Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 285343 |
| ensemblid | ENSG00000179152.20 |
| hgncid | 25241 |
| symbol | TCAIM |
| name | T cell activation inhibitor, mitochondrial |
| refseq_nuc | NM_173826.4 |
| refseq_prot | NP_776187.2 |
| ensembl_nuc | ENST00000342649.9 |
| ensembl_prot | ENSP00000341539.4 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 44338766 |
| end | 44409448 |
| strand | + |
| ver | v1.2 |
| region | chr3:44338766-44409448 |
| region5000 | chr3:44333766-44414448 |
| regionname0 | TCAIM_chr3_44338766_44409448 |
| regionname5000 | TCAIM_chr3_44333766_44414448 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 496 | 243 | 87 | 56 | 60 | 12 | 26 | 34 | TCAIM_chr3_44333766_44414448 | TCAIM | MFCHL others(491): Show |
chr3 | 44333766 | 44414448 |
| a0002 | 0/0 | 496 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | MFCHL others(491): Show |
chr3 | 44333766 | 44414448 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1488 | 234 | 84 | 55 | 56 | 11 | 26 | TCAIM_chr3_44333766_44414448 | TCAIM | ATGTT others(1483): Show |
chr3 | 44333766 | 44414448 | ||
| a0001c0003 | 0/0 | 1488 | 4 | 3 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | ATGTT others(1483): Show |
chr3 | 44333766 | 44414448 | ||
| a0001c0004 | 0/0 | 1488 | 4 | 0 | 0 | 4 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | ATGTT others(1483): Show |
chr3 | 44333766 | 44414448 | ||
| a0001c0005 | 0/0 | 1488 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | ATGTT others(1483): Show |
chr3 | 44333766 | 44414448 | ||
| a0002c0002 | 0/0 | 1488 | 5 | 5 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | ATGTT others(1483): Show |
chr3 | 44333766 | 44414448 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3370 | 145 | 37 | 35 | 46 | 7 | 19 | TCAIM_chr3_44333766_44414448 | TCAIM | CTTCT others(3365): Show |
chr3 | 44333766 | 44414448 |
| a0001c0001t0002 | 1/0 | 3370 | 29 | 20 | 7 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | CTTCT others(3365): Show |
chr3 | 44333766 | 44414448 |
| a0001c0001t0003 | 0/0 | 3371 | 23 | 4 | 6 | 5 | 3 | 5 | TCAIM_chr3_44333766_44414448 | TCAIM | CTCCT others(3366): Show |
chr3 | 44333766 | 44414448 |
| a0001c0001t0004 | 0/0 | 3354 | 7 | 7 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | CTTCT others(3349): Show |
chr3 | 44333766 | 44414448 |
| a0001c0001t0005 | 0/0 | 3370 | 6 | 6 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | CTTCT others(3365): Show |
chr3 | 44333766 | 44414448 |
| a0001c0001t0006 | 0/0 | 3370 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | CTTCT others(3365): Show |
chr3 | 44333766 | 44414448 |
| a0001c0001t0007 | 0/0 | 3371 | 4 | 4 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | CTCCT others(3366): Show |
chr3 | 44333766 | 44414448 |
| a0001c0001t0008 | 0/0 | 3371 | 4 | 1 | 3 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | CTCCT others(3366): Show |
chr3 | 44333766 | 44414448 |
| a0001c0001t0009 | 0/0 | 3370 | 2 | 0 | 2 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | CTCCT others(3365): Show |
chr3 | 44333766 | 44414448 |
| a0001c0001t0010 | 0/0 | 3371 | 2 | 2 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | CTCCT others(3366): Show |
chr3 | 44333766 | 44414448 |
| a0001c0001t0011 | 0/0 | 3370 | 2 | 0 | 0 | 2 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | CTTCT others(3365): Show |
chr3 | 44333766 | 44414448 |
| a0001c0001t0012 | 0/0 | 3371 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | CTCCT others(3366): Show |
chr3 | 44333766 | 44414448 |
| a0001c0001t0013 | 0/0 | 3370 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | CTTCT others(3365): Show |
chr3 | 44333766 | 44414448 |
| a0001c0001t0014 | 0/0 | 3370 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | CTTCT others(3365): Show |
chr3 | 44333766 | 44414448 |
| a0001c0001t0015 | 0/0 | 3370 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | CTTCT others(3365): Show |
chr3 | 44333766 | 44414448 |
| a0001c0001t0016 | 0/0 | 3370 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | CTTCT others(3365): Show |
chr3 | 44333766 | 44414448 |
| a0001c0001t0017 | 0/0 | 3370 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | CTTCT others(3365): Show |
chr3 | 44333766 | 44414448 |
| a0001c0001t0018 | 0/0 | 3371 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | CTTCT others(3366): Show |
chr3 | 44333766 | 44414448 |
| a0001c0001t0019 | 0/0 | 3370 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | CTTCT others(3365): Show |
chr3 | 44333766 | 44414448 |
| a0001c0001t0020 | 0/0 | 3370 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | CTTCT others(3365): Show |
chr3 | 44333766 | 44414448 |
| a0001c0003t0001 | 0/0 | 3370 | 4 | 3 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | CTTCT others(3365): Show |
chr3 | 44333766 | 44414448 |
| a0001c0004t0006 | 0/0 | 3370 | 4 | 0 | 0 | 4 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | CTTCT others(3365): Show |
chr3 | 44333766 | 44414448 |
| a0001c0005t0001 | 0/0 | 3370 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | CTTCT others(3365): Show |
chr3 | 44333766 | 44414448 |
| a0002c0002t0001 | 0/0 | 3370 | 5 | 5 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | CTTCT others(3365): Show |
chr3 | 44333766 | 44414448 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0105 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0002g0143 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0004g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0005g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0006g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0007g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0007g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0007g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0007g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0008g0003 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0008g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0008g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0009g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0009g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0010g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0010g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0011g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0011g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0012g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0013g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0014g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0015g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0016g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0017g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0018g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0019g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0001t0020g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0003t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0003t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0004t0006g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0004t0006g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0004t0006g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0004t0006g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0001c0005t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0002c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0002c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0002c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0002c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| a0002c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | GBR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0230 | EUR | GBR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG00423 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | CHS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG00558 | hp1 | a0001 | c0004 | t0006 | g0164 | EAS | CHS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | CHS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG00597 | hp2 | a0001 | c0004 | t0006 | g0166 | EAS | CHS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CHS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG00639 | hp2 | a0001 | c0001 | t0008 | g0003 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG00673 | hp2 | a0001 | c0004 | t0006 | g0165 | EAS | CHS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG00733 | hp1 | a0001 | c0001 | t0003 | g0060 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG00741 | hp2 | a0001 | c0001 | t0008 | g0067 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0135 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01109 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01167 | hp2 | a0001 | c0001 | t0018 | g0211 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01192 | hp2 | a0001 | c0001 | t0008 | g0078 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01257 | hp2 | a0001 | c0001 | t0009 | g0064 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01258 | hp1 | a0001 | c0001 | t0009 | g0063 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0069 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | IBS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0012 | EUR | IBS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | IBS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0054 | EUR | IBS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | IBS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01517 | hp2 | a0001 | c0001 | t0003 | g0059 | EUR | IBS | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0011 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0008 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01934 | hp1 | a0001 | c0005 | t0001 | g0131 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0057 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | KHV | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | KHV | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | KHV | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02145 | hp1 | a0001 | c0001 | t0008 | g0003 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0061 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0085 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02300 | hp2 | a0001 | c0001 | t0013 | g0039 | AMR | PEL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0090 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | KHV | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02572 | hp1 | a0001 | c0003 | t0001 | g0083 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02630 | hp1 | a0001 | c0001 | t0020 | g0015 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02698 | hp1 | a0001 | c0001 | t0017 | g0154 | SAS | PJL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0030 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0075 | SAS | PJL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0088 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02809 | hp2 | a0001 | c0003 | t0001 | g0026 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0089 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02895 | hp1 | a0001 | c0001 | t0007 | g0066 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0087 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02896 | hp1 | a0001 | c0001 | t0007 | g0065 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0086 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02922 | hp1 | a0001 | c0001 | t0010 | g0074 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0016 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0047 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0072 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0028 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0007 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03486 | hp1 | a0001 | c0001 | t0015 | g0010 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0079 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0048 | AFR | ESN | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | GWD | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03669 | hp2 | a0001 | c0001 | t0012 | g0082 | SAS | PJL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0070 | SAS | BEB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0081 | SAS | BEB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0071 | SAS | BEB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | STU | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | STU | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | STU | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | STU | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0051 | SAS | STU | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | YRI | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0040 | AFR | YRI | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | CHB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | CHB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0001 | AFR | YRI | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | YRI | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18947 | hp1 | a0001 | c0001 | t0016 | g0224 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18966 | hp2 | a0001 | c0004 | t0006 | g0171 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18970 | hp1 | a0001 | c0001 | t0006 | g0170 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18986 | hp1 | a0001 | c0001 | t0011 | g0229 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0073 | AFR | LWK | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA19043 | hp2 | a0001 | c0001 | t0014 | g0045 | AFR | LWK | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA19091 | hp1 | a0001 | c0001 | t0019 | g0189 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA19091 | hp2 | a0001 | c0001 | t0011 | g0187 | EAS | JPT | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA20129 | hp1 | a0001 | c0001 | t0010 | g0068 | AFR | ASW | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ASW | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | TSI | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | TSI | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0056 | EUR | TSI | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA20805 | hp2 | a0001 | c0003 | t0001 | g0091 | EUR | TSI | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | GIH | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | GIH | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0041 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02109 | hp2 | a0001 | c0001 | t0004 | g0084 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0001 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ACB | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0033 | AFR | MSL | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | LWK | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0105 | REF | REF | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0143 | REF | REF | TCAIM_chr3_44333766_44414448 | TCAIM | chr3 | 44333766 | 44414448 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:44407671 | G | T | 1 | a0002 | 5 | HG02257.hp1 HG02723.hp1 HG03139.hp2 others(2): Show |
missense_variant | MODERATE | c.1480G>T | p.Ala494Ser | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 1593/3370 | 1480/1491 | 494/496 | chr3 | 44407671 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:44367646 | T | C | 2 | a0001c0003 a0002c0002 |
9 | HG02257.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
synonymous_variant | LOW | c.510T>C | p.Phe170Phe | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/11 | 623/3370 | 510/1491 | 170/496 | chr3 | 44367646 | |||
| chr3:44400367 | T | C | 1 | a0001c0004 | 4 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(1): Show |
synonymous_variant | LOW | c.898T>C | p.Leu300Leu | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 9/11 | 1011/3370 | 898/1491 | 300/496 | chr3 | 44400367 | |||
| chr3:44400534 | T | C | 1 | a0001c0005 | 1 | HG01934.hp1 | synonymous_variant | LOW | c.1065T>C | p.Ser355Ser | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 9/11 | 1178/3370 | 1065/1491 | 355/496 | chr3 | 44400534 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:44338768 | T | C | 6 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0008 others(3): Show |
36 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
5_prime_UTR_variant | MODIFIER | c.-111T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/11 | 16015 | chr3 | 44338768 | ||||||
| chr3:44407879 | C | T | 1 | a0001c0001t0020 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*197C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 197 | chr3 | 44407879 | ||||||
| chr3:44407880 | G | A | 2 | a0001c0001t0006 a0001c0004t0006 |
5 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*198G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 198 | chr3 | 44407880 | ||||||
| chr3:44407893 | T | C | 1 | a0001c0001t0013 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*211T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 211 | chr3 | 44407893 | ||||||
| chr3:44408086 | C | T | 1 | a0001c0001t0012 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*404C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 404 | chr3 | 44408086 | ||||||
| chr3:44408090 | A | G | 1 | a0001c0001t0008 | 4 | HG00639.hp2 HG00741.hp2 HG01192.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*408A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 408 | chr3 | 44408090 | ||||||
| chr3:44408427 | C | T | 1 | a0001c0001t0004 | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*745C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 745 | chr3 | 44408427 | ||||||
| chr3:44408485 | C | T | 1 | a0001c0001t0019 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*803C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 803 | chr3 | 44408485 | ||||||
| chr3:44408579 | G | GT | 6 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0008 others(3): Show |
35 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*903dupT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 904 | INFO_REALIGN_3_PRIME | chr3 | 44408579 | |||||
| chr3:44408619 | G | C | 1 | a0001c0001t0007 | 4 | HG02895.hp1 HG02896.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*937G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 937 | chr3 | 44408619 | ||||||
| chr3:44408734 | A | C | 21 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(18): Show |
216 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*1052A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 1052 | chr3 | 44408734 | ||||||
| chr3:44408781 | G | A | 1 | a0001c0001t0015 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1099G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 1099 | chr3 | 44408781 | ||||||
| chr3:44408808 | C | T | 1 | a0001c0001t0011 | 2 | NA18986.hp1 NA19091.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1126C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 1126 | chr3 | 44408808 | ||||||
| chr3:44408923 | C | T | 1 | a0001c0001t0010 | 2 | HG02922.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1241C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 1241 | chr3 | 44408923 | ||||||
| chr3:44409035 | AGAAAGGA others(9): Show |
A | 1 | a0001c0001t0004 | 7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1357_*1372delAGGA others(12): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 1357 | INFO_REALIGN_3_PRIME | chr3 | 44409035 | |||||
| chr3:44409059 | A | G | 1 | a0001c0001t0017 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1377A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 1377 | chr3 | 44409059 | ||||||
| chr3:44409072 | A | G | 21 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(18): Show |
216 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*1390A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 1390 | chr3 | 44409072 | ||||||
| chr3:44409184 | A | G | 1 | a0001c0001t0014 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1502A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 1502 | chr3 | 44409184 | ||||||
| chr3:44409211 | G | A | 1 | a0001c0001t0016 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1529G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 1529 | chr3 | 44409211 | ||||||
| chr3:44409243 | T | C | 2 | a0001c0001t0005 a0001c0001t0015 |
7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1561T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 11/11 | 1561 | chr3 | 44409243 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:44338996 | A | C | 58 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0001g0188 others(55): Show |
58 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.-45+162A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44338996 | |||||||
| chr3:44339107 | C | CAA | 191 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(188): Show |
196 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.-45+273_-45+274ins others(2): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44339107 | |||||||
| chr3:44339253 | C | G | 1 | a0001c0001t0001g0184 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-45+419C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44339253 | |||||||
| chr3:44339292 | G | A | 6 | a0001c0001t0005g0001 a0001c0001t0005g0007 a0001c0001t0005g0008 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-45+458G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44339292 | |||||||
| chr3:44339378 | A | G | 6 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(3): Show |
6 | HG02647.hp2 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-45+544A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44339378 | |||||||
| chr3:44339391 | C | G | 1 | a0001c0001t0001g0242 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-45+557C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44339391 | |||||||
| chr3:44339475 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-45+641A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44339475 | |||||||
| chr3:44339934 | T | C | 1 | a0001c0001t0002g0012 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-45+1100T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44339934 | |||||||
| chr3:44339988 | A | G | 1 | a0001c0001t0003g0135 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-45+1154A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44339988 | |||||||
| chr3:44340418 | C | A | 191 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(188): Show |
196 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.-45+1584C>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44340418 | |||||||
| chr3:44340504 | A | T | 1 | a0001c0001t0001g0134 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-45+1670A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44340504 | |||||||
| chr3:44340553 | T | C | 1 | a0001c0001t0002g0013 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-45+1719T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44340553 | |||||||
| chr3:44340930 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-45+2096T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44340930 | |||||||
| chr3:44341430 | A | AT | 6 | a0001c0001t0005g0001 a0001c0001t0005g0007 a0001c0001t0005g0008 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-45+2602dupT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 44341430 | ||||||
| chr3:44341564 | C | T | 108 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0092 others(105): Show |
111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.-45+2730C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44341564 | |||||||
| chr3:44341645 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-45+2811G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44341645 | |||||||
| chr3:44341720 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-45+2886G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44341720 | |||||||
| chr3:44341752 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-45+2918A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44341752 | |||||||
| chr3:44341906 | G | A | 5 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
5 | HG02258.hp1 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.-45+3072G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44341906 | |||||||
| chr3:44342070 | T | C | 1 | a0001c0001t0020g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-45+3236T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44342070 | |||||||
| chr3:44342217 | C | A | 1 | a0001c0003t0001g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-45+3383C>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44342217 | |||||||
| chr3:44342327 | G | T | 109 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(106): Show |
112 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-45+3493G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44342327 | |||||||
| chr3:44342388 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-45+3554C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44342388 | |||||||
| chr3:44342414 | A | G | 6 | a0001c0001t0005g0001 a0001c0001t0005g0007 a0001c0001t0005g0008 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-45+3580A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44342414 | |||||||
| chr3:44342439 | C | T | 1 | a0001c0003t0001g0091 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-45+3605C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44342439 | |||||||
| chr3:44342728 | TA | T | 7 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-45+3897delA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 44342728 | ||||||
| chr3:44342888 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-45+4054G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44342888 | |||||||
| chr3:44342999 | C | T | 191 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(188): Show |
196 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.-45+4165C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44342999 | |||||||
| chr3:44343146 | AAAG | A | 15 | a0001c0001t0002g0002 a0001c0001t0002g0017 a0001c0001t0002g0018 others(12): Show |
16 | HG01192.hp1 HG01243.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-45+4318_-45+4320d others(5): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 44343146 | ||||||
| chr3:44343237 | C | T | 82 | a0001c0001t0001g0027 a0001c0001t0002g0002 a0001c0001t0002g0012 others(79): Show |
84 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(81): Show |
intron_variant | MODIFIER | c.-45+4403C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44343237 | |||||||
| chr3:44343284 | A | G | 197 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(194): Show |
202 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.-45+4450A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44343284 | |||||||
| chr3:44343317 | A | G | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG00438.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.-45+4483A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44343317 | |||||||
| chr3:44343398 | C | T | 1 | a0001c0003t0001g0083 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-45+4564C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44343398 | |||||||
| chr3:44343499 | A | G | 82 | a0001c0001t0001g0027 a0001c0001t0002g0002 a0001c0001t0002g0012 others(79): Show |
84 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(81): Show |
intron_variant | MODIFIER | c.-45+4665A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44343499 | |||||||
| chr3:44343582 | T | A | 1 | a0001c0001t0004g0089 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-45+4748T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44343582 | |||||||
| chr3:44343621 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-45+4787C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44343621 | |||||||
| chr3:44343902 | G | A | 7 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-45+5068G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44343902 | |||||||
| chr3:44344010 | T | C | 82 | a0001c0001t0001g0027 a0001c0001t0002g0002 a0001c0001t0002g0012 others(79): Show |
84 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(81): Show |
intron_variant | MODIFIER | c.-45+5176T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44344010 | |||||||
| chr3:44344023 | C | CT | 68 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0140 others(65): Show |
71 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(68): Show |
intron_variant | MODIFIER | c.-45+5207dupT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 44344023 | ||||||
| chr3:44344023 | C | CTT | 5 | a0001c0001t0002g0080 a0001c0001t0003g0081 a0001c0001t0008g0078 others(2): Show |
5 | HG01192.hp2 HG02055.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-45+5206_-45+5207d others(4): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 44344023 | ||||||
| chr3:44344023 | CT | C | 90 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(87): Show |
91 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.-45+5207delT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 44344023 | ||||||
| chr3:44344040 | T | G | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0011g0187 |
3 | NA18981.hp2 NA19056.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-45+5206T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44344040 | |||||||
| chr3:44344041 | T | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0011g0187 |
3 | NA18981.hp2 NA19056.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-45+5207T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44344041 | |||||||
| chr3:44344066 | G | A | 3 | a0001c0001t0001g0188 a0001c0001t0001g0190 a0001c0001t0019g0189 |
3 | HG02080.hp1 HG02080.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-45+5232G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44344066 | |||||||
| chr3:44344213 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-45+5379T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44344213 | |||||||
| chr3:44344291 | C | T | 1 | a0001c0001t0002g0077 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-45+5457C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44344291 | |||||||
| chr3:44344322 | G | A | 197 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(194): Show |
202 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.-45+5488G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44344322 | |||||||
| chr3:44344771 | G | A | 1 | a0001c0001t0008g0078 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-45+5937G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44344771 | |||||||
| chr3:44344813 | G | A | 204 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(201): Show |
209 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.-45+5979G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44344813 | |||||||
| chr3:44344906 | A | G | 37 | a0001c0001t0001g0027 a0001c0001t0003g0047 a0001c0001t0003g0048 others(34): Show |
38 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.-45+6072A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44344906 | |||||||
| chr3:44344998 | C | T | 7 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-45+6164C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44344998 | |||||||
| chr3:44345103 | A | G | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-45+6269A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44345103 | |||||||
| chr3:44345122 | C | T | 191 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(188): Show |
196 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(193): Show |
intron_variant | MODIFIER | c.-45+6288C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44345122 | |||||||
| chr3:44345141 | G | A | 4 | a0001c0003t0001g0016 a0001c0003t0001g0026 a0001c0003t0001g0083 others(1): Show |
4 | HG02572.hp1 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45+6307G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44345141 | |||||||
| chr3:44345154 | G | A | 5 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0030 others(2): Show |
5 | HG02257.hp1 HG02723.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-45+6320G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44345154 | |||||||
| chr3:44345205 | G | T | 1 | a0001c0001t0001g0093 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-45+6371G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44345205 | |||||||
| chr3:44345282 | T | C | 1 | a0001c0001t0020g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-45+6448T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44345282 | |||||||
| chr3:44345843 | C | G | 1 | a0001c0001t0002g0046 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-45+7009C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44345843 | |||||||
| chr3:44346080 | C | T | 1 | a0001c0001t0003g0076 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-45+7246C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44346080 | |||||||
| chr3:44346103 | TAAAAGTA | T | 6 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-45+7270_-45+7276d others(9): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44346103 | |||||||
| chr3:44346148 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-45+7314G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44346148 | |||||||
| chr3:44346292 | A | G | 1 | a0001c0001t0004g0088 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-45+7458A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44346292 | |||||||
| chr3:44346350 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-45+7516C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44346350 | |||||||
| chr3:44346436 | A | G | 4 | a0001c0003t0001g0016 a0001c0003t0001g0026 a0001c0003t0001g0083 others(1): Show |
4 | HG02572.hp1 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45+7602A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44346436 | |||||||
| chr3:44346609 | G | A | 4 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0049 others(1): Show |
4 | HG02486.hp2 HG02970.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-45+7775G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44346609 | |||||||
| chr3:44346644 | C | G | 1 | a0002c0002t0001g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-45+7810C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44346644 | |||||||
| chr3:44347094 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-44-7645G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44347094 | |||||||
| chr3:44347164 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-44-7575C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44347164 | |||||||
| chr3:44347168 | A | G | 2 | a0001c0001t0001g0233 a0001c0001t0001g0239 |
2 | HG02056.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.-44-7571A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44347168 | |||||||
| chr3:44347400 | A | G | 165 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(162): Show |
169 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.-44-7339A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44347400 | |||||||
| chr3:44347448 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-44-7291G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44347448 | |||||||
| chr3:44347505 | A | G | 36 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0142 others(33): Show |
37 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.-44-7234A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44347505 | |||||||
| chr3:44347710 | C | T | 35 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0049 others(32): Show |
36 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.-44-7029C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44347710 | |||||||
| chr3:44348042 | A | C | 1 | a0001c0001t0001g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-44-6697A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44348042 | |||||||
| chr3:44348293 | G | C | 1 | a0001c0001t0001g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-44-6446G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44348293 | |||||||
| chr3:44348703 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-44-6036G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44348703 | |||||||
| chr3:44348771 | C | T | 1 | a0001c0001t0003g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-44-5968C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44348771 | |||||||
| chr3:44348791 | G | C | 6 | a0001c0001t0005g0001 a0001c0001t0005g0007 a0001c0001t0005g0008 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44-5948G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44348791 | |||||||
| chr3:44348953 | G | A | 18 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0053 others(15): Show |
18 | HG00423.hp2 HG00733.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.-44-5786G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44348953 | |||||||
| chr3:44349013 | AG | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0144 a0001c0001t0001g0145 others(1): Show |
5 | HG01358.hp1 HG01975.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44-5725delG | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44349013 | |||||||
| chr3:44349127 | G | A | 1 | a0001c0001t0001g0005 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-44-5612G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44349127 | |||||||
| chr3:44349234 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-44-5505G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44349234 | |||||||
| chr3:44349566 | A | T | 1 | a0001c0001t0001g0232 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-44-5173A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44349566 | |||||||
| chr3:44349614 | A | G | 1 | a0001c0005t0001g0131 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-44-5125A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44349614 | |||||||
| chr3:44349693 | G | A | 4 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
4 | HG01106.hp1 HG02257.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-5046G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44349693 | |||||||
| chr3:44349773 | G | A | 2 | a0001c0001t0003g0051 a0001c0001t0003g0081 |
2 | HG03927.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.-44-4966G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44349773 | |||||||
| chr3:44349849 | G | A | 1 | a0001c0001t0003g0135 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-44-4890G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44349849 | |||||||
| chr3:44349850 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-44-4889T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44349850 | |||||||
| chr3:44349937 | G | A | 109 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(106): Show |
112 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-44-4802G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44349937 | |||||||
| chr3:44350077 | A | G | 7 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44-4662A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44350077 | |||||||
| chr3:44350161 | T | C | 2 | a0001c0001t0007g0065 a0001c0001t0007g0066 |
2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-44-4578T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44350161 | |||||||
| chr3:44350200 | G | T | 49 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0137 others(46): Show |
50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-44-4539G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44350200 | |||||||
| chr3:44350245 | G | T | 1 | a0001c0001t0001g0231 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-44-4494G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44350245 | |||||||
| chr3:44350403 | C | G | 1 | a0001c0001t0001g0230 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-44-4336C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44350403 | |||||||
| chr3:44350496 | G | A | 1 | a0001c0005t0001g0131 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-44-4243G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44350496 | |||||||
| chr3:44350815 | G | A | 2 | a0001c0001t0001g0188 a0001c0001t0001g0190 |
2 | HG02080.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.-44-3924G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44350815 | |||||||
| chr3:44350816 | A | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0190 |
2 | HG02080.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.-44-3923A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44350816 | |||||||
| chr3:44350887 | T | G | 1 | a0001c0001t0001g0005 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-44-3852T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44350887 | |||||||
| chr3:44350908 | G | T | 1 | a0001c0001t0014g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-44-3831G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44350908 | |||||||
| chr3:44351066 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-44-3673G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44351066 | |||||||
| chr3:44351192 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-44-3547T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44351192 | |||||||
| chr3:44351241 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-44-3498G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44351241 | |||||||
| chr3:44351258 | G | T | 1 | a0001c0001t0003g0075 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-44-3481G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44351258 | |||||||
| chr3:44351264 | C | A | 1 | a0001c0001t0001g0194 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-44-3475C>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44351264 | |||||||
| chr3:44351293 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-44-3446G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44351293 | |||||||
| chr3:44351347 | G | GT | 7 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44-3381dupT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 44351347 | ||||||
| chr3:44351382 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-44-3357T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44351382 | |||||||
| chr3:44351628 | G | A | 109 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(106): Show |
112 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.-44-3111G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44351628 | |||||||
| chr3:44351629 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA18986.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.-44-3110G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44351629 | |||||||
| chr3:44351644 | A | G | 158 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(155): Show |
162 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.-44-3095A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44351644 | |||||||
| chr3:44351815 | G | A | 7 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44-2924G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44351815 | |||||||
| chr3:44352087 | G | GTA | 6 | a0001c0001t0005g0001 a0001c0001t0005g0007 a0001c0001t0005g0008 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44-2638_-44-2637d others(4): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 44352087 | ||||||
| chr3:44352087 | GTA | G | 4 | a0001c0001t0001g0027 a0001c0001t0001g0125 a0001c0001t0001g0126 others(1): Show |
4 | HG02818.hp1 HG02922.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44-2638_-44-2637d others(4): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 44352087 | ||||||
| chr3:44352179 | C | T | 4 | a0001c0001t0007g0065 a0001c0001t0007g0066 a0001c0001t0007g0072 others(1): Show |
4 | HG02895.hp1 HG02896.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-2560C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44352179 | |||||||
| chr3:44352419 | G | A | 6 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(3): Show |
6 | HG02647.hp2 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-44-2320G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44352419 | |||||||
| chr3:44352641 | A | G | 1 | a0001c0003t0001g0016 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-44-2098A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44352641 | |||||||
| chr3:44352660 | G | A | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | NA18961.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.-44-2079G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44352660 | |||||||
| chr3:44352923 | C | CT | 8 | a0001c0001t0002g0013 a0001c0001t0004g0084 a0001c0001t0004g0085 others(5): Show |
8 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44-1800dupT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 44352923 | ||||||
| chr3:44352923 | C | CTTT | 99 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(96): Show |
101 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.-44-1802_-44-1800d others(5): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 44352923 | ||||||
| chr3:44352923 | C | CTTTT | 7 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0123 others(4): Show |
8 | HG00741.hp1 HG01099.hp2 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44-1803_-44-1800d others(6): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 44352923 | ||||||
| chr3:44352923 | CT | C | 5 | a0001c0001t0001g0027 a0001c0001t0001g0150 a0001c0001t0001g0152 others(2): Show |
5 | HG02896.hp1 HG02896.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44-1800delT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr3 | 44352923 | ||||||
| chr3:44352955 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0020g0015 |
2 | HG02630.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-44-1784C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44352955 | |||||||
| chr3:44352956 | G | C | 108 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0092 others(105): Show |
111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.-44-1783G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44352956 | |||||||
| chr3:44353092 | G | A | 1 | a0001c0001t0002g0013 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-44-1647G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44353092 | |||||||
| chr3:44353163 | C | G | 1 | a0001c0001t0004g0090 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-44-1576C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44353163 | |||||||
| chr3:44353233 | T | C | 1 | a0001c0001t0002g0032 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-44-1506T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44353233 | |||||||
| chr3:44353237 | TAGTATC | T | 99 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(96): Show |
100 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.-44-1501_-44-1496d others(8): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44353237 | |||||||
| chr3:44353395 | T | C | 2 | a0001c0001t0001g0192 a0001c0001t0001g0197 |
2 | HG03654.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-44-1344T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44353395 | |||||||
| chr3:44353404 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-44-1335T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44353404 | |||||||
| chr3:44354044 | A | G | 3 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0049 |
3 | HG02486.hp2 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-44-695A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44354044 | |||||||
| chr3:44354073 | A | C | 7 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44-666A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44354073 | |||||||
| chr3:44354128 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-44-611G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44354128 | |||||||
| chr3:44354324 | G | A | 202 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(199): Show |
207 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.-44-415G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44354324 | |||||||
| chr3:44354420 | T | C | 1 | a0001c0005t0001g0131 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-44-319T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 1/10 | chr3 | 44354420 | |||||||
| chr3:44354915 | T | C | 1 | a0001c0001t0020g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.29+104T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44354915 | |||||||
| chr3:44355194 | C | A | 3 | a0001c0003t0001g0016 a0001c0003t0001g0026 a0001c0003t0001g0083 |
3 | HG02572.hp1 HG02809.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.29+383C>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44355194 | |||||||
| chr3:44355246 | TA | T | 106 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0092 others(103): Show |
109 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.29+440delA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 44355246 | ||||||
| chr3:44355646 | G | A | 2 | a0001c0001t0003g0052 a0001c0001t0003g0053 |
2 | HG02040.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.29+835G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44355646 | |||||||
| chr3:44355676 | G | A | 1 | a0001c0001t0008g0067 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.29+865G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44355676 | |||||||
| chr3:44355732 | A | T | 35 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0049 others(32): Show |
36 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.29+921A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44355732 | |||||||
| chr3:44355797 | A | G | 2 | a0001c0001t0001g0152 a0001c0001t0001g0173 |
2 | NA19056.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.29+986A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44355797 | |||||||
| chr3:44355830 | C | G | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG02056.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.29+1019C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44355830 | |||||||
| chr3:44355878 | T | C | 6 | a0001c0001t0005g0001 a0001c0001t0005g0007 a0001c0001t0005g0008 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.29+1067T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44355878 | |||||||
| chr3:44355955 | G | C | 35 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0049 others(32): Show |
36 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.29+1144G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44355955 | |||||||
| chr3:44355968 | G | C | 158 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(155): Show |
162 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.29+1157G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44355968 | |||||||
| chr3:44356217 | G | C | 49 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0137 others(46): Show |
50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.29+1406G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44356217 | |||||||
| chr3:44356295 | G | A | 43 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0141 others(40): Show |
44 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.30-1446G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44356295 | |||||||
| chr3:44356336 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.30-1405G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44356336 | |||||||
| chr3:44356653 | G | C | 108 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0092 others(105): Show |
111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.30-1088G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44356653 | |||||||
| chr3:44356693 | TG | T | 7 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.30-1046delG | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 44356693 | ||||||
| chr3:44356736 | C | T | 43 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0141 others(40): Show |
44 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.30-1005C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44356736 | |||||||
| chr3:44356779 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.30-962A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44356779 | |||||||
| chr3:44356811 | C | CA | 22 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0097 others(19): Show |
23 | HG00738.hp1 HG01192.hp1 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.30-914dupA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 44356811 | ||||||
| chr3:44356824 | A | AC | 35 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0049 others(32): Show |
36 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.30-917_30-916insC | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44356824 | |||||||
| chr3:44356869 | G | A | 35 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0049 others(32): Show |
36 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.30-872G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44356869 | |||||||
| chr3:44356923 | G | A | 108 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0092 others(105): Show |
111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.30-818G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44356923 | |||||||
| chr3:44356930 | A | G | 9 | a0001c0003t0001g0016 a0001c0003t0001g0026 a0001c0003t0001g0083 others(6): Show |
9 | HG02257.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.30-811A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44356930 | |||||||
| chr3:44357019 | A | T | 1 | a0001c0001t0001g0231 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.30-722A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44357019 | |||||||
| chr3:44357129 | G | C | 100 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0092 others(97): Show |
102 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.30-612G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44357129 | |||||||
| chr3:44357343 | C | A | 1 | a0001c0001t0002g0033 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.30-398C>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44357343 | |||||||
| chr3:44357393 | A | AAGAG | 211 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(208): Show |
216 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.30-346_30-343dupGA others(2): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr3 | 44357393 | ||||||
| chr3:44357434 | A | G | 1 | a0001c0001t0020g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.30-307A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44357434 | |||||||
| chr3:44357616 | A | G | 2 | a0002c0002t0001g0029 a0002c0002t0001g0030 |
2 | HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.30-125A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 2/10 | chr3 | 44357616 | |||||||
| chr3:44358176 | T | C | 202 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(199): Show |
207 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(204): Show |
intron_variant | MODIFIER | c.165+300T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44358176 | |||||||
| chr3:44358488 | A | T | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG00438.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.165+612A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44358488 | |||||||
| chr3:44358669 | G | C | 1 | a0001c0005t0001g0131 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.165+793G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44358669 | |||||||
| chr3:44358739 | A | C | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.165+863A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44358739 | |||||||
| chr3:44359155 | G | A | 2 | a0001c0001t0001g0099 a0001c0001t0001g0100 |
2 | HG03831.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.165+1279G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44359155 | |||||||
| chr3:44359169 | T | C | 18 | a0001c0001t0003g0051 a0001c0001t0003g0052 a0001c0001t0003g0053 others(15): Show |
18 | HG00423.hp2 HG00733.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.165+1293T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44359169 | |||||||
| chr3:44359763 | C | T | 100 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0092 others(97): Show |
102 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.166-1602C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44359763 | |||||||
| chr3:44359869 | G | A | 1 | a0001c0001t0002g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.166-1496G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44359869 | |||||||
| chr3:44360011 | C | G | 9 | a0001c0003t0001g0016 a0001c0003t0001g0026 a0001c0003t0001g0083 others(6): Show |
9 | HG02257.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.166-1354C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44360011 | |||||||
| chr3:44360153 | C | T | 35 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0049 others(32): Show |
36 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.166-1212C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44360153 | |||||||
| chr3:44360440 | G | C | 1 | a0001c0001t0001g0138 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.166-925G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44360440 | |||||||
| chr3:44360571 | G | A | 158 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(155): Show |
162 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.166-794G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44360571 | |||||||
| chr3:44360761 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.166-604G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44360761 | |||||||
| chr3:44360772 | A | C | 108 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0092 others(105): Show |
111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.166-593A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44360772 | |||||||
| chr3:44360809 | C | T | 211 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(208): Show |
216 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.166-556C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44360809 | |||||||
| chr3:44360882 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.166-483A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44360882 | |||||||
| chr3:44360899 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.166-466C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 3/10 | chr3 | 44360899 | |||||||
| chr3:44361599 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.319+81T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44361599 | |||||||
| chr3:44361875 | A | G | 2 | a0001c0001t0009g0063 a0001c0001t0009g0064 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.319+357A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44361875 | |||||||
| chr3:44362200 | A | G | 49 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0137 others(46): Show |
50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.319+682A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44362200 | |||||||
| chr3:44362259 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.319+741C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44362259 | |||||||
| chr3:44362387 | C | T | 7 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.319+869C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44362387 | |||||||
| chr3:44362700 | C | T | 6 | a0001c0001t0005g0001 a0001c0001t0005g0007 a0001c0001t0005g0008 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.319+1182C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44362700 | |||||||
| chr3:44362909 | A | G | 1 | a0001c0001t0002g0034 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.319+1391A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44362909 | |||||||
| chr3:44363037 | C | T | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0174 |
3 | HG02257.hp2 HG04199.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.319+1519C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44363037 | |||||||
| chr3:44363229 | T | C | 1 | a0001c0001t0002g0080 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.319+1711T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44363229 | |||||||
| chr3:44363563 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.319+2045A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44363563 | |||||||
| chr3:44363655 | A | C | 3 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0062 |
3 | HG00423.hp2 HG02040.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.319+2137A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44363655 | |||||||
| chr3:44363920 | C | CT | 23 | a0001c0001t0001g0027 a0001c0001t0002g0018 a0001c0001t0002g0025 others(20): Show |
23 | HG00423.hp2 HG00741.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.319+2429dupT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44363920 | ||||||
| chr3:44363920 | C | CTT | 6 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(3): Show |
6 | HG02622.hp1 HG02717.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.319+2428_319+2429d others(4): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44363920 | ||||||
| chr3:44363920 | C | CTTT | 6 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0001g0173 others(3): Show |
6 | HG02258.hp1 HG02698.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.319+2427_319+2429d others(5): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44363920 | ||||||
| chr3:44363920 | C | CTTTT | 22 | a0001c0001t0001g0006 a0001c0001t0001g0140 a0001c0001t0001g0144 others(19): Show |
23 | HG00558.hp1 HG00609.hp1 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.319+2426_319+2429d others(6): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44363920 | ||||||
| chr3:44363920 | C | CTTTTT | 14 | a0001c0001t0001g0136 a0001c0001t0001g0146 a0001c0001t0001g0147 others(11): Show |
14 | HG00597.hp2 HG00642.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.319+2425_319+2429d others(7): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44363920 | ||||||
| chr3:44363920 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0142 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.319+2420_319+2429d others(12): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44363920 | ||||||
| chr3:44363920 | CT | C | 22 | a0001c0001t0001g0014 a0001c0001t0001g0092 a0001c0001t0001g0094 others(19): Show |
22 | HG00423.hp1 HG01257.hp2 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.319+2429delT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44363920 | ||||||
| chr3:44363920 | CTT | C | 89 | a0001c0001t0001g0004 a0001c0001t0001g0093 a0001c0001t0001g0095 others(86): Show |
91 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.319+2428_319+2429d others(4): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44363920 | ||||||
| chr3:44363951 | A | G | 110 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(107): Show |
113 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(110): Show |
intron_variant | MODIFIER | c.319+2433A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44363951 | |||||||
| chr3:44363975 | T | C | 158 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(155): Show |
162 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.319+2457T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44363975 | |||||||
| chr3:44364118 | G | A | 7 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.319+2600G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44364118 | |||||||
| chr3:44364162 | C | G | 1 | a0001c0001t0020g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.319+2644C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44364162 | |||||||
| chr3:44364212 | C | A | 1 | a0001c0001t0001g0234 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.319+2694C>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44364212 | |||||||
| chr3:44364212 | C | T | 7 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.319+2694C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44364212 | |||||||
| chr3:44364239 | T | A | 9 | a0001c0001t0001g0014 a0001c0001t0001g0137 a0001c0001t0001g0138 others(6): Show |
9 | HG02257.hp1 HG02622.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.319+2721T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44364239 | |||||||
| chr3:44364275 | T | A | 1 | a0001c0001t0014g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.319+2757T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44364275 | |||||||
| chr3:44364410 | T | C | 35 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0049 others(32): Show |
36 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.319+2892T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44364410 | |||||||
| chr3:44364627 | C | A | 158 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(155): Show |
162 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.320-2829C>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44364627 | |||||||
| chr3:44364745 | C | CA | 19 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0155 others(16): Show |
19 | HG00597.hp2 HG01109.hp1 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.320-2694dupA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44364745 | ||||||
| chr3:44364784 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.320-2672C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44364784 | |||||||
| chr3:44364913 | A | G | 1 | a0001c0001t0003g0071 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.320-2543A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44364913 | |||||||
| chr3:44365051 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | HG00733.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.320-2405T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44365051 | |||||||
| chr3:44365116 | TTTTTC | T | 108 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0092 others(105): Show |
111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.320-2337_320-2333d others(7): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44365116 | ||||||
| chr3:44365334 | C | CT | 6 | a0001c0001t0001g0096 a0001c0001t0001g0122 a0001c0001t0001g0126 others(3): Show |
6 | HG01358.hp1 HG01975.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.320-2109dupT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44365334 | ||||||
| chr3:44365409 | A | G | 1 | a0001c0001t0002g0041 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.320-2047A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44365409 | |||||||
| chr3:44365489 | C | T | 1 | a0001c0001t0002g0036 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.320-1967C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44365489 | |||||||
| chr3:44365618 | G | T | 5 | a0001c0001t0006g0170 a0001c0004t0006g0164 a0001c0004t0006g0165 others(2): Show |
5 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(2): Show |
intron_variant | MODIFIER | c.320-1838G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44365618 | |||||||
| chr3:44365754 | C | G | 6 | a0001c0001t0005g0001 a0001c0001t0005g0007 a0001c0001t0005g0008 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.320-1702C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44365754 | |||||||
| chr3:44365917 | T | A | 1 | a0001c0001t0001g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.320-1539T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44365917 | |||||||
| chr3:44365948 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.320-1508C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44365948 | |||||||
| chr3:44366218 | AT | A | 49 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0137 others(46): Show |
50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.320-1232delT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44366218 | ||||||
| chr3:44366463 | G | GT | 28 | a0001c0001t0001g0027 a0001c0001t0001g0125 a0001c0001t0001g0126 others(25): Show |
28 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.320-973dupT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44366463 | ||||||
| chr3:44366463 | GT | G | 86 | a0001c0001t0001g0004 a0001c0001t0001g0093 a0001c0001t0001g0094 others(83): Show |
88 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.320-973delT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44366463 | ||||||
| chr3:44366472 | T | G | 1 | a0001c0001t0001g0202 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.320-984T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44366472 | |||||||
| chr3:44366529 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.320-927G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44366529 | |||||||
| chr3:44366605 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.320-851C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44366605 | |||||||
| chr3:44366627 | AT | A | 157 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(154): Show |
161 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.320-817delT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44366627 | ||||||
| chr3:44366709 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.320-747G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44366709 | |||||||
| chr3:44366763 | G | T | 49 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0137 others(46): Show |
50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.320-693G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44366763 | |||||||
| chr3:44366802 | G | A | 4 | a0001c0001t0007g0065 a0001c0001t0007g0066 a0001c0001t0007g0072 others(1): Show |
4 | HG02895.hp1 HG02896.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.320-654G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44366802 | |||||||
| chr3:44366905 | T | G | 98 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(95): Show |
99 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.320-551T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44366905 | |||||||
| chr3:44366978 | T | C | 1 | a0001c0001t0004g0089 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.320-478T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44366978 | |||||||
| chr3:44367349 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.320-107C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | chr3 | 44367349 | |||||||
| chr3:44367372 | G | GT | 211 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(208): Show |
216 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.320-81dupT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr3 | 44367372 | ||||||
| chr3:44367958 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.572+250T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44367958 | |||||||
| chr3:44367984 | T | C | 49 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0137 others(46): Show |
50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.572+276T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44367984 | |||||||
| chr3:44368097 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.572+389C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44368097 | |||||||
| chr3:44368154 | T | C | 36 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0049 others(33): Show |
37 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.572+446T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44368154 | |||||||
| chr3:44368581 | T | C | 1 | a0001c0001t0011g0229 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.572+873T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44368581 | |||||||
| chr3:44369015 | C | T | 1 | a0001c0004t0006g0171 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.572+1307C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44369015 | |||||||
| chr3:44369374 | G | A | 36 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0142 others(33): Show |
37 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.572+1666G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44369374 | |||||||
| chr3:44369708 | C | G | 1 | a0001c0001t0001g0118 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.572+2000C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44369708 | |||||||
| chr3:44369942 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.572+2234G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44369942 | |||||||
| chr3:44370076 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.572+2368G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370076 | |||||||
| chr3:44370083 | ATTC | A | 108 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0092 others(105): Show |
111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.572+2378_572+2380d others(5): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44370083 | ||||||
| chr3:44370287 | C | G | 1 | a0001c0001t0020g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.572+2579C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370287 | |||||||
| chr3:44370380 | G | A | 1 | a0001c0001t0002g0042 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.572+2672G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370380 | |||||||
| chr3:44370413 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.572+2705G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370413 | |||||||
| chr3:44370455 | C | CA | 70 | a0001c0001t0001g0006 a0001c0001t0001g0093 a0001c0001t0001g0106 others(67): Show |
72 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.572+2764dupA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44370455 | ||||||
| chr3:44370455 | C | CAA | 7 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 others(4): Show |
7 | HG00597.hp2 HG01175.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.572+2763_572+2764d others(4): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44370455 | ||||||
| chr3:44370455 | CA | C | 6 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.572+2764delA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44370455 | ||||||
| chr3:44370618 | T | C | 9 | a0001c0003t0001g0016 a0001c0003t0001g0026 a0001c0003t0001g0083 others(6): Show |
9 | HG02257.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.572+2910T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370618 | |||||||
| chr3:44370641 | C | T | 1 | a0001c0001t0001g0216 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.572+2933C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370641 | |||||||
| chr3:44370669 | T | TG | 5 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0049 others(2): Show |
5 | HG02486.hp2 HG02735.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.572+2961_572+2962i others(3): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370669 | |||||||
| chr3:44370670 | T | G | 31 | a0001c0001t0001g0190 a0001c0001t0003g0050 a0001c0001t0003g0051 others(28): Show |
32 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.572+2962T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370670 | |||||||
| chr3:44370716 | G | A | 5 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.572+3008G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370716 | |||||||
| chr3:44370750 | C | CT | 36 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0049 others(33): Show |
37 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.572+3045dupT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44370750 | ||||||
| chr3:44370751 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.572+3043T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370751 | |||||||
| chr3:44370752 | TTC | T | 155 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
159 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.572+3046_572+3047d others(4): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44370752 | ||||||
| chr3:44370753 | TC | T | 3 | a0001c0001t0001g0093 a0001c0001t0001g0126 a0001c0001t0001g0141 |
3 | HG02647.hp1 HG02818.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.572+3046delC | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370753 | |||||||
| chr3:44370754 | C | T | 54 | a0001c0001t0001g0027 a0001c0001t0002g0037 a0001c0001t0003g0047 others(51): Show |
55 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.572+3046C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370754 | |||||||
| chr3:44370908 | A | AT | 112 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(109): Show |
115 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.572+3220dupT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44370908 | ||||||
| chr3:44370908 | A | ATT | 6 | a0001c0001t0001g0093 a0001c0001t0001g0121 a0001c0001t0001g0122 others(3): Show |
6 | HG00735.hp2 HG01106.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.572+3219_572+3220d others(4): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44370908 | ||||||
| chr3:44370908 | AT | A | 10 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(7): Show |
10 | HG01516.hp2 HG02647.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.572+3220delT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44370908 | ||||||
| chr3:44370972 | C | T | 1 | a0001c0001t0019g0189 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.572+3264C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370972 | |||||||
| chr3:44370998 | G | T | 6 | a0001c0001t0002g0013 a0001c0001t0002g0032 a0001c0001t0002g0040 others(3): Show |
6 | HG02572.hp2 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.572+3290G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44370998 | |||||||
| chr3:44371062 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.572+3354G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44371062 | |||||||
| chr3:44371154 | C | T | 6 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0180 others(3): Show |
6 | HG02647.hp2 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.572+3446C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44371154 | |||||||
| chr3:44371205 | C | T | 7 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.572+3497C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44371205 | |||||||
| chr3:44372004 | A | G | 10 | a0001c0001t0001g0014 a0001c0001t0004g0084 a0001c0001t0004g0085 others(7): Show |
10 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.572+4296A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372004 | |||||||
| chr3:44372006 | G | A | 9 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 others(6): Show |
9 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.572+4298G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372006 | |||||||
| chr3:44372009 | A | AGAAG | 6 | a0001c0001t0002g0013 a0001c0001t0002g0023 a0001c0001t0002g0033 others(3): Show |
6 | HG02300.hp2 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.572+4366_572+4369d others(6): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44372009 | ||||||
| chr3:44372009 | A | AGAAGGAA others(5): Show |
1 | a0001c0001t0002g0024 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.572+4358_572+4369d others(14): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44372009 | ||||||
| chr3:44372009 | AGAAG | A | 56 | a0001c0001t0001g0006 a0001c0001t0001g0094 a0001c0001t0001g0097 others(53): Show |
58 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.572+4366_572+4369d others(6): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44372009 | ||||||
| chr3:44372009 | AGAAGGAA others(1): Show |
A | 32 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0027 others(29): Show |
33 | HG00423.hp1 HG00558.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.572+4362_572+4369d others(10): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44372009 | ||||||
| chr3:44372009 | AGAAGGAA others(5): Show |
A | 24 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0107 others(21): Show |
24 | HG01099.hp2 HG01123.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.572+4358_572+4369d others(14): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44372009 | ||||||
| chr3:44372009 | AGAAGGAA others(9): Show |
A | 8 | a0001c0001t0001g0106 a0001c0001t0001g0125 a0001c0001t0001g0186 others(5): Show |
8 | HG00738.hp1 HG01099.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.572+4354_572+4369d others(18): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44372009 | ||||||
| chr3:44372009 | AGAAGGAA others(13): Show |
A | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0004t0006g0165 |
3 | HG00673.hp2 HG02922.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.572+4350_572+4369d others(22): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44372009 | ||||||
| chr3:44372011 | AAGGAAGG others(7): Show |
A | 6 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.572+4304_572+4317d others(16): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372011 | |||||||
| chr3:44372011 | AAGGAAGG others(11): Show |
A | 1 | a0001c0001t0004g0089 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.572+4304_572+4321d others(20): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372011 | |||||||
| chr3:44372040 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.572+4332A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372040 | |||||||
| chr3:44372053 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.572+4345G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372053 | |||||||
| chr3:44372064 | A | AGGAAGGA others(13): Show |
2 | a0001c0001t0001g0180 a0001c0001t0001g0182 |
2 | HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.572+4369_572+4370i others(22): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44372064 | ||||||
| chr3:44372064 | A | AGGAAGGA others(9): Show |
1 | a0001c0001t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.572+4369_572+4370i others(18): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44372064 | ||||||
| chr3:44372064 | A | AGGAAGGA others(5): Show |
7 | a0001c0001t0001g0152 a0001c0001t0001g0159 a0001c0001t0001g0173 others(4): Show |
7 | HG02486.hp1 HG02647.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.572+4367_572+4368i others(14): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44372064 | ||||||
| chr3:44372064 | A | AGGAAGGA others(1): Show |
6 | a0001c0001t0001g0147 a0001c0001t0001g0155 a0001c0001t0001g0156 others(3): Show |
6 | HG00609.hp1 HG01106.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.572+4363_572+4364i others(10): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44372064 | ||||||
| chr3:44372064 | A | AGGAG | 13 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0001t0001g0139 others(10): Show |
13 | HG00642.hp2 HG01175.hp2 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.572+4359_572+4360i others(6): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44372064 | ||||||
| chr3:44372064 | A | G | 20 | a0001c0001t0001g0006 a0001c0001t0001g0140 a0001c0001t0001g0141 others(17): Show |
21 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.572+4356A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372064 | |||||||
| chr3:44372077 | G | C | 139 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(136): Show |
142 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.572+4369G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372077 | |||||||
| chr3:44372077 | G | GGAAC | 20 | a0001c0001t0001g0098 a0001c0001t0001g0192 a0001c0001t0001g0214 others(17): Show |
21 | HG01123.hp2 HG01261.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.572+4369_572+4370i others(6): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372077 | |||||||
| chr3:44372077 | G | GGAAGGAA others(9): Show |
1 | a0002c0002t0001g0030 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.572+4369_572+4370i others(18): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372077 | |||||||
| chr3:44372120 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.572+4412C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372120 | |||||||
| chr3:44372134 | C | T | 2 | a0001c0001t0001g0186 a0001c0001t0001g0198 |
2 | HG00738.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.572+4426C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372134 | |||||||
| chr3:44372197 | G | C | 49 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0137 others(46): Show |
50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.572+4489G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372197 | |||||||
| chr3:44372337 | A | G | 158 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(155): Show |
162 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.572+4629A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372337 | |||||||
| chr3:44372511 | T | C | 1 | a0001c0001t0002g0043 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.572+4803T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372511 | |||||||
| chr3:44372566 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.572+4858C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372566 | |||||||
| chr3:44372570 | C | G | 2 | a0001c0003t0001g0026 a0001c0003t0001g0083 |
2 | HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.572+4862C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372570 | |||||||
| chr3:44372587 | C | CT | 6 | a0001c0001t0005g0001 a0001c0001t0005g0007 a0001c0001t0005g0008 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.572+4893dupT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44372587 | ||||||
| chr3:44372632 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.572+4924C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372632 | |||||||
| chr3:44372793 | G | A | 1 | a0001c0003t0001g0083 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.572+5085G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44372793 | |||||||
| chr3:44373115 | GTTTTTTT others(17): Show |
G | 1 | a0001c0001t0001g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.572+5414_572+5437d others(26): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44373115 | ||||||
| chr3:44373416 | G | C | 1 | a0001c0001t0001g0232 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.572+5708G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44373416 | |||||||
| chr3:44373492 | TA | T | 157 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(154): Show |
161 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.572+5797delA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44373492 | ||||||
| chr3:44373609 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.572+5901G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44373609 | |||||||
| chr3:44373746 | T | A | 1 | a0001c0001t0001g0141 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.572+6038T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44373746 | |||||||
| chr3:44374281 | GCTTT | G | 43 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0138 others(40): Show |
44 | HG00609.hp1 HG00642.hp2 HG01106.hp1 others(41): Show |
intron_variant | MODIFIER | c.572+6578_572+6581d others(6): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44374281 | ||||||
| chr3:44374282 | CTTTCT | C | 6 | a0001c0001t0001g0137 a0001c0001t0006g0170 a0001c0004t0006g0164 others(3): Show |
6 | HG00558.hp1 HG00597.hp2 HG00673.hp2 others(3): Show |
intron_variant | MODIFIER | c.572+6578_572+6582d others(7): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44374282 | ||||||
| chr3:44374286 | C | CT | 38 | a0001c0001t0001g0114 a0001c0001t0001g0118 a0001c0001t0001g0130 others(35): Show |
39 | HG00140.hp1 HG00423.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.572+6593dupT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44374286 | ||||||
| chr3:44374286 | CT | C | 12 | a0001c0001t0001g0125 a0001c0001t0001g0126 a0001c0001t0001g0128 others(9): Show |
12 | HG00642.hp1 HG02572.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.572+6593delT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44374286 | ||||||
| chr3:44374393 | G | A | 5 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0030 others(2): Show |
5 | HG02257.hp1 HG02723.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.572+6685G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44374393 | |||||||
| chr3:44374420 | T | C | 99 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(96): Show |
100 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.572+6712T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44374420 | |||||||
| chr3:44374494 | A | G | 36 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0049 others(33): Show |
37 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.572+6786A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44374494 | |||||||
| chr3:44374860 | A | G | 7 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.572+7152A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44374860 | |||||||
| chr3:44375015 | A | C | 2 | a0001c0001t0001g0192 a0001c0001t0001g0197 |
2 | HG03654.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.572+7307A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44375015 | |||||||
| chr3:44375373 | A | T | 3 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0049 |
3 | HG02486.hp2 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.572+7665A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44375373 | |||||||
| chr3:44375429 | G | A | 2 | a0001c0003t0001g0026 a0001c0003t0001g0083 |
2 | HG02572.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.572+7721G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44375429 | |||||||
| chr3:44375455 | A | T | 1 | a0001c0001t0003g0061 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.572+7747A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44375455 | |||||||
| chr3:44375535 | G | C | 99 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(96): Show |
100 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.572+7827G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44375535 | |||||||
| chr3:44375563 | T | G | 1 | a0001c0001t0001g0179 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.572+7855T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44375563 | |||||||
| chr3:44375737 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.572+8029C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44375737 | |||||||
| chr3:44375745 | T | C | 1 | a0001c0001t0003g0070 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.572+8037T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44375745 | |||||||
| chr3:44375977 | G | T | 1 | a0001c0001t0001g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.572+8269G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44375977 | |||||||
| chr3:44376024 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.572+8316G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44376024 | |||||||
| chr3:44376089 | T | C | 1 | a0001c0001t0007g0073 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.572+8381T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44376089 | |||||||
| chr3:44376242 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.572+8534T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44376242 | |||||||
| chr3:44376320 | A | G | 6 | a0001c0001t0005g0001 a0001c0001t0005g0007 a0001c0001t0005g0008 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.572+8612A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44376320 | |||||||
| chr3:44376498 | T | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0162 |
2 | HG02135.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.572+8790T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44376498 | |||||||
| chr3:44376572 | A | T | 6 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(3): Show |
6 | HG02258.hp1 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.572+8864A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44376572 | |||||||
| chr3:44376625 | A | G | 2 | a0001c0001t0001g0192 a0001c0001t0001g0197 |
2 | HG03654.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.572+8917A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44376625 | |||||||
| chr3:44376870 | C | T | 6 | a0001c0001t0005g0001 a0001c0001t0005g0007 a0001c0001t0005g0008 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.572+9162C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44376870 | |||||||
| chr3:44377045 | A | G | 158 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(155): Show |
162 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.572+9337A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44377045 | |||||||
| chr3:44377161 | C | T | 9 | a0001c0003t0001g0016 a0001c0003t0001g0026 a0001c0003t0001g0083 others(6): Show |
9 | HG02257.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.572+9453C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44377161 | |||||||
| chr3:44377200 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.572+9492A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44377200 | |||||||
| chr3:44377342 | C | G | 5 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0030 others(2): Show |
5 | HG02257.hp1 HG02723.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.572+9634C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44377342 | |||||||
| chr3:44377391 | T | C | 35 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0049 others(32): Show |
36 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.572+9683T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44377391 | |||||||
| chr3:44377404 | AGAAAGTT others(11): Show |
A | 1 | a0001c0001t0001g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.572+9698_572+9715d others(20): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44377404 | ||||||
| chr3:44377581 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.572+9873G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44377581 | |||||||
| chr3:44377742 | G | A | 5 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
5 | HG02258.hp1 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.572+10034G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44377742 | |||||||
| chr3:44378249 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.572+10541C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44378249 | |||||||
| chr3:44378391 | C | G | 1 | a0001c0001t0020g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.572+10683C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44378391 | |||||||
| chr3:44378459 | C | G | 108 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0092 others(105): Show |
111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.572+10751C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44378459 | |||||||
| chr3:44378546 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.572+10838G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44378546 | |||||||
| chr3:44378586 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.572+10878G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44378586 | |||||||
| chr3:44378643 | C | A | 1 | a0001c0001t0002g0013 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.572+10935C>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44378643 | |||||||
| chr3:44378746 | G | C | 43 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0141 others(40): Show |
44 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.572+11038G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44378746 | |||||||
| chr3:44378754 | T | C | 5 | a0001c0001t0003g0054 a0001c0001t0003g0056 a0001c0001t0003g0057 others(2): Show |
5 | HG00733.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.572+11046T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44378754 | |||||||
| chr3:44378760 | G | A | 1 | a0001c0001t0001g0005 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.572+11052G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44378760 | |||||||
| chr3:44378784 | G | A | 6 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.572+11076G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44378784 | |||||||
| chr3:44378796 | C | CA | 58 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0097 others(55): Show |
59 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.572+11103dupA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44378796 | ||||||
| chr3:44378796 | C | CAA | 4 | a0001c0001t0001g0006 a0001c0001t0001g0144 a0001c0001t0001g0145 others(1): Show |
5 | HG01358.hp1 HG01975.hp1 NA18961.hp1 others(2): Show |
intron_variant | MODIFIER | c.572+11102_572+1110 others(6): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44378796 | ||||||
| chr3:44378813 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.572+11105G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44378813 | |||||||
| chr3:44379206 | T | A | 1 | a0001c0001t0001g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.572+11498T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44379206 | |||||||
| chr3:44379206 | TAATA | T | 3 | a0001c0001t0001g0161 a0001c0001t0001g0168 a0001c0001t0001g0172 |
3 | HG01175.hp2 HG02683.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.572+11508_572+1151 others(8): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44379206 | ||||||
| chr3:44379270 | G | T | 1 | a0001c0001t0001g0150 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.572+11562G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44379270 | |||||||
| chr3:44379274 | G | C | 1 | a0001c0001t0001g0237 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.572+11566G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44379274 | |||||||
| chr3:44379294 | A | T | 1 | a0001c0001t0001g0237 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.572+11586A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44379294 | |||||||
| chr3:44379482 | A | G | 6 | a0001c0001t0005g0001 a0001c0001t0005g0007 a0001c0001t0005g0008 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.572+11774A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44379482 | |||||||
| chr3:44379501 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.572+11793G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44379501 | |||||||
| chr3:44379618 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.572+11910C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44379618 | |||||||
| chr3:44379672 | T | G | 1 | a0001c0001t0001g0221 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.572+11964T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44379672 | |||||||
| chr3:44379825 | G | A | 3 | a0001c0001t0001g0191 a0001c0001t0001g0214 a0001c0001t0001g0215 |
3 | HG01123.hp2 HG01358.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.572+12117G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44379825 | |||||||
| chr3:44379988 | C | T | 3 | a0001c0001t0001g0218 a0001c0001t0001g0240 a0001c0001t0001g0241 |
3 | HG00438.hp1 HG02040.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.572+12280C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44379988 | |||||||
| chr3:44380391 | A | T | 108 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0092 others(105): Show |
111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.573-12464A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44380391 | |||||||
| chr3:44380430 | A | G | 2 | a0001c0001t0001g0227 a0001c0001t0001g0228 |
2 | HG02056.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.573-12425A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44380430 | |||||||
| chr3:44380487 | T | C | 1 | a0001c0005t0001g0131 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.573-12368T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44380487 | |||||||
| chr3:44381262 | C | G | 1 | a0001c0001t0001g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.573-11593C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44381262 | |||||||
| chr3:44381744 | A | G | 1 | a0001c0001t0016g0224 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.573-11111A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44381744 | |||||||
| chr3:44381924 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.573-10931C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44381924 | |||||||
| chr3:44381959 | A | G | 1 | a0001c0001t0003g0071 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.573-10896A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44381959 | |||||||
| chr3:44381973 | T | A | 1 | a0001c0001t0001g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.573-10882T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44381973 | |||||||
| chr3:44381976 | G | A | 1 | a0001c0001t0002g0020 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.573-10879G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44381976 | |||||||
| chr3:44382179 | G | A | 11 | a0001c0001t0001g0191 a0001c0001t0001g0194 a0001c0001t0001g0203 others(8): Show |
11 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.573-10676G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44382179 | |||||||
| chr3:44382312 | C | T | 35 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0049 others(32): Show |
36 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.573-10543C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44382312 | |||||||
| chr3:44382440 | A | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0181 |
2 | HG02647.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.573-10415A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44382440 | |||||||
| chr3:44382536 | A | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.573-10319A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44382536 | |||||||
| chr3:44382566 | A | G | 5 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0122 others(2): Show |
5 | HG00735.hp1 HG01934.hp2 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.573-10289A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44382566 | |||||||
| chr3:44382692 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.573-10163G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44382692 | |||||||
| chr3:44382734 | A | G | 1 | a0001c0001t0003g0061 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.573-10121A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44382734 | |||||||
| chr3:44382873 | A | G | 109 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(106): Show |
112 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.573-9982A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44382873 | |||||||
| chr3:44383117 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.573-9738G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44383117 | |||||||
| chr3:44383187 | C | G | 1 | a0001c0001t0001g0220 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.573-9668C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44383187 | |||||||
| chr3:44383347 | C | G | 158 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(155): Show |
162 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.573-9508C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44383347 | |||||||
| chr3:44383475 | T | G | 1 | a0001c0001t0001g0098 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.573-9380T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44383475 | |||||||
| chr3:44383536 | A | G | 229 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(226): Show |
234 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.573-9319A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44383536 | |||||||
| chr3:44383557 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.573-9298C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44383557 | |||||||
| chr3:44383641 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.573-9214A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44383641 | |||||||
| chr3:44383685 | G | T | 211 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(208): Show |
216 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.573-9170G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44383685 | |||||||
| chr3:44383690 | G | A | 49 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0137 others(46): Show |
50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.573-9165G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44383690 | |||||||
| chr3:44383809 | C | CA | 5 | a0001c0001t0002g0023 a0001c0001t0002g0036 a0001c0001t0005g0008 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.573-9021dupA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44383809 | ||||||
| chr3:44383809 | C | CAAAA | 6 | a0001c0001t0020g0015 a0001c0003t0001g0016 a0002c0002t0001g0028 others(3): Show |
6 | HG02257.hp1 HG02630.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.573-9024_573-9021d others(6): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44383809 | ||||||
| chr3:44383809 | CA | C | 49 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0107 others(46): Show |
50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.573-9021delA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44383809 | ||||||
| chr3:44383809 | CAA | C | 94 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(91): Show |
95 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.573-9022_573-9021d others(4): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44383809 | ||||||
| chr3:44383809 | CAAAAA | C | 34 | a0001c0001t0001g0027 a0001c0001t0003g0047 a0001c0001t0003g0048 others(31): Show |
35 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.573-9025_573-9021d others(7): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44383809 | ||||||
| chr3:44383935 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.573-8920G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44383935 | |||||||
| chr3:44383947 | A | G | 1 | a0001c0001t0002g0040 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.573-8908A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44383947 | |||||||
| chr3:44384343 | G | C | 49 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0137 others(46): Show |
50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.573-8512G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44384343 | |||||||
| chr3:44384499 | C | T | 111 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(108): Show |
114 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.573-8356C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44384499 | |||||||
| chr3:44384546 | G | C | 1 | a0001c0001t0018g0211 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.573-8309G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44384546 | |||||||
| chr3:44384587 | A | G | 6 | a0001c0001t0005g0001 a0001c0001t0005g0007 a0001c0001t0005g0008 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.573-8268A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44384587 | |||||||
| chr3:44384634 | C | T | 1 | a0001c0001t0003g0069 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.573-8221C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44384634 | |||||||
| chr3:44384808 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.573-8047A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44384808 | |||||||
| chr3:44385542 | C | T | 1 | a0001c0001t0001g0005 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.573-7313C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44385542 | |||||||
| chr3:44385544 | G | A | 49 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0137 others(46): Show |
50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.573-7311G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44385544 | |||||||
| chr3:44385600 | G | A | 49 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0137 others(46): Show |
50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.573-7255G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44385600 | |||||||
| chr3:44386209 | C | CA | 73 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0093 others(70): Show |
76 | HG00639.hp2 HG00733.hp1 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.573-6623dupA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44386209 | ||||||
| chr3:44386209 | C | CAA | 39 | a0001c0001t0001g0096 a0001c0001t0001g0106 a0001c0001t0001g0136 others(36): Show |
39 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.573-6624_573-6623d others(4): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44386209 | ||||||
| chr3:44386209 | C | CAAA | 9 | a0001c0001t0001g0006 a0001c0001t0001g0138 a0001c0001t0001g0139 others(6): Show |
10 | HG01106.hp1 HG01175.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.573-6625_573-6623d others(5): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44386209 | ||||||
| chr3:44386479 | C | T | 6 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.573-6376C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44386479 | |||||||
| chr3:44386621 | G | T | 2 | a0001c0001t0001g0216 a0001c0001t0001g0220 |
2 | HG01261.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.573-6234G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44386621 | |||||||
| chr3:44386641 | C | T | 3 | a0001c0001t0001g0111 a0001c0001t0001g0117 a0001c0001t0001g0128 |
3 | HG00642.hp1 HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.573-6214C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44386641 | |||||||
| chr3:44386724 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.573-6131C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44386724 | |||||||
| chr3:44386738 | T | A | 100 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0092 others(97): Show |
102 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.573-6117T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44386738 | |||||||
| chr3:44386929 | G | A | 5 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
5 | HG02258.hp1 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.573-5926G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44386929 | |||||||
| chr3:44386945 | C | T | 98 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(95): Show |
99 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.573-5910C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44386945 | |||||||
| chr3:44386954 | G | A | 100 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0092 others(97): Show |
102 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.573-5901G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44386954 | |||||||
| chr3:44386955 | T | G | 1 | a0001c0001t0002g0032 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.573-5900T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44386955 | |||||||
| chr3:44386993 | C | T | 108 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0092 others(105): Show |
111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.573-5862C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44386993 | |||||||
| chr3:44386994 | G | A | 6 | a0001c0001t0002g0013 a0001c0001t0002g0032 a0001c0001t0002g0040 others(3): Show |
6 | HG02572.hp2 HG02886.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.573-5861G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44386994 | |||||||
| chr3:44387319 | C | T | 43 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0141 others(40): Show |
44 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.573-5536C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44387319 | |||||||
| chr3:44387430 | AG | A | 6 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.573-5422delG | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44387430 | ||||||
| chr3:44387643 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.573-5212C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44387643 | |||||||
| chr3:44387953 | T | G | 1 | a0001c0001t0020g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.573-4902T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44387953 | |||||||
| chr3:44387968 | A | T | 1 | a0001c0003t0001g0083 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.573-4887A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44387968 | |||||||
| chr3:44388022 | A | C | 5 | a0001c0001t0001g0126 a0001c0001t0001g0169 a0001c0001t0001g0203 others(2): Show |
5 | HG00597.hp2 HG02148.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.573-4833A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44388022 | |||||||
| chr3:44388200 | T | C | 2 | a0001c0001t0007g0065 a0001c0001t0007g0066 |
2 | HG02895.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.573-4655T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44388200 | |||||||
| chr3:44388441 | TAGAGTC | T | 6 | a0001c0001t0005g0001 a0001c0001t0005g0007 a0001c0001t0005g0008 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.573-4408_573-4403d others(8): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44388441 | ||||||
| chr3:44388694 | G | A | 1 | a0001c0001t0003g0081 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.573-4161G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44388694 | |||||||
| chr3:44388840 | G | A | 42 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0142 others(39): Show |
43 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.573-4015G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44388840 | |||||||
| chr3:44388998 | T | G | 1 | a0001c0001t0015g0010 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.573-3857T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44388998 | |||||||
| chr3:44389029 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.573-3826C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44389029 | |||||||
| chr3:44389042 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.573-3813G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44389042 | |||||||
| chr3:44389222 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0125 a0001c0001t0001g0126 |
3 | HG02818.hp1 HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.573-3633G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44389222 | |||||||
| chr3:44389503 | G | A | 2 | a0001c0001t0001g0195 a0001c0001t0001g0196 |
2 | NA18961.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.573-3352G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44389503 | |||||||
| chr3:44389688 | G | A | 4 | a0001c0003t0001g0016 a0001c0003t0001g0026 a0001c0003t0001g0083 others(1): Show |
4 | HG02572.hp1 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.573-3167G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44389688 | |||||||
| chr3:44389746 | T | TA | 105 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0092 others(102): Show |
108 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(105): Show |
intron_variant | MODIFIER | c.573-3097dupA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr3 | 44389746 | ||||||
| chr3:44390069 | A | G | 2 | a0001c0001t0001g0117 a0001c0001t0001g0128 |
2 | HG00642.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.573-2786A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44390069 | |||||||
| chr3:44390148 | A | G | 2 | a0002c0002t0001g0029 a0002c0002t0001g0030 |
2 | HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.573-2707A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44390148 | |||||||
| chr3:44390707 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.573-2148A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44390707 | |||||||
| chr3:44390737 | G | A | 36 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0142 others(33): Show |
37 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.573-2118G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44390737 | |||||||
| chr3:44390878 | C | T | 1 | a0001c0001t0001g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.573-1977C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44390878 | |||||||
| chr3:44390891 | A | T | 4 | a0001c0001t0001g0161 a0001c0001t0001g0168 a0001c0001t0001g0172 others(1): Show |
4 | HG01175.hp2 HG02683.hp2 HG02698.hp1 others(1): Show |
intron_variant | MODIFIER | c.573-1964A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44390891 | |||||||
| chr3:44391113 | G | A | 1 | a0001c0001t0004g0090 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.573-1742G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44391113 | |||||||
| chr3:44391218 | G | A | 6 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(3): Show |
6 | HG02258.hp1 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.573-1637G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44391218 | |||||||
| chr3:44391274 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.573-1581C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44391274 | |||||||
| chr3:44391338 | G | A | 6 | a0001c0001t0005g0001 a0001c0001t0005g0007 a0001c0001t0005g0008 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.573-1517G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44391338 | |||||||
| chr3:44391339 | C | T | 1 | a0001c0001t0001g0233 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.573-1516C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44391339 | |||||||
| chr3:44391345 | C | T | 1 | a0001c0001t0001g0231 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.573-1510C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44391345 | |||||||
| chr3:44391358 | T | A | 1 | a0001c0001t0003g0061 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.573-1497T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44391358 | |||||||
| chr3:44391394 | A | G | 158 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(155): Show |
162 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.573-1461A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44391394 | |||||||
| chr3:44391748 | A | T | 1 | a0001c0001t0001g0141 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.573-1107A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44391748 | |||||||
| chr3:44391990 | A | C | 1 | a0001c0001t0002g0044 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.573-865A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44391990 | |||||||
| chr3:44392075 | T | C | 1 | a0001c0001t0003g0060 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.573-780T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44392075 | |||||||
| chr3:44392145 | A | G | 3 | a0001c0001t0001g0180 a0001c0001t0001g0182 a0001c0001t0001g0183 |
3 | HG02818.hp2 HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.573-710A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44392145 | |||||||
| chr3:44392282 | G | C | 158 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(155): Show |
162 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.573-573G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44392282 | |||||||
| chr3:44392418 | C | T | 158 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(155): Show |
162 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(159): Show |
intron_variant | MODIFIER | c.573-437C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44392418 | |||||||
| chr3:44392766 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.573-89G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44392766 | |||||||
| chr3:44392819 | G | A | 8 | a0001c0001t0002g0012 a0001c0001t0002g0033 a0001c0001t0002g0035 others(5): Show |
8 | HG01123.hp1 HG01261.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.573-36G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 5/10 | chr3 | 44392819 | |||||||
| chr3:44393182 | G | T | 35 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0049 others(32): Show |
36 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.695+205G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44393182 | |||||||
| chr3:44393183 | C | T | 35 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0049 others(32): Show |
36 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.695+206C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44393183 | |||||||
| chr3:44393348 | C | G | 1 | a0001c0001t0001g0141 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.695+371C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44393348 | |||||||
| chr3:44393618 | C | T | 7 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.695+641C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44393618 | |||||||
| chr3:44393743 | C | T | 2 | a0001c0001t0003g0070 a0001c0001t0003g0075 |
2 | HG02735.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.695+766C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44393743 | |||||||
| chr3:44393788 | A | G | 99 | a0001c0001t0001g0004 a0001c0001t0001g0092 a0001c0001t0001g0093 others(96): Show |
100 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.695+811A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44393788 | |||||||
| chr3:44394066 | T | C | 1 | a0002c0002t0001g0079 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.695+1089T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394066 | |||||||
| chr3:44394110 | CT | C | 49 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0137 others(46): Show |
50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.695+1141delT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394110 | ||||||
| chr3:44394185 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG02818.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.695+1208G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394185 | |||||||
| chr3:44394346 | A | C | 1 | a0001c0001t0001g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.695+1369A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394346 | |||||||
| chr3:44394365 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.695+1388A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394365 | |||||||
| chr3:44394401 | G | A | 6 | a0001c0001t0005g0001 a0001c0001t0005g0007 a0001c0001t0005g0008 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.695+1424G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394401 | |||||||
| chr3:44394419 | G | T | 1 | a0001c0001t0001g0122 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.695+1442G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394419 | |||||||
| chr3:44394557 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.695+1580A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394557 | |||||||
| chr3:44394618 | G | A | 7 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.695+1641G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394618 | |||||||
| chr3:44394666 | C | A | 1 | a0001c0001t0001g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.695+1689C>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394666 | |||||||
| chr3:44394835 | A | G | 1 | a0001c0001t0003g0048 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.696-1565A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394835 | |||||||
| chr3:44394836 | G | T | 49 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0137 others(46): Show |
50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.696-1564G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394836 | |||||||
| chr3:44394864 | G | A | 3 | a0001c0001t0001g0180 a0001c0001t0001g0182 a0001c0001t0001g0183 |
3 | HG02818.hp2 HG03139.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.696-1536G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394864 | |||||||
| chr3:44394908 | AAAAAAAA others(14): Show |
A | 1 | a0001c0001t0001g0196 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.696-1490_696-1470d others(23): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394908 | ||||||
| chr3:44394909 | AAAAAAAA others(13): Show |
A | 3 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0134 |
3 | HG01099.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.696-1489_696-1470d others(22): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394909 | ||||||
| chr3:44394915 | AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0001g0215 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.696-1483_696-1474d others(12): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394915 | ||||||
| chr3:44394915 | AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0001g0146 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.696-1483_696-1470d others(16): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394915 | ||||||
| chr3:44394916 | AAAAAAAT others(8): Show |
A | 1 | a0001c0001t0003g0076 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.696-1482_696-1468d others(17): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394916 | ||||||
| chr3:44394917 | AAAAAATA others(5): Show |
A | 1 | a0001c0001t0001g0177 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.696-1481_696-1470d others(14): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394917 | ||||||
| chr3:44394917 | AAAAAATA others(9): Show |
A | 2 | a0001c0001t0001g0141 a0001c0001t0003g0052 |
2 | HG02040.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.696-1481_696-1466d others(18): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394917 | ||||||
| chr3:44394918 | AAAAATAT others(4): Show |
A | 3 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0132 |
3 | HG00733.hp2 HG03471.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.696-1480_696-1470d others(13): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394918 | ||||||
| chr3:44394918 | AAAAATAT others(6): Show |
A | 3 | a0001c0001t0001g0140 a0001c0001t0001g0149 a0001c0001t0007g0073 |
3 | HG03098.hp2 HG04199.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.696-1480_696-1468d others(15): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394918 | ||||||
| chr3:44394918 | AAAAATAT others(8): Show |
A | 3 | a0001c0001t0001g0136 a0001c0001t0001g0145 a0001c0001t0007g0072 |
3 | HG01975.hp1 HG03041.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.696-1480_696-1466d others(17): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394918 | ||||||
| chr3:44394918 | AAAAATAT others(16): Show |
A | 2 | a0002c0002t0001g0029 a0002c0002t0001g0030 |
2 | HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.696-1480_696-1458d others(25): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394918 | ||||||
| chr3:44394918 | AAAAATAT others(18): Show |
A | 2 | a0002c0002t0001g0028 a0002c0002t0001g0079 |
2 | HG03139.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.696-1480_696-1456d others(27): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394918 | ||||||
| chr3:44394919 | AAAATATA others(1): Show |
A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0116 others(2): Show |
5 | HG02717.hp2 HG02809.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.696-1479_696-1472d others(10): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394919 | ||||||
| chr3:44394919 | AAAATATA others(3): Show |
A | 2 | a0001c0001t0001g0127 a0001c0001t0011g0229 |
2 | HG02965.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.696-1479_696-1470d others(12): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394919 | ||||||
| chr3:44394919 | AAAATATA others(5): Show |
A | 3 | a0001c0001t0001g0119 a0001c0001t0001g0129 a0001c0001t0001g0176 |
3 | HG01891.hp1 HG02280.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.696-1479_696-1468d others(14): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394919 | ||||||
| chr3:44394919 | AAAATATA others(7): Show |
A | 8 | a0001c0001t0001g0006 a0001c0001t0001g0144 a0001c0001t0001g0152 others(5): Show |
9 | HG02523.hp2 HG02896.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.696-1479_696-1466d others(16): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394919 | ||||||
| chr3:44394920 | AAATATAT others(2): Show |
A | 14 | a0001c0001t0001g0186 a0001c0001t0001g0194 a0001c0001t0001g0198 others(11): Show |
14 | HG00423.hp1 HG00609.hp2 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.696-1478_696-1470d others(11): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394920 | ||||||
| chr3:44394920 | AAATATAT others(4): Show |
A | 13 | a0001c0001t0001g0096 a0001c0001t0001g0102 a0001c0001t0001g0108 others(10): Show |
13 | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.696-1478_696-1468d others(13): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394920 | ||||||
| chr3:44394920 | AAATATAT others(6): Show |
A | 8 | a0001c0001t0001g0148 a0001c0001t0001g0158 a0001c0001t0001g0168 others(5): Show |
8 | HG01175.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.696-1478_696-1466d others(15): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394920 | ||||||
| chr3:44394920 | AAATATAT others(8): Show |
A | 6 | a0001c0001t0001g0151 a0001c0001t0001g0175 a0001c0001t0003g0061 others(3): Show |
6 | HG02148.hp2 HG02735.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.696-1478_696-1464d others(17): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394920 | ||||||
| chr3:44394920 | AAATATAT others(16): Show |
A | 1 | a0002c0002t0001g0031 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.696-1478_696-1456d others(25): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394920 | ||||||
| chr3:44394921 | A | T | 4 | a0001c0001t0001g0125 a0001c0001t0002g0018 a0001c0001t0002g0021 others(1): Show |
4 | HG01192.hp1 HG03453.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.696-1479A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394921 | |||||||
| chr3:44394921 | AAT | A | 6 | a0001c0001t0002g0012 a0001c0001t0002g0032 a0001c0001t0002g0036 others(3): Show |
6 | HG01515.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.696-1442_696-1441d others(4): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394921 | ||||||
| chr3:44394921 | AATATATA others(1): Show |
A | 11 | a0001c0001t0001g0106 a0001c0001t0001g0181 a0001c0001t0001g0185 others(8): Show |
11 | HG00597.hp1 HG00735.hp2 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.696-1448_696-1441d others(10): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394921 | ||||||
| chr3:44394921 | AATATATA others(3): Show |
A | 8 | a0001c0001t0001g0093 a0001c0001t0001g0095 a0001c0001t0001g0099 others(5): Show |
8 | HG01167.hp2 HG02683.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.696-1450_696-1441d others(12): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394921 | ||||||
| chr3:44394921 | AATATATA others(5): Show |
A | 6 | a0001c0001t0001g0109 a0001c0001t0001g0155 a0001c0001t0001g0156 others(3): Show |
6 | HG02486.hp1 HG02818.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.696-1452_696-1441d others(14): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394921 | ||||||
| chr3:44394921 | AATATATA others(7): Show |
A | 27 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0153 others(24): Show |
27 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.696-1454_696-1441d others(16): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394921 | ||||||
| chr3:44394921 | AATATATA others(11): Show |
A | 1 | a0001c0001t0001g0126 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.696-1458_696-1441d others(20): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394921 | ||||||
| chr3:44394921 | AATATATA others(17): Show |
A | 1 | a0001c0001t0001g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.696-1464_696-1441d others(26): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394921 | ||||||
| chr3:44394922 | AT | A | 3 | a0001c0001t0002g0035 a0001c0001t0002g0042 a0001c0001t0002g0077 |
3 | HG01346.hp1 HG01361.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.696-1477delT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394922 | |||||||
| chr3:44394922 | ATAT | A | 6 | a0001c0001t0002g0040 a0001c0001t0002g0044 a0001c0001t0004g0084 others(3): Show |
6 | HG02109.hp2 HG02572.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.696-1477_696-1475d others(5): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394922 | |||||||
| chr3:44394922 | ATATATAT | A | 5 | a0001c0001t0001g0100 a0001c0001t0001g0200 a0001c0001t0001g0210 others(2): Show |
5 | HG02004.hp1 HG02572.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.696-1477_696-1471d others(9): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394922 | |||||||
| chr3:44394922 | ATATATAT others(2): Show |
A | 23 | a0001c0001t0001g0092 a0001c0001t0001g0107 a0001c0001t0001g0118 others(20): Show |
23 | HG00140.hp1 HG00140.hp2 HG00438.hp1 others(20): Show |
intron_variant | MODIFIER | c.696-1477_696-1469d others(11): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394922 | |||||||
| chr3:44394922 | ATATATAT others(4): Show |
A | 10 | a0001c0001t0001g0098 a0001c0001t0001g0101 a0001c0001t0001g0110 others(7): Show |
10 | HG00639.hp1 HG00735.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.696-1477_696-1467d others(13): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394922 | |||||||
| chr3:44394922 | ATATATAT others(6): Show |
A | 9 | a0001c0001t0001g0139 a0001c0001t0001g0147 a0001c0001t0003g0047 others(6): Show |
9 | HG00673.hp2 HG01106.hp1 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.696-1477_696-1465d others(15): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394922 | |||||||
| chr3:44394922 | ATATATAT others(8): Show |
A | 7 | a0001c0001t0001g0162 a0001c0001t0003g0049 a0001c0001t0003g0069 others(4): Show |
7 | HG00639.hp2 HG00741.hp2 HG01346.hp2 others(4): Show |
intron_variant | MODIFIER | c.696-1477_696-1463d others(17): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394922 | |||||||
| chr3:44394923 | T | A | 5 | a0001c0001t0002g0002 a0001c0001t0002g0020 a0001c0001t0002g0024 others(2): Show |
5 | HG01243.hp2 HG01952.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.696-1477T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394923 | |||||||
| chr3:44394925 | T | A | 8 | a0001c0001t0002g0012 a0001c0001t0002g0020 a0001c0001t0002g0032 others(5): Show |
8 | HG01515.hp2 HG02258.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.696-1475T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394925 | |||||||
| chr3:44394927 | T | A | 12 | a0001c0001t0002g0020 a0001c0001t0002g0032 a0001c0001t0002g0040 others(9): Show |
12 | HG02109.hp2 HG02258.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.696-1473T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394927 | |||||||
| chr3:44394929 | T | A | 3 | a0001c0001t0001g0205 a0001c0001t0002g0013 a0001c0001t0002g0044 |
3 | HG02572.hp2 HG02886.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.696-1471T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394929 | |||||||
| chr3:44394931 | T | A | 8 | a0001c0001t0001g0100 a0001c0001t0001g0181 a0001c0001t0001g0201 others(5): Show |
8 | HG00597.hp1 HG02004.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.696-1469T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394931 | |||||||
| chr3:44394933 | T | A | 16 | a0001c0001t0001g0093 a0001c0001t0001g0178 a0001c0001t0001g0179 others(13): Show |
16 | HG00438.hp1 HG00597.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.696-1467T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394933 | |||||||
| chr3:44394935 | T | A | 8 | a0001c0001t0001g0117 a0001c0001t0001g0133 a0001c0001t0001g0159 others(5): Show |
8 | HG00438.hp1 HG00735.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.696-1465T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394935 | |||||||
| chr3:44394936 | ATATATAT others(17): Show |
A | 1 | a0001c0001t0001g0122 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.696-1456_696-1433d others(26): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr3 | 44394936 | ||||||
| chr3:44394937 | T | A | 14 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(11): Show |
15 | HG00597.hp2 HG01106.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.696-1463T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394937 | |||||||
| chr3:44394939 | T | A | 8 | a0001c0001t0003g0048 a0001c0001t0003g0071 a0001c0001t0005g0001 others(5): Show |
9 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.696-1461T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394939 | |||||||
| chr3:44394941 | T | A | 1 | a0001c0001t0001g0126 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.696-1459T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394941 | |||||||
| chr3:44394948 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.696-1452A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394948 | |||||||
| chr3:44394958 | A | G | 1 | a0001c0001t0002g0043 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.696-1442A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44394958 | |||||||
| chr3:44395021 | C | T | 108 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0092 others(105): Show |
111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.696-1379C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44395021 | |||||||
| chr3:44395396 | A | C | 108 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0092 others(105): Show |
111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.696-1004A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44395396 | |||||||
| chr3:44395445 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.696-955A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44395445 | |||||||
| chr3:44395592 | G | T | 1 | a0001c0001t0020g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.696-808G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44395592 | |||||||
| chr3:44395673 | T | C | 1 | a0001c0001t0003g0049 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.696-727T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44395673 | |||||||
| chr3:44395756 | G | A | 1 | a0001c0001t0014g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.696-644G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44395756 | |||||||
| chr3:44395892 | T | C | 4 | a0001c0003t0001g0016 a0001c0003t0001g0026 a0001c0003t0001g0083 others(1): Show |
4 | HG02572.hp1 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.696-508T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44395892 | |||||||
| chr3:44395935 | C | T | 59 | a0001c0001t0001g0092 a0001c0001t0001g0185 a0001c0001t0001g0186 others(56): Show |
59 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.696-465C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44395935 | |||||||
| chr3:44395945 | C | T | 5 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
5 | HG02258.hp1 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.696-455C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44395945 | |||||||
| chr3:44395965 | C | T | 3 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0049 |
3 | HG02486.hp2 HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.696-435C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44395965 | |||||||
| chr3:44396178 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.696-222A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44396178 | |||||||
| chr3:44396220 | C | T | 4 | a0001c0001t0003g0052 a0001c0001t0003g0053 a0001c0001t0003g0058 others(1): Show |
4 | HG00423.hp2 HG02040.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.696-180C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44396220 | |||||||
| chr3:44396289 | G | A | 43 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0141 others(40): Show |
44 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.696-111G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44396289 | |||||||
| chr3:44396378 | A | C | 229 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(226): Show |
234 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.696-22A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 6/10 | chr3 | 44396378 | |||||||
| chr3:44396569 | C | CCAAATAA others(31): Show |
1 | a0001c0001t0001g0125 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.793+109_793+110ins others(38): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr3 | 44396569 | ||||||
| chr3:44396627 | T | G | 1 | a0001c0001t0001g0005 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.794-116T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 7/10 | chr3 | 44396627 | |||||||
| chr3:44396631 | A | C | 6 | a0001c0001t0005g0001 a0001c0001t0005g0007 a0001c0001t0005g0008 others(3): Show |
7 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.794-112A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 7/10 | chr3 | 44396631 | |||||||
| chr3:44396873 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.885+39C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44396873 | |||||||
| chr3:44397002 | A | G | 1 | a0001c0001t0001g0237 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.885+168A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44397002 | |||||||
| chr3:44397356 | T | G | 1 | a0001c0001t0001g0005 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.885+522T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44397356 | |||||||
| chr3:44397396 | A | C | 2 | a0001c0001t0001g0240 a0001c0001t0001g0241 |
2 | HG00438.hp1 HG02040.hp2 |
intron_variant | MODIFIER | c.885+562A>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44397396 | |||||||
| chr3:44397421 | C | G | 33 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0049 others(30): Show |
34 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.885+587C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44397421 | |||||||
| chr3:44397576 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.885+742A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44397576 | |||||||
| chr3:44397675 | G | A | 1 | a0001c0001t0004g0084 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.885+841G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44397675 | |||||||
| chr3:44397752 | A | G | 116 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(113): Show |
119 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.885+918A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44397752 | |||||||
| chr3:44397856 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0183 |
2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.885+1022C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44397856 | |||||||
| chr3:44397857 | G | A | 2 | a0001c0001t0010g0068 a0001c0001t0010g0074 |
2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.885+1023G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44397857 | |||||||
| chr3:44397909 | T | G | 102 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0092 others(99): Show |
104 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.885+1075T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44397909 | |||||||
| chr3:44398056 | C | G | 1 | a0001c0001t0001g0098 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.885+1222C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44398056 | |||||||
| chr3:44398066 | C | A | 1 | a0001c0001t0020g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.885+1232C>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44398066 | |||||||
| chr3:44398249 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.885+1415C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44398249 | |||||||
| chr3:44398250 | G | A | 3 | a0001c0001t0001g0108 a0001c0001t0009g0063 a0001c0001t0009g0064 |
3 | HG01257.hp2 HG01258.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.885+1416G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44398250 | |||||||
| chr3:44398279 | A | T | 108 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0092 others(105): Show |
111 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.885+1445A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44398279 | |||||||
| chr3:44398355 | G | A | 6 | a0001c0001t0001g0027 a0001c0001t0001g0137 a0001c0001t0001g0138 others(3): Show |
6 | HG02258.hp1 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.885+1521G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44398355 | |||||||
| chr3:44398360 | A | G | 211 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(208): Show |
216 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.885+1526A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44398360 | |||||||
| chr3:44398420 | ACT | A | 49 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0137 others(46): Show |
50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.885+1587_885+1588d others(4): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44398420 | |||||||
| chr3:44398445 | T | TTAGA | 27 | a0001c0001t0001g0005 a0001c0001t0001g0097 a0001c0001t0001g0100 others(24): Show |
28 | HG00423.hp2 HG00609.hp1 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.885+1662_885+1665d others(6): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr3 | 44398445 | ||||||
| chr3:44398445 | T | TTAGATAG others(1): Show |
9 | a0001c0001t0001g0107 a0001c0001t0001g0114 a0001c0001t0001g0145 others(6): Show |
9 | HG01975.hp1 HG02615.hp1 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.885+1658_885+1665d others(10): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr3 | 44398445 | ||||||
| chr3:44398445 | T | TTAGATAG others(5): Show |
5 | a0001c0001t0001g0125 a0001c0001t0001g0136 a0001c0001t0003g0054 others(2): Show |
5 | HG00673.hp2 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.885+1654_885+1665d others(14): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr3 | 44398445 | ||||||
| chr3:44398445 | TTAGA | T | 53 | a0001c0001t0001g0004 a0001c0001t0001g0094 a0001c0001t0001g0098 others(50): Show |
54 | HG00140.hp2 HG00597.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.885+1662_885+1665d others(6): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr3 | 44398445 | ||||||
| chr3:44398445 | TTAGATAG others(1): Show |
T | 46 | a0001c0001t0001g0006 a0001c0001t0001g0112 a0001c0001t0001g0113 others(43): Show |
48 | HG00140.hp1 HG00423.hp1 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.885+1658_885+1665d others(10): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr3 | 44398445 | ||||||
| chr3:44398445 | TTAGATAG others(5): Show |
T | 13 | a0001c0001t0001g0178 a0001c0001t0001g0200 a0001c0001t0001g0207 others(10): Show |
13 | HG00438.hp1 HG01928.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.885+1654_885+1665d others(14): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr3 | 44398445 | ||||||
| chr3:44398511 | C | T | 116 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(113): Show |
119 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.885+1677C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44398511 | |||||||
| chr3:44398679 | A | G | 1 | a0001c0001t0001g0014 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.886-1676A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44398679 | |||||||
| chr3:44398697 | C | A | 1 | a0001c0001t0020g0015 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.886-1658C>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44398697 | |||||||
| chr3:44399010 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.886-1345G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44399010 | |||||||
| chr3:44399071 | T | G | 1 | a0001c0001t0019g0189 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.886-1284T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44399071 | |||||||
| chr3:44399386 | G | A | 1 | a0001c0001t0001g0208 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.886-969G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44399386 | |||||||
| chr3:44399808 | G | A | 1 | a0001c0001t0003g0071 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.886-547G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44399808 | |||||||
| chr3:44399903 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.886-452C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 8/10 | chr3 | 44399903 | |||||||
| chr3:44400840 | A | G | 1 | a0001c0001t0002g0036 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1118+253A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 9/10 | chr3 | 44400840 | |||||||
| chr3:44400868 | T | A | 9 | a0001c0003t0001g0016 a0001c0003t0001g0026 a0001c0003t0001g0083 others(6): Show |
9 | HG02257.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1118+281T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 9/10 | chr3 | 44400868 | |||||||
| chr3:44401179 | C | G | 1 | a0001c0001t0001g0005 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1119-24C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 9/10 | chr3 | 44401179 | |||||||
| chr3:44401735 | C | A | 49 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0137 others(46): Show |
50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.1250+401C>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44401735 | |||||||
| chr3:44402037 | T | A | 1 | a0001c0001t0001g0190 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1250+703T>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44402037 | |||||||
| chr3:44402074 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.1250+740T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44402074 | |||||||
| chr3:44402284 | G | T | 49 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0137 others(46): Show |
50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.1250+950G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44402284 | |||||||
| chr3:44402420 | ATG | A | 34 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0003g0049 others(31): Show |
35 | HG00423.hp2 HG00639.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.1250+1088_1250+108 others(6): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr3 | 44402420 | ||||||
| chr3:44402610 | C | T | 1 | a0001c0001t0003g0135 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1250+1276C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44402610 | |||||||
| chr3:44402831 | G | A | 5 | a0002c0002t0001g0028 a0002c0002t0001g0029 a0002c0002t0001g0030 others(2): Show |
5 | HG02257.hp1 HG02723.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1250+1497G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44402831 | |||||||
| chr3:44403162 | G | A | 116 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(113): Show |
119 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.1250+1828G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44403162 | |||||||
| chr3:44403162 | G | C | 36 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0142 others(33): Show |
37 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.1250+1828G>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44403162 | |||||||
| chr3:44403255 | C | T | 9 | a0001c0003t0001g0016 a0001c0003t0001g0026 a0001c0003t0001g0083 others(6): Show |
9 | HG02257.hp1 HG02572.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1250+1921C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44403255 | |||||||
| chr3:44403415 | C | G | 7 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1250+2081C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44403415 | |||||||
| chr3:44403580 | G | A | 1 | a0001c0001t0001g0237 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1250+2246G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44403580 | |||||||
| chr3:44403641 | G | T | 1 | a0001c0001t0003g0075 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1250+2307G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44403641 | |||||||
| chr3:44403717 | G | A | 1 | a0001c0001t0003g0071 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1250+2383G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44403717 | |||||||
| chr3:44403849 | C | T | 116 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(113): Show |
119 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.1250+2515C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44403849 | |||||||
| chr3:44403860 | GATGGCCT others(3): Show |
G | 1 | a0001c0001t0004g0087 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1250+2527_1250+253 others(14): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44403860 | |||||||
| chr3:44404011 | C | G | 4 | a0001c0003t0001g0016 a0001c0003t0001g0026 a0001c0003t0001g0083 others(1): Show |
4 | HG02572.hp1 HG02809.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250+2677C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44404011 | |||||||
| chr3:44404368 | C | T | 49 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0137 others(46): Show |
50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.1250+3034C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44404368 | |||||||
| chr3:44404736 | T | C | 7 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-2706T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44404736 | |||||||
| chr3:44404808 | AT | A | 45 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0137 others(42): Show |
46 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(43): Show |
intron_variant | MODIFIER | c.1251-2627delT | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr3 | 44404808 | ||||||
| chr3:44405109 | C | CCAGCCTG others(10): Show |
1 | a0001c0001t0004g0087 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1251-2332_1251-233 others(21): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr3 | 44405109 | ||||||
| chr3:44405117 | C | G | 1 | a0001c0001t0004g0087 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1251-2325C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44405117 | |||||||
| chr3:44405122 | G | T | 1 | a0001c0001t0004g0087 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1251-2320G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44405122 | |||||||
| chr3:44405131 | G | A | 1 | a0001c0001t0004g0087 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1251-2311G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44405131 | |||||||
| chr3:44405132 | A | G | 1 | a0001c0001t0004g0087 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1251-2310A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44405132 | |||||||
| chr3:44405143 | C | A | 1 | a0001c0001t0004g0087 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1251-2299C>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44405143 | |||||||
| chr3:44405151 | T | C | 1 | a0001c0001t0004g0087 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1251-2291T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44405151 | |||||||
| chr3:44405163 | G | A | 1 | a0001c0001t0001g0005 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1251-2279G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44405163 | |||||||
| chr3:44405198 | C | G | 1 | a0001c0001t0001g0176 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1251-2244C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44405198 | |||||||
| chr3:44405345 | G | A | 7 | a0001c0001t0004g0084 a0001c0001t0004g0085 a0001c0001t0004g0086 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1251-2097G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44405345 | |||||||
| chr3:44405570 | A | G | 49 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0137 others(46): Show |
50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.1251-1872A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44405570 | |||||||
| chr3:44405605 | C | T | 6 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(3): Show |
6 | HG02258.hp1 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1251-1837C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44405605 | |||||||
| chr3:44405844 | TG | T | 116 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(113): Show |
119 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.1251-1595delG | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr3 | 44405844 | ||||||
| chr3:44405909 | G | A | 2 | a0001c0001t0001g0152 a0001c0001t0001g0173 |
2 | NA19056.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1251-1533G>A | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44405909 | |||||||
| chr3:44405951 | C | CA | 41 | a0001c0001t0002g0035 a0001c0001t0002g0046 a0001c0001t0002g0077 others(38): Show |
41 | HG00423.hp2 HG00733.hp1 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.1251-1470dupA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr3 | 44405951 | ||||||
| chr3:44405951 | CA | C | 161 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(158): Show |
165 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(162): Show |
intron_variant | MODIFIER | c.1251-1470delA | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr3 | 44405951 | ||||||
| chr3:44406044 | G | T | 1 | a0001c0001t0002g0042 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1251-1398G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44406044 | |||||||
| chr3:44406392 | C | G | 1 | a0001c0001t0001g0136 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1251-1050C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44406392 | |||||||
| chr3:44406482 | T | C | 211 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(208): Show |
216 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.1251-960T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44406482 | |||||||
| chr3:44406483 | A | T | 211 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(208): Show |
216 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.1251-959A>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44406483 | |||||||
| chr3:44406484 | T | G | 211 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(208): Show |
216 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.1251-958T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44406484 | |||||||
| chr3:44406486 | C | G | 211 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(208): Show |
216 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.1251-956C>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44406486 | |||||||
| chr3:44406489 | A | G | 211 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(208): Show |
216 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.1251-953A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44406489 | |||||||
| chr3:44406490 | GTA | G | 211 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(208): Show |
216 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.1251-951_1251-950d others(4): Show |
TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44406490 | |||||||
| chr3:44406493 | A | G | 211 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(208): Show |
216 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(213): Show |
intron_variant | MODIFIER | c.1251-949A>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44406493 | |||||||
| chr3:44406599 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1251-843T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44406599 | |||||||
| chr3:44406623 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1251-819T>C | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44406623 | |||||||
| chr3:44406628 | G | T | 49 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0137 others(46): Show |
50 | HG00558.hp1 HG00597.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.1251-814G>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44406628 | |||||||
| chr3:44406810 | C | T | 2 | a0001c0001t0001g0213 a0001c0001t0001g0236 |
2 | HG00438.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.1251-632C>T | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44406810 | |||||||
| chr3:44407161 | T | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0168 |
2 | HG02683.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1251-281T>G | TCAIM | ENSG00000179152.20 | transcript | ENST00000342649.9 | protein_coding | 10/10 | chr3 | 44407161 |