t0003g0244 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.411-7234G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89804558 | |||||||
| chr14:89804710 | C | G | 1 | a0001c0001t0010g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.411-7386G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89804710 | |||||||
| chr14:89804740 | C | T | 205 | a0001c0001t0001g0045 a0001c0001t0001g0096 a0001c0001t0001g0150 others(202): Show |
205 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.411-7416G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89804740 | |||||||
| chr14:89804869 | T | G | 1 | a0001c0002t0031g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.411-7545A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89804869 | |||||||
| chr14:89805042 | C | T | 2 | a0001c0001t0022g0064 a0001c0002t0001g0190 |
2 | HG03492.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.411-7718G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89805042 | |||||||
| chr14:89805249 | A | G | 1 | a0001c0001t0005g0121 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.411-7925T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89805249 | |||||||
| chr14:89805442 | T | C | 10 | a0001c0001t0010g0180 a0001c0003t0009g0022 a0001c0003t0037g0018 others(7): Show |
10 | HG02109.hp2 HG02451.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.411-8118A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89805442 | |||||||
| chr14:89805589 | G | T | 1 | a0001c0001t0001g0165 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.411-8265C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89805589 | |||||||
| chr14:89805608 | C | G | 62 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(59): Show |
62 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.411-8284G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89805608 | |||||||
| chr14:89805672 | C | T | 1 | a0001c0002t0001g0228 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.411-8348G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89805672 | |||||||
| chr14:89805779 | T | C | 153 | a0001c0001t0001g0045 a0001c0001t0001g0150 a0001c0001t0002g0029 others(150): Show |
153 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.411-8455A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89805779 | |||||||
| chr14:89806065 | G | A | 17 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(14): Show |
17 | HG00621.hp2 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.411-8741C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89806065 | |||||||
| chr14:89806122 | G | T | 2 | a0001c0001t0010g0236 a0001c0003t0012g0016 |
2 | HG02258.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.411-8798C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89806122 | |||||||
| chr14:89806251 | A | G | 1 | a0001c0002t0040g0118 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.411-8927T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89806251 | |||||||
| chr14:89806603 | C | T | 1 | a0001c0002t0031g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.411-9279G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89806603 | |||||||
| chr14:89806608 | C | T | 2 | a0001c0002t0020g0025 a0001c0004t0020g0283 |
2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.411-9284G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89806608 | |||||||
| chr14:89806624 | C | T | 90 | a0001c0001t0001g0045 a0001c0001t0001g0150 a0001c0001t0003g0042 others(87): Show |
90 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.411-9300G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89806624 | |||||||
| chr14:89806793 | C | G | 1 | a0001c0004t0020g0283 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.411-9469G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89806793 | |||||||
| chr14:89806807 | A | G | 1 | a0001c0004t0002g0276 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.411-9483T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89806807 | |||||||
| chr14:89806842 | G | A | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.411-9518C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89806842 | |||||||
| chr14:89806947 | G | A | 3 | a0001c0001t0001g0096 a0001c0003t0004g0019 a0001c0006t0004g0265 |
3 | HG02572.hp1 HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.411-9623C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89806947 | |||||||
| chr14:89807039 | T | C | 2 | a0001c0002t0002g0169 a0002c0005t0029g0260 |
2 | HG02897.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.411-9715A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89807039 | |||||||
| chr14:89807087 | C | T | 2 | a0002c0005t0003g0253 a0002c0005t0003g0258 |
2 | HG01109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.411-9763G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89807087 | |||||||
| chr14:89807403 | G | A | 1 | a0001c0002t0031g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.411-10079C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89807403 | |||||||
| chr14:89807591 | C | T | 10 | a0001c0001t0010g0180 a0001c0003t0009g0022 a0001c0003t0037g0018 others(7): Show |
10 | HG02109.hp2 HG02451.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.411-10267G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89807591 | |||||||
| chr14:89807703 | T | C | 2 | a0001c0002t0001g0168 a0001c0003t0025g0006 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.411-10379A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89807703 | |||||||
| chr14:89807737 | A | G | 45 | a0001c0001t0003g0042 a0001c0001t0003g0052 a0001c0001t0003g0057 others(42): Show |
45 | HG00621.hp1 HG00673.hp1 HG01081.hp1 others(42): Show |
intron_variant | MODIFIER | c.411-10413T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89807737 | |||||||
| chr14:89807818 | T | A | 2 | a0004c0010t0004g0040 a0004c0010t0004g0041 |
2 | HG01884.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.411-10494A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89807818 | |||||||
| chr14:89807881 | C | T | 10 | a0001c0001t0010g0180 a0001c0003t0009g0022 a0001c0003t0037g0018 others(7): Show |
10 | HG02109.hp2 HG02451.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.411-10557G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89807881 | |||||||
| chr14:89807921 | A | C | 1 | a0001c0004t0006g0284 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.411-10597T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89807921 | |||||||
| chr14:89807984 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.411-10660G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89807984 | |||||||
| chr14:89808004 | T | A | 5 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(2): Show |
5 | HG01884.hp2 HG02976.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.411-10680A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89808004 | |||||||
| chr14:89808212 | A | G | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | NA18954.hp2 NA18968.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.411-10888T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89808212 | |||||||
| chr14:89808297 | T | C | 27 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0053 others(24): Show |
27 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.411-10973A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89808297 | |||||||
| chr14:89808365 | G | C | 203 | a0001c0001t0001g0045 a0001c0001t0001g0096 a0001c0001t0001g0150 others(200): Show |
203 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.411-11041C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89808365 | |||||||
| chr14:89808517 | G | T | 1 | a0001c0001t0011g0130 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.411-11193C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89808517 | |||||||
| chr14:89808582 | C | T | 1 | a0001c0002t0001g0228 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.411-11258G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89808582 | |||||||
| chr14:89808927 | G | T | 1 | a0001c0004t0006g0284 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.411-11603C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89808927 | |||||||
| chr14:89809069 | G | A | 6 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(3): Show |
6 | HG01884.hp2 HG02976.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.411-11745C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89809069 | |||||||
| chr14:89809188 | T | C | 1 | a0001c0001t0001g0067 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.411-11864A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89809188 | |||||||
| chr14:89809209 | T | C | 1 | a0001c0002t0001g0228 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.411-11885A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89809209 | |||||||
| chr14:89809263 | G | A | 2 | a0001c0002t0002g0169 a0002c0005t0029g0260 |
2 | HG02897.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.411-11939C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89809263 | |||||||
| chr14:89809296 | A | T | 2 | a0001c0002t0020g0025 a0001c0004t0020g0283 |
2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.411-11972T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89809296 | |||||||
| chr14:89809378 | G | T | 1 | a0001c0001t0010g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.411-12054C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89809378 | |||||||
| chr14:89809440 | T | C | 4 | a0001c0001t0008g0175 a0001c0001t0008g0176 a0001c0001t0008g0177 others(1): Show |
4 | HG02280.hp2 HG02717.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-12116A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89809440 | |||||||
| chr14:89809496 | G | A | 2 | a0001c0003t0003g0013 a0001c0003t0003g0014 |
2 | HG03710.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.411-12172C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89809496 | |||||||
| chr14:89809701 | C | T | 1 | a0003c0008t0001g0266 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.411-12377G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89809701 | |||||||
| chr14:89809715 | T | A | 43 | a0001c0001t0003g0042 a0001c0001t0003g0052 a0001c0001t0003g0057 others(40): Show |
43 | HG00621.hp1 HG00673.hp1 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.411-12391A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89809715 | |||||||
| chr14:89809801 | G | A | 153 | a0001c0001t0001g0045 a0001c0001t0001g0150 a0001c0001t0002g0029 others(150): Show |
153 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.411-12477C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89809801 | |||||||
| chr14:89809838 | A | G | 1 | a0001c0001t0004g0110 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.411-12514T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89809838 | |||||||
| chr14:89809914 | A | G | 11 | a0001c0001t0010g0180 a0001c0002t0027g0172 a0001c0003t0009g0022 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.411-12590T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89809914 | |||||||
| chr14:89810140 | G | A | 2 | a0001c0001t0013g0028 a0001c0001t0013g0106 |
2 | HG01168.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.411-12816C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89810140 | |||||||
| chr14:89810290 | G | A | 2 | a0001c0004t0017g0281 a0002c0007t0017g0257 |
2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.411-12966C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89810290 | |||||||
| chr14:89810296 | G | C | 3 | a0001c0001t0001g0096 a0001c0003t0004g0019 a0001c0006t0004g0265 |
3 | HG02572.hp1 HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.411-12972C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89810296 | |||||||
| chr14:89810314 | G | A | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-12990C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89810314 | |||||||
| chr14:89810378 | T | C | 63 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0031 others(60): Show |
63 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.411-13054A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89810378 | |||||||
| chr14:89810506 | A | G | 193 | a0001c0001t0001g0045 a0001c0001t0001g0096 a0001c0001t0001g0150 others(190): Show |
193 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.411-13182T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89810506 | |||||||
| chr14:89810524 | G | A | 37 | a0001c0001t0001g0096 a0001c0001t0004g0054 a0001c0001t0004g0073 others(34): Show |
37 | HG00408.hp1 HG01099.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.411-13200C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89810524 | |||||||
| chr14:89810750 | C | T | 1 | a0001c0006t0014g0264 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.411-13426G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89810750 | |||||||
| chr14:89810755 | C | CA | 137 | a0001c0001t0001g0096 a0001c0001t0001g0150 a0001c0001t0002g0029 others(134): Show |
137 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.411-13432dupT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89810755 | |||||||
| chr14:89810755 | CA | C | 8 | a0001c0001t0001g0078 a0001c0001t0001g0144 a0001c0001t0004g0170 others(5): Show |
8 | HG01884.hp2 HG02976.hp1 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.411-13432delT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89810755 | |||||||
| chr14:89810756 | A | AG | 46 | a0001c0001t0003g0042 a0001c0001t0003g0052 a0001c0001t0003g0057 others(43): Show |
46 | HG00621.hp1 HG00673.hp1 HG01081.hp1 others(43): Show |
intron_variant | MODIFIER | c.411-13433_411-1343 others(5): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89810756 | |||||||
| chr14:89810811 | A | T | 3 | a0001c0001t0001g0096 a0001c0003t0004g0019 a0001c0006t0004g0265 |
3 | HG02572.hp1 HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.411-13487T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89810811 | |||||||
| chr14:89810832 | G | A | 37 | a0001c0001t0001g0096 a0001c0001t0004g0054 a0001c0001t0004g0073 others(34): Show |
37 | HG00408.hp1 HG01099.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.411-13508C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89810832 | |||||||
| chr14:89810922 | A | G | 2 | a0001c0001t0030g0043 a0005c0011t0009g0245 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.411-13598T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89810922 | |||||||
| chr14:89811320 | G | A | 1 | a0001c0002t0002g0169 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.411-13996C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89811320 | |||||||
| chr14:89811619 | G | A | 1 | a0001c0003t0021g0003 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.411-14295C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89811619 | |||||||
| chr14:89811686 | T | C | 1 | a0001c0002t0003g0194 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.411-14362A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89811686 | |||||||
| chr14:89811703 | G | C | 18 | a0001c0001t0004g0097 a0001c0001t0004g0170 a0001c0001t0004g0171 others(15): Show |
18 | HG00621.hp2 HG01081.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.411-14379C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89811703 | |||||||
| chr14:89811739 | T | C | 226 | a0001c0001t0001g0045 a0001c0001t0001g0096 a0001c0001t0001g0150 others(223): Show |
226 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.411-14415A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89811739 | |||||||
| chr14:89811778 | G | C | 2 | a0001c0001t0030g0043 a0005c0011t0009g0245 |
2 | HG02809.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.411-14454C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89811778 | |||||||
| chr14:89811783 | T | C | 1 | a0001c0003t0002g0021 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.411-14459A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89811783 | |||||||
| chr14:89812080 | T | C | 2 | a0001c0001t0010g0180 a0001c0002t0027g0172 |
2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.411-14756A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89812080 | |||||||
| chr14:89812236 | T | C | 27 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0053 others(24): Show |
27 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(24): Show |
intron_variant | MODIFIER | c.411-14912A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89812236 | |||||||
| chr14:89812559 | G | A | 11 | a0001c0001t0010g0180 a0001c0002t0027g0172 a0001c0003t0009g0022 others(8): Show |
11 | HG01891.hp1 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.411-15235C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89812559 | |||||||
| chr14:89812622 | G | A | 3 | a0001c0001t0014g0240 a0001c0006t0014g0264 a0001c0009t0014g0270 |
3 | HG02257.hp1 HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.411-15298C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89812622 | |||||||
| chr14:89812669 | G | C | 26 | a0001c0001t0005g0034 a0001c0001t0005g0035 a0001c0001t0005g0053 others(23): Show |
26 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.411-15345C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89812669 | |||||||
| chr14:89812677 | T | C | 1 | a0002c0005t0004g0249 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.411-15353A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89812677 | |||||||
| chr14:89812689 | T | C | 1 | a0001c0003t0008g0020 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.411-15365A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89812689 | |||||||
| chr14:89812751 | C | T | 2 | a0001c0001t0002g0157 a0001c0001t0002g0158 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.411-15427G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89812751 | |||||||
| chr14:89812790 | A | G | 5 | a0001c0001t0001g0096 a0001c0002t0020g0025 a0001c0003t0004g0019 others(2): Show |
5 | HG02572.hp1 HG02647.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.411-15466T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89812790 | |||||||
| chr14:89812849 | T | C | 2 | a0001c0001t0002g0109 a0001c0001t0002g0129 |
2 | HG02735.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.411-15525A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89812849 | |||||||
| chr14:89812904 | T | A | 1 | a0001c0001t0001g0098 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.411-15580A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89812904 | |||||||
| chr14:89813172 | C | T | 153 | a0001c0001t0001g0045 a0001c0001t0001g0150 a0001c0001t0002g0029 others(150): Show |
153 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.411-15848G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89813172 | |||||||
| chr14:89813300 | G | A | 1 | a0001c0001t0005g0146 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.411-15976C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89813300 | |||||||
| chr14:89813446 | A | T | 2 | a0002c0005t0003g0253 a0002c0005t0003g0258 |
2 | HG01109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.411-16122T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89813446 | |||||||
| chr14:89813548 | TCTTTCTT others(5): Show |
T | 9 | a0001c0001t0008g0175 a0001c0001t0008g0176 a0001c0001t0008g0177 others(6): Show |
9 | HG01070.hp1 HG01192.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.411-16236_411-1622 others(16): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89813548 | |||||||
| chr14:89813826 | T | G | 20 | a0001c0001t0005g0053 a0001c0001t0005g0055 a0001c0001t0005g0080 others(17): Show |
20 | HG00140.hp1 HG00438.hp2 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.411-16502A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89813826 | |||||||
| chr14:89813892 | C | T | 2 | a0001c0001t0001g0093 a0001c0001t0001g0143 |
2 | NA19004.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.411-16568G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89813892 | |||||||
| chr14:89813897 | T | C | 8 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0008g0179 others(5): Show |
8 | HG01070.hp1 HG01891.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.411-16573A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89813897 | |||||||
| chr14:89814071 | G | GA | 8 | a0001c0001t0001g0046 a0001c0001t0004g0097 a0001c0002t0001g0168 others(5): Show |
8 | HG00735.hp2 HG01081.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.411-16748dupT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89814071 | |||||||
| chr14:89814087 | CT | C | 148 | a0001c0001t0001g0060 a0001c0001t0001g0068 a0001c0001t0001g0143 others(145): Show |
148 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.411-16764delA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89814087 | |||||||
| chr14:89814137 | G | C | 1 | a0001c0002t0027g0172 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.411-16813C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89814137 | |||||||
| chr14:89814153 | G | A | 1 | a0001c0002t0020g0025 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.411-16829C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89814153 | |||||||
| chr14:89814447 | G | A | 1 | a0001c0001t0002g0071 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.411-17123C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89814447 | |||||||
| chr14:89814671 | T | C | 2 | a0001c0004t0017g0281 a0002c0007t0017g0257 |
2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.411-17347A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89814671 | |||||||
| chr14:89814682 | C | A | 42 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0033 others(39): Show |
42 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(39): Show |
intron_variant | MODIFIER | c.411-17358G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89814682 | |||||||
| chr14:89814682 | C | G | 2 | a0001c0003t0004g0019 a0001c0006t0004g0265 |
2 | HG02572.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.411-17358G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89814682 | |||||||
| chr14:89814692 | G | A | 1 | a0001c0003t0001g0017 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.411-17368C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89814692 | |||||||
| chr14:89814704 | C | CA | 14 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0150 others(11): Show |
14 | HG01070.hp1 HG01168.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.411-17381dupT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89814704 | |||||||
| chr14:89814704 | CA | C | 10 | a0001c0001t0001g0127 a0001c0003t0009g0022 a0001c0003t0037g0018 others(7): Show |
10 | HG01070.hp2 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.411-17381delT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89814704 | |||||||
| chr14:89814720 | A | C | 1 | a0001c0002t0003g0197 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.411-17396T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89814720 | |||||||
| chr14:89815060 | G | A | 1 | a0001c0002t0040g0118 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.411-17736C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89815060 | |||||||
| chr14:89815099 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0137 |
2 | HG02132.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.411-17775C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89815099 | |||||||
| chr14:89815185 | C | T | 2 | a0001c0002t0003g0191 a0001c0002t0024g0192 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.411-17861G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89815185 | |||||||
| chr14:89815190 | C | A | 1 | a0005c0011t0009g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.411-17866G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89815190 | |||||||
| chr14:89815214 | C | T | 1 | a0002c0005t0004g0249 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.411-17890G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89815214 | |||||||
| chr14:89815275 | T | C | 2 | a0001c0002t0003g0191 a0001c0002t0024g0192 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.411-17951A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89815275 | |||||||
| chr14:89815291 | C | T | 1 | a0001c0009t0001g0269 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.411-17967G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89815291 | |||||||
| chr14:89815339 | G | A | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.411-18015C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89815339 | |||||||
| chr14:89815453 | A | C | 2 | a0001c0004t0006g0284 a0003c0008t0001g0268 |
2 | HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.411-18129T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89815453 | |||||||
| chr14:89815523 | T | G | 18 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0044 others(15): Show |
18 | HG01070.hp1 HG01192.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.411-18199A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89815523 | |||||||
| chr14:89815575 | C | T | 22 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0044 others(19): Show |
22 | HG01070.hp1 HG01192.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.411-18251G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89815575 | |||||||
| chr14:89815615 | G | A | 6 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0010g0047 others(3): Show |
6 | HG01070.hp1 HG02486.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.411-18291C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89815615 | |||||||
| chr14:89815645 | C | T | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.411-18321G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89815645 | |||||||
| chr14:89815716 | G | A | 117 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(114): Show |
117 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.411-18392C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89815716 | |||||||
| chr14:89815938 | G | A | 2 | a0001c0001t0010g0047 a0001c0001t0010g0237 |
2 | HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.411-18614C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89815938 | |||||||
| chr14:89816436 | C | A | 85 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(82): Show |
85 | HG00408.hp2 HG00438.hp1 HG01070.hp1 others(82): Show |
intron_variant | MODIFIER | c.411-19112G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89816436 | |||||||
| chr14:89816855 | C | T | 2 | a0001c0001t0007g0231 a0001c0002t0031g0026 |
2 | HG02055.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.411-19531G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89816855 | |||||||
| chr14:89817063 | A | C | 1 | a0001c0002t0005g0206 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.411-19739T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89817063 | |||||||
| chr14:89817281 | CA | C | 3 | a0001c0001t0030g0043 a0001c0004t0017g0281 a0002c0007t0017g0257 |
3 | HG02922.hp1 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.411-19958delT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89817281 | |||||||
| chr14:89817527 | A | G | 1 | a0001c0001t0002g0030 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.411-20203T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89817527 | |||||||
| chr14:89817534 | T | C | 3 | a0001c0001t0010g0180 a0001c0002t0001g0228 a0001c0004t0023g0274 |
3 | HG02451.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.411-20210A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89817534 | |||||||
| chr14:89817696 | T | C | 11 | a0001c0001t0001g0067 a0001c0001t0001g0074 a0001c0001t0001g0082 others(8): Show |
11 | HG00408.hp2 HG01433.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.411-20372A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89817696 | |||||||
| chr14:89817704 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.411-20380T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89817704 | |||||||
| chr14:89817731 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.411-20407G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89817731 | |||||||
| chr14:89817796 | C | G | 24 | a0001c0001t0001g0096 a0001c0001t0001g0120 a0001c0001t0002g0156 others(21): Show |
24 | HG00323.hp1 HG00438.hp2 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.411-20472G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89817796 | |||||||
| chr14:89817879 | A | G | 143 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0068 others(140): Show |
143 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.411-20555T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89817879 | |||||||
| chr14:89817994 | AAAAT | A | 145 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0068 others(142): Show |
145 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.411-20674_411-2067 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89817994 | |||||||
| chr14:89818005 | A | G | 1 | a0001c0001t0005g0134 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.411-20681T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89818005 | |||||||
| chr14:89818019 | A | G | 121 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0068 others(118): Show |
121 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.411-20695T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89818019 | |||||||
| chr14:89818025 | A | T | 1 | a0003c0008t0001g0268 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.411-20701T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89818025 | |||||||
| chr14:89818166 | C | T | 2 | a0001c0002t0002g0169 a0003c0008t0026g0267 |
2 | HG02897.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.411-20842G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89818166 | |||||||
| chr14:89818201 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.411-20877T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89818201 | |||||||
| chr14:89818395 | A | G | 121 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0068 others(118): Show |
121 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.411-21071T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89818395 | |||||||
| chr14:89818404 | T | C | 23 | a0001c0001t0001g0096 a0001c0001t0001g0120 a0001c0001t0004g0145 others(20): Show |
23 | HG00438.hp2 HG00673.hp2 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.411-21080A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89818404 | |||||||
| chr14:89818540 | A | G | 1 | a0001c0003t0016g0024 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.411-21216T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89818540 | |||||||
| chr14:89818611 | A | G | 3 | a0001c0002t0004g0195 a0001c0002t0004g0204 a0001c0002t0019g0221 |
3 | HG00408.hp1 HG02027.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.411-21287T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89818611 | |||||||
| chr14:89818718 | G | T | 1 | a0001c0003t0021g0002 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.411-21394C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89818718 | |||||||
| chr14:89819049 | A | G | 2 | a0001c0001t0002g0044 a0001c0001t0006g0149 |
2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.411-21725T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89819049 | |||||||
| chr14:89819314 | T | C | 67 | a0001c0001t0001g0068 a0001c0001t0001g0098 a0001c0001t0001g0125 others(64): Show |
67 | HG00408.hp1 HG01109.hp2 HG01255.hp2 others(64): Show |
intron_variant | MODIFIER | c.411-21990A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89819314 | |||||||
| chr14:89819373 | G | A | 122 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0068 others(119): Show |
122 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.411-22049C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89819373 | |||||||
| chr14:89819422 | C | T | 233 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(230): Show |
233 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.411-22098G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89819422 | |||||||
| chr14:89819457 | TCAC | T | 143 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(140): Show |
143 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.411-22136_411-2213 others(7): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89819457 | |||||||
| chr14:89819579 | G | A | 8 | a0001c0001t0002g0114 a0001c0001t0039g0132 a0001c0002t0001g0168 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.411-22255C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89819579 | |||||||
| chr14:89819608 | A | AC | 11 | a0001c0001t0001g0233 a0001c0001t0002g0044 a0001c0001t0005g0034 others(8): Show |
11 | HG01192.hp1 HG02015.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.411-22285dupG | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89819608 | |||||||
| chr14:89819608 | A | C | 213 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0068 others(210): Show |
213 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(210): Show |
intron_variant | MODIFIER | c.411-22284T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89819608 | |||||||
| chr14:89819616 | C | A | 2 | a0001c0001t0001g0120 a0001c0001t0005g0121 |
2 | NA18952.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.411-22292G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89819616 | |||||||
| chr14:89819786 | G | A | 117 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0068 others(114): Show |
117 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.411-22462C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89819786 | |||||||
| chr14:89820371 | T | C | 12 | a0001c0001t0002g0044 a0001c0001t0006g0149 a0001c0001t0008g0175 others(9): Show |
12 | HG01192.hp1 HG01891.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.411-23047A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89820371 | |||||||
| chr14:89820376 | A | G | 117 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0068 others(114): Show |
117 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.411-23052T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89820376 | |||||||
| chr14:89820515 | C | T | 5 | a0001c0001t0014g0240 a0001c0002t0002g0169 a0001c0003t0004g0019 others(2): Show |
5 | HG02572.hp1 HG02723.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.411-23191G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89820515 | |||||||
| chr14:89820639 | G | A | 3 | a0001c0001t0007g0231 a0001c0002t0031g0026 a0001c0009t0014g0270 |
3 | HG02055.hp1 HG02257.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.411-23315C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89820639 | |||||||
| chr14:89820749 | GGT | G | 3 | a0001c0001t0010g0072 a0001c0001t0010g0122 a0001c0002t0010g0209 |
3 | HG03491.hp1 HG03669.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.411-23427_411-2342 others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89820749 | |||||||
| chr14:89820774 | T | C | 5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0150 others(2): Show |
5 | HG02258.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.411-23450A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89820774 | |||||||
| chr14:89820878 | T | C | 1 | a0001c0002t0031g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.411-23554A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89820878 | |||||||
| chr14:89820880 | T | TTA | 2 | a0001c0002t0003g0191 a0001c0002t0024g0192 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.411-23558_411-2355 others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89820880 | |||||||
| chr14:89820992 | T | C | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | NA18968.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.411-23668A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89820992 | |||||||
| chr14:89821198 | C | A | 2 | a0001c0002t0003g0191 a0001c0002t0024g0192 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.411-23874G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89821198 | |||||||
| chr14:89821205 | C | T | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0150 others(1): Show |
4 | HG02258.hp1 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.411-23881G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89821205 | |||||||
| chr14:89821225 | CTCAT | C | 3 | a0001c0001t0010g0236 a0001c0002t0002g0169 a0003c0008t0026g0267 |
3 | HG02559.hp1 HG02897.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.411-23905_411-2390 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89821225 | |||||||
| chr14:89821384 | A | T | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0150 others(1): Show |
4 | HG02258.hp1 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.411-24060T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89821384 | |||||||
| chr14:89821579 | T | C | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-24255A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89821579 | |||||||
| chr14:89821780 | C | T | 1 | a0003c0008t0001g0268 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.411-24456G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89821780 | |||||||
| chr14:89822149 | T | G | 1 | a0001c0001t0005g0128 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.411-24825A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89822149 | |||||||
| chr14:89822251 | A | T | 222 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(219): Show |
222 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.411-24927T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89822251 | |||||||
| chr14:89822344 | G | A | 13 | a0001c0001t0003g0075 a0001c0003t0001g0011 a0001c0003t0001g0012 others(10): Show |
13 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.411-25020C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89822344 | |||||||
| chr14:89822377 | A | C | 3 | a0001c0003t0002g0021 a0001c0003t0021g0002 a0001c0003t0021g0003 |
3 | HG00323.hp2 HG01168.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.411-25053T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89822377 | |||||||
| chr14:89822447 | C | T | 3 | a0001c0001t0022g0064 a0001c0003t0003g0013 a0001c0003t0003g0014 |
3 | HG03492.hp2 HG03710.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.411-25123G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89822447 | |||||||
| chr14:89822504 | G | A | 3 | a0001c0001t0010g0180 a0001c0002t0001g0228 a0001c0004t0023g0274 |
3 | HG02451.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.411-25180C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89822504 | |||||||
| chr14:89822627 | T | C | 157 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(154): Show |
157 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.411-25303A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89822627 | |||||||
| chr14:89822690 | G | C | 1 | a0003c0008t0001g0268 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.411-25366C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89822690 | |||||||
| chr14:89822730 | T | A | 3 | a0001c0001t0030g0043 a0001c0004t0017g0281 a0002c0007t0017g0257 |
3 | HG02922.hp1 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.411-25406A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89822730 | |||||||
| chr14:89822783 | T | C | 1 | a0005c0011t0009g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.411-25459A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89822783 | |||||||
| chr14:89822830 | G | A | 1 | a0003c0008t0001g0268 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.411-25506C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89822830 | |||||||
| chr14:89822864 | G | C | 3 | a0001c0001t0001g0120 a0001c0001t0005g0119 a0001c0001t0005g0121 |
3 | HG01496.hp2 NA18952.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.411-25540C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89822864 | |||||||
| chr14:89822931 | G | A | 5 | a0001c0001t0005g0115 a0001c0001t0005g0146 a0001c0001t0030g0043 others(2): Show |
5 | HG02922.hp1 HG02976.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.411-25607C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89822931 | |||||||
| chr14:89823228 | A | G | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0150 others(1): Show |
4 | HG02258.hp1 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.411-25904T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89823228 | |||||||
| chr14:89823235 | T | A | 1 | a0001c0004t0006g0284 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.411-25911A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89823235 | |||||||
| chr14:89823607 | G | A | 1 | a0001c0001t0014g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.411-26283C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89823607 | |||||||
| chr14:89823908 | C | T | 1 | a0001c0001t0002g0148 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.411-26584G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89823908 | |||||||
| chr14:89824108 | G | C | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0150 others(1): Show |
4 | HG02258.hp1 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.411-26784C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89824108 | |||||||
| chr14:89824116 | T | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0150 |
2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.411-26792A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89824116 | |||||||
| chr14:89824188 | C | T | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0150 others(1): Show |
4 | HG02258.hp1 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.411-26864G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89824188 | |||||||
| chr14:89824278 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.411-26954C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89824278 | |||||||
| chr14:89824332 | C | T | 1 | a0003c0008t0001g0268 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.411-27008G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89824332 | |||||||
| chr14:89824476 | G | A | 1 | a0003c0008t0026g0267 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.411-27152C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89824476 | |||||||
| chr14:89824781 | T | C | 5 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(2): Show |
5 | HG01884.hp2 HG02976.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.411-27457A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89824781 | |||||||
| chr14:89824791 | G | A | 3 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0012g0238 |
3 | HG02280.hp1 HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.411-27467C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89824791 | |||||||
| chr14:89825058 | C | T | 1 | a0001c0001t0010g0237 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.411-27734G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89825058 | |||||||
| chr14:89825102 | C | CA | 19 | a0001c0001t0001g0167 a0001c0001t0002g0030 a0001c0001t0002g0109 others(16): Show |
19 | HG00408.hp2 HG01175.hp2 HG01358.hp2 others(16): Show |
intron_variant | MODIFIER | c.411-27779dupT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89825102 | |||||||
| chr14:89825102 | CA | C | 12 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0096 others(9): Show |
12 | HG01891.hp2 HG01943.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.411-27779delT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89825102 | |||||||
| chr14:89825175 | A | C | 1 | a0003c0008t0026g0267 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.411-27851T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89825175 | |||||||
| chr14:89825330 | T | C | 1 | a0001c0003t0004g0005 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.411-28006A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89825330 | |||||||
| chr14:89825673 | T | C | 1 | a0001c0001t0001g0068 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.411-28349A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89825673 | |||||||
| chr14:89825780 | G | A | 1 | a0001c0001t0004g0151 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.411-28456C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89825780 | |||||||
| chr14:89825818 | G | A | 2 | a0001c0001t0008g0178 a0001c0001t0008g0239 |
2 | HG01192.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.411-28494C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89825818 | |||||||
| chr14:89826258 | G | T | 1 | a0001c0001t0034g0066 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.411-28934C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89826258 | |||||||
| chr14:89826320 | G | A | 2 | a0001c0002t0003g0191 a0001c0002t0024g0192 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.411-28996C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89826320 | |||||||
| chr14:89826620 | G | A | 1 | a0001c0002t0003g0065 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.411-29296C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89826620 | |||||||
| chr14:89826801 | G | T | 1 | a0001c0001t0011g0130 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.411-29477C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89826801 | |||||||
| chr14:89826807 | T | C | 1 | a0001c0001t0002g0049 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.411-29483A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89826807 | |||||||
| chr14:89827007 | T | C | 3 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0001c0001t0002g0162 |
3 | HG01515.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.411-29683A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89827007 | |||||||
| chr14:89827119 | G | T | 7 | a0001c0003t0009g0022 a0001c0004t0009g0271 a0001c0004t0009g0272 others(4): Show |
7 | HG02109.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.411-29795C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89827119 | |||||||
| chr14:89827433 | G | A | 19 | a0001c0001t0004g0097 a0001c0001t0004g0170 a0001c0001t0004g0171 others(16): Show |
19 | HG00735.hp2 HG01081.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.411-30109C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89827433 | |||||||
| chr14:89827514 | T | C | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0150 others(1): Show |
4 | HG02258.hp1 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.411-30190A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89827514 | |||||||
| chr14:89827519 | C | G | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0150 others(1): Show |
4 | HG02258.hp1 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.411-30195G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89827519 | |||||||
| chr14:89827556 | C | A | 1 | a0003c0008t0026g0267 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.411-30232G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89827556 | |||||||
| chr14:89827599 | C | T | 1 | a0001c0002t0020g0025 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.411-30275G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89827599 | |||||||
| chr14:89827628 | C | CT | 83 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(80): Show |
83 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.411-30305dupA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89827628 | |||||||
| chr14:89827628 | CT | C | 15 | a0001c0001t0001g0078 a0001c0001t0001g0140 a0001c0001t0004g0085 others(12): Show |
15 | HG02015.hp1 HG02559.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.411-30305delA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89827628 | |||||||
| chr14:89827764 | G | T | 1 | a0001c0002t0004g0205 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.411-30440C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89827764 | |||||||
| chr14:89827838 | G | A | 1 | a0001c0002t0042g0227 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.411-30514C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89827838 | |||||||
| chr14:89828107 | C | T | 2 | a0001c0002t0003g0182 a0001c0002t0003g0199 |
2 | NA18959.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.411-30783G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89828107 | |||||||
| chr14:89828134 | T | A | 2 | a0001c0001t0002g0044 a0001c0001t0006g0149 |
2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.411-30810A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89828134 | |||||||
| chr14:89828247 | GA | G | 7 | a0001c0001t0010g0236 a0001c0001t0014g0240 a0001c0002t0002g0169 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.411-30924delT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89828247 | |||||||
| chr14:89828501 | A | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0137 |
2 | HG02132.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.411-31177T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89828501 | |||||||
| chr14:89828508 | T | C | 1 | a0001c0009t0001g0269 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.411-31184A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89828508 | |||||||
| chr14:89828518 | C | T | 7 | a0001c0001t0010g0236 a0001c0001t0014g0240 a0001c0002t0002g0169 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.411-31194G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89828518 | |||||||
| chr14:89828839 | C | T | 44 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0001g0120 others(41): Show |
44 | HG00438.hp2 HG00673.hp2 HG01192.hp1 others(41): Show |
intron_variant | MODIFIER | c.411-31515G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89828839 | |||||||
| chr14:89828844 | G | A | 2 | a0001c0001t0002g0154 a0001c0001t0002g0155 |
2 | HG00735.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.411-31520C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89828844 | |||||||
| chr14:89828873 | G | C | 1 | a0003c0008t0001g0268 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.411-31549C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89828873 | |||||||
| chr14:89828874 | C | T | 1 | a0003c0008t0001g0268 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.411-31550G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89828874 | |||||||
| chr14:89829055 | T | C | 1 | a0002c0005t0004g0249 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.411-31731A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89829055 | |||||||
| chr14:89829353 | G | T | 158 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(155): Show |
158 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.411-32029C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89829353 | |||||||
| chr14:89829442 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.411-32118G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89829442 | |||||||
| chr14:89829621 | G | A | 1 | a0001c0001t0007g0079 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.411-32297C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89829621 | |||||||
| chr14:89829922 | C | T | 5 | a0001c0002t0003g0181 a0001c0002t0003g0189 a0001c0002t0003g0217 others(2): Show |
5 | NA18952.hp1 NA18970.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.411-32598G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89829922 | |||||||
| chr14:89830431 | C | T | 41 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0001g0120 others(38): Show |
41 | HG00438.hp2 HG00673.hp2 HG01192.hp1 others(38): Show |
intron_variant | MODIFIER | c.411-33107G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89830431 | |||||||
| chr14:89830469 | T | A | 1 | a0001c0001t0014g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.411-33145A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89830469 | |||||||
| chr14:89830596 | G | A | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0150 others(1): Show |
4 | HG02258.hp1 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.411-33272C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89830596 | |||||||
| chr14:89830667 | T | A | 158 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(155): Show |
158 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.411-33343A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89830667 | |||||||
| chr14:89830718 | T | C | 9 | a0001c0003t0004g0005 a0001c0003t0009g0022 a0001c0004t0009g0271 others(6): Show |
9 | HG02109.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.411-33394A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89830718 | |||||||
| chr14:89830861 | T | C | 1 | a0002c0005t0004g0249 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.411-33537A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89830861 | |||||||
| chr14:89831045 | T | G | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-33721A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89831045 | |||||||
| chr14:89831047 | A | T | 159 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(156): Show |
159 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.411-33723T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89831047 | |||||||
| chr14:89831084 | G | A | 1 | a0005c0011t0009g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.411-33760C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89831084 | |||||||
| chr14:89831225 | A | T | 159 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(156): Show |
159 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.411-33901T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89831225 | |||||||
| chr14:89831320 | A | G | 159 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(156): Show |
159 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.411-33996T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89831320 | |||||||
| chr14:89831344 | G | C | 159 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(156): Show |
159 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.411-34020C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89831344 | |||||||
| chr14:89831438 | C | T | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.411-34114G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89831438 | |||||||
| chr14:89831690 | C | T | 159 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(156): Show |
159 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.411-34366G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89831690 | |||||||
| chr14:89831779 | C | T | 52 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(49): Show |
52 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.411-34455G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89831779 | |||||||
| chr14:89831878 | C | G | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.411-34554G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89831878 | |||||||
| chr14:89831931 | C | T | 226 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(223): Show |
226 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.411-34607G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89831931 | |||||||
| chr14:89831955 | G | C | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.411-34631C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89831955 | |||||||
| chr14:89832220 | G | A | 3 | a0001c0001t0030g0043 a0001c0004t0017g0281 a0002c0007t0017g0257 |
3 | HG02922.hp1 HG02976.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.411-34896C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89832220 | |||||||
| chr14:89832370 | T | G | 51 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(48): Show |
51 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.411-35046A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89832370 | |||||||
| chr14:89832400 | T | G | 51 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(48): Show |
51 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.411-35076A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89832400 | |||||||
| chr14:89832450 | T | A | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-35126A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89832450 | |||||||
| chr14:89832554 | G | C | 1 | a0001c0003t0008g0020 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.411-35230C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89832554 | |||||||
| chr14:89832647 | C | T | 159 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(156): Show |
159 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.411-35323G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89832647 | |||||||
| chr14:89832730 | C | T | 37 | a0001c0001t0001g0068 a0001c0001t0001g0140 a0001c0001t0001g0141 others(34): Show |
37 | HG00323.hp2 HG01109.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.411-35406G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89832730 | |||||||
| chr14:89832884 | C | T | 1 | a0001c0001t0014g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.411-35560G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89832884 | |||||||
| chr14:89833028 | C | A | 1 | a0001c0006t0006g0263 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.411-35704G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89833028 | |||||||
| chr14:89833041 | A | C | 6 | a0001c0002t0020g0025 a0001c0004t0006g0284 a0001c0004t0020g0283 others(3): Show |
6 | HG02257.hp1 HG02559.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.411-35717T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89833041 | |||||||
| chr14:89833069 | C | T | 1 | a0001c0003t0004g0005 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.411-35745G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89833069 | |||||||
| chr14:89833194 | T | C | 1 | a0001c0002t0027g0172 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.411-35870A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89833194 | |||||||
| chr14:89833197 | C | T | 52 | a0001c0001t0001g0068 a0001c0001t0001g0140 a0001c0001t0001g0141 others(49): Show |
52 | HG00323.hp2 HG01109.hp2 HG01168.hp1 others(49): Show |
intron_variant | MODIFIER | c.411-35873G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89833197 | |||||||
| chr14:89833283 | G | A | 159 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(156): Show |
159 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.411-35959C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89833283 | |||||||
| chr14:89833302 | G | A | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0150 others(1): Show |
4 | HG02258.hp1 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.411-35978C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89833302 | |||||||
| chr14:89833399 | C | T | 7 | a0001c0001t0010g0236 a0001c0001t0014g0240 a0001c0002t0002g0169 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.411-36075G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89833399 | |||||||
| chr14:89833424 | C | T | 3 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0033 |
3 | HG00140.hp2 HG01099.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.411-36100G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89833424 | |||||||
| chr14:89833519 | A | C | 23 | a0001c0001t0001g0120 a0001c0001t0001g0125 a0001c0001t0003g0057 others(20): Show |
23 | HG00438.hp2 HG00673.hp2 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.411-36195T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89833519 | |||||||
| chr14:89833673 | A | G | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.411-36349T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89833673 | |||||||
| chr14:89834133 | T | TCACGAGG others(15): Show |
1 | a0001c0001t0002g0071 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.411-36831_411-3681 others(26): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834133 | |||||||
| chr14:89834137 | GAGGTCAG others(15): Show |
G | 1 | a0001c0001t0032g0235 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.411-36835_411-3681 others(26): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834137 | |||||||
| chr14:89834159 | A | G | 239 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(236): Show |
239 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.411-36835T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834159 | |||||||
| chr14:89834171 | T | C | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.411-36847A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834171 | |||||||
| chr14:89834245 | G | A | 88 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0068 others(85): Show |
88 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.411-36921C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834245 | |||||||
| chr14:89834308 | G | A | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.411-36984C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834308 | |||||||
| chr14:89834312 | G | A | 51 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(48): Show |
51 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.411-36988C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834312 | |||||||
| chr14:89834320 | G | A | 59 | a0001c0001t0001g0068 a0001c0001t0001g0127 a0001c0001t0002g0029 others(56): Show |
59 | HG00140.hp2 HG01070.hp2 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.411-36996C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834320 | |||||||
| chr14:89834331 | G | A | 5 | a0001c0002t0002g0207 a0001c0002t0002g0208 a0001c0002t0002g0220 others(2): Show |
5 | HG01074.hp1 HG01255.hp1 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.411-37007C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834331 | |||||||
| chr14:89834333 | A | G | 1 | a0001c0001t0010g0072 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.411-37009T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834333 | |||||||
| chr14:89834342 | C | T | 2 | a0001c0006t0014g0264 a0001c0009t0002g0273 |
2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.411-37018G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834342 | |||||||
| chr14:89834375 | C | CA | 35 | a0001c0001t0001g0150 a0001c0001t0002g0154 a0001c0001t0002g0155 others(32): Show |
35 | HG00323.hp2 HG00673.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.411-37052dupT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834375 | |||||||
| chr14:89834375 | C | CAA | 8 | a0001c0001t0001g0046 a0001c0001t0003g0052 a0001c0001t0010g0122 others(5): Show |
8 | HG02148.hp1 HG02486.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.411-37053_411-3705 others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834375 | |||||||
| chr14:89834375 | CA | C | 11 | a0001c0001t0005g0128 a0001c0001t0005g0146 a0001c0001t0008g0178 others(8): Show |
11 | HG00438.hp2 HG01192.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.411-37052delT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834375 | |||||||
| chr14:89834375 | CAA | C | 42 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0001g0120 others(39): Show |
42 | HG00140.hp2 HG00673.hp2 HG01099.hp2 others(39): Show |
intron_variant | MODIFIER | c.411-37053_411-3705 others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834375 | |||||||
| chr14:89834375 | CAAAAAAA others(8): Show |
C | 1 | a0001c0009t0014g0270 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.411-37066_411-3705 others(19): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834375 | |||||||
| chr14:89834398 | A | C | 35 | a0001c0001t0001g0120 a0001c0001t0001g0125 a0001c0001t0002g0031 others(32): Show |
35 | HG00140.hp2 HG00438.hp2 HG00673.hp2 others(32): Show |
intron_variant | MODIFIER | c.411-37074T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834398 | |||||||
| chr14:89834401 | A | C | 7 | a0001c0001t0001g0060 a0001c0001t0001g0096 a0001c0001t0001g0098 others(4): Show |
7 | HG02280.hp1 HG02647.hp2 NA18522.hp2 others(4): Show |
intron_variant | MODIFIER | c.411-37077T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834401 | |||||||
| chr14:89834403 | A | AAAAAC | 8 | a0001c0001t0002g0029 a0001c0001t0002g0044 a0001c0001t0002g0166 others(5): Show |
8 | HG01109.hp2 HG01261.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.411-37080_411-3707 others(9): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834403 | |||||||
| chr14:89834403 | A | AAAAC | 17 | a0001c0001t0001g0068 a0001c0001t0002g0030 a0001c0001t0002g0109 others(14): Show |
17 | HG01255.hp2 HG01433.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.411-37080_411-3707 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834403 | |||||||
| chr14:89834403 | A | AAAC | 16 | a0001c0001t0002g0038 a0001c0001t0002g0129 a0001c0001t0003g0104 others(13): Show |
16 | HG01192.hp2 HG01243.hp1 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.411-37080_411-3707 others(7): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834403 | |||||||
| chr14:89834403 | A | AAC | 54 | a0001c0001t0001g0058 a0001c0001t0001g0076 a0001c0001t0001g0078 others(51): Show |
54 | HG00621.hp1 HG00621.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.411-37080_411-3707 others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834403 | |||||||
| chr14:89834403 | A | AC | 39 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0074 others(36): Show |
39 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(36): Show |
intron_variant | MODIFIER | c.411-37080dupG | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834403 | |||||||
| chr14:89834403 | A | G | 1 | a0001c0003t0004g0005 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.411-37079T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834403 | |||||||
| chr14:89834594 | C | T | 142 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(139): Show |
142 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.411-37270G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834594 | |||||||
| chr14:89834612 | C | A | 1 | a0001c0001t0002g0129 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.411-37288G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834612 | |||||||
| chr14:89834691 | A | G | 166 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(163): Show |
166 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.411-37367T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834691 | |||||||
| chr14:89834882 | G | A | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.411-37558C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834882 | |||||||
| chr14:89834904 | G | A | 1 | a0001c0001t0014g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.411-37580C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834904 | |||||||
| chr14:89834970 | A | C | 21 | a0001c0001t0001g0068 a0001c0001t0002g0029 a0001c0001t0002g0030 others(18): Show |
21 | HG01109.hp2 HG01255.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.411-37646T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89834970 | |||||||
| chr14:89835054 | T | A | 1 | a0001c0001t0001g0125 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.411-37730A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835054 | |||||||
| chr14:89835102 | ATTTGCT | A | 4 | a0001c0002t0002g0229 a0001c0002t0002g0230 a0001c0004t0023g0274 others(1): Show |
4 | HG03225.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.411-37784_411-3777 others(10): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835102 | |||||||
| chr14:89835279 | C | G | 12 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0150 others(9): Show |
12 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.411-37955G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835279 | |||||||
| chr14:89835296 | T | C | 3 | a0001c0002t0031g0026 a0001c0004t0017g0281 a0002c0007t0017g0257 |
3 | HG02647.hp1 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.411-37972A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835296 | |||||||
| chr14:89835433 | A | G | 105 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(102): Show |
105 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.411-38109T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835433 | |||||||
| chr14:89835493 | C | T | 18 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0150 others(15): Show |
18 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.411-38169G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835493 | |||||||
| chr14:89835497 | T | C | 21 | a0001c0001t0001g0068 a0001c0001t0002g0029 a0001c0001t0002g0030 others(18): Show |
21 | HG01109.hp2 HG01255.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.411-38173A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835497 | |||||||
| chr14:89835569 | G | A | 2 | a0001c0002t0003g0191 a0001c0002t0024g0192 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.411-38245C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835569 | |||||||
| chr14:89835585 | C | CGT | 15 | a0001c0001t0001g0074 a0001c0001t0001g0144 a0001c0001t0002g0033 others(12): Show |
15 | HG00140.hp1 HG00140.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.411-38263_411-3826 others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835585 | |||||||
| chr14:89835585 | C | CGTGT | 19 | a0001c0001t0001g0060 a0001c0001t0002g0049 a0001c0001t0002g0154 others(16): Show |
19 | HG01099.hp1 HG01175.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.411-38265_411-3826 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835585 | |||||||
| chr14:89835585 | C | CGTGTGT | 11 | a0001c0001t0001g0082 a0001c0001t0002g0030 a0001c0001t0003g0059 others(8): Show |
11 | HG01884.hp2 HG01934.hp1 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.411-38267_411-3826 others(10): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835585 | |||||||
| chr14:89835585 | C | CGTGTGTG others(1): Show |
22 | a0001c0001t0001g0077 a0001c0001t0001g0127 a0001c0001t0001g0142 others(19): Show |
22 | HG00408.hp2 HG00438.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.411-38269_411-3826 others(12): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835585 | |||||||
| chr14:89835585 | C | CGTGTGTG others(3): Show |
18 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0002g0044 others(15): Show |
18 | HG00408.hp1 HG02071.hp1 HG02132.hp2 others(15): Show |
intron_variant | MODIFIER | c.411-38271_411-3826 others(14): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835585 | |||||||
| chr14:89835585 | C | CGTGTGTG others(5): Show |
8 | a0001c0001t0002g0114 a0001c0001t0002g0166 a0001c0001t0008g0176 others(5): Show |
8 | HG01943.hp1 HG02280.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.411-38273_411-3826 others(16): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835585 | |||||||
| chr14:89835585 | C | CGTGTGTG others(7): Show |
11 | a0001c0001t0002g0029 a0001c0001t0008g0177 a0001c0001t0033g0050 others(8): Show |
11 | HG00673.hp1 HG01255.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.411-38275_411-3826 others(18): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835585 | |||||||
| chr14:89835585 | C | CGTGTGTG others(9): Show |
7 | a0001c0001t0003g0101 a0001c0001t0004g0085 a0001c0001t0039g0132 others(4): Show |
7 | HG02015.hp1 HG02109.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.411-38277_411-3826 others(20): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835585 | |||||||
| chr14:89835585 | C | CGTGTGTG others(11): Show |
2 | a0001c0002t0002g0169 a0001c0002t0004g0195 |
2 | HG02897.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.411-38279_411-3826 others(22): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835585 | |||||||
| chr14:89835585 | C | CGTGTGTG others(13): Show |
2 | a0001c0001t0001g0068 a0001c0001t0018g0048 |
2 | HG01109.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.411-38281_411-3826 others(24): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835585 | |||||||
| chr14:89835585 | C | CGTGTGTG others(15): Show |
1 | a0001c0002t0004g0193 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.411-38283_411-3826 others(26): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835585 | |||||||
| chr14:89835585 | C | CGTGTGTG others(17): Show |
1 | a0001c0001t0004g0097 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.411-38285_411-3826 others(28): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835585 | |||||||
| chr14:89835585 | C | CGTGTGTG others(19): Show |
1 | a0001c0001t0028g0084 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.411-38287_411-3826 others(30): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835585 | |||||||
| chr14:89835585 | C | CGTGTGTG others(23): Show |
1 | a0002c0007t0004g0261 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.411-38291_411-3826 others(34): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835585 | |||||||
| chr14:89835585 | CGT | C | 34 | a0001c0001t0001g0139 a0001c0001t0001g0165 a0001c0001t0002g0031 others(31): Show |
34 | HG00323.hp2 HG01099.hp2 HG01168.hp1 others(31): Show |
intron_variant | MODIFIER | c.411-38263_411-3826 others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835585 | |||||||
| chr14:89835585 | CGTGT | C | 23 | a0001c0001t0001g0067 a0001c0001t0001g0078 a0001c0001t0001g0095 others(20): Show |
23 | HG00621.hp1 HG00735.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.411-38265_411-3826 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835585 | |||||||
| chr14:89835585 | CGTGTGT | C | 5 | a0001c0001t0001g0093 a0001c0001t0001g0143 a0001c0001t0011g0094 others(2): Show |
5 | HG02559.hp2 HG02622.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.411-38267_411-3826 others(10): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835585 | |||||||
| chr14:89835585 | CGTGTGTG others(1): Show |
C | 4 | a0001c0001t0001g0096 a0001c0001t0032g0235 a0001c0002t0002g0246 others(1): Show |
4 | HG01070.hp1 HG02647.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.411-38269_411-3826 others(12): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835585 | |||||||
| chr14:89835585 | CGTGTGTG others(3): Show |
C | 9 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0005g0092 others(6): Show |
9 | HG02723.hp1 HG02970.hp2 HG03130.hp1 others(6): Show |
intron_variant | MODIFIER | c.411-38271_411-3826 others(14): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835585 | |||||||
| chr14:89835585 | CGTGTGTG others(5): Show |
C | 5 | a0001c0001t0005g0053 a0001c0001t0005g0138 a0001c0001t0006g0037 others(2): Show |
5 | HG01261.hp2 HG02257.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.411-38273_411-3826 others(16): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835585 | |||||||
| chr14:89835585 | CGTGTGTG others(7): Show |
C | 30 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0120 others(27): Show |
30 | HG00438.hp2 HG00673.hp2 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.411-38275_411-3826 others(18): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835585 | |||||||
| chr14:89835585 | CGTGTGTG others(9): Show |
C | 2 | a0001c0002t0042g0227 a0001c0003t0012g0016 |
2 | HG02258.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.411-38277_411-3826 others(20): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835585 | |||||||
| chr14:89835585 | CGTGTGTG others(15): Show |
C | 1 | a0003c0008t0001g0268 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.411-38283_411-3826 others(26): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835585 | |||||||
| chr14:89835628 | G | GTGTGTGT others(5): Show |
1 | a0001c0002t0031g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.411-38305_411-3830 others(16): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835628 | |||||||
| chr14:89835640 | GTGT | G | 3 | a0001c0001t0012g0089 a0001c0001t0013g0106 a0001c0002t0006g0225 |
3 | HG00621.hp2 HG01358.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.411-38319_411-3831 others(7): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835640 | |||||||
| chr14:89835643 | T | TG | 3 | a0001c0001t0005g0035 a0001c0001t0011g0130 a0001c0003t0003g0014 |
3 | HG02056.hp2 HG04228.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.411-38320_411-3831 others(5): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835643 | |||||||
| chr14:89835643 | T | TGTGTGTG | 3 | a0001c0001t0004g0145 a0001c0002t0043g0001 a0002c0005t0003g0253 |
3 | HG01109.hp1 HG04204.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.411-38320_411-3831 others(11): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835643 | |||||||
| chr14:89835643 | T | TGTGTGTG others(2): Show |
4 | a0001c0002t0005g0187 a0001c0002t0019g0218 a0001c0003t0037g0018 others(1): Show |
4 | HG02965.hp1 HG02965.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-38320_411-3831 others(13): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835643 | |||||||
| chr14:89835643 | T | TGTGTGTG others(4): Show |
1 | a0002c0005t0002g0250 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.411-38320_411-3831 others(15): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835643 | |||||||
| chr14:89835649 | A | G | 1 | a0001c0009t0014g0270 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.411-38325T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835649 | |||||||
| chr14:89835672 | G | A | 52 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(49): Show |
52 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(49): Show |
intron_variant | MODIFIER | c.411-38348C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835672 | |||||||
| chr14:89835719 | C | T | 133 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0068 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.411-38395G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835719 | |||||||
| chr14:89835834 | G | C | 6 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(3): Show |
6 | HG01884.hp2 HG02976.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.411-38510C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835834 | |||||||
| chr14:89835907 | C | T | 19 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(16): Show |
19 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.411-38583G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89835907 | |||||||
| chr14:89836086 | T | C | 1 | a0001c0001t0007g0036 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.411-38762A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89836086 | |||||||
| chr14:89836137 | T | C | 21 | a0001c0001t0001g0068 a0001c0001t0002g0029 a0001c0001t0002g0030 others(18): Show |
21 | HG01109.hp2 HG01255.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.411-38813A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89836137 | |||||||
| chr14:89836245 | T | C | 1 | a0001c0004t0017g0281 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.411-38921A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89836245 | |||||||
| chr14:89836252 | G | C | 7 | a0001c0001t0010g0236 a0001c0001t0014g0240 a0001c0002t0002g0169 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.411-38928C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89836252 | |||||||
| chr14:89836309 | T | C | 21 | a0001c0001t0001g0068 a0001c0001t0002g0029 a0001c0001t0002g0030 others(18): Show |
21 | HG01109.hp2 HG01255.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.411-38985A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89836309 | |||||||
| chr14:89836652 | T | G | 43 | a0001c0001t0001g0120 a0001c0001t0001g0125 a0001c0001t0003g0057 others(40): Show |
43 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.411-39328A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89836652 | |||||||
| chr14:89836721 | T | C | 128 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0068 others(125): Show |
128 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.411-39397A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89836721 | |||||||
| chr14:89836769 | A | T | 133 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0068 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.411-39445T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89836769 | |||||||
| chr14:89836932 | T | C | 110 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(107): Show |
110 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.411-39608A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89836932 | |||||||
| chr14:89836958 | G | C | 1 | a0001c0003t0004g0005 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.411-39634C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89836958 | |||||||
| chr14:89837009 | G | A | 2 | a0001c0002t0003g0191 a0001c0002t0024g0192 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.411-39685C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89837009 | |||||||
| chr14:89837009 | G | T | 18 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(15): Show |
18 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.411-39685C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89837009 | |||||||
| chr14:89837038 | G | T | 6 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0234 others(3): Show |
6 | HG01070.hp1 HG03195.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.411-39714C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89837038 | |||||||
| chr14:89837039 | A | G | 133 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0068 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.411-39715T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89837039 | |||||||
| chr14:89837091 | T | A | 133 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0068 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.411-39767A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89837091 | |||||||
| chr14:89837101 | T | C | 133 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0068 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.411-39777A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89837101 | |||||||
| chr14:89837169 | T | C | 3 | a0001c0002t0031g0026 a0001c0004t0017g0281 a0002c0007t0017g0257 |
3 | HG02647.hp1 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.411-39845A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89837169 | |||||||
| chr14:89837213 | C | G | 3 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0012g0238 |
3 | HG02280.hp1 HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.411-39889G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89837213 | |||||||
| chr14:89837710 | C | T | 3 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0012g0238 |
3 | HG02280.hp1 HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.411-40386G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89837710 | |||||||
| chr14:89837739 | G | A | 105 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(102): Show |
105 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.411-40415C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89837739 | |||||||
| chr14:89837846 | C | T | 2 | a0001c0001t0003g0057 a0001c0001t0034g0066 |
2 | NA19066.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.411-40522G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89837846 | |||||||
| chr14:89837963 | A | G | 14 | a0001c0001t0001g0120 a0001c0001t0001g0125 a0001c0001t0005g0053 others(11): Show |
14 | HG00438.hp2 HG01496.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.411-40639T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89837963 | |||||||
| chr14:89838051 | T | C | 43 | a0001c0001t0001g0120 a0001c0001t0001g0125 a0001c0001t0003g0057 others(40): Show |
43 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.411-40727A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89838051 | |||||||
| chr14:89838110 | G | A | 2 | a0001c0002t0003g0191 a0001c0002t0024g0192 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.411-40786C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89838110 | |||||||
| chr14:89838227 | ACT | A | 3 | a0001c0002t0003g0212 a0001c0002t0003g0213 a0001c0002t0003g0214 |
3 | NA18973.hp1 NA18983.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.411-40905_411-4090 others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89838227 | |||||||
| chr14:89838358 | G | A | 98 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(95): Show |
98 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.411-41034C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89838358 | |||||||
| chr14:89838454 | A | C | 132 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0068 others(129): Show |
132 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.411-41130T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89838454 | |||||||
| chr14:89838525 | AAG | A | 43 | a0001c0001t0001g0120 a0001c0001t0001g0125 a0001c0001t0003g0057 others(40): Show |
43 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.411-41203_411-4120 others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89838525 | |||||||
| chr14:89838593 | A | G | 1 | a0005c0011t0009g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.411-41269T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89838593 | |||||||
| chr14:89838603 | A | G | 3 | a0001c0002t0031g0026 a0001c0004t0017g0281 a0002c0007t0017g0257 |
3 | HG02647.hp1 HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.411-41279T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89838603 | |||||||
| chr14:89838676 | C | T | 1 | a0001c0001t0010g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.411-41352G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89838676 | |||||||
| chr14:89838767 | G | C | 3 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0012g0238 |
3 | HG02280.hp1 HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.411-41443C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89838767 | |||||||
| chr14:89838789 | T | A | 1 | a0001c0006t0006g0263 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.411-41465A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89838789 | |||||||
| chr14:89838902 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.411-41578C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89838902 | |||||||
| chr14:89839135 | G | A | 1 | a0002c0005t0002g0250 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.411-41811C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89839135 | |||||||
| chr14:89839265 | C | A | 2 | a0001c0002t0003g0191 a0001c0002t0024g0192 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.411-41941G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89839265 | |||||||
| chr14:89839316 | A | G | 154 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0068 others(151): Show |
154 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.411-41992T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89839316 | |||||||
| chr14:89839536 | C | A | 1 | a0001c0001t0002g0049 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.411-42212G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89839536 | |||||||
| chr14:89839568 | A | C | 1 | a0001c0009t0014g0270 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.411-42244T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89839568 | |||||||
| chr14:89839689 | T | C | 1 | a0001c0006t0014g0264 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.411-42365A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89839689 | |||||||
| chr14:89839858 | G | A | 133 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0068 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.411-42534C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89839858 | |||||||
| chr14:89839879 | A | G | 5 | a0001c0001t0010g0236 a0001c0002t0001g0168 a0001c0002t0002g0169 others(2): Show |
5 | HG02559.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.411-42555T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89839879 | |||||||
| chr14:89839922 | C | T | 19 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(16): Show |
19 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.411-42598G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89839922 | |||||||
| chr14:89840038 | G | C | 127 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0068 others(124): Show |
127 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.411-42714C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89840038 | |||||||
| chr14:89840165 | T | A | 21 | a0001c0001t0001g0068 a0001c0001t0002g0029 a0001c0001t0002g0030 others(18): Show |
21 | HG01109.hp2 HG01255.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.411-42841A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89840165 | |||||||
| chr14:89840209 | T | C | 1 | a0005c0011t0009g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.411-42885A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89840209 | |||||||
| chr14:89840315 | A | G | 2 | a0002c0005t0004g0249 a0005c0011t0009g0245 |
2 | HG02809.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.411-42991T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89840315 | |||||||
| chr14:89840461 | C | T | 1 | a0001c0001t0005g0035 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.411-43137G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89840461 | |||||||
| chr14:89840727 | T | C | 43 | a0001c0001t0001g0120 a0001c0001t0001g0125 a0001c0001t0003g0057 others(40): Show |
43 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.411-43403A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89840727 | |||||||
| chr14:89841127 | G | A | 2 | a0001c0001t0001g0127 a0001c0001t0007g0126 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.411-43803C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89841127 | |||||||
| chr14:89841155 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.411-43831A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89841155 | |||||||
| chr14:89841448 | G | A | 1 | a0001c0001t0014g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.411-44124C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89841448 | |||||||
| chr14:89841517 | A | T | 2 | a0001c0002t0003g0191 a0001c0002t0024g0192 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.411-44193T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89841517 | |||||||
| chr14:89841852 | A | C | 6 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0234 others(3): Show |
6 | HG01070.hp1 HG03195.hp2 NA18968.hp2 others(3): Show |
intron_variant | MODIFIER | c.411-44528T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89841852 | |||||||
| chr14:89842005 | G | T | 3 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0012g0238 |
3 | HG02280.hp1 HG02647.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.411-44681C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89842005 | |||||||
| chr14:89842078 | T | C | 1 | a0001c0002t0001g0228 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.411-44754A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89842078 | |||||||
| chr14:89842439 | A | G | 143 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(140): Show |
143 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.411-45115T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89842439 | |||||||
| chr14:89842506 | C | T | 1 | a0001c0003t0004g0005 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.411-45182G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89842506 | |||||||
| chr14:89842556 | C | A | 7 | a0001c0003t0009g0022 a0001c0004t0009g0271 a0001c0004t0009g0272 others(4): Show |
7 | HG02109.hp2 HG02451.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.411-45232G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89842556 | |||||||
| chr14:89842597 | A | AATATG | 9 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0010g0236 others(6): Show |
9 | HG01109.hp1 HG02071.hp1 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.411-45278_411-4527 others(9): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89842597 | |||||||
| chr14:89842597 | A | AATATGAT others(3): Show |
1 | a0001c0001t0032g0235 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.411-45283_411-4527 others(14): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89842597 | |||||||
| chr14:89842597 | AATATG | A | 94 | a0001c0001t0001g0045 a0001c0001t0001g0058 a0001c0001t0001g0067 others(91): Show |
94 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.411-45278_411-4527 others(9): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89842597 | |||||||
| chr14:89842597 | AATATGAT others(3): Show |
A | 82 | a0001c0001t0001g0046 a0001c0001t0001g0068 a0001c0001t0001g0120 others(79): Show |
82 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.411-45283_411-4527 others(14): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89842597 | |||||||
| chr14:89842597 | AATATGAT others(8): Show |
A | 3 | a0001c0001t0002g0044 a0001c0001t0006g0149 a0001c0003t0004g0005 |
3 | HG02572.hp2 HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.411-45288_411-4527 others(19): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89842597 | |||||||
| chr14:89842623 | A | G | 1 | a0001c0002t0003g0194 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.411-45299T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89842623 | |||||||
| chr14:89842632 | G | A | 4 | a0001c0001t0005g0124 a0001c0002t0031g0026 a0001c0004t0017g0281 others(1): Show |
4 | HG02647.hp1 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.411-45308C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89842632 | |||||||
| chr14:89842637 | G | A | 169 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(166): Show |
169 | HG00140.hp2 HG00408.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.411-45313C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89842637 | |||||||
| chr14:89842637 | G | GATATA | 14 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0005g0086 others(11): Show |
14 | HG00140.hp1 HG00323.hp2 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.411-45318_411-4531 others(9): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89842637 | |||||||
| chr14:89842637 | G | GATATGAT others(3): Show |
4 | a0001c0001t0001g0096 a0001c0001t0012g0238 a0001c0003t0004g0019 others(1): Show |
4 | HG02572.hp1 HG02647.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-45314_411-4531 others(14): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89842637 | |||||||
| chr14:89842637 | G | GATATGAT others(8): Show |
1 | a0001c0009t0014g0270 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.411-45314_411-4531 others(19): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89842637 | |||||||
| chr14:89842637 | G | GATATGAT others(13): Show |
1 | a0001c0001t0001g0098 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.411-45314_411-4531 others(24): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89842637 | |||||||
| chr14:89842807 | T | C | 15 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0150 others(12): Show |
15 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.411-45483A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89842807 | |||||||
| chr14:89842913 | A | G | 1 | a0001c0001t0010g0237 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.411-45589T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89842913 | |||||||
| chr14:89842929 | C | T | 7 | a0001c0001t0010g0236 a0001c0001t0014g0240 a0001c0002t0002g0169 others(4): Show |
7 | HG02559.hp1 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.411-45605G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89842929 | |||||||
| chr14:89842939 | C | T | 138 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(135): Show |
138 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.411-45615G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89842939 | |||||||
| chr14:89842961 | A | G | 14 | a0001c0001t0003g0075 a0001c0001t0003g0088 a0001c0001t0004g0145 others(11): Show |
14 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.411-45637T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89842961 | |||||||
| chr14:89843131 | T | C | 70 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0001g0120 others(67): Show |
70 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.411-45807A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89843131 | |||||||
| chr14:89843148 | C | T | 1 | a0001c0004t0017g0281 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.411-45824G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89843148 | |||||||
| chr14:89843214 | C | A | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.411-45890G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89843214 | |||||||
| chr14:89843364 | AAAGT | A | 102 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(99): Show |
102 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.411-46044_411-4604 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89843364 | |||||||
| chr14:89843448 | C | T | 2 | a0001c0001t0002g0049 a0001c0001t0002g0071 |
2 | HG01515.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.411-46124G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89843448 | |||||||
| chr14:89843689 | T | G | 3 | a0001c0003t0004g0019 a0001c0003t0037g0018 a0001c0006t0004g0265 |
3 | HG02572.hp1 HG02965.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.411-46365A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89843689 | |||||||
| chr14:89843782 | C | T | 114 | a0001c0001t0001g0045 a0001c0001t0001g0058 a0001c0001t0001g0067 others(111): Show |
114 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.411-46458G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89843782 | |||||||
| chr14:89843815 | C | T | 4 | a0001c0001t0014g0240 a0001c0003t0004g0019 a0001c0003t0037g0018 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-46491G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89843815 | |||||||
| chr14:89843936 | G | A | 4 | a0001c0001t0001g0060 a0001c0001t0003g0059 a0001c0001t0003g0061 others(1): Show |
4 | NA18986.hp2 NA18989.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.411-46612C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89843936 | |||||||
| chr14:89844242 | A | T | 1 | a0001c0001t0005g0113 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.411-46918T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89844242 | |||||||
| chr14:89844357 | T | G | 1 | a0001c0001t0010g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.411-47033A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89844357 | |||||||
| chr14:89844551 | C | T | 1 | a0003c0008t0001g0266 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.411-47227G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89844551 | |||||||
| chr14:89844606 | T | C | 1 | a0001c0002t0002g0246 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.411-47282A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89844606 | |||||||
| chr14:89844739 | C | T | 104 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(101): Show |
104 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.411-47415G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89844739 | |||||||
| chr14:89844930 | C | A | 120 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(117): Show |
120 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.411-47606G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89844930 | |||||||
| chr14:89844935 | T | C | 180 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(177): Show |
180 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(177): Show |
intron_variant | MODIFIER | c.411-47611A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89844935 | |||||||
| chr14:89844971 | C | T | 6 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0012g0238 others(3): Show |
6 | HG02280.hp1 HG02602.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.411-47647G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89844971 | |||||||
| chr14:89845162 | T | C | 1 | a0001c0001t0005g0134 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.411-47838A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89845162 | |||||||
| chr14:89845278 | C | T | 1 | a0001c0001t0013g0108 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.411-47954G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89845278 | |||||||
| chr14:89845628 | C | T | 5 | a0001c0002t0020g0025 a0001c0004t0006g0284 a0001c0004t0020g0283 others(2): Show |
5 | HG02257.hp1 HG02559.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.411-48304G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89845628 | |||||||
| chr14:89845671 | G | A | 95 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(92): Show |
95 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.411-48347C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89845671 | |||||||
| chr14:89845718 | T | C | 1 | a0001c0001t0002g0109 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.411-48394A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89845718 | |||||||
| chr14:89845784 | T | A | 120 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(117): Show |
120 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.411-48460A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89845784 | |||||||
| chr14:89845917 | G | T | 104 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(101): Show |
104 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.411-48593C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89845917 | |||||||
| chr14:89845954 | G | A | 6 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0012g0238 others(3): Show |
6 | HG02280.hp1 HG02602.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.411-48630C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89845954 | |||||||
| chr14:89845956 | A | T | 1 | a0001c0001t0002g0166 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.411-48632T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89845956 | |||||||
| chr14:89845984 | G | T | 2 | a0001c0001t0018g0048 a0001c0001t0033g0050 |
2 | HG01109.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.411-48660C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89845984 | |||||||
| chr14:89846133 | T | A | 5 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0148 others(2): Show |
5 | HG01261.hp1 HG01934.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.411-48809A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89846133 | |||||||
| chr14:89846137 | G | A | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-48813C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89846137 | |||||||
| chr14:89846320 | A | G | 1 | a0002c0005t0002g0250 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.411-48996T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89846320 | |||||||
| chr14:89846335 | A | G | 2 | a0001c0002t0003g0191 a0001c0002t0024g0192 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.411-49011T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89846335 | |||||||
| chr14:89846380 | G | T | 1 | a0001c0001t0018g0048 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.411-49056C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89846380 | |||||||
| chr14:89846618 | C | T | 2 | a0001c0002t0031g0026 a0001c0004t0017g0281 |
2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.411-49294G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89846618 | |||||||
| chr14:89846628 | T | C | 105 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(102): Show |
105 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.411-49304A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89846628 | |||||||
| chr14:89846758 | C | T | 1 | a0003c0008t0001g0268 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.411-49434G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89846758 | |||||||
| chr14:89846829 | C | A | 120 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(117): Show |
120 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.411-49505G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89846829 | |||||||
| chr14:89846870 | A | G | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-49546T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89846870 | |||||||
| chr14:89847122 | T | C | 39 | a0001c0001t0001g0127 a0001c0001t0002g0031 a0001c0001t0002g0032 others(36): Show |
39 | HG00140.hp2 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.411-49798A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89847122 | |||||||
| chr14:89847165 | A | G | 15 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0150 others(12): Show |
15 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.411-49841T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89847165 | |||||||
| chr14:89847430 | T | C | 1 | a0005c0011t0009g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.411-50106A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89847430 | |||||||
| chr14:89847460 | C | T | 106 | a0001c0001t0001g0060 a0001c0001t0001g0096 a0001c0001t0001g0098 others(103): Show |
106 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.411-50136G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89847460 | |||||||
| chr14:89847654 | G | A | 120 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(117): Show |
120 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.411-50330C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89847654 | |||||||
| chr14:89847675 | G | T | 1 | a0001c0009t0001g0269 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.411-50351C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89847675 | |||||||
| chr14:89847681 | G | A | 45 | a0001c0001t0001g0120 a0001c0001t0001g0125 a0001c0001t0003g0057 others(42): Show |
45 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.411-50357C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89847681 | |||||||
| chr14:89847741 | C | CA | 13 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(10): Show |
13 | HG00735.hp1 HG01070.hp1 HG03195.hp2 others(10): Show |
intron_variant | MODIFIER | c.411-50418dupT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89847741 | |||||||
| chr14:89847741 | CA | C | 55 | a0001c0001t0001g0060 a0001c0001t0001g0096 a0001c0001t0001g0098 others(52): Show |
55 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.411-50418delT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89847741 | |||||||
| chr14:89847741 | CAAAAAAA | C | 6 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0023 others(3): Show |
6 | NA18959.hp1 NA18973.hp2 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.411-50424_411-5041 others(11): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89847741 | |||||||
| chr14:89847756 | A | G | 7 | a0001c0001t0014g0240 a0001c0002t0002g0169 a0001c0002t0027g0172 others(4): Show |
7 | HG01891.hp1 HG02572.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.411-50432T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89847756 | |||||||
| chr14:89847757 | AAAG | A | 77 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(74): Show |
77 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(74): Show |
intron_variant | MODIFIER | c.411-50436_411-5043 others(7): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89847757 | |||||||
| chr14:89847758 | AAG | A | 36 | a0001c0001t0001g0127 a0001c0001t0002g0031 a0001c0001t0002g0032 others(33): Show |
36 | HG00140.hp2 HG01070.hp2 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.411-50436_411-5043 others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89847758 | |||||||
| chr14:89847759 | AG | A | 6 | a0001c0001t0002g0038 a0001c0001t0002g0136 a0001c0001t0004g0110 others(3): Show |
6 | HG01175.hp1 HG01243.hp1 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.411-50436delC | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89847759 | |||||||
| chr14:89847912 | A | C | 18 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(15): Show |
18 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.411-50588T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89847912 | |||||||
| chr14:89848035 | C | T | 2 | a0001c0002t0003g0191 a0001c0002t0024g0192 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.411-50711G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89848035 | |||||||
| chr14:89848371 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.411-51047A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89848371 | |||||||
| chr14:89848512 | G | A | 1 | a0001c0001t0010g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.411-51188C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89848512 | |||||||
| chr14:89848636 | T | C | 1 | a0001c0004t0020g0283 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.411-51312A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89848636 | |||||||
| chr14:89848709 | T | C | 2 | a0001c0001t0001g0120 a0001c0001t0005g0121 |
2 | NA18952.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.411-51385A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89848709 | |||||||
| chr14:89848788 | G | A | 10 | a0001c0001t0002g0039 a0001c0001t0002g0109 a0001c0001t0004g0107 others(7): Show |
10 | HG01099.hp1 HG01168.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.411-51464C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89848788 | |||||||
| chr14:89848816 | A | T | 91 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(88): Show |
91 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.411-51492T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89848816 | |||||||
| chr14:89848830 | T | G | 120 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(117): Show |
120 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.411-51506A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89848830 | |||||||
| chr14:89848849 | C | T | 104 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(101): Show |
104 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.411-51525G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89848849 | |||||||
| chr14:89848972 | A | C | 1 | a0001c0001t0008g0175 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.411-51648T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89848972 | |||||||
| chr14:89848984 | G | A | 119 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(116): Show |
119 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.411-51660C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89848984 | |||||||
| chr14:89849043 | C | A | 6 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0012g0238 others(3): Show |
6 | HG02280.hp1 HG02602.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.411-51719G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89849043 | |||||||
| chr14:89849044 | TA | T | 6 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0012g0238 others(3): Show |
6 | HG02280.hp1 HG02602.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.411-51721delT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89849044 | |||||||
| chr14:89849049 | A | T | 6 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0012g0238 others(3): Show |
6 | HG02280.hp1 HG02602.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.411-51725T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89849049 | |||||||
| chr14:89849164 | T | C | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-51840A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89849164 | |||||||
| chr14:89849384 | A | G | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-52060T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89849384 | |||||||
| chr14:89849449 | AG | A | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-52126delC | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89849449 | |||||||
| chr14:89849535 | T | C | 1 | a0002c0005t0004g0249 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.411-52211A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89849535 | |||||||
| chr14:89849572 | A | G | 1 | a0001c0002t0004g0185 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.411-52248T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89849572 | |||||||
| chr14:89849583 | T | C | 4 | a0001c0004t0009g0271 a0001c0004t0009g0272 a0001c0004t0009g0275 others(1): Show |
4 | HG02486.hp1 HG03225.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-52259A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89849583 | |||||||
| chr14:89849606 | G | GT | 69 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0098 others(66): Show |
69 | HG00323.hp2 HG00438.hp2 HG00673.hp1 others(66): Show |
intron_variant | MODIFIER | c.411-52283dupA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89849606 | |||||||
| chr14:89849606 | G | GTT | 87 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(84): Show |
87 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.411-52284_411-5228 others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89849606 | |||||||
| chr14:89849606 | G | GTTT | 14 | a0001c0001t0002g0081 a0001c0001t0005g0035 a0001c0001t0007g0126 others(11): Show |
14 | HG01071.hp1 HG01071.hp2 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.411-52285_411-5228 others(7): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89849606 | |||||||
| chr14:89849610 | T | G | 1 | a0001c0001t0014g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.411-52286A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89849610 | |||||||
| chr14:89849684 | G | T | 1 | a0005c0011t0009g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.411-52360C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89849684 | |||||||
| chr14:89849897 | C | T | 104 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(101): Show |
104 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.411-52573G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89849897 | |||||||
| chr14:89849945 | T | G | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-52621A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89849945 | |||||||
| chr14:89850053 | T | G | 20 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(17): Show |
20 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.411-52729A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89850053 | |||||||
| chr14:89850229 | C | G | 8 | a0001c0001t0008g0175 a0001c0001t0008g0176 a0001c0001t0008g0177 others(5): Show |
8 | HG01192.hp1 HG02280.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.411-52905G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89850229 | |||||||
| chr14:89850270 | T | C | 2 | a0001c0002t0003g0191 a0001c0002t0024g0192 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.411-52946A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89850270 | |||||||
| chr14:89850345 | G | A | 1 | a0001c0009t0014g0270 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.411-53021C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89850345 | |||||||
| chr14:89850479 | G | T | 3 | a0001c0001t0004g0054 a0001c0001t0004g0073 a0001c0001t0015g0103 |
3 | HG01928.hp2 NA18949.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.411-53155C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89850479 | |||||||
| chr14:89850670 | A | G | 15 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0150 others(12): Show |
15 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.411-53346T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89850670 | |||||||
| chr14:89850689 | G | A | 120 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(117): Show |
120 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.411-53365C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89850689 | |||||||
| chr14:89850734 | C | T | 100 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(97): Show |
100 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.411-53410G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89850734 | |||||||
| chr14:89850942 | T | G | 1 | a0001c0001t0011g0130 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.411-53618A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89850942 | |||||||
| chr14:89851447 | A | G | 15 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0150 others(12): Show |
15 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.411-54123T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89851447 | |||||||
| chr14:89851669 | A | C | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-54345T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89851669 | |||||||
| chr14:89851898 | T | C | 1 | a0001c0003t0004g0005 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.411-54574A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89851898 | |||||||
| chr14:89851959 | C | T | 4 | a0001c0001t0014g0240 a0001c0003t0004g0019 a0001c0003t0037g0018 others(1): Show |
4 | HG02572.hp1 HG02723.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-54635G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89851959 | |||||||
| chr14:89852184 | A | G | 14 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0150 others(11): Show |
14 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.411-54860T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89852184 | |||||||
| chr14:89852186 | T | C | 39 | a0001c0001t0001g0127 a0001c0001t0002g0031 a0001c0001t0002g0032 others(36): Show |
39 | HG00140.hp2 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.411-54862A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89852186 | |||||||
| chr14:89852301 | C | T | 1 | a0001c0001t0008g0176 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.411-54977G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89852301 | |||||||
| chr14:89852430 | C | T | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-55106G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89852430 | |||||||
| chr14:89852560 | C | T | 107 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(104): Show |
107 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.411-55236G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89852560 | |||||||
| chr14:89852632 | A | G | 1 | a0001c0006t0014g0264 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.411-55308T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89852632 | |||||||
| chr14:89852837 | C | T | 1 | a0001c0002t0042g0227 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.411-55513G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89852837 | |||||||
| chr14:89853073 | A | G | 1 | a0001c0001t0010g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.411-55749T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89853073 | |||||||
| chr14:89853317 | T | C | 2 | a0001c0002t0003g0191 a0001c0002t0024g0192 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.411-55993A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89853317 | |||||||
| chr14:89853432 | T | C | 1 | a0001c0001t0004g0107 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.411-56108A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89853432 | |||||||
| chr14:89853618 | G | A | 2 | a0001c0002t0031g0026 a0001c0004t0017g0281 |
2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.411-56294C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89853618 | |||||||
| chr14:89853625 | A | G | 108 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(105): Show |
108 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.411-56301T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89853625 | |||||||
| chr14:89853639 | A | G | 1 | a0001c0002t0027g0172 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.411-56315T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89853639 | |||||||
| chr14:89854196 | C | CA | 6 | a0001c0001t0001g0077 a0001c0001t0004g0085 a0001c0003t0004g0005 others(3): Show |
6 | HG00438.hp1 HG01891.hp2 HG02015.hp1 others(3): Show |
intron_variant | MODIFIER | c.411-56873dupT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89854196 | |||||||
| chr14:89854196 | CA | C | 16 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0150 others(13): Show |
16 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.411-56873delT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89854196 | |||||||
| chr14:89854211 | T | A | 18 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(15): Show |
18 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.411-56887A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89854211 | |||||||
| chr14:89854219 | C | G | 1 | a0001c0001t0004g0152 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.411-56895G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89854219 | |||||||
| chr14:89854237 | AT | A | 145 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(142): Show |
145 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.411-56914delA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89854237 | |||||||
| chr14:89854263 | T | G | 18 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(15): Show |
18 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.411-56939A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89854263 | |||||||
| chr14:89854302 | A | G | 230 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(227): Show |
230 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(227): Show |
intron_variant | MODIFIER | c.411-56978T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89854302 | |||||||
| chr14:89854316 | T | C | 19 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(16): Show |
19 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.411-56992A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89854316 | |||||||
| chr14:89854328 | G | A | 1 | a0005c0011t0009g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.411-57004C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89854328 | |||||||
| chr14:89854330 | T | G | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.411-57006A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89854330 | |||||||
| chr14:89854474 | A | G | 4 | a0001c0002t0002g0229 a0001c0002t0002g0230 a0001c0004t0023g0274 others(1): Show |
4 | HG03225.hp2 HG03453.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.411-57150T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89854474 | |||||||
| chr14:89854509 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.411-57185C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89854509 | |||||||
| chr14:89854654 | G | A | 113 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(110): Show |
113 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.411-57330C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89854654 | |||||||
| chr14:89854755 | A | C | 19 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(16): Show |
19 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.411-57431T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89854755 | |||||||
| chr14:89854799 | G | A | 1 | a0003c0008t0001g0268 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.411-57475C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89854799 | |||||||
| chr14:89854832 | A | G | 113 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(110): Show |
113 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.411-57508T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89854832 | |||||||
| chr14:89854987 | A | G | 19 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(16): Show |
19 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.411-57663T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89854987 | |||||||
| chr14:89854997 | G | C | 19 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(16): Show |
19 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.411-57673C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89854997 | |||||||
| chr14:89855077 | T | C | 133 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(130): Show |
133 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.411-57753A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89855077 | |||||||
| chr14:89855166 | GCTT | G | 5 | a0001c0002t0020g0025 a0001c0004t0006g0284 a0001c0004t0020g0283 others(2): Show |
5 | HG02257.hp1 HG02559.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.411-57845_411-5784 others(7): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89855166 | |||||||
| chr14:89855173 | T | C | 1 | a0001c0002t0002g0246 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.411-57849A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89855173 | |||||||
| chr14:89855312 | C | T | 5 | a0001c0002t0003g0182 a0001c0002t0003g0199 a0001c0002t0004g0185 others(2): Show |
5 | HG02004.hp1 NA18959.hp2 NA18991.hp1 others(2): Show |
intron_variant | MODIFIER | c.411-57988G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89855312 | |||||||
| chr14:89855325 | A | G | 113 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(110): Show |
113 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.411-58001T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89855325 | |||||||
| chr14:89855420 | G | A | 113 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(110): Show |
113 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.411-58096C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89855420 | |||||||
| chr14:89855431 | G | C | 1 | a0003c0008t0001g0268 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.411-58107C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89855431 | |||||||
| chr14:89855474 | T | G | 19 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(16): Show |
19 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.411-58150A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89855474 | |||||||
| chr14:89855545 | G | A | 1 | a0001c0001t0008g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.411-58221C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89855545 | |||||||
| chr14:89855587 | CAACT | C | 64 | a0001c0001t0001g0068 a0001c0001t0001g0120 a0001c0001t0001g0125 others(61): Show |
64 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.411-58267_411-5826 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89855587 | |||||||
| chr14:89855611 | A | AT | 15 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0150 others(12): Show |
15 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.411-58288dupA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89855611 | |||||||
| chr14:89855750 | T | C | 19 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(16): Show |
19 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.411-58426A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89855750 | |||||||
| chr14:89856178 | TTCTC | T | 17 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(14): Show |
17 | HG00323.hp2 HG01168.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.411-58858_411-5885 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89856178 | |||||||
| chr14:89856184 | CTCTCTCT others(3): Show |
C | 18 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0150 others(15): Show |
18 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.411-58870_411-5886 others(14): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89856184 | |||||||
| chr14:89856192 | C | CT | 100 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(97): Show |
100 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.411-58869dupA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89856192 | |||||||
| chr14:89856192 | C | CTT | 6 | a0001c0001t0001g0093 a0001c0001t0001g0127 a0001c0001t0004g0170 others(3): Show |
6 | HG01070.hp2 HG01884.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.411-58870_411-5886 others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89856192 | |||||||
| chr14:89856192 | CT | C | 7 | a0001c0002t0019g0218 a0001c0002t0020g0025 a0001c0004t0006g0284 others(4): Show |
7 | HG01891.hp2 HG02257.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.411-58869delA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89856192 | |||||||
| chr14:89856205 | T | C | 1 | a0001c0001t0030g0043 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.411-58881A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89856205 | |||||||
| chr14:89856294 | T | C | 112 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(109): Show |
112 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.411-58970A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89856294 | |||||||
| chr14:89856393 | T | A | 1 | a0001c0001t0005g0053 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.411-59069A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89856393 | |||||||
| chr14:89856410 | G | C | 1 | a0001c0004t0017g0281 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.411-59086C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89856410 | |||||||
| chr14:89856478 | C | T | 1 | a0002c0005t0004g0249 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.411-59154G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89856478 | |||||||
| chr14:89856589 | A | G | 1 | a0001c0003t0004g0019 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.411-59265T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89856589 | |||||||
| chr14:89856645 | A | T | 4 | a0001c0001t0001g0060 a0001c0001t0003g0059 a0001c0001t0003g0061 others(1): Show |
4 | NA18986.hp2 NA18989.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.411-59321T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89856645 | |||||||
| chr14:89856714 | T | C | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-59390A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89856714 | |||||||
| chr14:89857038 | C | G | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0150 others(1): Show |
4 | HG02258.hp1 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.411-59714G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89857038 | |||||||
| chr14:89857051 | G | C | 159 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(156): Show |
159 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.411-59727C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89857051 | |||||||
| chr14:89857357 | C | T | 1 | a0001c0003t0004g0005 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.411-60033G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89857357 | |||||||
| chr14:89857511 | C | CT | 164 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(161): Show |
164 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(161): Show |
intron_variant | MODIFIER | c.411-60188dupA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89857511 | |||||||
| chr14:89857799 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0137 |
2 | HG02132.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.411-60475C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89857799 | |||||||
| chr14:89857991 | GACCCTGG others(16): Show |
G | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.411-60690_411-6066 others(27): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89857991 | |||||||
| chr14:89858031 | T | C | 1 | a0001c0001t0008g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.411-60707A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89858031 | |||||||
| chr14:89858139 | C | T | 102 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(99): Show |
102 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.411-60815G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89858139 | |||||||
| chr14:89858336 | C | T | 5 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0007g0231 others(2): Show |
5 | HG02055.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.411-61012G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89858336 | |||||||
| chr14:89858355 | C | T | 5 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.411-61031G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89858355 | |||||||
| chr14:89858512 | C | A | 5 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.411-61188G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89858512 | |||||||
| chr14:89858529 | G | A | 5 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0234 others(2): Show |
5 | HG01070.hp1 HG03195.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.411-61205C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89858529 | |||||||
| chr14:89858599 | C | A | 5 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.411-61275G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89858599 | |||||||
| chr14:89858656 | A | AT | 122 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(119): Show |
122 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.411-61333dupA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89858656 | |||||||
| chr14:89858656 | A | ATT | 20 | a0001c0001t0002g0109 a0001c0001t0002g0136 a0001c0001t0002g0157 others(17): Show |
20 | HG01175.hp1 HG01175.hp2 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.411-61334_411-6133 others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89858656 | |||||||
| chr14:89858834 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.411-61510T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89858834 | |||||||
| chr14:89858903 | G | A | 5 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.411-61579C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89858903 | |||||||
| chr14:89859083 | C | T | 1 | a0003c0008t0026g0267 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.411-61759G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89859083 | |||||||
| chr14:89859191 | T | C | 5 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.411-61867A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89859191 | |||||||
| chr14:89859213 | C | T | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.411-61889G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89859213 | |||||||
| chr14:89859680 | T | C | 5 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.411-62356A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89859680 | |||||||
| chr14:89859681 | G | A | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-62357C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89859681 | |||||||
| chr14:89859824 | T | G | 2 | a0001c0002t0003g0191 a0001c0002t0024g0192 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.411-62500A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89859824 | |||||||
| chr14:89860065 | C | T | 3 | a0001c0002t0002g0169 a0001c0002t0027g0172 a0003c0008t0026g0267 |
3 | HG01891.hp1 HG02897.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.411-62741G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89860065 | |||||||
| chr14:89860104 | C | T | 1 | a0001c0001t0038g0069 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.411-62780G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89860104 | |||||||
| chr14:89860343 | G | A | 13 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0012g0238 others(10): Show |
13 | HG01891.hp1 HG02280.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.411-63019C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89860343 | |||||||
| chr14:89860366 | A | AAAAC | 8 | a0001c0001t0002g0136 a0001c0001t0006g0063 a0001c0001t0010g0072 others(5): Show |
8 | HG01175.hp1 HG01243.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.411-63046_411-6304 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89860366 | |||||||
| chr14:89860366 | A | AAAACAAA others(9): Show |
5 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.411-63058_411-6304 others(20): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89860366 | |||||||
| chr14:89860366 | AAAAC | A | 7 | a0001c0002t0002g0169 a0001c0002t0027g0172 a0001c0003t0004g0019 others(4): Show |
7 | HG01891.hp1 HG02572.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.411-63046_411-6304 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89860366 | |||||||
| chr14:89860374 | C | CAAAA | 14 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0150 others(11): Show |
14 | HG02109.hp2 HG02258.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.411-63051_411-6305 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89860374 | |||||||
| chr14:89860394 | T | A | 1 | a0001c0001t0005g0115 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.411-63070A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89860394 | |||||||
| chr14:89860403 | G | T | 1 | a0001c0001t0003g0088 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.411-63079C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89860403 | |||||||
| chr14:89860451 | G | A | 1 | a0003c0008t0001g0268 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.411-63127C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89860451 | |||||||
| chr14:89860556 | G | GA | 3 | a0001c0003t0004g0019 a0001c0003t0037g0018 a0001c0006t0004g0265 |
3 | HG02572.hp1 HG02965.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.411-63233dupT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89860556 | |||||||
| chr14:89860606 | T | G | 5 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.411-63282A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89860606 | |||||||
| chr14:89860630 | A | G | 2 | a0002c0005t0029g0260 a0002c0007t0004g0261 |
2 | HG01081.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.411-63306T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89860630 | |||||||
| chr14:89860804 | T | G | 2 | a0001c0002t0003g0191 a0001c0002t0024g0192 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.411-63480A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89860804 | |||||||
| chr14:89860998 | A | G | 3 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0033 |
3 | HG00140.hp2 HG01099.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.411-63674T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89860998 | |||||||
| chr14:89861004 | T | C | 1 | a0003c0008t0001g0268 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.411-63680A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89861004 | |||||||
| chr14:89861106 | C | T | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.411-63782G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89861106 | |||||||
| chr14:89861117 | C | T | 1 | a0001c0001t0008g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.411-63793G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89861117 | |||||||
| chr14:89861290 | A | G | 5 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.411-63966T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89861290 | |||||||
| chr14:89861468 | A | T | 1 | a0001c0001t0028g0084 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.411-64144T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89861468 | |||||||
| chr14:89861508 | C | G | 1 | a0001c0002t0006g0225 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.411-64184G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89861508 | |||||||
| chr14:89861645 | C | A | 1 | a0001c0001t0008g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.411-64321G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89861645 | |||||||
| chr14:89861646 | T | C | 1 | a0001c0001t0008g0178 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.411-64322A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89861646 | |||||||
| chr14:89861653 | G | A | 5 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.411-64329C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89861653 | |||||||
| chr14:89861801 | T | C | 11 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0004g0170 others(8): Show |
11 | HG01884.hp2 HG01891.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.411-64477A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89861801 | |||||||
| chr14:89861813 | G | GC | 6 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0012g0238 others(3): Show |
6 | HG02280.hp1 HG02602.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.411-64490dupG | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89861813 | |||||||
| chr14:89861875 | G | A | 2 | a0001c0002t0031g0026 a0001c0004t0017g0281 |
2 | HG02647.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.411-64551C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89861875 | |||||||
| chr14:89861895 | T | C | 39 | a0001c0001t0001g0127 a0001c0001t0002g0031 a0001c0001t0002g0032 others(36): Show |
39 | HG00140.hp2 HG01070.hp2 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.411-64571A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89861895 | |||||||
| chr14:89862293 | A | G | 1 | a0001c0001t0022g0064 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.411-64969T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89862293 | |||||||
| chr14:89862312 | A | AT | 5 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0234 others(2): Show |
5 | HG01070.hp1 HG03195.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.411-64989dupA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89862312 | |||||||
| chr14:89862312 | AT | A | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0150 others(1): Show |
4 | HG02258.hp1 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.411-64989delA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89862312 | |||||||
| chr14:89862321 | T | A | 1 | a0001c0004t0017g0281 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.411-64997A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89862321 | |||||||
| chr14:89862527 | T | C | 1 | a0001c0003t0004g0005 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.411-65203A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89862527 | |||||||
| chr14:89862649 | C | T | 231 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(228): Show |
231 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(228): Show |
intron_variant | MODIFIER | c.411-65325G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89862649 | |||||||
| chr14:89862653 | T | C | 1 | a0001c0001t0004g0151 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.411-65329A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89862653 | |||||||
| chr14:89862723 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.411-65399T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89862723 | |||||||
| chr14:89862724 | T | G | 134 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(131): Show |
134 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.411-65400A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89862724 | |||||||
| chr14:89862834 | A | G | 44 | a0001c0001t0001g0120 a0001c0001t0001g0125 a0001c0001t0003g0057 others(41): Show |
44 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.411-65510T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89862834 | |||||||
| chr14:89862882 | G | T | 3 | a0001c0001t0003g0083 a0001c0001t0005g0034 a0001c0001t0005g0035 |
3 | HG02015.hp2 HG02056.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.411-65558C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89862882 | |||||||
| chr14:89862988 | A | G | 110 | a0001c0001t0001g0058 a0001c0001t0001g0067 a0001c0001t0001g0070 others(107): Show |
110 | HG00140.hp1 HG00140.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.411-65664T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89862988 | |||||||
| chr14:89863108 | GA | G | 12 | a0001c0001t0003g0088 a0001c0003t0001g0011 a0001c0003t0001g0012 others(9): Show |
12 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.411-65785delT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89863108 | |||||||
| chr14:89863477 | T | C | 13 | a0001c0001t0001g0098 a0001c0001t0004g0097 a0001c0001t0004g0170 others(10): Show |
13 | HG02280.hp1 HG02451.hp2 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.411-66153A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89863477 | |||||||
| chr14:89863483 | T | C | 79 | a0001c0001t0001g0058 a0001c0001t0001g0095 a0001c0001t0001g0098 others(76): Show |
79 | HG00323.hp2 HG00408.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.411-66159A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89863483 | |||||||
| chr14:89863489 | C | T | 3 | a0001c0001t0022g0064 a0001c0003t0003g0013 a0001c0003t0003g0014 |
3 | HG03492.hp2 HG03710.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.411-66165G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89863489 | |||||||
| chr14:89863685 | T | C | 12 | a0001c0001t0007g0231 a0001c0001t0008g0239 a0001c0002t0031g0026 others(9): Show |
12 | HG02055.hp1 HG02109.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.411-66361A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89863685 | |||||||
| chr14:89863823 | A | G | 1 | a0001c0001t0014g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.411-66499T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89863823 | |||||||
| chr14:89863856 | G | A | 1 | a0001c0001t0002g0129 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.411-66532C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89863856 | |||||||
| chr14:89863976 | A | G | 24 | a0001c0001t0003g0088 a0001c0001t0004g0054 a0001c0002t0002g0246 others(21): Show |
24 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.411-66652T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89863976 | |||||||
| chr14:89864159 | A | T | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.411-66835T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89864159 | |||||||
| chr14:89864222 | C | T | 2 | a0001c0002t0002g0247 a0001c0002t0003g0248 |
2 | HG02602.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.411-66898G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89864222 | |||||||
| chr14:89864383 | T | C | 8 | a0001c0002t0001g0168 a0001c0002t0002g0169 a0001c0002t0027g0172 others(5): Show |
8 | HG01081.hp2 HG01891.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.411-67059A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89864383 | |||||||
| chr14:89864469 | G | A | 1 | a0001c0003t0001g0017 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.410+67072C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89864469 | |||||||
| chr14:89864477 | T | C | 1 | a0001c0001t0002g0129 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.410+67064A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89864477 | |||||||
| chr14:89864561 | G | A | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.410+66980C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89864561 | |||||||
| chr14:89864659 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.410+66882C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89864659 | |||||||
| chr14:89864745 | C | A | 8 | a0001c0002t0001g0228 a0001c0002t0002g0229 a0001c0002t0002g0230 others(5): Show |
8 | HG02451.hp2 HG02602.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.410+66796G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89864745 | |||||||
| chr14:89864767 | T | A | 3 | a0001c0006t0006g0263 a0001c0006t0009g0262 a0001c0006t0014g0264 |
3 | HG02486.hp2 HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.410+66774A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89864767 | |||||||
| chr14:89864770 | A | T | 1 | a0001c0006t0014g0264 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.410+66771T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89864770 | |||||||
| chr14:89865085 | G | A | 5 | a0001c0002t0001g0168 a0001c0002t0002g0169 a0001c0002t0027g0172 others(2): Show |
5 | HG01891.hp1 HG02809.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.410+66456C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89865085 | |||||||
| chr14:89865112 | C | T | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.410+66429G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89865112 | |||||||
| chr14:89865368 | C | T | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+66173G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89865368 | |||||||
| chr14:89865452 | C | G | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+66089G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89865452 | |||||||
| chr14:89865547 | G | A | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+65994C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89865547 | |||||||
| chr14:89865574 | T | G | 1 | a0001c0001t0001g0143 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.410+65967A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89865574 | |||||||
| chr14:89865618 | C | T | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.410+65923G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89865618 | |||||||
| chr14:89865619 | G | A | 1 | a0001c0001t0010g0072 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.410+65922C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89865619 | |||||||
| chr14:89865630 | T | C | 22 | a0001c0001t0003g0088 a0001c0003t0001g0011 a0001c0003t0001g0012 others(19): Show |
22 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.410+65911A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89865630 | |||||||
| chr14:89865725 | C | T | 22 | a0001c0001t0003g0088 a0001c0003t0001g0011 a0001c0003t0001g0012 others(19): Show |
22 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.410+65816G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89865725 | |||||||
| chr14:89865824 | T | C | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+65717A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89865824 | |||||||
| chr14:89865831 | A | AT | 244 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(241): Show |
244 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.410+65709dupA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89865831 | |||||||
| chr14:89865859 | G | A | 1 | a0001c0001t0004g0097 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.410+65682C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89865859 | |||||||
| chr14:89865958 | A | G | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+65583T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89865958 | |||||||
| chr14:89865981 | T | C | 1 | a0001c0001t0002g0166 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.410+65560A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89865981 | |||||||
| chr14:89866009 | T | C | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+65532A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89866009 | |||||||
| chr14:89866200 | T | C | 1 | a0001c0001t0010g0122 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.410+65341A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89866200 | |||||||
| chr14:89866343 | C | T | 2 | a0001c0001t0008g0175 a0001c0001t0008g0176 |
2 | HG02280.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.410+65198G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89866343 | |||||||
| chr14:89866707 | C | G | 1 | a0001c0003t0003g0015 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.410+64834G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89866707 | |||||||
| chr14:89866717 | T | C | 2 | a0001c0001t0010g0236 a0001c0001t0010g0237 |
2 | HG02559.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.410+64824A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89866717 | |||||||
| chr14:89866804 | T | G | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.410+64737A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89866804 | |||||||
| chr14:89866805 | TTTTTTA | T | 22 | a0001c0001t0003g0088 a0001c0003t0001g0011 a0001c0003t0001g0012 others(19): Show |
22 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.410+64730_410+6473 others(10): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89866805 | |||||||
| chr14:89866971 | G | A | 2 | a0001c0001t0008g0239 a0001c0001t0012g0238 |
2 | HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.410+64570C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89866971 | |||||||
| chr14:89867296 | G | T | 1 | a0005c0011t0009g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.410+64245C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89867296 | |||||||
| chr14:89867518 | G | A | 142 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(139): Show |
142 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.410+64023C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89867518 | |||||||
| chr14:89867602 | G | A | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+63939C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89867602 | |||||||
| chr14:89867635 | T | G | 1 | a0001c0001t0001g0139 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.410+63906A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89867635 | |||||||
| chr14:89867915 | C | T | 235 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(232): Show |
235 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.410+63626G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89867915 | |||||||
| chr14:89868003 | C | T | 2 | a0001c0001t0002g0154 a0001c0001t0002g0155 |
2 | HG00735.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.410+63538G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89868003 | |||||||
| chr14:89868266 | G | A | 1 | a0001c0009t0002g0273 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.410+63275C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89868266 | |||||||
| chr14:89868361 | G | A | 1 | a0001c0001t0010g0122 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.410+63180C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89868361 | |||||||
| chr14:89868465 | A | C | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+63076T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89868465 | |||||||
| chr14:89868497 | G | A | 5 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(2): Show |
5 | HG01884.hp2 HG02257.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.410+63044C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89868497 | |||||||
| chr14:89868620 | G | A | 1 | a0001c0002t0003g0065 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.410+62921C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89868620 | |||||||
| chr14:89868708 | A | G | 244 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(241): Show |
244 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.410+62833T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89868708 | |||||||
| chr14:89868829 | A | G | 1 | a0001c0006t0014g0264 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.410+62712T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89868829 | |||||||
| chr14:89868896 | G | A | 1 | a0001c0006t0014g0264 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.410+62645C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89868896 | |||||||
| chr14:89869027 | C | T | 4 | a0001c0001t0001g0060 a0001c0001t0003g0059 a0001c0001t0003g0061 others(1): Show |
4 | NA18986.hp2 NA18989.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.410+62514G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89869027 | |||||||
| chr14:89869038 | CA | C | 34 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0003g0088 others(31): Show |
34 | HG00323.hp2 HG01070.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.410+62502delT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89869038 | |||||||
| chr14:89869200 | C | T | 199 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(196): Show |
199 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.410+62341G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89869200 | |||||||
| chr14:89869390 | T | C | 1 | a0001c0002t0004g0200 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.410+62151A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89869390 | |||||||
| chr14:89869516 | T | C | 1 | a0001c0001t0014g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.410+62025A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89869516 | |||||||
| chr14:89869628 | C | T | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+61913G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89869628 | |||||||
| chr14:89869816 | C | T | 3 | a0001c0001t0003g0042 a0001c0001t0012g0089 a0001c0001t0015g0027 |
3 | HG00621.hp2 NA18955.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.410+61725G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89869816 | |||||||
| chr14:89869850 | C | T | 3 | a0001c0001t0003g0042 a0001c0001t0012g0089 a0001c0001t0015g0027 |
3 | HG00621.hp2 NA18955.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.410+61691G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89869850 | |||||||
| chr14:89869905 | T | C | 9 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0234 others(6): Show |
9 | HG01070.hp1 HG02559.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.410+61636A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89869905 | |||||||
| chr14:89870046 | A | G | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+61495T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89870046 | |||||||
| chr14:89870232 | A | G | 1 | a0001c0001t0003g0088 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.410+61309T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89870232 | |||||||
| chr14:89870415 | C | T | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+61126G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89870415 | |||||||
| chr14:89870560 | T | C | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.410+60981A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89870560 | |||||||
| chr14:89870574 | T | C | 24 | a0001c0001t0003g0088 a0001c0001t0008g0239 a0001c0001t0012g0238 others(21): Show |
24 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.410+60967A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89870574 | |||||||
| chr14:89870660 | G | A | 5 | a0001c0004t0001g0277 a0001c0004t0001g0278 a0001c0004t0002g0276 others(2): Show |
5 | HG02258.hp2 HG02622.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.410+60881C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89870660 | |||||||
| chr14:89870710 | T | A | 1 | a0001c0001t0003g0101 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.410+60831A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89870710 | |||||||
| chr14:89870767 | TA | T | 158 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(155): Show |
158 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.410+60773delT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89870767 | |||||||
| chr14:89870767 | TAA | T | 66 | a0001c0001t0001g0074 a0001c0001t0001g0127 a0001c0001t0001g0140 others(63): Show |
66 | HG00735.hp2 HG01070.hp2 HG01074.hp1 others(63): Show |
intron_variant | MODIFIER | c.410+60772_410+6077 others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89870767 | |||||||
| chr14:89870814 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.410+60727C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89870814 | |||||||
| chr14:89870854 | C | T | 4 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 others(1): Show |
4 | HG02258.hp1 HG03017.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+60687G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89870854 | |||||||
| chr14:89870898 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.410+60643G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89870898 | |||||||
| chr14:89870924 | A | C | 1 | a0001c0001t0004g0073 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.410+60617T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89870924 | |||||||
| chr14:89871088 | G | C | 1 | a0001c0001t0004g0073 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.410+60453C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89871088 | |||||||
| chr14:89871496 | A | C | 16 | a0001c0001t0001g0120 a0001c0001t0001g0125 a0001c0001t0001g0137 others(13): Show |
16 | HG00438.hp2 HG01496.hp2 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.410+60045T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89871496 | |||||||
| chr14:89871524 | C | T | 3 | a0001c0001t0018g0048 a0001c0001t0018g0100 a0001c0001t0033g0050 |
3 | HG01109.hp2 HG01255.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.410+60017G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89871524 | |||||||
| chr14:89871645 | T | C | 7 | a0001c0001t0007g0231 a0001c0004t0009g0271 a0001c0004t0009g0272 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.410+59896A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89871645 | |||||||
| chr14:89871860 | T | C | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+59681A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89871860 | |||||||
| chr14:89871937 | C | G | 1 | a0001c0001t0014g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.410+59604G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89871937 | |||||||
| chr14:89872225 | G | T | 239 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(236): Show |
239 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.410+59316C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89872225 | |||||||
| chr14:89872347 | G | T | 1 | a0001c0003t0004g0005 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.410+59194C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89872347 | |||||||
| chr14:89872359 | A | G | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+59182T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89872359 | |||||||
| chr14:89872526 | C | T | 5 | a0001c0004t0009g0271 a0001c0004t0009g0272 a0001c0004t0009g0275 others(2): Show |
5 | HG02109.hp2 HG02486.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.410+59015G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89872526 | |||||||
| chr14:89872609 | T | A | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.410+58932A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89872609 | |||||||
| chr14:89872749 | C | G | 2 | a0001c0001t0002g0044 a0001c0001t0006g0149 |
2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.410+58792G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89872749 | |||||||
| chr14:89872782 | G | GACAC | 9 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0234 others(6): Show |
9 | HG01070.hp1 HG02559.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.410+58755_410+5875 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89872782 | |||||||
| chr14:89872812 | C | A | 143 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(140): Show |
143 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(140): Show |
intron_variant | MODIFIER | c.410+58729G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89872812 | |||||||
| chr14:89872854 | G | GAC | 92 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0039 others(89): Show |
92 | HG00323.hp2 HG00673.hp1 HG00735.hp2 others(89): Show |
intron_variant | MODIFIER | c.410+58685_410+5868 others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89872854 | |||||||
| chr14:89872854 | G | GACAC | 3 | a0001c0001t0012g0238 a0001c0004t0006g0284 a0001c0004t0020g0283 |
3 | HG02559.hp2 HG03195.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.410+58683_410+5868 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89872854 | |||||||
| chr14:89872854 | GACAC | G | 3 | a0001c0001t0022g0064 a0001c0003t0003g0013 a0001c0003t0003g0014 |
3 | HG03492.hp2 HG03710.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.410+58683_410+5868 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89872854 | |||||||
| chr14:89872958 | C | A | 3 | a0001c0003t0004g0019 a0001c0003t0008g0020 a0001c0003t0037g0018 |
3 | HG02572.hp1 HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.410+58583G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89872958 | |||||||
| chr14:89873009 | G | T | 1 | a0003c0008t0026g0267 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.410+58532C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89873009 | |||||||
| chr14:89873087 | A | C | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+58454T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89873087 | |||||||
| chr14:89873151 | C | T | 1 | a0001c0001t0003g0147 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.410+58390G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89873151 | |||||||
| chr14:89873654 | T | C | 2 | a0001c0001t0002g0038 a0001c0001t0006g0037 |
2 | HG01261.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.410+57887A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89873654 | |||||||
| chr14:89873767 | C | T | 3 | a0001c0003t0002g0021 a0001c0003t0021g0002 a0001c0003t0021g0003 |
3 | HG00323.hp2 HG01168.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.410+57774G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89873767 | |||||||
| chr14:89874186 | G | T | 1 | a0001c0001t0002g0148 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.410+57355C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89874186 | |||||||
| chr14:89874338 | C | T | 17 | a0001c0001t0002g0114 a0001c0001t0008g0175 a0001c0001t0008g0176 others(14): Show |
17 | HG00735.hp2 HG01109.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.410+57203G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89874338 | |||||||
| chr14:89874449 | C | G | 4 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0234 others(1): Show |
4 | HG01070.hp1 NA18968.hp2 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+57092G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89874449 | |||||||
| chr14:89874725 | G | A | 1 | a0001c0002t0002g0222 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.410+56816C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89874725 | |||||||
| chr14:89874784 | C | T | 6 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0234 others(3): Show |
6 | HG01070.hp1 HG02559.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.410+56757G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89874784 | |||||||
| chr14:89875150 | G | A | 195 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(192): Show |
195 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.410+56391C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89875150 | |||||||
| chr14:89875221 | GAACTGCC others(23): Show |
G | 1 | a0001c0001t0002g0109 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.410+56290_410+5631 others(34): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89875221 | |||||||
| chr14:89875237 | G | T | 1 | a0001c0001t0011g0056 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.410+56304C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89875237 | |||||||
| chr14:89875308 | A | G | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+56233T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89875308 | |||||||
| chr14:89875321 | C | A | 240 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(237): Show |
240 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.410+56220G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89875321 | |||||||
| chr14:89875461 | G | A | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+56080C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89875461 | |||||||
| chr14:89875473 | T | C | 1 | a0001c0001t0004g0073 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.410+56068A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89875473 | |||||||
| chr14:89875494 | A | G | 253 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(250): Show |
253 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.410+56047T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89875494 | |||||||
| chr14:89875831 | C | G | 6 | a0001c0001t0008g0175 a0001c0001t0008g0176 a0001c0001t0008g0177 others(3): Show |
6 | HG01192.hp1 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.410+55710G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89875831 | |||||||
| chr14:89875838 | G | A | 1 | a0001c0001t0008g0179 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.410+55703C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89875838 | |||||||
| chr14:89875854 | G | C | 1 | a0002c0005t0002g0259 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.410+55687C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89875854 | |||||||
| chr14:89875868 | G | A | 7 | a0001c0001t0007g0231 a0001c0004t0009g0271 a0001c0004t0009g0272 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.410+55673C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89875868 | |||||||
| chr14:89875974 | T | G | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+55567A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89875974 | |||||||
| chr14:89876133 | C | CT | 5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0150 others(2): Show |
5 | HG02615.hp1 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.410+55407dupA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89876133 | |||||||
| chr14:89876246 | G | A | 13 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0234 others(10): Show |
13 | HG01070.hp1 HG02258.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.410+55295C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89876246 | |||||||
| chr14:89876436 | G | A | 1 | a0001c0003t0001g0012 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.410+55105C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89876436 | |||||||
| chr14:89876458 | G | A | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+55083C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89876458 | |||||||
| chr14:89876484 | T | C | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+55057A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89876484 | |||||||
| chr14:89876552 | T | C | 5 | a0001c0004t0001g0277 a0001c0004t0001g0278 a0001c0004t0002g0276 others(2): Show |
5 | HG02258.hp2 HG02622.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.410+54989A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89876552 | |||||||
| chr14:89876588 | T | C | 2 | a0002c0005t0002g0250 a0002c0005t0004g0249 |
2 | HG02055.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.410+54953A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89876588 | |||||||
| chr14:89876687 | G | A | 2 | a0001c0001t0008g0239 a0001c0001t0012g0238 |
2 | HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.410+54854C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89876687 | |||||||
| chr14:89876852 | A | G | 224 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(221): Show |
224 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.410+54689T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89876852 | |||||||
| chr14:89876865 | C | T | 3 | a0001c0001t0001g0090 a0001c0006t0006g0263 a0001c0006t0009g0262 |
3 | HG02486.hp2 HG02630.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.410+54676G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89876865 | |||||||
| chr14:89876866 | G | A | 1 | a0001c0006t0014g0264 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.410+54675C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89876866 | |||||||
| chr14:89876916 | G | GC | 23 | a0001c0001t0003g0088 a0001c0003t0001g0011 a0001c0003t0001g0012 others(20): Show |
23 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.410+54624dupG | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89876916 | |||||||
| chr14:89876932 | G | A | 1 | a0002c0007t0017g0257 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.410+54609C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89876932 | |||||||
| chr14:89877044 | GT | G | 19 | a0001c0002t0001g0190 a0001c0002t0002g0116 a0001c0002t0002g0117 others(16): Show |
19 | HG00673.hp1 HG01074.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.410+54496delA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89877044 | |||||||
| chr14:89877047 | T | A | 19 | a0001c0002t0001g0190 a0001c0002t0002g0116 a0001c0002t0002g0117 others(16): Show |
19 | HG00673.hp1 HG01074.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.410+54494A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89877047 | |||||||
| chr14:89877146 | T | TTCCTCCC others(3): Show |
1 | a0001c0003t0016g0024 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.410+54394_410+5439 others(14): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89877146 | |||||||
| chr14:89877149 | C | T | 1 | a0001c0003t0016g0024 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.410+54392G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89877149 | |||||||
| chr14:89877151 | T | C | 1 | a0001c0003t0016g0024 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.410+54390A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89877151 | |||||||
| chr14:89877228 | C | T | 1 | a0001c0001t0002g0039 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.410+54313G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89877228 | |||||||
| chr14:89877805 | C | T | 3 | a0001c0009t0001g0269 a0001c0009t0002g0273 a0001c0009t0014g0270 |
3 | HG02257.hp1 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.410+53736G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89877805 | |||||||
| chr14:89878003 | C | T | 2 | a0001c0002t0001g0190 a0001c0002t0003g0183 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.410+53538G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89878003 | |||||||
| chr14:89878041 | C | T | 25 | a0001c0001t0003g0088 a0001c0001t0003g0091 a0001c0003t0001g0011 others(22): Show |
25 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.410+53500G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89878041 | |||||||
| chr14:89878223 | G | T | 1 | a0001c0004t0017g0281 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.410+53318C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89878223 | |||||||
| chr14:89878324 | T | G | 5 | a0001c0002t0001g0168 a0001c0002t0002g0169 a0001c0002t0027g0172 others(2): Show |
5 | HG01891.hp1 HG02809.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.410+53217A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89878324 | |||||||
| chr14:89878350 | G | A | 3 | a0001c0002t0003g0197 a0001c0006t0006g0263 a0001c0006t0009g0262 |
3 | HG02132.hp2 HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+53191C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89878350 | |||||||
| chr14:89878418 | T | C | 9 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(6): Show |
9 | HG01884.hp2 HG01891.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.410+53123A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89878418 | |||||||
| chr14:89878498 | A | G | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+53043T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89878498 | |||||||
| chr14:89878560 | A | T | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+52981T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89878560 | |||||||
| chr14:89878601 | A | T | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+52940T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89878601 | |||||||
| chr14:89878637 | A | G | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+52904T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89878637 | |||||||
| chr14:89878663 | T | C | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+52878A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89878663 | |||||||
| chr14:89878701 | G | A | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+52840C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89878701 | |||||||
| chr14:89878861 | CTCT | C | 24 | a0001c0001t0003g0088 a0001c0003t0001g0011 a0001c0003t0001g0012 others(21): Show |
24 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.410+52677_410+5267 others(7): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89878861 | |||||||
| chr14:89879062 | C | T | 24 | a0001c0001t0003g0088 a0001c0003t0001g0011 a0001c0003t0001g0012 others(21): Show |
24 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.410+52479G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89879062 | |||||||
| chr14:89879074 | C | T | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+52467G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89879074 | |||||||
| chr14:89879324 | T | C | 1 | a0001c0001t0004g0107 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.410+52217A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89879324 | |||||||
| chr14:89879573 | C | G | 24 | a0001c0001t0003g0088 a0001c0003t0001g0011 a0001c0003t0001g0012 others(21): Show |
24 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.410+51968G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89879573 | |||||||
| chr14:89879667 | C | T | 1 | a0001c0006t0014g0264 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.410+51874G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89879667 | |||||||
| chr14:89879805 | C | G | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+51736G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89879805 | |||||||
| chr14:89879945 | T | C | 2 | a0001c0001t0002g0029 a0001c0001t0002g0030 |
2 | HG01261.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.410+51596A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89879945 | |||||||
| chr14:89880054 | T | C | 223 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(220): Show |
223 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.410+51487A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89880054 | |||||||
| chr14:89880095 | G | A | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+51446C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89880095 | |||||||
| chr14:89880159 | G | A | 2 | a0001c0001t0013g0028 a0001c0001t0013g0106 |
2 | HG01168.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.410+51382C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89880159 | |||||||
| chr14:89880221 | T | A | 1 | a0001c0002t0031g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.410+51320A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89880221 | |||||||
| chr14:89880291 | G | A | 7 | a0001c0001t0007g0231 a0001c0004t0009g0271 a0001c0004t0009g0272 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.410+51250C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89880291 | |||||||
| chr14:89880301 | C | T | 4 | a0001c0002t0002g0246 a0001c0002t0002g0247 a0001c0002t0003g0248 others(1): Show |
4 | HG02602.hp2 HG02738.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.410+51240G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89880301 | |||||||
| chr14:89880439 | C | T | 2 | a0001c0001t0002g0081 a0001c0001t0004g0073 |
2 | HG01071.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.410+51102G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89880439 | |||||||
| chr14:89880631 | A | C | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+50910T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89880631 | |||||||
| chr14:89880961 | G | T | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+50580C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89880961 | |||||||
| chr14:89880980 | G | A | 1 | a0001c0004t0017g0281 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.410+50561C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89880980 | |||||||
| chr14:89881098 | C | CTATT | 3 | a0001c0001t0002g0051 a0001c0001t0003g0052 a0001c0001t0003g0244 |
3 | HG01081.hp1 HG01943.hp2 HG02148.hp1 |
intron_variant | MODIFIER | c.410+50439_410+5044 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881098 | |||||||
| chr14:89881452 | C | CATATATA others(3): Show |
2 | a0001c0001t0001g0068 a0001c0003t0012g0016 |
2 | HG02258.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.410+50079_410+5008 others(14): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881452 | |||||||
| chr14:89881452 | C | CATATATA others(5): Show |
4 | a0001c0001t0001g0120 a0001c0001t0001g0137 a0001c0001t0005g0121 others(1): Show |
4 | HG02132.hp1 HG03540.hp2 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.410+50077_410+5008 others(16): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881452 | |||||||
| chr14:89881452 | C | CATATATA others(7): Show |
16 | a0001c0001t0001g0045 a0001c0001t0001g0067 a0001c0001t0001g0125 others(13): Show |
16 | HG00438.hp2 HG01515.hp1 HG02630.hp1 others(13): Show |
intron_variant | MODIFIER | c.410+50075_410+5008 others(18): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881452 | |||||||
| chr14:89881452 | C | CATATATA others(9): Show |
1 | a0001c0001t0005g0146 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.410+50088_410+5008 others(20): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881452 | |||||||
| chr14:89881452 | C | CATATATA others(11): Show |
2 | a0001c0001t0001g0046 a0001c0001t0030g0043 |
2 | HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.410+50088_410+5008 others(22): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881452 | |||||||
| chr14:89881452 | C | CATATATA others(13): Show |
1 | a0001c0001t0001g0144 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.410+50088_410+5008 others(24): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881452 | |||||||
| chr14:89881452 | C | CATATATA others(19): Show |
21 | a0001c0001t0003g0088 a0001c0003t0001g0011 a0001c0003t0001g0012 others(18): Show |
21 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.410+50088_410+5008 others(30): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881452 | |||||||
| chr14:89881452 | C | CATATATA others(21): Show |
1 | a0001c0003t0001g0017 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.410+50088_410+5008 others(32): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881452 | |||||||
| chr14:89881452 | C | CATATATA others(17): Show |
5 | a0001c0001t0001g0082 a0001c0001t0001g0143 a0001c0004t0023g0274 others(2): Show |
5 | HG02055.hp2 HG03130.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.410+50088_410+5008 others(28): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881452 | |||||||
| chr14:89881452 | C | CATATATA others(19): Show |
7 | a0001c0001t0002g0114 a0001c0001t0005g0035 a0001c0001t0007g0231 others(4): Show |
7 | HG00673.hp2 HG02055.hp1 HG02056.hp1 others(4): Show |
intron_variant | MODIFIER | c.410+50088_410+5008 others(30): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881452 | |||||||
| chr14:89881452 | C | CATATATA others(33): Show |
1 | a0001c0006t0014g0264 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.410+50088_410+5008 others(44): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881452 | |||||||
| chr14:89881452 | C | CATATATA others(21): Show |
6 | a0001c0001t0001g0070 a0001c0001t0008g0179 a0001c0001t0012g0238 others(3): Show |
6 | HG01358.hp1 HG02622.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.410+50088_410+5008 others(32): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881452 | |||||||
| chr14:89881452 | C | CATATATA others(23): Show |
16 | a0001c0001t0001g0077 a0001c0001t0001g0095 a0001c0001t0002g0030 others(13): Show |
16 | HG00323.hp1 HG00438.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.410+50088_410+5008 others(34): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881452 | |||||||
| chr14:89881452 | C | CATATATA others(25): Show |
51 | a0001c0001t0001g0058 a0001c0001t0001g0127 a0001c0001t0001g0140 others(48): Show |
51 | HG00140.hp2 HG00408.hp2 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.410+50088_410+5008 others(36): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881452 | |||||||
| chr14:89881452 | C | CATATATA others(27): Show |
22 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0167 others(19): Show |
22 | HG00621.hp2 HG00735.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.410+50088_410+5008 others(38): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881452 | |||||||
| chr14:89881452 | C | CATATATA others(29): Show |
17 | a0001c0001t0001g0093 a0001c0001t0001g0102 a0001c0001t0001g0232 others(14): Show |
17 | HG00140.hp1 HG01109.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.410+50088_410+5008 others(40): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881452 | |||||||
| chr14:89881452 | C | CATATATA others(31): Show |
14 | a0001c0001t0001g0060 a0001c0001t0001g0074 a0001c0001t0002g0039 others(11): Show |
14 | HG01168.hp2 HG01891.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.410+50088_410+5008 others(42): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881452 | |||||||
| chr14:89881452 | C | CATATATA others(33): Show |
10 | a0001c0001t0001g0090 a0001c0001t0001g0096 a0001c0001t0001g0139 others(7): Show |
10 | HG00735.hp2 HG01243.hp1 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.410+50088_410+5008 others(44): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881452 | |||||||
| chr14:89881452 | C | CATATATA others(35): Show |
8 | a0001c0001t0001g0098 a0001c0001t0002g0038 a0001c0001t0004g0163 others(5): Show |
8 | HG01192.hp1 HG02015.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.410+50088_410+5008 others(46): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881452 | |||||||
| chr14:89881452 | C | CATATATA others(37): Show |
4 | a0001c0001t0002g0109 a0001c0001t0004g0097 a0001c0001t0004g0145 others(1): Show |
4 | HG03710.hp1 HG04184.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.410+50088_410+5008 others(48): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881452 | |||||||
| chr14:89881452 | C | CGCATATA others(35): Show |
1 | a0001c0002t0042g0227 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.410+50088_410+5008 others(46): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881452 | |||||||
| chr14:89881452 | C | CGCATATA others(41): Show |
1 | a0001c0002t0003g0191 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.410+50088_410+5008 others(52): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881452 | |||||||
| chr14:89881452 | C | CGCATATA others(43): Show |
1 | a0001c0002t0024g0192 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.410+50088_410+5008 others(54): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881452 | |||||||
| chr14:89881452 | CAT | C | 5 | a0001c0002t0001g0168 a0001c0002t0002g0169 a0001c0002t0027g0172 others(2): Show |
5 | HG01891.hp1 HG02809.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.410+50087_410+5008 others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881452 | |||||||
| chr14:89881457 | A | G | 5 | a0001c0002t0001g0168 a0001c0002t0002g0169 a0001c0002t0027g0172 others(2): Show |
5 | HG01891.hp1 HG02809.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.410+50084T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881457 | |||||||
| chr14:89881466 | T | TATATATA others(26): Show |
1 | a0001c0001t0003g0164 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.410+50074_410+5007 others(37): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881466 | |||||||
| chr14:89881466 | T | TATATATA others(34): Show |
1 | a0001c0001t0004g0085 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.410+50074_410+5007 others(45): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881466 | |||||||
| chr14:89881509 | A | G | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+50032T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881509 | |||||||
| chr14:89881550 | T | C | 1 | a0005c0011t0009g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.410+49991A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881550 | |||||||
| chr14:89881699 | T | C | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+49842A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881699 | |||||||
| chr14:89881842 | T | C | 7 | a0001c0001t0007g0231 a0001c0004t0009g0271 a0001c0004t0009g0272 others(4): Show |
7 | HG02055.hp1 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.410+49699A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881842 | |||||||
| chr14:89881872 | C | T | 1 | a0001c0001t0008g0179 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.410+49669G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881872 | |||||||
| chr14:89881886 | A | G | 1 | a0001c0001t0010g0047 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.410+49655T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881886 | |||||||
| chr14:89881926 | G | A | 3 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0001c0001t0002g0162 |
3 | HG01515.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.410+49615C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881926 | |||||||
| chr14:89881969 | T | C | 1 | a0001c0001t0005g0092 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.410+49572A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89881969 | |||||||
| chr14:89882005 | G | C | 244 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(241): Show |
244 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.410+49536C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89882005 | |||||||
| chr14:89882071 | C | T | 20 | a0001c0002t0001g0190 a0001c0002t0002g0116 a0001c0002t0002g0117 others(17): Show |
20 | HG00673.hp1 HG01074.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.410+49470G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89882071 | |||||||
| chr14:89882102 | A | G | 3 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0033 |
3 | HG00140.hp2 HG01099.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.410+49439T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89882102 | |||||||
| chr14:89882145 | C | T | 1 | a0001c0001t0008g0178 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.410+49396G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89882145 | |||||||
| chr14:89882159 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.410+49382A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89882159 | |||||||
| chr14:89882236 | C | T | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+49305G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89882236 | |||||||
| chr14:89882315 | C | G | 220 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(217): Show |
220 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.410+49226G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89882315 | |||||||
| chr14:89882634 | C | T | 2 | a0001c0001t0002g0081 a0001c0001t0004g0073 |
2 | HG01071.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.410+48907G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89882634 | |||||||
| chr14:89882736 | T | C | 176 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(173): Show |
176 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.410+48805A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89882736 | |||||||
| chr14:89882784 | T | C | 1 | a0001c0001t0028g0084 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.410+48757A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89882784 | |||||||
| chr14:89882794 | G | A | 5 | a0001c0002t0001g0168 a0001c0002t0002g0169 a0001c0002t0027g0172 others(2): Show |
5 | HG01891.hp1 HG02809.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.410+48747C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89882794 | |||||||
| chr14:89882807 | G | A | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+48734C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89882807 | |||||||
| chr14:89882850 | C | T | 223 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(220): Show |
223 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.410+48691G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89882850 | |||||||
| chr14:89882866 | G | C | 2 | a0001c0001t0013g0028 a0001c0001t0013g0106 |
2 | HG01168.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.410+48675C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89882866 | |||||||
| chr14:89882983 | G | A | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+48558C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89882983 | |||||||
| chr14:89882987 | G | A | 1 | a0001c0002t0001g0190 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.410+48554C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89882987 | |||||||
| chr14:89883002 | C | A | 1 | a0001c0001t0014g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.410+48539G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89883002 | |||||||
| chr14:89883117 | C | T | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+48424G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89883117 | |||||||
| chr14:89883733 | C | A | 1 | a0001c0001t0008g0177 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.410+47808G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89883733 | |||||||
| chr14:89883753 | C | T | 141 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(138): Show |
141 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.410+47788G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89883753 | |||||||
| chr14:89883864 | A | G | 220 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(217): Show |
220 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.410+47677T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89883864 | |||||||
| chr14:89884026 | C | T | 1 | a0001c0001t0004g0163 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.410+47515G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89884026 | |||||||
| chr14:89884043 | C | A | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+47498G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89884043 | |||||||
| chr14:89884500 | C | A | 1 | a0001c0009t0014g0270 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.410+47041G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89884500 | |||||||
| chr14:89884686 | G | A | 1 | a0001c0002t0003g0065 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.410+46855C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89884686 | |||||||
| chr14:89884902 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.410+46639C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89884902 | |||||||
| chr14:89884999 | G | A | 9 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(6): Show |
9 | HG01884.hp2 HG01891.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.410+46542C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89884999 | |||||||
| chr14:89885118 | G | A | 5 | a0001c0004t0009g0271 a0001c0004t0009g0272 a0001c0004t0009g0275 others(2): Show |
5 | HG02109.hp2 HG02486.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.410+46423C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89885118 | |||||||
| chr14:89885347 | C | A | 19 | a0001c0002t0001g0190 a0001c0002t0002g0116 a0001c0002t0002g0117 others(16): Show |
19 | HG00673.hp1 HG01074.hp1 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.410+46194G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89885347 | |||||||
| chr14:89885471 | G | A | 1 | a0001c0001t0014g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.410+46070C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89885471 | |||||||
| chr14:89885524 | G | A | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+46017C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89885524 | |||||||
| chr14:89885626 | G | A | 24 | a0001c0001t0003g0088 a0001c0003t0001g0011 a0001c0003t0001g0012 others(21): Show |
24 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.410+45915C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89885626 | |||||||
| chr14:89885685 | AAGAGAGA others(3): Show |
A | 5 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0234 others(2): Show |
5 | HG02559.hp1 HG03195.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.410+45846_410+4585 others(14): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89885685 | |||||||
| chr14:89885727 | A | AAGAGAGA others(21): Show |
2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+45813_410+4581 others(32): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89885727 | |||||||
| chr14:89885739 | G | A | 1 | a0001c0001t0004g0085 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.410+45802C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89885739 | |||||||
| chr14:89885743 | A | G | 1 | a0001c0001t0004g0085 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.410+45798T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89885743 | |||||||
| chr14:89885747 | A | G | 1 | a0001c0001t0004g0085 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.410+45794T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89885747 | |||||||
| chr14:89885758 | GGAAA | G | 214 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0067 others(211): Show |
214 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.410+45779_410+4578 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89885758 | |||||||
| chr14:89885808 | AAAAG | A | 5 | a0001c0002t0001g0168 a0001c0002t0002g0169 a0001c0002t0027g0172 others(2): Show |
5 | HG01891.hp1 HG02809.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.410+45729_410+4573 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89885808 | |||||||
| chr14:89885852 | T | C | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+45689A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89885852 | |||||||
| chr14:89885882 | C | CT | 49 | a0001c0001t0001g0120 a0001c0001t0001g0125 a0001c0001t0001g0127 others(46): Show |
49 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.410+45658dupA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89885882 | |||||||
| chr14:89885888 | T | C | 1 | a0001c0001t0032g0235 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.410+45653A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89885888 | |||||||
| chr14:89885891 | TC | T | 13 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(10): Show |
13 | HG01256.hp1 HG01884.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.410+45649delG | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89885891 | |||||||
| chr14:89885892 | C | T | 207 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(204): Show |
207 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(204): Show |
intron_variant | MODIFIER | c.410+45649G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89885892 | |||||||
| chr14:89886324 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.410+45217A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89886324 | |||||||
| chr14:89886374 | C | T | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+45167G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89886374 | |||||||
| chr14:89886527 | AAAAAAAA others(11): Show |
A | 2 | a0001c0001t0008g0239 a0001c0001t0012g0238 |
2 | HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.410+44996_410+4501 others(22): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89886527 | |||||||
| chr14:89886540 | AAAAAG | A | 19 | a0001c0001t0001g0141 a0001c0001t0002g0031 a0001c0001t0002g0114 others(16): Show |
19 | HG00735.hp2 HG01099.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.410+44996_410+4500 others(9): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89886540 | |||||||
| chr14:89886541 | AAAAG | A | 136 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(133): Show |
136 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.410+44996_410+4499 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89886541 | |||||||
| chr14:89886542 | AAAG | A | 54 | a0001c0001t0001g0060 a0001c0001t0001g0098 a0001c0001t0001g0102 others(51): Show |
54 | HG01081.hp2 HG01109.hp2 HG01168.hp1 others(51): Show |
intron_variant | MODIFIER | c.410+44996_410+4499 others(7): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89886542 | |||||||
| chr14:89886543 | AAG | A | 10 | a0001c0001t0004g0163 a0001c0001t0004g0170 a0001c0001t0004g0171 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.410+44996_410+4499 others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89886543 | |||||||
| chr14:89886544 | AG | A | 9 | a0001c0002t0001g0228 a0001c0002t0002g0229 a0001c0002t0002g0230 others(6): Show |
9 | HG02132.hp2 HG02451.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.410+44996delC | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89886544 | |||||||
| chr14:89886545 | G | A | 51 | a0001c0002t0001g0188 a0001c0002t0001g0190 a0001c0002t0001g0196 others(48): Show |
51 | HG00408.hp1 HG00673.hp1 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.410+44996C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89886545 | |||||||
| chr14:89886612 | T | C | 27 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(24): Show |
27 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.410+44929A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89886612 | |||||||
| chr14:89886767 | G | C | 7 | a0001c0003t0008g0008 a0002c0005t0003g0253 a0002c0005t0003g0258 others(4): Show |
7 | HG00735.hp2 HG01109.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.410+44774C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89886767 | |||||||
| chr14:89886787 | A | G | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+44754T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89886787 | |||||||
| chr14:89886811 | C | T | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+44730G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89886811 | |||||||
| chr14:89886840 | C | T | 2 | a0001c0002t0002g0116 a0001c0002t0040g0118 |
2 | HG03017.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.410+44701G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89886840 | |||||||
| chr14:89886887 | T | C | 2 | a0001c0001t0001g0046 a0001c0001t0030g0043 |
2 | HG03098.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.410+44654A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89886887 | |||||||
| chr14:89887068 | A | T | 243 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(240): Show |
243 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.410+44473T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89887068 | |||||||
| chr14:89887100 | A | C | 3 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0033 |
3 | HG00140.hp2 HG01099.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.410+44441T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89887100 | |||||||
| chr14:89887383 | A | G | 2 | a0001c0004t0006g0284 a0001c0004t0020g0283 |
2 | HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.410+44158T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89887383 | |||||||
| chr14:89887482 | ATAAT | A | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+44055_410+4405 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89887482 | |||||||
| chr14:89887562 | G | C | 27 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(24): Show |
27 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.410+43979C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89887562 | |||||||
| chr14:89887574 | C | T | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+43967G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89887574 | |||||||
| chr14:89887581 | A | T | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.410+43960T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89887581 | |||||||
| chr14:89887684 | A | G | 3 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0001c0001t0002g0162 |
3 | HG01515.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.410+43857T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89887684 | |||||||
| chr14:89887702 | A | G | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+43839T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89887702 | |||||||
| chr14:89887855 | G | A | 2 | a0001c0002t0001g0215 a0001c0002t0001g0216 |
2 | NA18942.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.410+43686C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89887855 | |||||||
| chr14:89887936 | AT | A | 27 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(24): Show |
27 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.410+43604delA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89887936 | |||||||
| chr14:89887955 | T | C | 6 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0023 others(3): Show |
6 | NA18959.hp1 NA18973.hp2 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.410+43586A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89887955 | |||||||
| chr14:89887985 | A | G | 1 | a0001c0003t0003g0015 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.410+43556T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89887985 | |||||||
| chr14:89888241 | T | C | 6 | a0001c0001t0008g0175 a0001c0001t0008g0176 a0001c0001t0008g0177 others(3): Show |
6 | HG01192.hp1 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.410+43300A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89888241 | |||||||
| chr14:89888362 | A | G | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+43179T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89888362 | |||||||
| chr14:89888420 | C | T | 1 | a0001c0002t0002g0247 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.410+43121G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89888420 | |||||||
| chr14:89888687 | ATATCAAG others(16): Show |
A | 1 | a0001c0001t0005g0113 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.410+42831_410+4285 others(27): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89888687 | |||||||
| chr14:89888840 | A | C | 20 | a0001c0001t0002g0114 a0001c0001t0008g0175 a0001c0001t0008g0176 others(17): Show |
20 | HG00735.hp2 HG01109.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.410+42701T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89888840 | |||||||
| chr14:89888866 | C | T | 5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0150 others(2): Show |
5 | HG02615.hp1 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.410+42675G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89888866 | |||||||
| chr14:89888964 | G | C | 1 | a0001c0004t0020g0283 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.410+42577C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89888964 | |||||||
| chr14:89888979 | C | T | 3 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0004g0097 |
3 | HG02280.hp1 HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.410+42562G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89888979 | |||||||
| chr14:89889073 | A | G | 1 | a0001c0002t0004g0195 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.410+42468T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89889073 | |||||||
| chr14:89889190 | T | G | 1 | a0001c0003t0008g0020 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.410+42351A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89889190 | |||||||
| chr14:89889341 | T | A | 2 | a0001c0001t0008g0239 a0001c0001t0012g0238 |
2 | HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.410+42200A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89889341 | |||||||
| chr14:89889647 | G | A | 109 | a0001c0001t0003g0088 a0001c0001t0004g0170 a0001c0001t0004g0171 others(106): Show |
109 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(106): Show |
intron_variant | MODIFIER | c.410+41894C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89889647 | |||||||
| chr14:89889908 | C | T | 9 | a0001c0001t0007g0231 a0001c0001t0014g0240 a0001c0003t0001g0012 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.410+41633G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89889908 | |||||||
| chr14:89889923 | C | T | 27 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(24): Show |
27 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.410+41618G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89889923 | |||||||
| chr14:89889925 | T | C | 1 | a0001c0001t0013g0112 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.410+41616A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89889925 | |||||||
| chr14:89890039 | C | T | 17 | a0001c0001t0002g0114 a0001c0001t0008g0175 a0001c0001t0008g0176 others(14): Show |
17 | HG00735.hp2 HG01109.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.410+41502G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89890039 | |||||||
| chr14:89890054 | A | G | 8 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0234 others(5): Show |
8 | HG01070.hp1 HG02559.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.410+41487T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89890054 | |||||||
| chr14:89890193 | G | C | 1 | a0001c0001t0008g0178 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.410+41348C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89890193 | |||||||
| chr14:89890195 | A | C | 2 | a0001c0001t0005g0034 a0001c0001t0005g0035 |
2 | HG02015.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.410+41346T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89890195 | |||||||
| chr14:89890275 | C | T | 210 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0120 others(207): Show |
210 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.410+41266G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89890275 | |||||||
| chr14:89890344 | C | T | 2 | a0001c0002t0003g0191 a0001c0002t0024g0192 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+41197G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89890344 | |||||||
| chr14:89890426 | G | A | 136 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(133): Show |
136 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(133): Show |
intron_variant | MODIFIER | c.410+41115C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89890426 | |||||||
| chr14:89890556 | G | C | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+40985C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89890556 | |||||||
| chr14:89890558 | A | T | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+40983T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89890558 | |||||||
| chr14:89890822 | A | G | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+40719T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89890822 | |||||||
| chr14:89890969 | C | T | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+40572G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89890969 | |||||||
| chr14:89891569 | C | T | 1 | a0002c0005t0029g0260 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.410+39972G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89891569 | |||||||
| chr14:89891682 | C | A | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+39859G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89891682 | |||||||
| chr14:89891715 | G | A | 1 | a0001c0006t0014g0264 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.410+39826C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89891715 | |||||||
| chr14:89891832 | G | A | 1 | a0001c0002t0005g0187 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.410+39709C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89891832 | |||||||
| chr14:89891880 | C | T | 1 | a0001c0001t0014g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.410+39661G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89891880 | |||||||
| chr14:89891961 | G | A | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+39580C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89891961 | |||||||
| chr14:89892073 | G | A | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+39468C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89892073 | |||||||
| chr14:89892139 | G | A | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+39402C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89892139 | |||||||
| chr14:89892344 | T | C | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+39197A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89892344 | |||||||
| chr14:89892359 | G | C | 1 | a0002c0005t0002g0259 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.410+39182C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89892359 | |||||||
| chr14:89892376 | C | T | 1 | a0001c0004t0017g0281 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.410+39165G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89892376 | |||||||
| chr14:89892494 | G | C | 5 | a0001c0002t0001g0168 a0001c0002t0002g0169 a0001c0002t0027g0172 others(2): Show |
5 | HG01891.hp1 HG02809.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.410+39047C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89892494 | |||||||
| chr14:89892639 | C | T | 2 | a0001c0002t0001g0215 a0001c0002t0001g0216 |
2 | NA18942.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.410+38902G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89892639 | |||||||
| chr14:89892678 | G | A | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+38863C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89892678 | |||||||
| chr14:89892796 | G | A | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+38745C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89892796 | |||||||
| chr14:89893118 | T | C | 12 | a0001c0001t0007g0231 a0001c0004t0001g0277 a0001c0004t0001g0278 others(9): Show |
12 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.410+38423A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89893118 | |||||||
| chr14:89893145 | G | A | 2 | a0001c0001t0001g0120 a0001c0001t0005g0121 |
2 | NA18952.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.410+38396C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89893145 | |||||||
| chr14:89893152 | T | G | 3 | a0001c0009t0001g0269 a0001c0009t0002g0273 a0001c0009t0014g0270 |
3 | HG02257.hp1 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.410+38389A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89893152 | |||||||
| chr14:89893217 | A | G | 250 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(247): Show |
250 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.410+38324T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89893217 | |||||||
| chr14:89893225 | A | G | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+38316T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89893225 | |||||||
| chr14:89893255 | C | T | 3 | a0001c0003t0004g0005 a0001c0003t0012g0016 a0001c0003t0025g0006 |
3 | HG02258.hp1 HG02897.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.410+38286G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89893255 | |||||||
| chr14:89893309 | G | T | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+38232C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89893309 | |||||||
| chr14:89893376 | C | T | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+38165G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89893376 | |||||||
| chr14:89893435 | C | T | 31 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(28): Show |
31 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.410+38106G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89893435 | |||||||
| chr14:89893473 | C | T | 66 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(63): Show |
66 | HG00408.hp1 HG00673.hp1 HG01074.hp1 others(63): Show |
intron_variant | MODIFIER | c.410+38068G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89893473 | |||||||
| chr14:89893547 | C | T | 10 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0044 others(7): Show |
10 | HG01109.hp2 HG01255.hp2 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.410+37994G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89893547 | |||||||
| chr14:89893562 | T | C | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+37979A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89893562 | |||||||
| chr14:89893577 | TA | T | 25 | a0001c0001t0003g0088 a0001c0003t0001g0011 a0001c0003t0001g0012 others(22): Show |
25 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.410+37963delT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89893577 | |||||||
| chr14:89893681 | C | T | 1 | a0001c0003t0037g0018 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.410+37860G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89893681 | |||||||
| chr14:89893702 | T | A | 1 | a0002c0005t0003g0258 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.410+37839A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89893702 | |||||||
| chr14:89893709 | T | C | 1 | a0001c0006t0004g0265 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.410+37832A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89893709 | |||||||
| chr14:89893786 | A | AAAC | 30 | a0001c0002t0001g0188 a0001c0002t0001g0196 a0001c0002t0001g0215 others(27): Show |
30 | HG00408.hp1 HG02004.hp1 HG02027.hp2 others(27): Show |
intron_variant | MODIFIER | c.410+37754_410+3775 others(7): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89893786 | |||||||
| chr14:89893786 | A | AC | 35 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(32): Show |
35 | HG00673.hp1 HG01074.hp1 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.410+37754_410+3775 others(5): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89893786 | |||||||
| chr14:89893786 | A | C | 4 | a0001c0001t0004g0145 a0001c0001t0014g0240 a0001c0003t0012g0016 others(1): Show |
4 | HG02258.hp1 HG02723.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+37755T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89893786 | |||||||
| chr14:89893862 | A | ACATATAT others(60): Show |
1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.410+37678_410+3767 others(71): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89893862 | |||||||
| chr14:89893863 | T | A | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.410+37678A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89893863 | |||||||
| chr14:89893866 | A | T | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.410+37675T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89893866 | |||||||
| chr14:89893868 | A | T | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.410+37673T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89893868 | |||||||
| chr14:89893869 | C | A | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.410+37672G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89893869 | |||||||
| chr14:89893876 | TAC | T | 3 | a0001c0009t0001g0269 a0001c0009t0002g0273 a0001c0009t0014g0270 |
3 | HG02257.hp1 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.410+37663_410+3766 others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89893876 | |||||||
| chr14:89893878 | C | T | 138 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(135): Show |
138 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(135): Show |
intron_variant | MODIFIER | c.410+37663G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89893878 | |||||||
| chr14:89893884 | C | T | 3 | a0001c0009t0001g0269 a0001c0009t0002g0273 a0001c0009t0014g0270 |
3 | HG02257.hp1 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.410+37657G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89893884 | |||||||
| chr14:89894103 | C | G | 1 | a0001c0001t0010g0122 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.410+37438G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89894103 | |||||||
| chr14:89894111 | C | T | 2 | a0001c0001t0002g0136 a0001c0001t0005g0135 |
2 | HG01175.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.410+37430G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89894111 | |||||||
| chr14:89894214 | T | G | 1 | a0001c0001t0005g0086 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.410+37327A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89894214 | |||||||
| chr14:89894228 | G | C | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+37313C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89894228 | |||||||
| chr14:89894266 | T | A | 3 | a0001c0001t0008g0175 a0001c0001t0008g0176 a0001c0001t0008g0177 |
3 | HG02280.hp2 HG02717.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.410+37275A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89894266 | |||||||
| chr14:89894336 | T | A | 4 | a0001c0002t0002g0208 a0001c0002t0002g0243 a0001c0002t0003g0194 others(1): Show |
4 | HG01255.hp1 HG01934.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.410+37205A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89894336 | |||||||
| chr14:89894449 | A | G | 1 | a0001c0001t0014g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.410+37092T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89894449 | |||||||
| chr14:89894557 | A | C | 1 | a0001c0001t0010g0072 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.410+36984T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89894557 | |||||||
| chr14:89894771 | A | G | 142 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(139): Show |
142 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(139): Show |
intron_variant | MODIFIER | c.410+36770T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89894771 | |||||||
| chr14:89894800 | C | G | 1 | a0001c0001t0001g0096 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.410+36741G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89894800 | |||||||
| chr14:89895083 | T | C | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+36458A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89895083 | |||||||
| chr14:89895107 | G | T | 8 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0234 others(5): Show |
8 | HG01070.hp1 HG02559.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.410+36434C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89895107 | |||||||
| chr14:89895219 | T | A | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+36322A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89895219 | |||||||
| chr14:89895398 | C | T | 210 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0120 others(207): Show |
210 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(207): Show |
intron_variant | MODIFIER | c.410+36143G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89895398 | |||||||
| chr14:89895509 | C | A | 1 | a0001c0001t0005g0115 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.410+36032G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89895509 | |||||||
| chr14:89895509 | C | T | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+36032G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89895509 | |||||||
| chr14:89895542 | A | G | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+35999T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89895542 | |||||||
| chr14:89895889 | G | T | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+35652C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89895889 | |||||||
| chr14:89895975 | T | C | 1 | a0001c0001t0001g0082 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.410+35566A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89895975 | |||||||
| chr14:89896011 | A | G | 60 | a0001c0002t0001g0188 a0001c0002t0001g0190 a0001c0002t0001g0196 others(57): Show |
60 | HG00408.hp1 HG00673.hp1 HG01074.hp1 others(57): Show |
intron_variant | MODIFIER | c.410+35530T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89896011 | |||||||
| chr14:89896100 | T | C | 20 | a0001c0001t0002g0114 a0001c0001t0008g0175 a0001c0001t0008g0176 others(17): Show |
20 | HG00735.hp2 HG01109.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.410+35441A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89896100 | |||||||
| chr14:89896113 | C | T | 58 | a0001c0002t0001g0188 a0001c0002t0001g0190 a0001c0002t0001g0196 others(55): Show |
58 | HG00408.hp1 HG00673.hp1 HG01074.hp1 others(55): Show |
intron_variant | MODIFIER | c.410+35428G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89896113 | |||||||
| chr14:89896124 | G | A | 1 | a0001c0001t0008g0179 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.410+35417C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89896124 | |||||||
| chr14:89896156 | C | A | 25 | a0001c0001t0003g0088 a0001c0003t0001g0011 a0001c0003t0001g0012 others(22): Show |
25 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.410+35385G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89896156 | |||||||
| chr14:89896244 | C | T | 1 | a0001c0001t0004g0145 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.410+35297G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89896244 | |||||||
| chr14:89896279 | TCACAGGA others(14): Show |
T | 16 | a0001c0001t0001g0120 a0001c0001t0001g0125 a0001c0001t0001g0137 others(13): Show |
16 | HG00438.hp2 HG01496.hp2 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.410+35241_410+3526 others(25): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89896279 | |||||||
| chr14:89896337 | C | T | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+35204G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89896337 | |||||||
| chr14:89896346 | T | C | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+35195A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89896346 | |||||||
| chr14:89896378 | A | G | 1 | a0001c0001t0001g0125 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.410+35163T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89896378 | |||||||
| chr14:89896389 | C | CA | 12 | a0001c0001t0004g0107 a0001c0004t0001g0277 a0001c0004t0001g0278 others(9): Show |
12 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.410+35151dupT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89896389 | |||||||
| chr14:89896597 | AG | A | 4 | a0001c0002t0001g0168 a0001c0002t0002g0169 a0001c0002t0027g0172 others(1): Show |
4 | HG01891.hp1 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+34943delC | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89896597 | |||||||
| chr14:89896779 | C | T | 1 | a0001c0001t0018g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.410+34762G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89896779 | |||||||
| chr14:89896827 | G | A | 1 | a0001c0003t0016g0010 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.410+34714C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89896827 | |||||||
| chr14:89897119 | C | T | 1 | a0001c0002t0003g0191 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.410+34422G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89897119 | |||||||
| chr14:89897207 | A | AT | 51 | a0001c0001t0002g0114 a0001c0001t0003g0083 a0001c0001t0003g0088 others(48): Show |
51 | HG00323.hp2 HG00621.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.410+34333dupA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89897207 | |||||||
| chr14:89897207 | AT | A | 11 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(8): Show |
11 | HG01884.hp2 HG01891.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.410+34333delA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89897207 | |||||||
| chr14:89897441 | C | T | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+34100G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89897441 | |||||||
| chr14:89897458 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.410+34083C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89897458 | |||||||
| chr14:89897495 | C | T | 25 | a0001c0001t0003g0088 a0001c0003t0001g0011 a0001c0003t0001g0012 others(22): Show |
25 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.410+34046G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89897495 | |||||||
| chr14:89897505 | C | T | 1 | a0001c0001t0004g0145 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.410+34036G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89897505 | |||||||
| chr14:89897639 | G | A | 25 | a0001c0001t0003g0088 a0001c0003t0001g0011 a0001c0003t0001g0012 others(22): Show |
25 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.410+33902C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89897639 | |||||||
| chr14:89897794 | C | T | 8 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0234 others(5): Show |
8 | HG01070.hp1 HG02559.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.410+33747G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89897794 | |||||||
| chr14:89898035 | TTCTAGCT others(7): Show |
T | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+33492_410+3350 others(18): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89898035 | |||||||
| chr14:89898126 | C | T | 1 | a0001c0009t0002g0273 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.410+33415G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89898126 | |||||||
| chr14:89898222 | G | A | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+33319C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89898222 | |||||||
| chr14:89898352 | CGTTTTT | C | 40 | a0001c0001t0002g0114 a0001c0002t0001g0188 a0001c0002t0001g0196 others(37): Show |
40 | HG00408.hp1 HG00735.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.410+33183_410+3318 others(10): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89898352 | |||||||
| chr14:89898361 | T | C | 1 | a0001c0001t0010g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.410+33180A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89898361 | |||||||
| chr14:89898521 | T | C | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+33020A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89898521 | |||||||
| chr14:89898631 | C | T | 1 | a0001c0002t0001g0190 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.410+32910G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89898631 | |||||||
| chr14:89898657 | G | A | 22 | a0001c0001t0003g0088 a0001c0001t0010g0072 a0001c0003t0001g0011 others(19): Show |
22 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.410+32884C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89898657 | |||||||
| chr14:89898666 | C | CT | 93 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0120 others(90): Show |
93 | HG00140.hp2 HG00438.hp2 HG00673.hp2 others(90): Show |
intron_variant | MODIFIER | c.410+32874dupA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89898666 | |||||||
| chr14:89898666 | C | CTT | 22 | a0001c0001t0003g0088 a0001c0001t0006g0149 a0001c0003t0001g0012 others(19): Show |
22 | HG00323.hp2 HG01081.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.410+32873_410+3287 others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89898666 | |||||||
| chr14:89898666 | CT | C | 61 | a0001c0001t0001g0090 a0001c0001t0003g0061 a0001c0001t0003g0062 others(58): Show |
61 | HG00408.hp1 HG00673.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.410+32874delA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89898666 | |||||||
| chr14:89898666 | CTT | C | 9 | a0001c0002t0001g0168 a0001c0002t0001g0190 a0001c0002t0001g0216 others(6): Show |
9 | HG01256.hp2 HG02896.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.410+32873_410+3287 others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89898666 | |||||||
| chr14:89898925 | C | T | 2 | a0001c0002t0003g0191 a0001c0002t0024g0192 |
2 | HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+32616G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89898925 | |||||||
| chr14:89898988 | A | T | 1 | a0001c0001t0004g0107 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.410+32553T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89898988 | |||||||
| chr14:89899049 | A | G | 3 | a0001c0006t0006g0263 a0001c0006t0009g0262 a0001c0006t0014g0264 |
3 | HG02486.hp2 HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.410+32492T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89899049 | |||||||
| chr14:89899169 | A | G | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+32372T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89899169 | |||||||
| chr14:89899405 | C | G | 4 | a0001c0002t0001g0168 a0001c0002t0002g0169 a0001c0002t0027g0172 others(1): Show |
4 | HG01891.hp1 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+32136G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89899405 | |||||||
| chr14:89899471 | C | T | 2 | a0001c0001t0008g0239 a0001c0001t0012g0238 |
2 | HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.410+32070G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89899471 | |||||||
| chr14:89899517 | C | T | 12 | a0001c0001t0007g0231 a0001c0004t0001g0277 a0001c0004t0001g0278 others(9): Show |
12 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.410+32024G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89899517 | |||||||
| chr14:89899976 | G | A | 1 | a0001c0001t0006g0133 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.410+31565C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89899976 | |||||||
| chr14:89900031 | TTCTA | T | 25 | a0001c0001t0003g0088 a0001c0003t0001g0011 a0001c0003t0001g0012 others(22): Show |
25 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.410+31506_410+3150 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89900031 | |||||||
| chr14:89900245 | C | A | 1 | a0001c0002t0031g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.410+31296G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89900245 | |||||||
| chr14:89900281 | G | A | 4 | a0001c0002t0001g0168 a0001c0002t0002g0169 a0001c0002t0027g0172 others(1): Show |
4 | HG01891.hp1 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+31260C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89900281 | |||||||
| chr14:89900444 | T | C | 2 | a0001c0001t0002g0081 a0001c0001t0004g0073 |
2 | HG01071.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.410+31097A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89900444 | |||||||
| chr14:89900557 | A | G | 1 | a0001c0001t0005g0119 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.410+30984T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89900557 | |||||||
| chr14:89900912 | A | G | 74 | a0001c0001t0004g0145 a0001c0001t0004g0170 a0001c0001t0004g0171 others(71): Show |
74 | HG00408.hp1 HG00673.hp1 HG01074.hp1 others(71): Show |
intron_variant | MODIFIER | c.410+30629T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89900912 | |||||||
| chr14:89901403 | T | C | 3 | a0001c0001t0008g0175 a0001c0001t0008g0176 a0001c0001t0008g0177 |
3 | HG02280.hp2 HG02717.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.410+30138A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89901403 | |||||||
| chr14:89901550 | A | G | 9 | a0001c0002t0001g0196 a0001c0002t0003g0181 a0001c0002t0003g0189 others(6): Show |
9 | HG02132.hp2 NA18952.hp1 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.410+29991T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89901550 | |||||||
| chr14:89902018 | C | CCT | 142 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(139): Show |
142 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(139): Show |
intron_variant | MODIFIER | c.410+29522_410+2952 others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89902018 | |||||||
| chr14:89902042 | A | G | 1 | a0001c0001t0005g0115 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.410+29499T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89902042 | |||||||
| chr14:89902476 | C | G | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+29065G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89902476 | |||||||
| chr14:89902562 | G | T | 25 | a0001c0001t0003g0088 a0001c0003t0001g0011 a0001c0003t0001g0012 others(22): Show |
25 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.410+28979C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89902562 | |||||||
| chr14:89902563 | C | T | 25 | a0001c0001t0003g0088 a0001c0003t0001g0011 a0001c0003t0001g0012 others(22): Show |
25 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.410+28978G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89902563 | |||||||
| chr14:89902646 | T | C | 3 | a0001c0003t0004g0019 a0001c0003t0008g0020 a0001c0003t0037g0018 |
3 | HG02572.hp1 HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.410+28895A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89902646 | |||||||
| chr14:89902712 | A | G | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+28829T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89902712 | |||||||
| chr14:89902815 | G | A | 1 | a0001c0009t0002g0273 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.410+28726C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89902815 | |||||||
| chr14:89903013 | C | A | 37 | a0001c0002t0001g0188 a0001c0002t0001g0196 a0001c0002t0001g0215 others(34): Show |
37 | HG00408.hp1 HG02004.hp1 HG02027.hp2 others(34): Show |
intron_variant | MODIFIER | c.410+28528G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89903013 | |||||||
| chr14:89903197 | C | T | 1 | a0001c0001t0008g0175 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.410+28344G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89903197 | |||||||
| chr14:89903405 | C | T | 45 | a0001c0001t0001g0120 a0001c0001t0001g0125 a0001c0001t0001g0127 others(42): Show |
45 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.410+28136G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89903405 | |||||||
| chr14:89903537 | A | G | 4 | a0001c0002t0001g0168 a0001c0002t0002g0169 a0001c0002t0027g0172 others(1): Show |
4 | HG01891.hp1 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+28004T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89903537 | |||||||
| chr14:89903573 | A | AG | 24 | a0001c0001t0001g0095 a0001c0001t0001g0167 a0001c0001t0002g0051 others(21): Show |
24 | HG00408.hp2 HG00735.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.410+27967dupC | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89903573 | |||||||
| chr14:89903573 | AG | A | 31 | a0001c0002t0001g0190 a0001c0002t0001g0228 a0001c0002t0002g0116 others(28): Show |
31 | HG00673.hp1 HG01074.hp1 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.410+27967delC | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89903573 | |||||||
| chr14:89903575 | G | C | 1 | a0001c0001t0014g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.410+27966C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89903575 | |||||||
| chr14:89903576 | G | T | 6 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0234 others(3): Show |
6 | HG01070.hp1 HG02559.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.410+27965C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89903576 | |||||||
| chr14:89903709 | C | G | 12 | a0001c0001t0007g0231 a0001c0004t0001g0277 a0001c0004t0001g0278 others(9): Show |
12 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.410+27832G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89903709 | |||||||
| chr14:89903793 | A | G | 12 | a0001c0001t0007g0231 a0001c0004t0001g0277 a0001c0004t0001g0278 others(9): Show |
12 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.410+27748T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89903793 | |||||||
| chr14:89903927 | C | A | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+27614G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89903927 | |||||||
| chr14:89903954 | A | G | 28 | a0001c0001t0003g0088 a0001c0003t0001g0011 a0001c0003t0001g0012 others(25): Show |
28 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.410+27587T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89903954 | |||||||
| chr14:89903977 | G | GT | 12 | a0001c0001t0007g0231 a0001c0004t0001g0277 a0001c0004t0001g0278 others(9): Show |
12 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.410+27563dupA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89903977 | |||||||
| chr14:89904068 | GCTGCACC others(17): Show |
G | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+27449_410+2747 others(28): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89904068 | |||||||
| chr14:89904084 | C | T | 5 | a0001c0001t0008g0175 a0001c0001t0008g0176 a0001c0001t0008g0177 others(2): Show |
5 | HG02280.hp2 HG02717.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.410+27457G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89904084 | |||||||
| chr14:89904244 | T | C | 4 | a0001c0001t0003g0091 a0001c0001t0003g0104 a0001c0001t0004g0105 others(1): Show |
4 | HG01346.hp2 HG01981.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+27297A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89904244 | |||||||
| chr14:89904660 | T | C | 3 | a0001c0001t0005g0086 a0001c0001t0005g0087 a0001c0001t0006g0063 |
3 | HG00140.hp1 HG01243.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.410+26881A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89904660 | |||||||
| chr14:89904754 | G | A | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+26787C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89904754 | |||||||
| chr14:89904779 | G | A | 1 | a0001c0001t0003g0164 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.410+26762C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89904779 | |||||||
| chr14:89904867 | T | C | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+26674A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89904867 | |||||||
| chr14:89904913 | A | G | 2 | a0001c0003t0001g0012 a0001c0003t0016g0009 |
2 | NA18959.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.410+26628T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89904913 | |||||||
| chr14:89905174 | T | C | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+26367A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89905174 | |||||||
| chr14:89905236 | T | C | 2 | a0001c0002t0001g0168 a0001c0002t0002g0169 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.410+26305A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89905236 | |||||||
| chr14:89905319 | T | C | 2 | a0001c0004t0006g0284 a0001c0004t0020g0283 |
2 | HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.410+26222A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89905319 | |||||||
| chr14:89905493 | C | T | 1 | a0001c0009t0001g0269 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.410+26048G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89905493 | |||||||
| chr14:89905638 | G | A | 2 | a0001c0001t0001g0098 a0001c0001t0004g0097 |
2 | HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.410+25903C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89905638 | |||||||
| chr14:89906087 | T | C | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+25454A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89906087 | |||||||
| chr14:89906172 | A | AAAAT | 35 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(32): Show |
35 | HG00323.hp1 HG00408.hp1 HG00621.hp2 others(32): Show |
intron_variant | MODIFIER | c.410+25365_410+2536 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89906172 | |||||||
| chr14:89906172 | AAAAT | A | 48 | a0001c0001t0001g0068 a0001c0001t0001g0074 a0001c0001t0001g0077 others(45): Show |
48 | HG00323.hp2 HG00438.hp1 HG00673.hp2 others(45): Show |
intron_variant | MODIFIER | c.410+25365_410+2536 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89906172 | |||||||
| chr14:89906172 | AAAATAAA others(1): Show |
A | 31 | a0001c0001t0003g0088 a0001c0002t0003g0065 a0001c0002t0004g0185 others(28): Show |
31 | HG00673.hp1 HG01081.hp2 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.410+25361_410+2536 others(12): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89906172 | |||||||
| chr14:89906172 | AAAATAAA others(5): Show |
A | 9 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(6): Show |
9 | HG01884.hp2 HG01891.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.410+25357_410+2536 others(16): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89906172 | |||||||
| chr14:89906181 | A | C | 1 | a0001c0003t0021g0002 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.410+25360T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89906181 | |||||||
| chr14:89906217 | AAATT | A | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+25320_410+2532 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89906217 | |||||||
| chr14:89906401 | C | A | 20 | a0001c0001t0002g0114 a0001c0001t0008g0175 a0001c0001t0008g0176 others(17): Show |
20 | HG00735.hp2 HG01109.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.410+25140G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89906401 | |||||||
| chr14:89907044 | C | T | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+24497G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89907044 | |||||||
| chr14:89907360 | C | T | 1 | a0001c0009t0002g0273 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.410+24181G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89907360 | |||||||
| chr14:89907402 | G | A | 1 | a0004c0010t0004g0041 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.410+24139C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89907402 | |||||||
| chr14:89907496 | T | A | 78 | a0001c0001t0004g0145 a0001c0001t0007g0231 a0001c0001t0014g0240 others(75): Show |
78 | HG00408.hp1 HG00673.hp1 HG01074.hp1 others(75): Show |
intron_variant | MODIFIER | c.410+24045A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89907496 | |||||||
| chr14:89907537 | T | C | 8 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(5): Show |
8 | HG01884.hp2 HG01891.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.410+24004A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89907537 | |||||||
| chr14:89907560 | C | T | 3 | a0001c0006t0006g0263 a0001c0006t0009g0262 a0001c0006t0014g0264 |
3 | HG02486.hp2 HG02630.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.410+23981G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89907560 | |||||||
| chr14:89907626 | G | C | 27 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(24): Show |
27 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.410+23915C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89907626 | |||||||
| chr14:89907637 | A | G | 3 | a0001c0003t0003g0013 a0001c0003t0003g0014 a0001c0003t0003g0015 |
3 | HG03710.hp2 HG03834.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.410+23904T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89907637 | |||||||
| chr14:89908166 | C | T | 3 | a0001c0003t0004g0019 a0001c0003t0008g0020 a0001c0003t0037g0018 |
3 | HG02572.hp1 HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.410+23375G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89908166 | |||||||
| chr14:89908199 | G | C | 1 | a0001c0009t0001g0269 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.410+23342C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89908199 | |||||||
| chr14:89908407 | C | T | 1 | a0001c0009t0001g0269 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.410+23134G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89908407 | |||||||
| chr14:89908453 | T | C | 104 | a0001c0001t0004g0145 a0001c0001t0007g0231 a0001c0001t0014g0240 others(101): Show |
104 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(101): Show |
intron_variant | MODIFIER | c.410+23088A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89908453 | |||||||
| chr14:89908505 | T | C | 6 | a0001c0002t0003g0182 a0001c0002t0003g0199 a0001c0002t0004g0185 others(3): Show |
6 | HG02004.hp1 NA18947.hp2 NA18959.hp2 others(3): Show |
intron_variant | MODIFIER | c.410+23036A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89908505 | |||||||
| chr14:89908526 | T | C | 1 | a0003c0008t0001g0268 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.410+23015A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89908526 | |||||||
| chr14:89908647 | C | T | 4 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 others(1): Show |
4 | HG02630.hp1 HG03017.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+22894G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89908647 | |||||||
| chr14:89908648 | A | G | 141 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(138): Show |
141 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(138): Show |
intron_variant | MODIFIER | c.410+22893T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89908648 | |||||||
| chr14:89908686 | C | T | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+22855G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89908686 | |||||||
| chr14:89908916 | G | A | 79 | a0001c0001t0004g0145 a0001c0001t0007g0231 a0001c0001t0014g0240 others(76): Show |
79 | HG00408.hp1 HG00673.hp1 HG01074.hp1 others(76): Show |
intron_variant | MODIFIER | c.410+22625C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89908916 | |||||||
| chr14:89909014 | G | A | 3 | a0001c0002t0001g0228 a0001c0002t0002g0229 a0001c0002t0002g0230 |
3 | HG02451.hp2 HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.410+22527C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89909014 | |||||||
| chr14:89909173 | T | C | 1 | a0001c0002t0004g0201 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.410+22368A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89909173 | |||||||
| chr14:89909494 | A | C | 25 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0017 others(22): Show |
25 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.410+22047T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89909494 | |||||||
| chr14:89909495 | G | T | 25 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0017 others(22): Show |
25 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.410+22046C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89909495 | |||||||
| chr14:89909504 | CG | C | 130 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(127): Show |
130 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(127): Show |
intron_variant | MODIFIER | c.410+22036delC | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89909504 | |||||||
| chr14:89909506 | G | A | 25 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0017 others(22): Show |
25 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.410+22035C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89909506 | |||||||
| chr14:89909555 | T | G | 4 | a0001c0002t0001g0168 a0001c0002t0002g0169 a0001c0002t0027g0172 others(1): Show |
4 | HG01891.hp1 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+21986A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89909555 | |||||||
| chr14:89909560 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.410+21981C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89909560 | |||||||
| chr14:89909648 | T | TC | 114 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(111): Show |
114 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(111): Show |
intron_variant | MODIFIER | c.410+21892dupG | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89909648 | |||||||
| chr14:89909649 | C | CT | 27 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(24): Show |
27 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(24): Show |
intron_variant | MODIFIER | c.410+21891dupA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89909649 | |||||||
| chr14:89909752 | A | G | 1 | a0001c0002t0004g0204 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.410+21789T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89909752 | |||||||
| chr14:89909759 | T | C | 62 | a0001c0001t0004g0145 a0001c0002t0001g0188 a0001c0002t0001g0190 others(59): Show |
62 | HG00408.hp1 HG00673.hp1 HG01074.hp1 others(59): Show |
intron_variant | MODIFIER | c.410+21782A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89909759 | |||||||
| chr14:89909816 | C | T | 93 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(90): Show |
93 | HG00408.hp1 HG00673.hp1 HG00735.hp2 others(90): Show |
intron_variant | MODIFIER | c.410+21725G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89909816 | |||||||
| chr14:89909864 | C | G | 21 | a0001c0001t0007g0231 a0001c0001t0014g0240 a0001c0002t0001g0168 others(18): Show |
21 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.410+21677G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89909864 | |||||||
| chr14:89909874 | G | C | 23 | a0001c0001t0007g0231 a0001c0001t0014g0240 a0001c0002t0001g0168 others(20): Show |
23 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.410+21667C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89909874 | |||||||
| chr14:89909876 | C | A | 19 | a0001c0001t0002g0114 a0001c0001t0008g0175 a0001c0001t0008g0176 others(16): Show |
19 | HG00735.hp2 HG01109.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.410+21665G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89909876 | |||||||
| chr14:89909879 | A | C | 1 | a0001c0001t0001g0165 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.410+21662T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89909879 | |||||||
| chr14:89909913 | C | T | 4 | a0001c0002t0001g0168 a0001c0002t0002g0169 a0001c0002t0027g0172 others(1): Show |
4 | HG01891.hp1 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+21628G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89909913 | |||||||
| chr14:89909917 | G | A | 3 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0234 |
3 | NA18968.hp2 NA19009.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.410+21624C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89909917 | |||||||
| chr14:89909971 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.410+21570G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89909971 | |||||||
| chr14:89910155 | A | G | 1 | a0001c0001t0003g0164 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.410+21386T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89910155 | |||||||
| chr14:89910156 | A | T | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+21385T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89910156 | |||||||
| chr14:89910251 | C | T | 1 | a0001c0001t0002g0038 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.410+21290G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89910251 | |||||||
| chr14:89910319 | C | T | 43 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(40): Show |
43 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.410+21222G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89910319 | |||||||
| chr14:89910325 | C | T | 4 | a0001c0002t0001g0168 a0001c0002t0002g0169 a0001c0002t0027g0172 others(1): Show |
4 | HG01891.hp1 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+21216G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89910325 | |||||||
| chr14:89910332 | T | C | 1 | a0001c0003t0002g0021 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.410+21209A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89910332 | |||||||
| chr14:89910335 | C | T | 43 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(40): Show |
43 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.410+21206G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89910335 | |||||||
| chr14:89910363 | T | C | 138 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(135): Show |
138 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(135): Show |
intron_variant | MODIFIER | c.410+21178A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89910363 | |||||||
| chr14:89910372 | C | T | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+21169G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89910372 | |||||||
| chr14:89910397 | A | C | 1 | a0001c0004t0020g0283 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.410+21144T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89910397 | |||||||
| chr14:89910459 | G | A | 1 | a0001c0002t0003g0210 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.410+21082C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89910459 | |||||||
| chr14:89910497 | T | C | 1 | a0001c0001t0004g0160 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.410+21044A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89910497 | |||||||
| chr14:89910578 | C | A | 62 | a0001c0001t0004g0145 a0001c0002t0001g0188 a0001c0002t0001g0190 others(59): Show |
62 | HG00408.hp1 HG00673.hp1 HG01074.hp1 others(59): Show |
intron_variant | MODIFIER | c.410+20963G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89910578 | |||||||
| chr14:89910598 | A | AATAC | 44 | a0001c0001t0001g0046 a0001c0001t0001g0067 a0001c0001t0001g0077 others(41): Show |
44 | HG00438.hp1 HG00673.hp2 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.410+20939_410+2094 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89910598 | |||||||
| chr14:89910598 | A | AATACATA others(1): Show |
8 | a0001c0001t0001g0076 a0001c0001t0001g0139 a0001c0001t0002g0148 others(5): Show |
8 | HG01168.hp2 HG02698.hp1 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.410+20935_410+2094 others(12): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89910598 | |||||||
| chr14:89910598 | A | C | 2 | a0001c0001t0002g0049 a0001c0001t0005g0138 |
2 | HG03239.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.410+20943T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89910598 | |||||||
| chr14:89910598 | AATAC | A | 18 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0033 others(15): Show |
18 | HG00140.hp2 HG01099.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.410+20939_410+2094 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89910598 | |||||||
| chr14:89910598 | AATACATA others(1): Show |
A | 77 | a0001c0001t0004g0145 a0001c0002t0001g0188 a0001c0002t0001g0196 others(74): Show |
77 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(74): Show |
intron_variant | MODIFIER | c.410+20935_410+2094 others(12): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89910598 | |||||||
| chr14:89910598 | AATACATA others(9): Show |
A | 3 | a0001c0001t0002g0136 a0001c0001t0005g0135 a0001c0002t0010g0209 |
3 | HG01175.hp1 HG01243.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.410+20927_410+2094 others(20): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89910598 | |||||||
| chr14:89910598 | AATACATA others(21): Show |
A | 47 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(44): Show |
47 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.410+20915_410+2094 others(32): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89910598 | |||||||
| chr14:89910824 | G | A | 47 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(44): Show |
47 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.410+20717C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89910824 | |||||||
| chr14:89910970 | C | T | 141 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(138): Show |
141 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(138): Show |
intron_variant | MODIFIER | c.410+20571G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89910970 | |||||||
| chr14:89911014 | T | C | 1 | a0001c0001t0008g0239 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.410+20527A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89911014 | |||||||
| chr14:89911277 | G | T | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+20264C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89911277 | |||||||
| chr14:89911384 | G | C | 1 | a0001c0001t0001g0096 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.410+20157C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89911384 | |||||||
| chr14:89911423 | C | T | 281 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(278): Show |
281 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.410+20118G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89911423 | |||||||
| chr14:89911482 | G | A | 47 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(44): Show |
47 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.410+20059C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89911482 | |||||||
| chr14:89911614 | C | A | 48 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(45): Show |
48 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.410+19927G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89911614 | |||||||
| chr14:89911998 | T | C | 8 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0234 others(5): Show |
8 | HG01070.hp1 HG02559.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.410+19543A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89911998 | |||||||
| chr14:89912389 | C | CT | 45 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(42): Show |
45 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.410+19151dupA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89912389 | |||||||
| chr14:89912576 | C | G | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+18965G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89912576 | |||||||
| chr14:89912894 | T | C | 5 | a0001c0004t0009g0271 a0001c0004t0009g0272 a0001c0004t0009g0275 others(2): Show |
5 | HG02109.hp2 HG02486.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.410+18647A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89912894 | |||||||
| chr14:89912916 | C | T | 9 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0234 others(6): Show |
9 | HG01070.hp1 HG02559.hp1 HG03195.hp2 others(6): Show |
intron_variant | MODIFIER | c.410+18625G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89912916 | |||||||
| chr14:89912918 | C | A | 3 | a0001c0002t0001g0228 a0001c0002t0002g0229 a0001c0002t0002g0230 |
3 | HG02451.hp2 HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.410+18623G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89912918 | |||||||
| chr14:89912931 | G | A | 11 | a0001c0004t0001g0277 a0001c0004t0001g0278 a0001c0004t0002g0276 others(8): Show |
11 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.410+18610C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89912931 | |||||||
| chr14:89913271 | C | T | 47 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(44): Show |
47 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.410+18270G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89913271 | |||||||
| chr14:89913274 | A | G | 1 | a0001c0003t0016g0010 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.410+18267T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89913274 | |||||||
| chr14:89913304 | T | C | 1 | a0003c0008t0001g0268 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.410+18237A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89913304 | |||||||
| chr14:89913326 | A | T | 25 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0017 others(22): Show |
25 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.410+18215T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89913326 | |||||||
| chr14:89913533 | A | G | 1 | a0001c0002t0020g0025 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.410+18008T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89913533 | |||||||
| chr14:89913964 | C | T | 47 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(44): Show |
47 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.410+17577G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89913964 | |||||||
| chr14:89914115 | T | TC | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+17425dupG | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89914115 | |||||||
| chr14:89914278 | C | T | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+17263G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89914278 | |||||||
| chr14:89914323 | G | A | 1 | a0001c0002t0040g0118 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.410+17218C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89914323 | |||||||
| chr14:89914494 | G | A | 3 | a0001c0002t0001g0196 a0001c0002t0003g0197 a0001c0002t0005g0187 |
3 | HG02132.hp2 NA18954.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.410+17047C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89914494 | |||||||
| chr14:89914502 | A | G | 2 | a0001c0001t0008g0239 a0001c0001t0012g0238 |
2 | HG03209.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.410+17039T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89914502 | |||||||
| chr14:89914559 | C | T | 47 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(44): Show |
47 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.410+16982G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89914559 | |||||||
| chr14:89914641 | C | T | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+16900G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89914641 | |||||||
| chr14:89914700 | G | A | 1 | a0003c0008t0001g0266 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.410+16841C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89914700 | |||||||
| chr14:89914717 | G | A | 47 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(44): Show |
47 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(44): Show |
intron_variant | MODIFIER | c.410+16824C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89914717 | |||||||
| chr14:89914892 | C | T | 1 | a0001c0004t0017g0281 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.410+16649G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89914892 | |||||||
| chr14:89915232 | T | C | 2 | a0002c0005t0002g0250 a0002c0005t0004g0249 |
2 | HG02055.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.410+16309A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89915232 | |||||||
| chr14:89915243 | A | G | 142 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(139): Show |
142 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(139): Show |
intron_variant | MODIFIER | c.410+16298T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89915243 | |||||||
| chr14:89915448 | T | C | 3 | a0001c0009t0001g0269 a0001c0009t0002g0273 a0001c0009t0014g0270 |
3 | HG02257.hp1 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.410+16093A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89915448 | |||||||
| chr14:89915540 | A | C | 1 | a0001c0002t0003g0211 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.410+16001T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89915540 | |||||||
| chr14:89915736 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.410+15805G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89915736 | |||||||
| chr14:89915855 | G | A | 1 | a0001c0001t0007g0036 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.410+15686C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89915855 | |||||||
| chr14:89916049 | G | T | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+15492C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89916049 | |||||||
| chr14:89916156 | GA | G | 106 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(103): Show |
106 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(103): Show |
intron_variant | MODIFIER | c.410+15384delT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89916156 | |||||||
| chr14:89916156 | GAA | G | 31 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(28): Show |
31 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.410+15383_410+1538 others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89916156 | |||||||
| chr14:89916216 | GA | G | 43 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(40): Show |
43 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.410+15324delT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89916216 | |||||||
| chr14:89916219 | G | C | 43 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(40): Show |
43 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.410+15322C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89916219 | |||||||
| chr14:89916220 | T | A | 43 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(40): Show |
43 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.410+15321A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89916220 | |||||||
| chr14:89916454 | C | T | 1 | a0001c0002t0020g0025 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.410+15087G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89916454 | |||||||
| chr14:89916457 | T | A | 1 | a0001c0003t0001g0017 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.410+15084A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89916457 | |||||||
| chr14:89916507 | C | G | 72 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(69): Show |
72 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(69): Show |
intron_variant | MODIFIER | c.410+15034G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89916507 | |||||||
| chr14:89916542 | T | C | 8 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(5): Show |
8 | HG01884.hp2 HG01891.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.410+14999A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89916542 | |||||||
| chr14:89916547 | C | A | 2 | a0001c0004t0006g0284 a0001c0004t0020g0283 |
2 | HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.410+14994G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89916547 | |||||||
| chr14:89916670 | G | A | 1 | a0001c0004t0017g0281 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.410+14871C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89916670 | |||||||
| chr14:89916708 | C | A | 24 | a0001c0002t0001g0190 a0001c0002t0002g0116 a0001c0002t0002g0117 others(21): Show |
24 | HG00673.hp1 HG01074.hp1 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.410+14833G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89916708 | |||||||
| chr14:89916742 | T | A | 43 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(40): Show |
43 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.410+14799A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89916742 | |||||||
| chr14:89916775 | C | T | 1 | a0001c0001t0008g0178 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.410+14766G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89916775 | |||||||
| chr14:89916814 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.410+14727C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89916814 | |||||||
| chr14:89916925 | T | C | 1 | a0001c0001t0002g0071 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.410+14616A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89916925 | |||||||
| chr14:89916976 | T | A | 43 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(40): Show |
43 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.410+14565A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89916976 | |||||||
| chr14:89917053 | C | CGT | 35 | a0001c0001t0001g0058 a0001c0001t0001g0068 a0001c0001t0001g0074 others(32): Show |
35 | HG00140.hp1 HG01071.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.410+14486_410+1448 others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917053 | |||||||
| chr14:89917053 | C | CGTGT | 13 | a0001c0001t0001g0067 a0001c0001t0001g0076 a0001c0001t0001g0077 others(10): Show |
13 | HG00438.hp1 HG01175.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.410+14484_410+1448 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917053 | |||||||
| chr14:89917053 | CGT | C | 45 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0090 others(42): Show |
45 | HG00140.hp2 HG00408.hp2 HG00621.hp2 others(42): Show |
intron_variant | MODIFIER | c.410+14486_410+1448 others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917053 | |||||||
| chr14:89917053 | CGTGT | C | 13 | a0001c0001t0001g0070 a0001c0001t0001g0137 a0001c0001t0001g0143 others(10): Show |
13 | HG00323.hp1 HG01081.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.410+14484_410+1448 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917053 | |||||||
| chr14:89917053 | CGTGTGT | C | 23 | a0001c0001t0001g0120 a0001c0001t0002g0039 a0001c0001t0005g0119 others(20): Show |
23 | HG00673.hp1 HG01074.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.410+14482_410+1448 others(10): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917053 | |||||||
| chr14:89917053 | CGTGTGTG others(1): Show |
C | 6 | a0001c0001t0022g0064 a0001c0002t0003g0191 a0001c0002t0024g0192 others(3): Show |
6 | HG01884.hp1 HG02257.hp1 HG03017.hp2 others(3): Show |
intron_variant | MODIFIER | c.410+14480_410+1448 others(12): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917053 | |||||||
| chr14:89917053 | CGTGTGTG others(3): Show |
C | 7 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(4): Show |
7 | HG01884.hp2 HG02976.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.410+14478_410+1448 others(14): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917053 | |||||||
| chr14:89917053 | CGTGTGTG others(5): Show |
C | 38 | a0001c0001t0001g0093 a0001c0001t0005g0092 a0001c0001t0011g0094 others(35): Show |
38 | HG00408.hp1 HG02004.hp1 HG02027.hp2 others(35): Show |
intron_variant | MODIFIER | c.410+14476_410+1448 others(16): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917053 | |||||||
| chr14:89917053 | CGTGTGTG others(9): Show |
C | 1 | a0001c0002t0031g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.410+14472_410+1448 others(20): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917053 | |||||||
| chr14:89917064 | GTGTGTGT others(27): Show |
G | 6 | a0001c0001t0008g0175 a0001c0001t0008g0176 a0001c0001t0008g0177 others(3): Show |
6 | HG01192.hp1 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.410+14443_410+1447 others(38): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917064 | |||||||
| chr14:89917080 | GTGTGTGT others(11): Show |
G | 10 | a0001c0004t0001g0277 a0001c0004t0001g0278 a0001c0004t0002g0276 others(7): Show |
10 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.410+14443_410+1446 others(22): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917080 | |||||||
| chr14:89917082 | GTGTGTGT others(9): Show |
G | 2 | a0001c0003t0004g0005 a0001c0004t0023g0274 |
2 | HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.410+14443_410+1445 others(20): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917082 | |||||||
| chr14:89917084 | GTGTGTGT others(7): Show |
G | 3 | a0001c0001t0010g0237 a0001c0001t0014g0240 a0001c0004t0006g0284 |
3 | HG02559.hp2 HG02723.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.410+14443_410+1445 others(18): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917084 | |||||||
| chr14:89917086 | GTGTGTGT others(5): Show |
G | 5 | a0001c0001t0007g0231 a0001c0003t0002g0021 a0001c0003t0021g0002 others(2): Show |
5 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.410+14443_410+1445 others(16): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917086 | |||||||
| chr14:89917088 | GTGTGTGT others(3): Show |
G | 23 | a0001c0001t0002g0114 a0001c0001t0010g0236 a0001c0003t0001g0011 others(20): Show |
23 | HG01109.hp1 HG01433.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.410+14443_410+1445 others(14): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917088 | |||||||
| chr14:89917090 | GTGTGTGT others(1): Show |
G | 8 | a0001c0003t0003g0015 a0001c0003t0009g0022 a0001c0003t0012g0016 others(5): Show |
8 | HG00735.hp2 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.410+14443_410+1445 others(12): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917090 | |||||||
| chr14:89917092 | GTGTGTA | G | 8 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0234 others(5): Show |
8 | HG01081.hp2 HG02896.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.410+14443_410+1444 others(10): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917092 | |||||||
| chr14:89917098 | A | G | 1 | a0001c0001t0032g0235 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.410+14443T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917098 | |||||||
| chr14:89917264 | G | T | 43 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(40): Show |
43 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.410+14277C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917264 | |||||||
| chr14:89917268 | CT | C | 4 | a0001c0002t0001g0168 a0001c0002t0002g0169 a0001c0002t0027g0172 others(1): Show |
4 | HG01891.hp1 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+14272delA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917268 | |||||||
| chr14:89917309 | G | A | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.410+14232C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917309 | |||||||
| chr14:89917524 | C | T | 7 | a0001c0002t0001g0168 a0001c0002t0002g0169 a0001c0002t0003g0191 others(4): Show |
7 | HG01891.hp1 HG02809.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.410+14017G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917524 | |||||||
| chr14:89917527 | C | T | 4 | a0001c0002t0001g0168 a0001c0002t0002g0169 a0001c0002t0027g0172 others(1): Show |
4 | HG01891.hp1 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+14014G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917527 | |||||||
| chr14:89917618 | A | C | 10 | a0001c0002t0002g0207 a0001c0002t0002g0208 a0001c0002t0002g0222 others(7): Show |
10 | HG01074.hp1 HG01255.hp1 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.410+13923T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917618 | |||||||
| chr14:89917620 | T | C | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.410+13921A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917620 | |||||||
| chr14:89917733 | T | C | 141 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(138): Show |
141 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(138): Show |
intron_variant | MODIFIER | c.410+13808A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917733 | |||||||
| chr14:89917734 | G | A | 37 | a0001c0002t0001g0188 a0001c0002t0001g0196 a0001c0002t0001g0215 others(34): Show |
37 | HG00408.hp1 HG02004.hp1 HG02027.hp2 others(34): Show |
intron_variant | MODIFIER | c.410+13807C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917734 | |||||||
| chr14:89917845 | C | T | 72 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(69): Show |
72 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(69): Show |
intron_variant | MODIFIER | c.410+13696G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89917845 | |||||||
| chr14:89918046 | A | G | 72 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(69): Show |
72 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(69): Show |
intron_variant | MODIFIER | c.410+13495T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89918046 | |||||||
| chr14:89918048 | A | G | 1 | a0001c0003t0008g0020 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.410+13493T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89918048 | |||||||
| chr14:89918273 | T | C | 72 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(69): Show |
72 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(69): Show |
intron_variant | MODIFIER | c.410+13268A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89918273 | |||||||
| chr14:89918339 | C | G | 140 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(137): Show |
140 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(137): Show |
intron_variant | MODIFIER | c.410+13202G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89918339 | |||||||
| chr14:89918342 | C | A | 3 | a0001c0003t0004g0019 a0001c0003t0008g0020 a0001c0003t0037g0018 |
3 | HG02572.hp1 HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.410+13199G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89918342 | |||||||
| chr14:89918409 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.410+13132G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89918409 | |||||||
| chr14:89918508 | C | T | 48 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0196 others(45): Show |
48 | HG00408.hp1 HG01891.hp1 HG02004.hp1 others(45): Show |
intron_variant | MODIFIER | c.410+13033G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89918508 | |||||||
| chr14:89918618 | G | C | 1 | a0001c0003t0016g0024 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.410+12923C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89918618 | |||||||
| chr14:89918969 | G | A | 1 | a0001c0002t0003g0065 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.410+12572C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89918969 | |||||||
| chr14:89919084 | T | C | 1 | a0003c0008t0001g0266 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.410+12457A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89919084 | |||||||
| chr14:89919123 | A | C | 8 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0234 others(5): Show |
8 | HG01070.hp1 HG02559.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.410+12418T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89919123 | |||||||
| chr14:89919194 | GAGAGAGA others(3): Show |
G | 1 | a0001c0002t0004g0202 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.410+12337_410+1234 others(14): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89919194 | |||||||
| chr14:89919204 | CAGAG | C | 114 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(111): Show |
114 | HG00408.hp1 HG00673.hp1 HG00735.hp2 others(111): Show |
intron_variant | MODIFIER | c.410+12333_410+1233 others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89919204 | |||||||
| chr14:89919204 | CAGAGAG | C | 25 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0017 others(22): Show |
25 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.410+12331_410+1233 others(10): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89919204 | |||||||
| chr14:89919208 | G | C | 1 | a0001c0002t0004g0202 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.410+12333C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89919208 | |||||||
| chr14:89919277 | AAAG | A | 3 | a0001c0009t0001g0269 a0001c0009t0002g0273 a0001c0009t0014g0270 |
3 | HG02257.hp1 HG03453.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.410+12261_410+1226 others(7): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89919277 | |||||||
| chr14:89919490 | T | C | 1 | a0003c0008t0026g0267 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.410+12051A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89919490 | |||||||
| chr14:89919681 | T | C | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.410+11860A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89919681 | |||||||
| chr14:89919690 | C | T | 3 | a0001c0002t0003g0212 a0001c0002t0003g0213 a0001c0002t0003g0214 |
3 | NA18973.hp1 NA18983.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.410+11851G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89919690 | |||||||
| chr14:89919791 | G | C | 25 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0017 others(22): Show |
25 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.410+11750C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89919791 | |||||||
| chr14:89919798 | C | T | 4 | a0001c0001t0001g0060 a0001c0001t0003g0059 a0001c0001t0003g0061 others(1): Show |
4 | NA18986.hp2 NA18989.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.410+11743G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89919798 | |||||||
| chr14:89919988 | A | C | 1 | a0001c0001t0010g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.410+11553T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89919988 | |||||||
| chr14:89920317 | T | C | 19 | a0001c0001t0002g0114 a0001c0001t0008g0175 a0001c0001t0008g0176 others(16): Show |
19 | HG00735.hp2 HG01109.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.410+11224A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89920317 | |||||||
| chr14:89920457 | T | C | 1 | a0001c0004t0017g0281 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.410+11084A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89920457 | |||||||
| chr14:89920561 | C | T | 140 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(137): Show |
140 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(137): Show |
intron_variant | MODIFIER | c.410+10980G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89920561 | |||||||
| chr14:89920619 | C | T | 1 | a0001c0001t0011g0153 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.410+10922G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89920619 | |||||||
| chr14:89920722 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.410+10819C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89920722 | |||||||
| chr14:89920780 | T | C | 61 | a0001c0002t0001g0188 a0001c0002t0001g0190 a0001c0002t0001g0196 others(58): Show |
61 | HG00408.hp1 HG00673.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.410+10761A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89920780 | |||||||
| chr14:89920790 | C | T | 68 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(65): Show |
68 | HG00408.hp1 HG00673.hp1 HG01074.hp1 others(65): Show |
intron_variant | MODIFIER | c.410+10751G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89920790 | |||||||
| chr14:89920791 | G | A | 48 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(45): Show |
48 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.410+10750C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89920791 | |||||||
| chr14:89920836 | G | C | 72 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(69): Show |
72 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(69): Show |
intron_variant | MODIFIER | c.410+10705C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89920836 | |||||||
| chr14:89920890 | C | A | 61 | a0001c0002t0001g0188 a0001c0002t0001g0190 a0001c0002t0001g0196 others(58): Show |
61 | HG00408.hp1 HG00673.hp1 HG01074.hp1 others(58): Show |
intron_variant | MODIFIER | c.410+10651G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89920890 | |||||||
| chr14:89920983 | T | G | 1 | a0001c0001t0001g0139 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.410+10558A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89920983 | |||||||
| chr14:89921014 | G | A | 1 | a0001c0001t0007g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.410+10527C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89921014 | |||||||
| chr14:89921063 | T | TAAAAAAA others(2): Show |
24 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0017 others(21): Show |
24 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.410+10469_410+1047 others(13): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89921063 | |||||||
| chr14:89921063 | TA | T | 68 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(65): Show |
68 | HG00408.hp1 HG00673.hp1 HG01074.hp1 others(65): Show |
intron_variant | MODIFIER | c.410+10477delT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89921063 | |||||||
| chr14:89921072 | A | AAAAAAAA others(4): Show |
13 | a0001c0001t0007g0231 a0001c0004t0001g0277 a0001c0004t0001g0278 others(10): Show |
13 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.410+10468_410+1046 others(15): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89921072 | |||||||
| chr14:89921072 | A | AAAAAAAA others(3): Show |
30 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(27): Show |
30 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.410+10468_410+1046 others(14): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89921072 | |||||||
| chr14:89921085 | A | G | 5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0002g0044 others(2): Show |
5 | HG02615.hp2 HG02630.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.410+10456T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89921085 | |||||||
| chr14:89921157 | T | A | 209 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0120 others(206): Show |
209 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.410+10384A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89921157 | |||||||
| chr14:89921316 | G | C | 1 | a0001c0002t0001g0190 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.410+10225C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89921316 | |||||||
| chr14:89921599 | G | A | 1 | a0001c0001t0010g0072 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.410+9942C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89921599 | |||||||
| chr14:89921625 | T | G | 2 | a0001c0009t0002g0273 a0001c0009t0014g0270 |
2 | HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.410+9916A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89921625 | |||||||
| chr14:89921769 | C | T | 140 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(137): Show |
140 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(137): Show |
intron_variant | MODIFIER | c.410+9772G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89921769 | |||||||
| chr14:89922082 | C | T | 3 | a0001c0002t0003g0212 a0001c0002t0003g0213 a0001c0002t0003g0214 |
3 | NA18973.hp1 NA18983.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.410+9459G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89922082 | |||||||
| chr14:89922258 | C | T | 1 | a0001c0001t0007g0123 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.410+9283G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89922258 | |||||||
| chr14:89922440 | A | G | 1 | a0001c0001t0032g0235 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.410+9101T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89922440 | |||||||
| chr14:89922544 | G | C | 1 | a0001c0001t0008g0176 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.410+8997C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89922544 | |||||||
| chr14:89922554 | A | G | 140 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(137): Show |
140 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(137): Show |
intron_variant | MODIFIER | c.410+8987T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89922554 | |||||||
| chr14:89922557 | C | T | 25 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0017 others(22): Show |
25 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.410+8984G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89922557 | |||||||
| chr14:89922562 | G | C | 1 | a0001c0001t0001g0058 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.410+8979C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89922562 | |||||||
| chr14:89922628 | G | T | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+8913C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89922628 | |||||||
| chr14:89922636 | T | C | 8 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0234 others(5): Show |
8 | HG01070.hp1 HG02559.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.410+8905A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89922636 | |||||||
| chr14:89922695 | A | G | 4 | a0001c0002t0001g0228 a0001c0002t0002g0229 a0001c0002t0002g0230 others(1): Show |
4 | HG02451.hp2 HG02809.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.410+8846T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89922695 | |||||||
| chr14:89922895 | A | G | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+8646T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89922895 | |||||||
| chr14:89922927 | T | A | 6 | a0002c0005t0003g0253 a0002c0005t0003g0258 a0002c0005t0007g0251 others(3): Show |
6 | HG00735.hp2 HG01109.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.410+8614A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89922927 | |||||||
| chr14:89923073 | T | C | 2 | a0002c0005t0002g0250 a0002c0005t0004g0249 |
2 | HG02055.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.410+8468A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89923073 | |||||||
| chr14:89923171 | A | G | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+8370T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89923171 | |||||||
| chr14:89923259 | C | T | 140 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(137): Show |
140 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(137): Show |
intron_variant | MODIFIER | c.410+8282G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89923259 | |||||||
| chr14:89923321 | A | G | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+8220T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89923321 | |||||||
| chr14:89923625 | G | C | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+7916C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89923625 | |||||||
| chr14:89923642 | T | C | 3 | a0001c0001t0002g0071 a0001c0001t0010g0072 a0001c0001t0018g0100 |
3 | HG01515.hp2 HG03239.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.410+7899A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89923642 | |||||||
| chr14:89923654 | T | C | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+7887A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89923654 | |||||||
| chr14:89923770 | A | G | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+7771T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89923770 | |||||||
| chr14:89923995 | A | ATTAG | 140 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(137): Show |
140 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(137): Show |
intron_variant | MODIFIER | c.410+7545_410+7546i others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89923995 | |||||||
| chr14:89924033 | T | C | 1 | a0001c0001t0005g0034 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.410+7508A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89924033 | |||||||
| chr14:89924084 | T | C | 25 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0017 others(22): Show |
25 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.410+7457A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89924084 | |||||||
| chr14:89924113 | A | C | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+7428T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89924113 | |||||||
| chr14:89924202 | A | G | 1 | a0001c0001t0007g0234 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.410+7339T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89924202 | |||||||
| chr14:89924212 | T | C | 1 | a0001c0001t0008g0177 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.410+7329A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89924212 | |||||||
| chr14:89924222 | A | G | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+7319T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89924222 | |||||||
| chr14:89924287 | T | C | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+7254A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89924287 | |||||||
| chr14:89924297 | C | T | 20 | a0001c0002t0001g0190 a0001c0002t0002g0116 a0001c0002t0002g0117 others(17): Show |
20 | HG00673.hp1 HG01074.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.410+7244G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89924297 | |||||||
| chr14:89924395 | T | C | 68 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(65): Show |
68 | HG00408.hp1 HG00673.hp1 HG01074.hp1 others(65): Show |
intron_variant | MODIFIER | c.410+7146A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89924395 | |||||||
| chr14:89924455 | T | C | 1 | a0001c0006t0014g0264 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.410+7086A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89924455 | |||||||
| chr14:89924604 | A | G | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+6937T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89924604 | |||||||
| chr14:89924624 | T | A | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+6917A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89924624 | |||||||
| chr14:89924728 | T | G | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+6813A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89924728 | |||||||
| chr14:89924769 | T | C | 1 | a0001c0002t0031g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.410+6772A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89924769 | |||||||
| chr14:89924887 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0006g0149 |
2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.410+6654G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89924887 | |||||||
| chr14:89925251 | T | A | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+6290A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89925251 | |||||||
| chr14:89925295 | G | A | 2 | a0001c0002t0004g0204 a0001c0002t0019g0221 |
2 | HG00408.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.410+6246C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89925295 | |||||||
| chr14:89925516 | T | C | 3 | a0001c0002t0001g0228 a0001c0002t0002g0229 a0001c0002t0002g0230 |
3 | HG02451.hp2 HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.410+6025A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89925516 | |||||||
| chr14:89925542 | A | G | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+5999T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89925542 | |||||||
| chr14:89925648 | C | CT | 41 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(38): Show |
41 | HG00735.hp2 HG01070.hp1 HG01192.hp1 others(38): Show |
intron_variant | MODIFIER | c.410+5892dupA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89925648 | |||||||
| chr14:89925648 | C | CTTTCTT | 25 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0017 others(22): Show |
25 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.410+5892_410+5893i others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89925648 | |||||||
| chr14:89925648 | C | CTTTTTTT | 63 | a0001c0002t0001g0188 a0001c0002t0001g0190 a0001c0002t0001g0196 others(60): Show |
63 | HG00408.hp1 HG00673.hp1 HG01074.hp1 others(60): Show |
intron_variant | MODIFIER | c.410+5886_410+5892d others(9): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89925648 | |||||||
| chr14:89925711 | C | T | 141 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(138): Show |
141 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(138): Show |
intron_variant | MODIFIER | c.410+5830G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89925711 | |||||||
| chr14:89925748 | C | T | 1 | a0001c0006t0014g0264 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.410+5793G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89925748 | |||||||
| chr14:89925786 | C | T | 4 | a0001c0002t0002g0246 a0001c0002t0002g0247 a0001c0002t0003g0248 others(1): Show |
4 | HG02602.hp2 HG02738.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.410+5755G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89925786 | |||||||
| chr14:89925793 | G | T | 1 | a0001c0006t0014g0264 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.410+5748C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89925793 | |||||||
| chr14:89925898 | G | A | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+5643C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89925898 | |||||||
| chr14:89925915 | G | T | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+5626C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89925915 | |||||||
| chr14:89925924 | G | A | 25 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0017 others(22): Show |
25 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.410+5617C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89925924 | |||||||
| chr14:89925950 | T | G | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+5591A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89925950 | |||||||
| chr14:89926170 | T | G | 2 | a0001c0001t0002g0148 a0001c0001t0002g0166 |
2 | HG02698.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.410+5371A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89926170 | |||||||
| chr14:89926222 | T | C | 1 | a0001c0001t0008g0179 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.410+5319A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89926222 | |||||||
| chr14:89926426 | G | A | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+5115C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89926426 | |||||||
| chr14:89926691 | T | C | 1 | a0001c0003t0008g0008 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.410+4850A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89926691 | |||||||
| chr14:89926712 | T | C | 22 | a0001c0001t0002g0114 a0001c0001t0008g0175 a0001c0001t0008g0176 others(19): Show |
22 | HG00735.hp2 HG01109.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.410+4829A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89926712 | |||||||
| chr14:89926793 | A | T | 6 | a0002c0005t0003g0253 a0002c0005t0003g0258 a0002c0005t0007g0251 others(3): Show |
6 | HG00735.hp2 HG01109.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.410+4748T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89926793 | |||||||
| chr14:89926806 | T | C | 1 | a0005c0011t0009g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.410+4735A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89926806 | |||||||
| chr14:89926848 | A | G | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+4693T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89926848 | |||||||
| chr14:89927087 | T | TCAAA | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+4453_410+4454i others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89927087 | |||||||
| chr14:89927178 | T | C | 25 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0017 others(22): Show |
25 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.410+4363A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89927178 | |||||||
| chr14:89927291 | T | C | 12 | a0001c0001t0007g0231 a0001c0004t0001g0277 a0001c0004t0001g0278 others(9): Show |
12 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.410+4250A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89927291 | |||||||
| chr14:89927365 | C | T | 25 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0017 others(22): Show |
25 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.410+4176G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89927365 | |||||||
| chr14:89927454 | G | A | 23 | a0001c0003t0001g0011 a0001c0003t0001g0017 a0001c0003t0001g0023 others(20): Show |
23 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.410+4087C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89927454 | |||||||
| chr14:89927454 | G | T | 2 | a0001c0003t0001g0012 a0001c0003t0016g0009 |
2 | NA18959.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.410+4087C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89927454 | |||||||
| chr14:89927479 | TGC | T | 8 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0234 others(5): Show |
8 | HG01070.hp1 HG02559.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.410+4060_410+4061d others(4): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89927479 | |||||||
| chr14:89927511 | G | A | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+4030C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89927511 | |||||||
| chr14:89927561 | A | G | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+3980T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89927561 | |||||||
| chr14:89927566 | T | C | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+3975A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89927566 | |||||||
| chr14:89927578 | C | A | 22 | a0001c0001t0002g0114 a0001c0001t0008g0175 a0001c0001t0008g0176 others(19): Show |
22 | HG00735.hp2 HG01109.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.410+3963G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89927578 | |||||||
| chr14:89927700 | G | A | 141 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(138): Show |
141 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(138): Show |
intron_variant | MODIFIER | c.410+3841C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89927700 | |||||||
| chr14:89927725 | CT | C | 21 | a0001c0001t0001g0167 a0001c0002t0001g0190 a0001c0002t0002g0116 others(18): Show |
21 | HG00673.hp1 HG01074.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.410+3815delA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89927725 | |||||||
| chr14:89927751 | C | T | 4 | a0001c0004t0009g0271 a0001c0004t0009g0272 a0001c0004t0009g0275 others(1): Show |
4 | HG02109.hp2 HG02486.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+3790G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89927751 | |||||||
| chr14:89927761 | G | A | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0002g0044 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+3780C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89927761 | |||||||
| chr14:89927785 | G | A | 20 | a0001c0002t0001g0190 a0001c0002t0002g0116 a0001c0002t0002g0117 others(17): Show |
20 | HG00673.hp1 HG01074.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.410+3756C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89927785 | |||||||
| chr14:89927866 | C | T | 20 | a0001c0002t0001g0190 a0001c0002t0002g0116 a0001c0002t0002g0117 others(17): Show |
20 | HG00673.hp1 HG01074.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.410+3675G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89927866 | |||||||
| chr14:89927974 | C | T | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+3567G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89927974 | |||||||
| chr14:89928046 | C | T | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+3495G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89928046 | |||||||
| chr14:89928057 | T | C | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+3484A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89928057 | |||||||
| chr14:89928075 | G | A | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+3466C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89928075 | |||||||
| chr14:89928170 | G | A | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+3371C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89928170 | |||||||
| chr14:89928254 | C | T | 1 | a0001c0001t0003g0147 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.410+3287G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89928254 | |||||||
| chr14:89928440 | T | C | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+3101A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89928440 | |||||||
| chr14:89928583 | T | G | 20 | a0001c0002t0001g0190 a0001c0002t0002g0116 a0001c0002t0002g0117 others(17): Show |
20 | HG00673.hp1 HG01074.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.410+2958A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89928583 | |||||||
| chr14:89928639 | T | C | 20 | a0001c0002t0001g0190 a0001c0002t0002g0116 a0001c0002t0002g0117 others(17): Show |
20 | HG00673.hp1 HG01074.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.410+2902A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89928639 | |||||||
| chr14:89928682 | TTA | T | 48 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(45): Show |
48 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.410+2857_410+2858d others(4): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89928682 | |||||||
| chr14:89928746 | TATTA | T | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+2791_410+2794d others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89928746 | |||||||
| chr14:89928797 | TTA | T | 2 | a0001c0002t0003g0198 a0001c0002t0004g0205 |
2 | HG02165.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.410+2742_410+2743d others(4): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89928797 | |||||||
| chr14:89928881 | T | C | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+2660A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89928881 | |||||||
| chr14:89928897 | C | A | 4 | a0001c0002t0001g0168 a0001c0002t0002g0169 a0001c0002t0027g0172 others(1): Show |
4 | HG01891.hp1 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+2644G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89928897 | |||||||
| chr14:89928994 | C | G | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA18968.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.410+2547G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89928994 | |||||||
| chr14:89929030 | C | CATAT | 22 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0017 others(19): Show |
22 | HG00323.hp2 HG01081.hp2 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.410+2507_410+2510d others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929030 | |||||||
| chr14:89929030 | C | CATATAT | 3 | a0001c0003t0003g0013 a0001c0003t0008g0008 a0002c0007t0017g0257 |
3 | HG02976.hp2 HG03130.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.410+2505_410+2510d others(8): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929030 | |||||||
| chr14:89929030 | C | CATATATA others(51): Show |
3 | a0001c0002t0001g0228 a0001c0002t0002g0229 a0001c0002t0002g0230 |
3 | HG02451.hp2 HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.410+2510_410+2511i others(60): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929030 | |||||||
| chr14:89929031 | A | ATATATAT others(24): Show |
1 | a0001c0002t0031g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.410+2509_410+2510i others(33): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929031 | |||||||
| chr14:89929031 | A | ATATATAT others(49): Show |
6 | a0001c0002t0001g0196 a0001c0002t0003g0181 a0001c0002t0003g0217 others(3): Show |
6 | NA18954.hp1 NA18970.hp2 NA18974.hp1 others(3): Show |
intron_variant | MODIFIER | c.410+2509_410+2510i others(58): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929031 | |||||||
| chr14:89929031 | A | ATATATAT others(47): Show |
1 | a0001c0002t0005g0187 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.410+2509_410+2510i others(56): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929031 | |||||||
| chr14:89929031 | A | ATATATAT others(47): Show |
4 | a0001c0002t0003g0189 a0001c0002t0003g0197 a0001c0002t0003g0213 others(1): Show |
4 | HG02132.hp2 NA18952.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+2509_410+2510i others(56): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929031 | |||||||
| chr14:89929031 | A | ATATATAT others(45): Show |
1 | a0001c0002t0003g0212 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.410+2509_410+2510i others(54): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929031 | |||||||
| chr14:89929031 | A | ATATATAT others(18): Show |
5 | a0001c0002t0001g0168 a0001c0002t0002g0169 a0001c0002t0027g0172 others(2): Show |
5 | HG01891.hp1 HG02809.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.410+2509_410+2510i others(27): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929031 | |||||||
| chr14:89929031 | A | ATATATAT others(57): Show |
3 | a0001c0002t0002g0246 a0001c0002t0002g0247 a0001c0002t0003g0248 |
3 | HG02602.hp2 HG02738.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.410+2509_410+2510i others(66): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929031 | |||||||
| chr14:89929031 | A | ATATATAT others(47): Show |
3 | a0001c0002t0001g0215 a0001c0002t0001g0216 a0001c0002t0004g0205 |
3 | HG02165.hp1 NA18942.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.410+2509_410+2510i others(56): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929031 | |||||||
| chr14:89929031 | A | ATATATAT others(45): Show |
9 | a0001c0002t0003g0182 a0001c0002t0003g0198 a0001c0002t0003g0199 others(6): Show |
9 | HG02004.hp1 NA18943.hp1 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.410+2509_410+2510i others(54): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929031 | |||||||
| chr14:89929031 | A | ATATATAT others(43): Show |
1 | a0001c0002t0001g0188 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.410+2509_410+2510i others(52): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929031 | |||||||
| chr14:89929031 | A | ATATATAT others(16): Show |
2 | a0001c0009t0001g0269 a0001c0009t0014g0270 |
2 | HG02257.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.410+2509_410+2510i others(25): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929031 | |||||||
| chr14:89929031 | A | ATATATAT others(53): Show |
1 | a0001c0002t0020g0025 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.410+2509_410+2510i others(62): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929031 | |||||||
| chr14:89929031 | A | ATATATAT others(49): Show |
1 | a0005c0011t0009g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.410+2509_410+2510i others(58): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929031 | |||||||
| chr14:89929031 | A | ATATATAT others(43): Show |
3 | a0001c0002t0004g0203 a0001c0002t0004g0204 a0001c0002t0019g0221 |
3 | HG00408.hp1 HG02027.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.410+2509_410+2510i others(52): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929031 | |||||||
| chr14:89929031 | A | ATATATAT others(41): Show |
1 | a0001c0002t0004g0195 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.410+2509_410+2510i others(50): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929031 | |||||||
| chr14:89929031 | A | ATATATAT others(14): Show |
3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+2509_410+2510i others(23): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929031 | |||||||
| chr14:89929031 | A | ATATATAT others(23): Show |
20 | a0001c0002t0001g0190 a0001c0002t0002g0116 a0001c0002t0002g0117 others(17): Show |
20 | HG00673.hp1 HG01074.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.410+2509_410+2510i others(32): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929031 | |||||||
| chr14:89929046 | C | T | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+2495G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929046 | |||||||
| chr14:89929048 | C | T | 73 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0196 others(70): Show |
73 | HG00323.hp2 HG00408.hp1 HG01081.hp2 others(70): Show |
intron_variant | MODIFIER | c.410+2493G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929048 | |||||||
| chr14:89929061 | T | G | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+2480A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929061 | |||||||
| chr14:89929068 | G | A | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+2473C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929068 | |||||||
| chr14:89929069 | G | GAGAT | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+2471_410+2472i others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929069 | |||||||
| chr14:89929171 | C | A | 2 | a0001c0001t0013g0028 a0001c0001t0013g0106 |
2 | HG01168.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.410+2370G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929171 | |||||||
| chr14:89929250 | C | A | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+2291G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929250 | |||||||
| chr14:89929366 | T | A | 1 | a0003c0008t0001g0266 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.410+2175A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929366 | |||||||
| chr14:89929403 | T | A | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+2138A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929403 | |||||||
| chr14:89929463 | A | T | 141 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(138): Show |
141 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(138): Show |
intron_variant | MODIFIER | c.410+2078T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929463 | |||||||
| chr14:89929840 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.410+1701T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929840 | |||||||
| chr14:89929882 | A | T | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+1659T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929882 | |||||||
| chr14:89929960 | G | T | 141 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0114 others(138): Show |
141 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(138): Show |
intron_variant | MODIFIER | c.410+1581C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89929960 | |||||||
| chr14:89930206 | T | C | 1 | a0002c0007t0017g0257 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.410+1335A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89930206 | |||||||
| chr14:89930230 | T | A | 61 | a0001c0001t0001g0120 a0001c0001t0001g0125 a0001c0001t0001g0127 others(58): Show |
61 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.410+1311A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89930230 | |||||||
| chr14:89930247 | G | A | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+1294C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89930247 | |||||||
| chr14:89930320 | TAA | T | 4 | a0001c0001t0002g0029 a0001c0001t0002g0030 a0001c0001t0002g0148 others(1): Show |
4 | HG01261.hp1 HG01934.hp1 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.410+1219_410+1220d others(4): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89930320 | |||||||
| chr14:89930471 | T | C | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+1070A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89930471 | |||||||
| chr14:89930479 | A | G | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+1062T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89930479 | |||||||
| chr14:89930527 | TA | T | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+1013delT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89930527 | |||||||
| chr14:89930814 | G | A | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+727C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89930814 | |||||||
| chr14:89931003 | T | C | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+538A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89931003 | |||||||
| chr14:89931060 | C | A | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+481G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89931060 | |||||||
| chr14:89931101 | G | A | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+440C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89931101 | |||||||
| chr14:89931137 | A | C | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+404T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89931137 | |||||||
| chr14:89931163 | T | C | 1 | a0001c0002t0010g0209 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.410+378A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89931163 | |||||||
| chr14:89931246 | G | A | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.410+295C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89931246 | |||||||
| chr14:89931283 | C | T | 1 | a0001c0001t0002g0154 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.410+258G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89931283 | |||||||
| chr14:89931287 | C | T | 1 | a0001c0001t0001g0067 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.410+254G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89931287 | |||||||
| chr14:89931331 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.410+210C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89931331 | |||||||
| chr14:89931374 | C | A | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.410+167G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89931374 | |||||||
| chr14:89931374 | C | T | 90 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(87): Show |
90 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.410+167G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89931374 | |||||||
| chr14:89931454 | T | A | 1 | a0001c0001t0005g0035 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.410+87A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 5/5 | chr14 | 89931454 | |||||||
| chr14:89931643 | C | T | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.320-12G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 4/5 | chr14 | 89931643 | |||||||
| chr14:89931649 | A | G | 4 | a0001c0002t0001g0168 a0001c0002t0002g0169 a0001c0002t0027g0172 others(1): Show |
4 | HG01891.hp1 HG02809.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.320-18T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 4/5 | chr14 | 89931649 | |||||||
| chr14:89931929 | C | T | 11 | a0001c0004t0001g0277 a0001c0004t0001g0278 a0001c0004t0002g0276 others(8): Show |
11 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.320-298G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 4/5 | chr14 | 89931929 | |||||||
| chr14:89932020 | ATATTGC | A | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.320-395_320-390del others(6): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 4/5 | chr14 | 89932020 | |||||||
| chr14:89932196 | A | G | 13 | a0001c0001t0007g0231 a0001c0001t0014g0240 a0001c0004t0001g0277 others(10): Show |
13 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.319+330T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 4/5 | chr14 | 89932196 | |||||||
| chr14:89932198 | T | C | 1 | a0001c0001t0003g0147 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.319+328A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 4/5 | chr14 | 89932198 | |||||||
| chr14:89932319 | T | C | 11 | a0001c0001t0001g0150 a0001c0001t0002g0029 a0001c0001t0002g0030 others(8): Show |
11 | HG01109.hp2 HG01255.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.319+207A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 4/5 | chr14 | 89932319 | |||||||
| chr14:89932339 | T | C | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.319+187A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 4/5 | chr14 | 89932339 | |||||||
| chr14:89932367 | G | A | 1 | a0001c0001t0005g0115 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.319+159C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 4/5 | chr14 | 89932367 | |||||||
| chr14:89932489 | A | C | 1 | a0001c0001t0001g0096 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.319+37T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 4/5 | chr14 | 89932489 | |||||||
| chr14:89932490 | A | AT | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.319+35dupA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 4/5 | chr14 | 89932490 | |||||||
| chr14:89932714 | T | C | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.218-87A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89932714 | |||||||
| chr14:89932758 | A | T | 1 | a0001c0001t0002g0031 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.218-131T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89932758 | |||||||
| chr14:89932825 | T | C | 93 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(90): Show |
93 | HG00323.hp2 HG00408.hp1 HG00673.hp1 others(90): Show |
intron_variant | MODIFIER | c.218-198A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89932825 | |||||||
| chr14:89933184 | G | A | 4 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0001c0001t0002g0159 others(1): Show |
4 | HG01515.hp1 HG03491.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.218-557C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89933184 | |||||||
| chr14:89933190 | A | T | 1 | a0001c0001t0003g0075 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.218-563T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89933190 | |||||||
| chr14:89933224 | C | A | 52 | a0001c0002t0001g0168 a0001c0002t0001g0190 a0001c0002t0002g0116 others(49): Show |
52 | HG00323.hp2 HG00673.hp1 HG01074.hp1 others(49): Show |
intron_variant | MODIFIER | c.218-597G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89933224 | |||||||
| chr14:89933377 | T | C | 103 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(100): Show |
103 | HG00323.hp2 HG00408.hp1 HG01074.hp1 others(100): Show |
intron_variant | MODIFIER | c.218-750A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89933377 | |||||||
| chr14:89933389 | A | G | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.218-762T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89933389 | |||||||
| chr14:89933419 | A | ACT | 103 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(100): Show |
103 | HG00323.hp2 HG00408.hp1 HG01074.hp1 others(100): Show |
intron_variant | MODIFIER | c.218-794_218-793dup others(2): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89933419 | |||||||
| chr14:89933442 | A | T | 103 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(100): Show |
103 | HG00323.hp2 HG00408.hp1 HG01074.hp1 others(100): Show |
intron_variant | MODIFIER | c.218-815T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89933442 | |||||||
| chr14:89933528 | A | G | 103 | a0001c0002t0001g0168 a0001c0002t0001g0188 a0001c0002t0001g0190 others(100): Show |
103 | HG00323.hp2 HG00408.hp1 HG01074.hp1 others(100): Show |
intron_variant | MODIFIER | c.218-901T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89933528 | |||||||
| chr14:89933748 | G | A | 25 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(22): Show |
25 | HG00735.hp2 HG01192.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.218-1121C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89933748 | |||||||
| chr14:89933755 | T | C | 1 | a0001c0001t0014g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.218-1128A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89933755 | |||||||
| chr14:89933763 | C | T | 3 | a0001c0003t0004g0005 a0001c0003t0012g0016 a0001c0003t0025g0006 |
3 | HG02258.hp1 HG02897.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.218-1136G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89933763 | |||||||
| chr14:89933975 | G | A | 3 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0004g0097 |
3 | HG02280.hp1 HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.218-1348C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89933975 | |||||||
| chr14:89933983 | T | C | 10 | a0001c0004t0006g0284 a0001c0004t0020g0283 a0002c0005t0002g0250 others(7): Show |
10 | HG00735.hp2 HG02055.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.218-1356A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89933983 | |||||||
| chr14:89933985 | T | G | 10 | a0001c0004t0006g0284 a0001c0004t0020g0283 a0002c0005t0002g0250 others(7): Show |
10 | HG00735.hp2 HG02055.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.218-1358A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89933985 | |||||||
| chr14:89934082 | C | T | 49 | a0001c0001t0001g0074 a0001c0001t0001g0242 a0001c0001t0004g0073 others(46): Show |
49 | HG00408.hp1 HG01074.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.218-1455G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89934082 | |||||||
| chr14:89934109 | C | A | 2 | a0002c0005t0002g0250 a0002c0005t0004g0249 |
2 | HG02055.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.218-1482G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89934109 | |||||||
| chr14:89934153 | CAGA | C | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.218-1529_218-1527d others(5): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89934153 | |||||||
| chr14:89934199 | C | T | 48 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0234 others(45): Show |
48 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.218-1572G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89934199 | |||||||
| chr14:89934431 | T | G | 3 | a0001c0002t0001g0228 a0001c0002t0002g0229 a0001c0002t0002g0230 |
3 | HG02451.hp2 HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.218-1804A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89934431 | |||||||
| chr14:89934445 | A | G | 52 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0231 others(49): Show |
52 | HG00735.hp2 HG01070.hp1 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.218-1818T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89934445 | |||||||
| chr14:89934552 | G | A | 6 | a0001c0001t0008g0175 a0001c0001t0008g0176 a0001c0001t0008g0177 others(3): Show |
6 | HG01192.hp1 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.218-1925C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89934552 | |||||||
| chr14:89934632 | AATTAGCA others(1): Show |
A | 3 | a0001c0002t0001g0168 a0001c0002t0002g0169 a0001c0002t0027g0172 |
3 | HG01891.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.218-2013_218-2006d others(10): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89934632 | |||||||
| chr14:89934648 | A | AT | 52 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0231 others(49): Show |
52 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.218-2022dupA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89934648 | |||||||
| chr14:89934659 | T | C | 1 | a0001c0004t0002g0279 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.218-2032A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89934659 | |||||||
| chr14:89934769 | C | T | 52 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0231 others(49): Show |
52 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(49): Show |
intron_variant | MODIFIER | c.218-2142G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89934769 | |||||||
| chr14:89935058 | G | T | 44 | a0001c0001t0007g0231 a0001c0003t0001g0011 a0001c0003t0001g0012 others(41): Show |
44 | HG00323.hp2 HG00735.hp2 HG01081.hp2 others(41): Show |
intron_variant | MODIFIER | c.218-2431C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89935058 | |||||||
| chr14:89935145 | G | T | 21 | a0001c0001t0007g0231 a0001c0006t0004g0265 a0001c0006t0006g0263 others(18): Show |
21 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.218-2518C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89935145 | |||||||
| chr14:89935349 | C | CAAG | 21 | a0001c0001t0007g0231 a0001c0006t0004g0265 a0001c0006t0006g0263 others(18): Show |
21 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.218-2725_218-2723d others(5): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89935349 | |||||||
| chr14:89935391 | A | T | 3 | a0001c0001t0001g0120 a0001c0001t0005g0119 a0001c0001t0005g0121 |
3 | HG01496.hp2 NA18952.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.218-2764T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89935391 | |||||||
| chr14:89935397 | G | GT | 59 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0070 others(56): Show |
59 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.218-2771dupA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89935397 | |||||||
| chr14:89935397 | GT | G | 117 | a0001c0001t0001g0096 a0001c0001t0001g0098 a0001c0001t0001g0232 others(114): Show |
117 | HG00323.hp2 HG00408.hp1 HG00735.hp2 others(114): Show |
intron_variant | MODIFIER | c.218-2771delA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89935397 | |||||||
| chr14:89935451 | G | A | 2 | a0001c0004t0006g0284 a0001c0004t0020g0283 |
2 | HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.218-2824C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89935451 | |||||||
| chr14:89935544 | C | T | 37 | a0001c0001t0007g0231 a0001c0004t0001g0277 a0001c0004t0001g0278 others(34): Show |
37 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.218-2917G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89935544 | |||||||
| chr14:89935595 | G | C | 21 | a0001c0001t0007g0231 a0001c0006t0004g0265 a0001c0006t0006g0263 others(18): Show |
21 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.218-2968C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89935595 | |||||||
| chr14:89935601 | A | G | 21 | a0001c0001t0007g0231 a0001c0006t0004g0265 a0001c0006t0006g0263 others(18): Show |
21 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.218-2974T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89935601 | |||||||
| chr14:89935684 | G | A | 21 | a0001c0001t0007g0231 a0001c0006t0004g0265 a0001c0006t0006g0263 others(18): Show |
21 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.218-3057C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89935684 | |||||||
| chr14:89935758 | C | T | 1 | a0001c0001t0014g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.218-3131G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89935758 | |||||||
| chr14:89935873 | C | T | 2 | a0001c0004t0006g0284 a0001c0004t0020g0283 |
2 | HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.218-3246G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89935873 | |||||||
| chr14:89935874 | G | A | 23 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0017 others(20): Show |
23 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.218-3247C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89935874 | |||||||
| chr14:89935966 | C | T | 1 | a0001c0001t0013g0112 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.218-3339G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89935966 | |||||||
| chr14:89936016 | A | T | 20 | a0001c0006t0004g0265 a0001c0006t0006g0263 a0001c0006t0009g0262 others(17): Show |
20 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.218-3389T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89936016 | |||||||
| chr14:89936026 | A | C | 22 | a0001c0003t0001g0012 a0001c0003t0001g0017 a0001c0003t0001g0023 others(19): Show |
22 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.218-3399T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89936026 | |||||||
| chr14:89936085 | CT | C | 21 | a0001c0001t0007g0231 a0001c0006t0004g0265 a0001c0006t0006g0263 others(18): Show |
21 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.218-3459delA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89936085 | |||||||
| chr14:89936088 | T | G | 1 | a0001c0001t0001g0046 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.218-3461A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89936088 | |||||||
| chr14:89936362 | TTTATTTT others(76): Show |
T | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-3818_218-3736d others(85): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89936362 | |||||||
| chr14:89936467 | C | T | 3 | a0001c0002t0002g0116 a0001c0002t0002g0117 a0001c0002t0040g0118 |
3 | HG01358.hp2 HG03017.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.218-3840G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89936467 | |||||||
| chr14:89936492 | G | C | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-3865C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89936492 | |||||||
| chr14:89936523 | T | A | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-3896A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89936523 | |||||||
| chr14:89936531 | A | G | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-3904T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89936531 | |||||||
| chr14:89936644 | C | T | 1 | a0001c0002t0004g0193 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.218-4017G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89936644 | |||||||
| chr14:89936658 | A | T | 1 | a0001c0001t0013g0106 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.218-4031T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89936658 | |||||||
| chr14:89936666 | G | C | 2 | a0003c0008t0001g0268 a0003c0008t0026g0267 |
2 | HG01891.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.218-4039C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89936666 | |||||||
| chr14:89936825 | T | A | 3 | a0001c0002t0001g0168 a0001c0002t0002g0169 a0001c0002t0027g0172 |
3 | HG01891.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.218-4198A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89936825 | |||||||
| chr14:89936946 | A | G | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-4319T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89936946 | |||||||
| chr14:89936975 | C | T | 1 | a0001c0002t0004g0223 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.218-4348G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89936975 | |||||||
| chr14:89937080 | C | T | 272 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(269): Show |
272 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.218-4453G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89937080 | |||||||
| chr14:89937126 | T | G | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-4499A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89937126 | |||||||
| chr14:89937134 | T | A | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-4507A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89937134 | |||||||
| chr14:89937143 | A | G | 27 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0231 others(24): Show |
27 | HG00735.hp2 HG01070.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.218-4516T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89937143 | |||||||
| chr14:89937163 | A | G | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-4536T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89937163 | |||||||
| chr14:89937164 | G | A | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-4537C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89937164 | |||||||
| chr14:89937218 | T | C | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-4591A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89937218 | |||||||
| chr14:89937219 | C | T | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-4592G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89937219 | |||||||
| chr14:89937220 | T | C | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-4593A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89937220 | |||||||
| chr14:89937256 | A | C | 1 | a0001c0001t0034g0066 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.218-4629T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89937256 | |||||||
| chr14:89937256 | A | G | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-4629T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89937256 | |||||||
| chr14:89937259 | T | A | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-4632A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89937259 | |||||||
| chr14:89937260 | G | T | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-4633C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89937260 | |||||||
| chr14:89937375 | T | C | 1 | a0001c0001t0003g0164 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.218-4748A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89937375 | |||||||
| chr14:89937387 | G | T | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-4760C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89937387 | |||||||
| chr14:89937409 | G | C | 6 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0234 others(3): Show |
6 | HG01070.hp1 HG02559.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.218-4782C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89937409 | |||||||
| chr14:89937629 | G | A | 27 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0231 others(24): Show |
27 | HG00735.hp2 HG01070.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.218-5002C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89937629 | |||||||
| chr14:89937658 | T | C | 1 | a0002c0007t0017g0257 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.218-5031A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89937658 | |||||||
| chr14:89937833 | A | C | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-5206T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89937833 | |||||||
| chr14:89937835 | A | T | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-5208T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89937835 | |||||||
| chr14:89937840 | T | A | 23 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0017 others(20): Show |
23 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.218-5213A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89937840 | |||||||
| chr14:89937862 | C | CATGTATA others(14): Show |
1 | a0001c0001t0005g0115 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.218-5256_218-5236d others(23): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89937862 | |||||||
| chr14:89937893 | T | G | 3 | a0001c0002t0003g0212 a0001c0002t0003g0213 a0001c0002t0003g0214 |
3 | NA18973.hp1 NA18983.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.218-5266A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89937893 | |||||||
| chr14:89937895 | G | T | 37 | a0001c0001t0001g0045 a0001c0001t0002g0044 a0001c0001t0004g0170 others(34): Show |
37 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.218-5268C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89937895 | |||||||
| chr14:89937897 | G | T | 1 | a0001c0006t0014g0264 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.218-5270C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89937897 | |||||||
| chr14:89937945 | C | A | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-5318G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89937945 | |||||||
| chr14:89938117 | A | T | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-5490T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89938117 | |||||||
| chr14:89938149 | C | A | 27 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0231 others(24): Show |
27 | HG00735.hp2 HG01070.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.218-5522G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89938149 | |||||||
| chr14:89938201 | G | A | 27 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0231 others(24): Show |
27 | HG00735.hp2 HG01070.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.218-5574C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89938201 | |||||||
| chr14:89938213 | G | A | 1 | a0001c0001t0015g0099 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.218-5586C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89938213 | |||||||
| chr14:89938323 | G | C | 3 | a0001c0001t0001g0045 a0001c0001t0002g0044 a0001c0001t0030g0043 |
3 | HG02615.hp2 HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.218-5696C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89938323 | |||||||
| chr14:89938372 | A | T | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-5745T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89938372 | |||||||
| chr14:89938452 | C | T | 58 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0004g0170 others(55): Show |
58 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.218-5825G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89938452 | |||||||
| chr14:89938605 | T | C | 3 | a0001c0001t0001g0045 a0001c0001t0002g0044 a0001c0001t0030g0043 |
3 | HG02615.hp2 HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.218-5978A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89938605 | |||||||
| chr14:89938711 | C | G | 3 | a0001c0002t0003g0191 a0001c0002t0024g0192 a0001c0002t0042g0227 |
3 | HG03017.hp2 HG03669.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.218-6084G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89938711 | |||||||
| chr14:89938769 | A | G | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-6142T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89938769 | |||||||
| chr14:89938806 | C | G | 1 | a0001c0002t0003g0065 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.218-6179G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89938806 | |||||||
| chr14:89938816 | A | G | 29 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0231 others(26): Show |
29 | HG00735.hp2 HG01070.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.218-6189T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89938816 | |||||||
| chr14:89938841 | T | C | 8 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0234 others(5): Show |
8 | HG01070.hp1 HG02559.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.218-6214A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89938841 | |||||||
| chr14:89938882 | T | A | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-6255A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89938882 | |||||||
| chr14:89938886 | C | A | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-6259G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89938886 | |||||||
| chr14:89938888 | A | C | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-6261T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89938888 | |||||||
| chr14:89938889 | A | T | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-6262T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89938889 | |||||||
| chr14:89938893 | C | T | 1 | a0001c0004t0023g0274 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.218-6266G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89938893 | |||||||
| chr14:89938896 | G | T | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-6269C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89938896 | |||||||
| chr14:89938919 | A | G | 1 | a0001c0002t0003g0065 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.218-6292T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89938919 | |||||||
| chr14:89938961 | A | T | 27 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0231 others(24): Show |
27 | HG00735.hp2 HG01070.hp1 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.218-6334T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89938961 | |||||||
| chr14:89938971 | C | CA | 21 | a0001c0001t0001g0102 a0001c0001t0003g0101 a0001c0001t0003g0104 others(18): Show |
21 | HG01192.hp1 HG01346.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.218-6345dupT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89938971 | |||||||
| chr14:89938971 | CA | C | 47 | a0001c0001t0006g0063 a0001c0001t0010g0236 a0001c0001t0010g0237 others(44): Show |
47 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.218-6345delT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89938971 | |||||||
| chr14:89938971 | CAA | C | 12 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(9): Show |
12 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.218-6346_218-6345d others(4): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89938971 | |||||||
| chr14:89938998 | G | C | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.218-6371C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89938998 | |||||||
| chr14:89939028 | C | T | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-6401G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89939028 | |||||||
| chr14:89939029 | T | C | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-6402A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89939029 | |||||||
| chr14:89939074 | C | T | 58 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0004g0170 others(55): Show |
58 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(55): Show |
intron_variant | MODIFIER | c.218-6447G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89939074 | |||||||
| chr14:89939101 | G | C | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-6474C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89939101 | |||||||
| chr14:89939103 | T | G | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-6476A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89939103 | |||||||
| chr14:89939105 | C | T | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-6478G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89939105 | |||||||
| chr14:89939211 | C | T | 4 | a0001c0001t0001g0060 a0001c0001t0003g0059 a0001c0001t0003g0061 others(1): Show |
4 | NA18986.hp2 NA18989.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.218-6584G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89939211 | |||||||
| chr14:89939250 | T | C | 20 | a0001c0006t0004g0265 a0001c0006t0006g0263 a0001c0006t0009g0262 others(17): Show |
20 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.218-6623A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89939250 | |||||||
| chr14:89939262 | T | C | 1 | a0002c0005t0003g0258 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.218-6635A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89939262 | |||||||
| chr14:89939277 | T | A | 1 | a0001c0003t0002g0004 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.218-6650A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89939277 | |||||||
| chr14:89939277 | T | TA | 100 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(97): Show |
100 | HG00323.hp2 HG00408.hp1 HG01074.hp1 others(97): Show |
intron_variant | MODIFIER | c.218-6651dupT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89939277 | |||||||
| chr14:89939357 | T | C | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.218-6730A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89939357 | |||||||
| chr14:89939442 | G | A | 1 | a0001c0002t0031g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.218-6815C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89939442 | |||||||
| chr14:89939502 | G | A | 1 | a0001c0002t0041g0226 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.218-6875C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89939502 | |||||||
| chr14:89939547 | C | T | 19 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0017 others(16): Show |
19 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.218-6920G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89939547 | |||||||
| chr14:89939655 | T | A | 1 | a0001c0001t0003g0147 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.218-7028A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89939655 | |||||||
| chr14:89939658 | T | G | 209 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0120 others(206): Show |
209 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.218-7031A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89939658 | |||||||
| chr14:89939697 | G | A | 1 | a0001c0006t0014g0264 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.218-7070C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89939697 | |||||||
| chr14:89939808 | A | G | 28 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0231 others(25): Show |
28 | HG00735.hp2 HG01070.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.218-7181T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89939808 | |||||||
| chr14:89939973 | G | A | 1 | a0001c0004t0017g0281 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.218-7346C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89939973 | |||||||
| chr14:89939989 | G | A | 23 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0017 others(20): Show |
23 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.218-7362C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89939989 | |||||||
| chr14:89940027 | G | A | 2 | a0001c0009t0002g0273 a0001c0009t0014g0270 |
2 | HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.218-7400C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89940027 | |||||||
| chr14:89940309 | C | T | 272 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0058 others(269): Show |
272 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.218-7682G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89940309 | |||||||
| chr14:89940326 | G | A | 1 | a0001c0001t0013g0112 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.218-7699C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89940326 | |||||||
| chr14:89940535 | A | T | 1 | a0001c0002t0031g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.218-7908T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89940535 | |||||||
| chr14:89940573 | T | C | 1 | a0001c0001t0005g0113 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.218-7946A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89940573 | |||||||
| chr14:89940803 | A | G | 28 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0231 others(25): Show |
28 | HG00735.hp2 HG01070.hp1 HG01081.hp2 others(25): Show |
intron_variant | MODIFIER | c.218-8176T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89940803 | |||||||
| chr14:89940978 | C | T | 47 | a0001c0002t0001g0188 a0001c0002t0001g0190 a0001c0002t0001g0196 others(44): Show |
47 | HG00408.hp1 HG01074.hp1 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.218-8351G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89940978 | |||||||
| chr14:89941027 | T | C | 26 | a0001c0001t0002g0154 a0001c0001t0002g0155 a0001c0001t0002g0156 others(23): Show |
26 | HG00323.hp1 HG00323.hp2 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.218-8400A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89941027 | |||||||
| chr14:89941062 | A | T | 1 | a0001c0009t0014g0270 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.218-8435T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89941062 | |||||||
| chr14:89941163 | T | C | 4 | a0001c0002t0001g0228 a0001c0002t0002g0229 a0001c0002t0002g0230 others(1): Show |
4 | HG02451.hp2 HG02809.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.218-8536A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89941163 | |||||||
| chr14:89941337 | C | T | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.218-8710G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89941337 | |||||||
| chr14:89941475 | G | A | 209 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0120 others(206): Show |
209 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.217+8622C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89941475 | |||||||
| chr14:89941574 | C | A | 1 | a0001c0003t0016g0024 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.217+8523G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89941574 | |||||||
| chr14:89941575 | T | C | 1 | a0001c0003t0016g0024 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.217+8522A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89941575 | |||||||
| chr14:89941584 | C | CT | 69 | a0001c0001t0001g0058 a0001c0001t0001g0232 a0001c0001t0001g0233 others(66): Show |
69 | HG00408.hp1 HG00735.hp2 HG01070.hp1 others(66): Show |
intron_variant | MODIFIER | c.217+8512dupA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89941584 | |||||||
| chr14:89941584 | CT | C | 30 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(27): Show |
30 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.217+8512delA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89941584 | |||||||
| chr14:89941681 | G | A | 1 | a0002c0005t0029g0260 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.217+8416C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89941681 | |||||||
| chr14:89941995 | T | C | 64 | a0001c0001t0001g0120 a0001c0001t0001g0125 a0001c0001t0001g0127 others(61): Show |
64 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.217+8102A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89941995 | |||||||
| chr14:89942311 | T | C | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.217+7786A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89942311 | |||||||
| chr14:89942411 | T | C | 2 | a0001c0001t0001g0045 a0001c0001t0002g0044 |
2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.217+7686A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89942411 | |||||||
| chr14:89942580 | G | C | 7 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(4): Show |
7 | HG01884.hp2 HG01891.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.217+7517C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89942580 | |||||||
| chr14:89942581 | G | A | 1 | a0001c0003t0012g0016 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.217+7516C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89942581 | |||||||
| chr14:89942666 | A | G | 1 | a0005c0011t0009g0245 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.217+7431T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89942666 | |||||||
| chr14:89942870 | G | C | 1 | a0001c0002t0002g0246 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.217+7227C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89942870 | |||||||
| chr14:89943135 | C | A | 1 | a0001c0002t0042g0227 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.217+6962G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89943135 | |||||||
| chr14:89943213 | G | C | 1 | a0001c0004t0020g0283 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.217+6884C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89943213 | |||||||
| chr14:89943232 | C | T | 5 | a0001c0001t0003g0057 a0001c0001t0004g0054 a0001c0001t0005g0055 others(2): Show |
5 | HG00673.hp2 HG02027.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.217+6865G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89943232 | |||||||
| chr14:89943247 | G | GT | 9 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(6): Show |
9 | HG01884.hp2 HG01891.hp1 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.217+6849dupA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89943247 | |||||||
| chr14:89943247 | G | GTT | 22 | a0001c0003t0001g0011 a0001c0003t0001g0017 a0001c0003t0001g0023 others(19): Show |
22 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.217+6848_217+6849d others(4): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89943247 | |||||||
| chr14:89943271 | G | C | 20 | a0001c0006t0004g0265 a0001c0006t0006g0263 a0001c0006t0009g0262 others(17): Show |
20 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.217+6826C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89943271 | |||||||
| chr14:89943656 | C | T | 3 | a0001c0003t0004g0019 a0001c0003t0008g0020 a0001c0003t0037g0018 |
3 | HG02572.hp1 HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.217+6441G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89943656 | |||||||
| chr14:89943828 | A | AAC | 3 | a0001c0001t0002g0039 a0004c0010t0004g0040 a0004c0010t0004g0041 |
3 | HG01884.hp1 HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.217+6267_217+6268d others(4): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89943828 | |||||||
| chr14:89943894 | G | T | 1 | a0001c0001t0002g0039 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.217+6203C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89943894 | |||||||
| chr14:89943899 | T | C | 1 | a0001c0003t0001g0017 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.217+6198A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89943899 | |||||||
| chr14:89944100 | C | T | 60 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0004g0170 others(57): Show |
60 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.217+5997G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89944100 | |||||||
| chr14:89944155 | G | A | 1 | a0001c0001t0010g0237 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.217+5942C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89944155 | |||||||
| chr14:89944230 | A | G | 6 | a0001c0001t0008g0175 a0001c0001t0008g0176 a0001c0001t0008g0177 others(3): Show |
6 | HG01192.hp1 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.217+5867T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89944230 | |||||||
| chr14:89944309 | A | T | 47 | a0001c0002t0001g0188 a0001c0002t0001g0190 a0001c0002t0001g0196 others(44): Show |
47 | HG00408.hp1 HG01074.hp1 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.217+5788T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89944309 | |||||||
| chr14:89944513 | T | C | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.217+5584A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89944513 | |||||||
| chr14:89944573 | T | C | 1 | a0001c0001t0014g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.217+5524A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89944573 | |||||||
| chr14:89944770 | T | C | 30 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0231 others(27): Show |
30 | HG00735.hp2 HG01070.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.217+5327A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89944770 | |||||||
| chr14:89944856 | T | TTAATAAA others(32): Show |
26 | a0001c0001t0001g0150 a0001c0001t0002g0029 a0001c0001t0002g0030 others(23): Show |
26 | HG00735.hp2 HG01109.hp2 HG01255.hp2 others(23): Show |
intron_variant | MODIFIER | c.217+5202_217+5240d others(41): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89944856 | |||||||
| chr14:89944856 | T | TTAATAAA others(71): Show |
1 | a0003c0008t0001g0268 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.217+5240_217+5241i others(80): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89944856 | |||||||
| chr14:89944856 | T | TTAATAAA others(71): Show |
17 | a0001c0001t0008g0239 a0001c0001t0012g0238 a0001c0001t0014g0240 others(14): Show |
17 | HG01081.hp2 HG01109.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.217+5163_217+5240d others(80): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89944856 | |||||||
| chr14:89944856 | TTAATAAA others(32): Show |
T | 8 | a0001c0001t0005g0053 a0001c0001t0008g0175 a0001c0001t0008g0176 others(5): Show |
8 | HG01192.hp1 HG02273.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.217+5202_217+5240d others(41): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89944856 | |||||||
| chr14:89944909 | A | ATTAGATT others(22): Show |
1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.217+5187_217+5188i others(31): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89944909 | |||||||
| chr14:89944910 | A | T | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.217+5187T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89944910 | |||||||
| chr14:89944931 | CTAA | C | 3 | a0001c0002t0001g0168 a0001c0002t0002g0169 a0001c0002t0027g0172 |
3 | HG01891.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.217+5163_217+5165d others(5): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89944931 | |||||||
| chr14:89944936 | AAT | A | 10 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(7): Show |
10 | HG01884.hp2 HG02976.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.217+5159_217+5160d others(4): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89944936 | |||||||
| chr14:89944936 | AATAAATC others(34): Show |
A | 2 | a0001c0003t0001g0017 a0001c0003t0002g0004 |
2 | HG01433.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.217+5120_217+5160d others(43): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89944936 | |||||||
| chr14:89944952 | T | C | 3 | a0001c0003t0003g0013 a0001c0003t0003g0014 a0001c0003t0003g0015 |
3 | HG03710.hp2 HG03834.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.217+5145A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89944952 | |||||||
| chr14:89944958 | AT | A | 6 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(3): Show |
6 | HG01884.hp2 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.217+5138delA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89944958 | |||||||
| chr14:89944970 | CTAA | C | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.217+5124_217+5126d others(5): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89944970 | |||||||
| chr14:89944970 | CTAATAAT others(35): Show |
C | 3 | a0001c0002t0001g0168 a0001c0002t0002g0169 a0001c0002t0027g0172 |
3 | HG01891.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.217+5085_217+5126d others(44): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89944970 | |||||||
| chr14:89944975 | AAT | A | 18 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0023 others(15): Show |
18 | HG02258.hp1 HG02451.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.217+5120_217+5121d others(4): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89944975 | |||||||
| chr14:89944976 | A | AAATCTAA others(67): Show |
3 | a0001c0003t0002g0021 a0001c0003t0021g0002 a0001c0003t0021g0003 |
3 | HG00323.hp2 HG01168.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.217+5120_217+5121i others(76): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89944976 | |||||||
| chr14:89944977 | T | A | 3 | a0001c0003t0002g0021 a0001c0003t0021g0002 a0001c0003t0021g0003 |
3 | HG00323.hp2 HG01168.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.217+5120A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89944977 | |||||||
| chr14:89945009 | CTAA | C | 4 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(1): Show |
4 | HG01884.hp2 HG02976.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.217+5085_217+5087d others(5): Show |
EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89945009 | |||||||
| chr14:89945112 | T | C | 29 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(26): Show |
29 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.217+4985A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89945112 | |||||||
| chr14:89945118 | C | T | 30 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0231 others(27): Show |
30 | HG00735.hp2 HG01070.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.217+4979G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89945118 | |||||||
| chr14:89945250 | A | G | 1 | a0001c0001t0004g0160 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.217+4847T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89945250 | |||||||
| chr14:89945259 | G | A | 1 | a0001c0001t0011g0153 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.217+4838C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89945259 | |||||||
| chr14:89945357 | A | G | 1 | a0001c0002t0003g0189 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.217+4740T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89945357 | |||||||
| chr14:89945437 | A | G | 2 | a0001c0003t0004g0019 a0001c0003t0037g0018 |
2 | HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.217+4660T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89945437 | |||||||
| chr14:89945629 | T | C | 2 | a0001c0004t0006g0284 a0001c0004t0020g0283 |
2 | HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.217+4468A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89945629 | |||||||
| chr14:89945912 | A | AT | 11 | a0001c0001t0001g0046 a0001c0001t0002g0051 a0001c0001t0002g0162 others(8): Show |
11 | HG01081.hp1 HG01515.hp1 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.217+4184dupA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89945912 | |||||||
| chr14:89945919 | T | C | 3 | a0001c0002t0001g0228 a0001c0002t0002g0229 a0001c0002t0002g0230 |
3 | HG02451.hp2 HG03225.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.217+4178A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89945919 | |||||||
| chr14:89945922 | T | A | 1 | a0001c0003t0012g0016 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.217+4175A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89945922 | |||||||
| chr14:89945924 | TA | T | 6 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0002t0001g0168 others(3): Show |
6 | HG01884.hp2 HG02273.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.217+4172delT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89945924 | |||||||
| chr14:89945925 | A | AT | 20 | a0001c0006t0006g0263 a0001c0006t0009g0262 a0001c0006t0014g0264 others(17): Show |
20 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.217+4171dupA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89945925 | |||||||
| chr14:89945925 | A | T | 49 | a0001c0001t0004g0173 a0001c0001t0004g0174 a0001c0002t0001g0188 others(46): Show |
49 | HG00408.hp1 HG01074.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.217+4172T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89945925 | |||||||
| chr14:89945930 | T | A | 3 | a0001c0001t0002g0039 a0004c0010t0004g0040 a0004c0010t0004g0041 |
3 | HG01884.hp1 HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.217+4167A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89945930 | |||||||
| chr14:89945931 | T | A | 3 | a0001c0001t0002g0154 a0001c0001t0002g0155 a0001c0001t0002g0156 |
3 | HG00323.hp1 HG00735.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.217+4166A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89945931 | |||||||
| chr14:89946029 | G | A | 20 | a0001c0006t0004g0265 a0001c0006t0006g0263 a0001c0006t0009g0262 others(17): Show |
20 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.217+4068C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89946029 | |||||||
| chr14:89946075 | T | C | 7 | a0001c0001t0002g0031 a0001c0001t0002g0032 a0001c0001t0002g0033 others(4): Show |
7 | HG00140.hp2 HG01099.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.217+4022A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89946075 | |||||||
| chr14:89946125 | G | T | 30 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0231 others(27): Show |
30 | HG00735.hp2 HG01070.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.217+3972C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89946125 | |||||||
| chr14:89946192 | G | C | 3 | a0001c0001t0004g0160 a0001c0001t0007g0036 a0001c0001t0007g0161 |
3 | HG01074.hp2 HG01175.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.217+3905C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89946192 | |||||||
| chr14:89946443 | C | T | 3 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0234 |
3 | NA18968.hp2 NA19009.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.217+3654G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89946443 | |||||||
| chr14:89946611 | C | T | 3 | a0001c0001t0002g0049 a0001c0001t0018g0048 a0001c0001t0033g0050 |
3 | HG01109.hp2 HG01255.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.217+3486G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89946611 | |||||||
| chr14:89946659 | A | G | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.217+3438T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89946659 | |||||||
| chr14:89946707 | T | C | 1 | a0001c0001t0002g0162 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.217+3390A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89946707 | |||||||
| chr14:89946710 | C | T | 60 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0004g0170 others(57): Show |
60 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.217+3387G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89946710 | |||||||
| chr14:89946733 | C | CT | 32 | a0001c0001t0001g0046 a0001c0001t0010g0047 a0001c0002t0001g0168 others(29): Show |
32 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.217+3363dupA | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89946733 | |||||||
| chr14:89946868 | A | C | 2 | a0002c0005t0002g0250 a0002c0005t0004g0249 |
2 | HG02055.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.217+3229T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89946868 | |||||||
| chr14:89946901 | T | C | 8 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0234 others(5): Show |
8 | HG01070.hp1 HG02559.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.217+3196A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89946901 | |||||||
| chr14:89946977 | T | C | 1 | a0001c0002t0002g0220 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.217+3120A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89946977 | |||||||
| chr14:89947002 | C | T | 30 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(27): Show |
30 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.217+3095G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89947002 | |||||||
| chr14:89947007 | T | C | 30 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0231 others(27): Show |
30 | HG00735.hp2 HG01070.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.217+3090A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89947007 | |||||||
| chr14:89947055 | T | C | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.217+3042A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89947055 | |||||||
| chr14:89947061 | G | A | 23 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0017 others(20): Show |
23 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.217+3036C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89947061 | |||||||
| chr14:89947099 | T | C | 1 | a0001c0004t0006g0284 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.217+2998A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89947099 | |||||||
| chr14:89947179 | C | G | 3 | a0001c0001t0001g0045 a0001c0001t0002g0044 a0001c0001t0030g0043 |
3 | HG02615.hp2 HG02886.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.217+2918G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89947179 | |||||||
| chr14:89947302 | T | C | 1 | a0001c0001t0010g0180 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.217+2795A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89947302 | |||||||
| chr14:89947640 | C | T | 7 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(4): Show |
7 | HG01884.hp2 HG01891.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.217+2457G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89947640 | |||||||
| chr14:89947787 | C | T | 1 | a0001c0002t0003g0182 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.217+2310G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89947787 | |||||||
| chr14:89947930 | C | G | 1 | a0001c0001t0014g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.217+2167G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89947930 | |||||||
| chr14:89948009 | C | T | 1 | a0001c0001t0003g0042 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.217+2088G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89948009 | |||||||
| chr14:89948702 | T | C | 30 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0231 others(27): Show |
30 | HG00735.hp2 HG01070.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.217+1395A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89948702 | |||||||
| chr14:89948723 | C | T | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.217+1374G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89948723 | |||||||
| chr14:89948855 | G | T | 3 | a0001c0001t0002g0039 a0004c0010t0004g0040 a0004c0010t0004g0041 |
3 | HG01884.hp1 HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.217+1242C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89948855 | |||||||
| chr14:89948881 | CA | C | 23 | a0001c0001t0007g0231 a0001c0001t0014g0240 a0001c0002t0003g0181 others(20): Show |
23 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.217+1215delT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89948881 | |||||||
| chr14:89948895 | T | C | 30 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(27): Show |
30 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.217+1202A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89948895 | |||||||
| chr14:89948986 | T | C | 9 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0234 others(6): Show |
9 | HG01070.hp1 HG02559.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.217+1111A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89948986 | |||||||
| chr14:89949059 | T | C | 30 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0231 others(27): Show |
30 | HG00735.hp2 HG01070.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.217+1038A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89949059 | |||||||
| chr14:89949205 | C | A | 1 | a0001c0003t0016g0024 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.217+892G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89949205 | |||||||
| chr14:89949269 | T | A | 2 | a0001c0001t0003g0164 a0001c0001t0004g0163 |
2 | HG00621.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.217+828A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89949269 | |||||||
| chr14:89949318 | G | A | 7 | a0001c0001t0004g0170 a0001c0001t0004g0171 a0001c0001t0004g0173 others(4): Show |
7 | HG01884.hp2 HG01891.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.217+779C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89949318 | |||||||
| chr14:89949404 | G | A | 1 | a0001c0002t0019g0221 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.217+693C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89949404 | |||||||
| chr14:89949443 | C | T | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.217+654G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89949443 | |||||||
| chr14:89949490 | G | T | 3 | a0001c0001t0008g0175 a0001c0001t0008g0176 a0001c0001t0008g0177 |
3 | HG02280.hp2 HG02717.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.217+607C>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89949490 | |||||||
| chr14:89949965 | T | C | 30 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0231 others(27): Show |
30 | HG00735.hp2 HG01070.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.217+132A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 3/5 | chr14 | 89949965 | |||||||
| chr14:89950173 | T | C | 23 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0017 others(20): Show |
23 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.172-31A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89950173 | |||||||
| chr14:89950263 | G | A | 23 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0017 others(20): Show |
23 | HG00323.hp2 HG01168.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.172-121C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89950263 | |||||||
| chr14:89950564 | A | G | 2 | a0001c0001t0002g0038 a0001c0001t0006g0037 |
2 | HG01261.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.172-422T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89950564 | |||||||
| chr14:89950579 | G | A | 1 | a0002c0005t0029g0260 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.172-437C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89950579 | |||||||
| chr14:89950605 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.172-463C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89950605 | |||||||
| chr14:89950624 | T | G | 1 | a0001c0003t0001g0017 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.172-482A>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89950624 | |||||||
| chr14:89950748 | G | A | 1 | a0001c0001t0014g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.172-606C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89950748 | |||||||
| chr14:89950759 | G | A | 1 | a0001c0001t0014g0240 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.172-617C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89950759 | |||||||
| chr14:89950912 | C | T | 1 | a0001c0001t0007g0036 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.172-770G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89950912 | |||||||
| chr14:89950992 | C | T | 2 | a0001c0001t0005g0034 a0001c0001t0005g0035 |
2 | HG02015.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.172-850G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89950992 | |||||||
| chr14:89951036 | T | A | 3 | a0001c0003t0004g0019 a0001c0003t0008g0020 a0001c0003t0037g0018 |
3 | HG02572.hp1 HG02622.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.172-894A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89951036 | |||||||
| chr14:89951102 | G | A | 1 | a0001c0001t0002g0166 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.172-960C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89951102 | |||||||
| chr14:89951164 | G | A | 48 | a0001c0002t0001g0188 a0001c0002t0001g0190 a0001c0002t0001g0196 others(45): Show |
48 | HG00408.hp1 HG01074.hp1 HG01255.hp1 others(45): Show |
intron_variant | MODIFIER | c.172-1022C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89951164 | |||||||
| chr14:89951401 | A | G | 30 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0231 others(27): Show |
30 | HG00735.hp2 HG01070.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.172-1259T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89951401 | |||||||
| chr14:89951620 | G | A | 60 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0004g0170 others(57): Show |
60 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.172-1478C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89951620 | |||||||
| chr14:89951685 | A | G | 1 | a0001c0002t0002g0246 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.172-1543T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89951685 | |||||||
| chr14:89951756 | A | C | 33 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0002g0031 others(30): Show |
33 | HG00140.hp2 HG00735.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.172-1614T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89951756 | |||||||
| chr14:89951758 | A | C | 1 | a0003c0008t0026g0267 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.172-1616T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89951758 | |||||||
| chr14:89951782 | G | A | 1 | a0002c0007t0004g0261 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.172-1640C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89951782 | |||||||
| chr14:89951885 | A | G | 2 | a0001c0001t0001g0232 a0001c0001t0001g0233 |
2 | NA18968.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.172-1743T>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89951885 | |||||||
| chr14:89952046 | T | C | 1 | a0001c0001t0001g0167 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.171+1860A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89952046 | |||||||
| chr14:89952080 | A | T | 2 | a0001c0001t0002g0029 a0001c0001t0002g0030 |
2 | HG01261.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.171+1826T>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89952080 | |||||||
| chr14:89952118 | C | T | 60 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0004g0170 others(57): Show |
60 | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(57): Show |
intron_variant | MODIFIER | c.171+1788G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89952118 | |||||||
| chr14:89952151 | A | C | 1 | a0001c0001t0007g0231 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.171+1755T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89952151 | |||||||
| chr14:89952197 | G | A | 5 | a0001c0002t0002g0222 a0001c0002t0004g0223 a0001c0002t0006g0224 others(2): Show |
5 | HG01256.hp2 HG01433.hp2 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.171+1709C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89952197 | |||||||
| chr14:89952510 | C | T | 1 | a0001c0001t0013g0028 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.171+1396G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89952510 | |||||||
| chr14:89952515 | C | T | 2 | a0001c0006t0006g0263 a0001c0006t0009g0262 |
2 | HG02486.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.171+1391G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89952515 | |||||||
| chr14:89952605 | T | C | 30 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0231 others(27): Show |
30 | HG00735.hp2 HG01070.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.171+1301A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89952605 | |||||||
| chr14:89952844 | T | C | 131 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0004g0170 others(128): Show |
131 | HG00323.hp2 HG00408.hp1 HG00735.hp2 others(128): Show |
intron_variant | MODIFIER | c.171+1062A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89952844 | |||||||
| chr14:89952908 | C | G | 1 | a0001c0001t0015g0027 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.171+998G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89952908 | |||||||
| chr14:89952946 | C | G | 1 | a0001c0002t0031g0026 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.171+960G>C | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89952946 | |||||||
| chr14:89952947 | G | A | 1 | a0001c0002t0042g0227 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.171+959C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89952947 | |||||||
| chr14:89953036 | G | C | 4 | a0001c0002t0001g0228 a0001c0002t0002g0229 a0001c0002t0002g0230 others(1): Show |
4 | HG02451.hp2 HG02809.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.171+870C>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89953036 | |||||||
| chr14:89953128 | G | A | 30 | a0001c0001t0001g0232 a0001c0001t0001g0233 a0001c0001t0007g0231 others(27): Show |
30 | HG00735.hp2 HG01070.hp1 HG01081.hp2 others(27): Show |
intron_variant | MODIFIER | c.171+778C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89953128 | |||||||
| chr14:89953207 | G | GA | 8 | a0001c0001t0001g0242 a0001c0001t0005g0241 a0001c0002t0002g0243 others(5): Show |
8 | HG01256.hp1 HG02027.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.171+698dupT | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89953207 | |||||||
| chr14:89953221 | A | C | 1 | a0003c0008t0001g0266 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.171+685T>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89953221 | |||||||
| chr14:89953222 | C | A | 15 | a0001c0006t0004g0265 a0001c0006t0014g0264 a0002c0005t0002g0250 others(12): Show |
15 | HG00735.hp2 HG01081.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.171+684G>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89953222 | |||||||
| chr14:89953473 | G | A | 1 | a0001c0001t0003g0244 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.171+433C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89953473 | |||||||
| chr14:89953698 | T | C | 16 | a0001c0004t0001g0277 a0001c0004t0001g0278 a0001c0004t0002g0276 others(13): Show |
16 | HG02109.hp2 HG02257.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.171+208A>G | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89953698 | |||||||
| chr14:89953783 | C | T | 1 | a0001c0002t0020g0025 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.171+123G>A | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89953783 | |||||||
| chr14:89953812 | T | A | 2 | a0001c0004t0006g0284 a0001c0004t0020g0283 |
2 | HG02559.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.171+94A>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 2/5 | chr14 | 89953812 | |||||||
| chr14:89954211 | G | A | 3 | a0001c0002t0002g0246 a0001c0002t0002g0247 a0001c0002t0003g0248 |
3 | HG02602.hp2 HG02738.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.76-210C>T | EFCAB11 | ENSG00000140025.16 | transcript | ENST00000316738.12 | protein_coding | 1/5 | chr14 | 89954211 |