Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9112 |
| ensemblid | ENSG00000182979.18 |
| hgncid | 7410 |
| symbol | MTA1 |
| name | metastasis associated 1 |
| refseq_nuc | NM_004689.4 |
| refseq_prot | NP_004680.2 |
| ensembl_nuc | ENST00000331320.12 |
| ensembl_prot | ENSP00000333633.7 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 105419827 |
| end | 105470729 |
| strand | + |
| ver | v1.2 |
| region | chr14:105419827-105470729 |
| region5000 | chr14:105414827-105475729 |
| regionname0 | MTA1_chr14_105419827_105470729 |
| regionname5000 | MTA1_chr14_105414827_105475729 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 715 | 156 | 41 | 42 | 44 | 10 | 18 | 26 | MTA1_chr14_105414827_105475729 | MTA1 | MAANM others(710): Show |
chr14 | 105414827 | 105475729 |
| a0002 | 0/0 | 715 | 78 | 1 | 14 | 50 | 2 | 11 | 32 | MTA1_chr14_105414827_105475729 | MTA1 | MAANM others(710): Show |
chr14 | 105414827 | 105475729 |
| a0003 | 1/0 | 715 | 39 | 34 | 4 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | MAANM others(710): Show |
chr14 | 105414827 | 105475729 |
| a0004 | 0/0 | 550 | 14 | 3 | 4 | 3 | 0 | 4 | 2 | MTA1_chr14_105414827_105475729 | MTA1 | MAANM others(545): Show |
chr14 | 105414827 | 105475729 |
| a0005 | 0/0 | 550 | 10 | 0 | 3 | 4 | 0 | 3 | 3 | MTA1_chr14_105414827_105475729 | MTA1 | MAANM others(545): Show |
chr14 | 105414827 | 105475729 |
| a0006 | 0/0 | 715 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | MAANM others(710): Show |
chr14 | 105414827 | 105475729 |
| a0007 | 0/0 | 715 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | MAANM others(710): Show |
chr14 | 105414827 | 105475729 |
| a0008 | 0/0 | 715 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | MAANM others(710): Show |
chr14 | 105414827 | 105475729 |
| a0009 | 0/0 | 715 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | MAANM others(710): Show |
chr14 | 105414827 | 105475729 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2145 | 150 | 40 | 40 | 43 | 9 | 17 | MTA1_chr14_105414827_105475729 | MTA1 | ATGGC others(2140): Show |
chr14 | 105414827 | 105475729 | ||
| a0001c0011 | 0/0 | 2145 | 2 | 0 | 0 | 1 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | ATGGC others(2140): Show |
chr14 | 105414827 | 105475729 | ||
| a0001c0012 | 0/0 | 2145 | 2 | 1 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | ATGGC others(2140): Show |
chr14 | 105414827 | 105475729 | ||
| a0001c0017 | 0/0 | 2145 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | ATGGC others(2140): Show |
chr14 | 105414827 | 105475729 | ||
| a0001c0019 | 0/0 | 2145 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | ATGGC others(2140): Show |
chr14 | 105414827 | 105475729 | ||
| a0002c0002 | 0/0 | 2145 | 77 | 1 | 14 | 49 | 2 | 11 | MTA1_chr14_105414827_105475729 | MTA1 | ATGGC others(2140): Show |
chr14 | 105414827 | 105475729 | ||
| a0002c0015 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | ATGGC others(2140): Show |
chr14 | 105414827 | 105475729 | ||
| a0003c0004 | 0/0 | 2145 | 12 | 10 | 2 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | ATGGC others(2140): Show |
chr14 | 105414827 | 105475729 | ||
| a0003c0006 | 0/0 | 2145 | 9 | 9 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | ATGGC others(2140): Show |
chr14 | 105414827 | 105475729 | ||
| a0003c0007 | 0/0 | 2145 | 9 | 8 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | ATGGC others(2140): Show |
chr14 | 105414827 | 105475729 | ||
| a0003c0008 | 1/0 | 2145 | 5 | 4 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | ATGGC others(2140): Show |
chr14 | 105414827 | 105475729 | ||
| a0003c0009 | 0/0 | 2145 | 3 | 2 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | ATGGC others(2140): Show |
chr14 | 105414827 | 105475729 | ||
| a0003c0014 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | ATGGC others(2140): Show |
chr14 | 105414827 | 105475729 | ||
| a0004c0003 | 0/0 | 2146 | 14 | 3 | 4 | 3 | 0 | 4 | MTA1_chr14_105414827_105475729 | MTA1 | ATGGC others(2141): Show |
chr14 | 105414827 | 105475729 | ||
| a0005c0005 | 0/0 | 2146 | 10 | 0 | 3 | 4 | 0 | 3 | MTA1_chr14_105414827_105475729 | MTA1 | ATGGC others(2141): Show |
chr14 | 105414827 | 105475729 | ||
| a0006c0010 | 0/0 | 2145 | 3 | 3 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | ATGGC others(2140): Show |
chr14 | 105414827 | 105475729 | ||
| a0007c0013 | 0/0 | 2145 | 2 | 1 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | ATGGC others(2140): Show |
chr14 | 105414827 | 105475729 | ||
| a0008c0018 | 0/0 | 2145 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | ATGGC others(2140): Show |
chr14 | 105414827 | 105475729 | ||
| a0009c0016 | 0/0 | 2145 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | ATGGC others(2140): Show |
chr14 | 105414827 | 105475729 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2871 | 142 | 35 | 39 | 42 | 8 | 17 | MTA1_chr14_105414827_105475729 | MTA1 | CTCTT others(2866): Show |
chr14 | 105414827 | 105475729 |
| a0001c0001t0002 | 0/0 | 2871 | 6 | 5 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | CTCTT others(2866): Show |
chr14 | 105414827 | 105475729 |
| a0001c0001t0003 | 0/0 | 2871 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | CTCTT others(2866): Show |
chr14 | 105414827 | 105475729 |
| a0001c0001t0007 | 0/0 | 2852 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | CTCTT others(2847): Show |
chr14 | 105414827 | 105475729 |
| a0001c0011t0001 | 0/0 | 2871 | 2 | 0 | 0 | 1 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | CTCTT others(2866): Show |
chr14 | 105414827 | 105475729 |
| a0001c0012t0001 | 0/0 | 2871 | 2 | 1 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | CTCTT others(2866): Show |
chr14 | 105414827 | 105475729 |
| a0001c0017t0001 | 0/0 | 2871 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | CTCTT others(2866): Show |
chr14 | 105414827 | 105475729 |
| a0001c0019t0001 | 0/0 | 2871 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | CTCTT others(2866): Show |
chr14 | 105414827 | 105475729 |
| a0002c0002t0001 | 0/0 | 2871 | 76 | 1 | 14 | 48 | 2 | 11 | MTA1_chr14_105414827_105475729 | MTA1 | CTCTT others(2866): Show |
chr14 | 105414827 | 105475729 |
| a0002c0002t0004 | 0/0 | 2871 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | CTCTT others(2866): Show |
chr14 | 105414827 | 105475729 |
| a0002c0015t0001 | 0/0 | 2871 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | CTCTT others(2866): Show |
chr14 | 105414827 | 105475729 |
| a0003c0004t0001 | 0/0 | 2871 | 12 | 10 | 2 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | CTCTT others(2866): Show |
chr14 | 105414827 | 105475729 |
| a0003c0006t0001 | 0/0 | 2871 | 8 | 8 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | CTCTT others(2866): Show |
chr14 | 105414827 | 105475729 |
| a0003c0006t0005 | 0/0 | 2871 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | CTCTT others(2866): Show |
chr14 | 105414827 | 105475729 |
| a0003c0007t0001 | 0/0 | 2871 | 9 | 8 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | CTCTT others(2866): Show |
chr14 | 105414827 | 105475729 |
| a0003c0008t0001 | 1/0 | 2871 | 5 | 4 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | CTCTT others(2866): Show |
chr14 | 105414827 | 105475729 |
| a0003c0009t0001 | 0/0 | 2871 | 3 | 2 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | CTCTT others(2866): Show |
chr14 | 105414827 | 105475729 |
| a0003c0014t0001 | 0/0 | 2871 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | CTCTT others(2866): Show |
chr14 | 105414827 | 105475729 |
| a0004c0003t0001 | 0/0 | 2872 | 14 | 3 | 4 | 3 | 0 | 4 | MTA1_chr14_105414827_105475729 | MTA1 | CTCTT others(2867): Show |
chr14 | 105414827 | 105475729 |
| a0005c0005t0001 | 0/0 | 2872 | 10 | 0 | 3 | 4 | 0 | 3 | MTA1_chr14_105414827_105475729 | MTA1 | CTCTT others(2867): Show |
chr14 | 105414827 | 105475729 |
| a0006c0010t0001 | 0/0 | 2871 | 3 | 3 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | CTCTT others(2866): Show |
chr14 | 105414827 | 105475729 |
| a0007c0013t0001 | 0/0 | 2871 | 2 | 1 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | CTCTT others(2866): Show |
chr14 | 105414827 | 105475729 |
| a0008c0018t0006 | 0/0 | 2871 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | CTCTT others(2866): Show |
chr14 | 105414827 | 105475729 |
| a0009c0016t0001 | 0/0 | 2871 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | CTCTT others(2866): Show |
chr14 | 105414827 | 105475729 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0017 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0193 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0001t0007g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0011t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0011t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0012t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0012t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0017t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0001c0019t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0001 | 0/0 | 10 | 0 | 0 | 9 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0002t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0002c0015t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0004t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0004t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0004t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0004t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0004t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0004t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0004t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0004t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0004t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0004t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0004t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0006t0001g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0006t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0006t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0006t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0006t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0006t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0007t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0007t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0007t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0007t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0007t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0007t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0007t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0007t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0007t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0008t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0008t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0008t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0008t0001g0035 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0008t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0009t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0009t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0009t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0003c0014t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0004c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0004c0003t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0004c0003t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0004c0003t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0004c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0004c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0004c0003t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0004c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0004c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0004c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0004c0003t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0004c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0004c0003t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0004c0003t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0005c0005t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0005c0005t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0005c0005t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0005c0005t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0005c0005t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0005c0005t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0005c0005t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0005c0005t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0005c0005t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0005c0005t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0006c0010t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0006c0010t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0006c0010t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0007c0013t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0007c0013t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0008c0018t0006g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| a0009c0016t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0255 | EUR | GBR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0227 | EUR | GBR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0258 | EUR | GBR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00280 | hp1 | a0001 | c0011 | t0001 | g0210 | EUR | FIN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0259 | EUR | FIN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0221 | EUR | FIN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0247 | EUR | FIN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0156 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00544 | hp1 | a0004 | c0003 | t0001 | g0186 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0178 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00597 | hp1 | a0005 | c0005 | t0001 | g0161 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0174 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0235 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00639 | hp1 | a0004 | c0003 | t0001 | g0078 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00639 | hp2 | a0001 | c0012 | t0001 | g0242 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00642 | hp2 | a0004 | c0003 | t0001 | g0117 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00673 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00735 | hp2 | a0003 | c0009 | t0001 | g0030 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0146 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01099 | hp2 | a0004 | c0003 | t0001 | g0262 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01106 | hp2 | a0002 | c0002 | t0001 | g0269 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01167 | hp1 | a0003 | c0007 | t0001 | g0063 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01167 | hp2 | a0003 | c0004 | t0001 | g0006 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0226 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01169 | hp1 | a0003 | c0004 | t0001 | g0006 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01192 | hp1 | a0005 | c0005 | t0001 | g0132 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01192 | hp2 | a0005 | c0005 | t0001 | g0216 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0225 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0196 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0160 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0138 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0072 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01433 | hp2 | a0004 | c0003 | t0001 | g0213 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01496 | hp1 | a0007 | c0013 | t0001 | g0037 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0194 | AMR | CLM | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0094 | EUR | IBS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0250 | EUR | IBS | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01891 | hp1 | a0003 | c0014 | t0001 | g0031 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0245 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01943 | hp1 | a0002 | c0002 | t0001 | g0075 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01981 | hp2 | a0005 | c0005 | t0001 | g0069 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0123 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02004 | hp1 | a0002 | c0002 | t0001 | g0144 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02015 | hp2 | a0001 | c0011 | t0001 | g0203 | EAS | KHV | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02040 | hp2 | a0002 | c0002 | t0004 | g0145 | EAS | KHV | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02055 | hp2 | a0003 | c0004 | t0001 | g0109 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0154 | EAS | KHV | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0101 | EAS | KHV | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02132 | hp2 | a0001 | c0001 | t0007 | g0022 | EAS | KHV | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02148 | hp1 | a0001 | c0019 | t0001 | g0206 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0139 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | CDX | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | CDX | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02257 | hp1 | a0003 | c0004 | t0001 | g0110 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0140 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02280 | hp1 | a0004 | c0003 | t0001 | g0041 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02280 | hp2 | a0003 | c0007 | t0001 | g0003 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02572 | hp1 | a0008 | c0018 | t0006 | g0003 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02572 | hp2 | a0003 | c0006 | t0001 | g0029 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0001 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02615 | hp1 | a0003 | c0007 | t0001 | g0058 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02615 | hp2 | a0003 | c0006 | t0001 | g0028 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02622 | hp1 | a0003 | c0007 | t0001 | g0061 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02622 | hp2 | a0003 | c0004 | t0001 | g0003 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02698 | hp1 | a0002 | c0002 | t0001 | g0158 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02717 | hp1 | a0007 | c0013 | t0001 | g0038 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02717 | hp2 | a0004 | c0003 | t0001 | g0039 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02809 | hp2 | a0003 | c0006 | t0005 | g0027 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02818 | hp1 | a0003 | c0007 | t0001 | g0057 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02818 | hp2 | a0003 | c0004 | t0001 | g0048 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02895 | hp1 | a0003 | c0009 | t0001 | g0026 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02896 | hp1 | a0006 | c0010 | t0001 | g0147 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02897 | hp1 | a0006 | c0010 | t0001 | g0126 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0098 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02922 | hp1 | a0006 | c0010 | t0001 | g0165 | AFR | ESN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02922 | hp2 | a0003 | c0006 | t0001 | g0002 | AFR | ESN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02965 | hp1 | a0003 | c0006 | t0001 | g0002 | AFR | ESN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02970 | hp1 | a0003 | c0004 | t0001 | g0120 | AFR | ESN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02970 | hp2 | a0003 | c0007 | t0001 | g0062 | AFR | ESN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0066 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03098 | hp1 | a0003 | c0008 | t0001 | g0020 | AFR | MSL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03130 | hp1 | a0003 | c0009 | t0001 | g0025 | AFR | ESN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03130 | hp2 | a0003 | c0004 | t0001 | g0054 | AFR | ESN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03195 | hp2 | a0003 | c0006 | t0001 | g0002 | AFR | ESN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | MSL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | MSL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03225 | hp2 | a0003 | c0007 | t0001 | g0060 | AFR | MSL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03453 | hp1 | a0003 | c0006 | t0001 | g0033 | AFR | MSL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | MSL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0246 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0015 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0256 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03516 | hp1 | a0003 | c0007 | t0001 | g0059 | AFR | ESN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03579 | hp1 | a0003 | c0004 | t0001 | g0055 | AFR | MSL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03579 | hp2 | a0003 | c0007 | t0001 | g0065 | AFR | MSL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03654 | hp2 | a0004 | c0003 | t0001 | g0112 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0148 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | STU | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0015 | SAS | STU | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03704 | hp2 | a0001 | c0017 | t0001 | g0050 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0104 | SAS | PJL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03831 | hp1 | a0005 | c0005 | t0001 | g0102 | SAS | BEB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03831 | hp2 | a0005 | c0005 | t0001 | g0159 | SAS | BEB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | BEB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0157 | SAS | BEB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG04184 | hp2 | a0004 | c0003 | t0001 | g0085 | SAS | BEB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0133 | SAS | STU | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | STU | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG04204 | hp1 | a0004 | c0003 | t0001 | g0106 | SAS | STU | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG04204 | hp2 | a0005 | c0005 | t0001 | g0143 | SAS | STU | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG04228 | hp1 | a0004 | c0003 | t0001 | g0251 | SAS | STU | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | STU | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | YRI | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | CHB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | CHB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | YRI | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18906 | hp2 | a0003 | c0006 | t0001 | g0002 | AFR | YRI | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18939 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18942 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0188 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18953 | hp2 | a0004 | c0003 | t0001 | g0205 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18969 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0218 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18975 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18982 | hp1 | a0005 | c0005 | t0001 | g0187 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18989 | hp2 | a0005 | c0005 | t0001 | g0222 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18998 | hp2 | a0005 | c0005 | t0001 | g0087 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0234 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19003 | hp2 | a0009 | c0016 | t0001 | g0090 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19009 | hp1 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19030 | hp1 | a0001 | c0012 | t0001 | g0043 | AFR | LWK | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | LWK | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19043 | hp1 | a0003 | c0008 | t0001 | g0018 | AFR | LWK | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19074 | hp1 | a0002 | c0015 | t0001 | g0131 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19077 | hp2 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0183 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19090 | hp2 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19091 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | YRI | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA19240 | hp2 | a0003 | c0004 | t0001 | g0032 | AFR | YRI | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ASW | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ASW | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | TSI | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02109 | hp1 | a0003 | c0004 | t0001 | g0064 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02109 | hp2 | a0004 | c0003 | t0001 | g0260 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG02559 | hp2 | a0003 | c0006 | t0001 | g0034 | AFR | ACB | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03471 | hp1 | a0003 | c0008 | t0001 | g0019 | AFR | MSL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| HG03471 | hp2 | a0003 | c0008 | t0001 | g0052 | AFR | MSL | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA18955 | hp2 | a0004 | c0003 | t0001 | g0128 | EAS | JPT | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA20300 | hp1 | a0002 | c0002 | t0001 | g0142 | AFR | USA | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA20300 | hp2 | a0003 | c0004 | t0001 | g0056 | AFR | USA | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | LWK | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | LWK | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0193 | REF | REF | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| homoSapiens | grch38p0 | a0003 | c0008 | t0001 | g0035 | REF | REF | MTA1_chr14_105414827_105475729 | MTA1 | chr14 | 105414827 | 105475729 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:105464069 | G | A | 3 | a0002 a0005 a0009 |
89 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(86): Show |
missense_variant | MODERATE | c.1114G>A | p.Val372Ile | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 13/21 | 1323/2871 | 1114/2148 | 372/715 | chr14 | 105464069 | |||
| chr14:105465102 | C | G | 1 | a0009 | 1 | NA19003.hp2 | missense_variant | MODERATE | c.1543C>G | p.Arg515Gly | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/21 | 1752/2871 | 1543/2148 | 515/715 | chr14 | 105465102 | |||
| chr14:105465151 | G | A | 1 | a0008 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.1592G>A | p.Arg531His | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/21 | 1801/2871 | 1592/2148 | 531/715 | chr14 | 105465151 | |||
| chr14:105466438 | G | GC | 2 | a0004 a0005 |
24 | HG00544.hp1 HG00597.hp1 HG00639.hp1 others(21): Show |
frameshift_variant | HIGH | c.1644dupC | p.Lys549fs | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 17/21 | 1854/2871 | 1645/2148 | 549/715 | INFO_REALIGN_3_PRIME | chr14 | 105466438 | ||
| chr14:105466467 | G | A | 1 | a0006 | 3 | HG02896.hp1 HG02897.hp1 HG02922.hp1 |
missense_variant | MODERATE | c.1666G>A | p.Val556Met | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 17/21 | 1875/2871 | 1666/2148 | 556/715 | chr14 | 105466467 | |||
| chr14:105469487 | G | A | 7 | a0001 a0002 a0004 others(4): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
missense_variant | MODERATE | c.1834G>A | p.Ala612Thr | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 19/21 | 2043/2871 | 1834/2148 | 612/715 | chr14 | 105469487 | |||
| chr14:105470169 | C | T | 1 | a0007 | 2 | HG01496.hp1 HG02717.hp1 |
missense_variant | MODERATE | c.2102C>T | p.Pro701Leu | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 21/21 | 2311/2871 | 2102/2148 | 701/715 | chr14 | 105470169 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:105445466 | C | A | 3 | a0003c0006 a0003c0009 a0003c0014 |
13 | HG00735.hp2 HG01891.hp1 HG02559.hp2 others(10): Show |
synonymous_variant | LOW | c.145C>A | p.Arg49Arg | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/21 | 354/2871 | 145/2148 | 49/715 | chr14 | 105445466 | |||
| chr14:105450083 | C | T | 18 | a0001c0001 a0001c0011 a0001c0012 others(15): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
synonymous_variant | LOW | c.267C>T | p.Asn89Asn | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 5/21 | 476/2871 | 267/2148 | 89/715 | chr14 | 105450083 | |||
| chr14:105454240 | G | A | 1 | a0002c0015 | 1 | NA19074.hp1 | synonymous_variant | LOW | c.480G>A | p.Leu160Leu | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/21 | 689/2871 | 480/2148 | 160/715 | chr14 | 105454240 | |||
| chr14:105463249 | C | T | 1 | a0003c0014 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.1008C>T | p.Tyr336Tyr | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 11/21 | 1217/2871 | 1008/2148 | 336/715 | chr14 | 105463249 | |||
| chr14:105464772 | C | T | 4 | a0001c0019 a0003c0007 a0003c0009 others(1): Show |
14 | HG00735.hp2 HG01167.hp1 HG02148.hp1 others(11): Show |
synonymous_variant | LOW | c.1443C>T | p.Ile481Ile | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 15/21 | 1652/2871 | 1443/2148 | 481/715 | chr14 | 105464772 | |||
| chr14:105464817 | G | A | 1 | a0001c0011 | 2 | HG00280.hp1 HG02015.hp2 |
synonymous_variant | LOW | c.1488G>A | p.Ala496Ala | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 15/21 | 1697/2871 | 1488/2148 | 496/715 | chr14 | 105464817 | |||
| chr14:105465101 | G | C | 1 | a0009c0016 | 1 | NA19003.hp2 | synonymous_variant | LOW | c.1542G>C | p.Ala514Ala | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/21 | 1751/2871 | 1542/2148 | 514/715 | chr14 | 105465101 | |||
| chr14:105469963 | C | T | 1 | a0001c0017 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.1968C>T | p.Asp656Asp | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 20/21 | 2177/2871 | 1968/2148 | 656/715 | chr14 | 105469963 | |||
| chr14:105470179 | G | A | 1 | a0001c0012 | 2 | HG00639.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.2112G>A | p.Ala704Ala | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 21/21 | 2321/2871 | 2112/2148 | 704/715 | chr14 | 105470179 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:105419980 | C | A | 1 | a0001c0001t0003 | 1 | HG00323.hp2 | 5_prime_UTR_variant | MODIFIER | c.-56C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/21 | 56 | chr14 | 105419980 | ||||||
| chr14:105470237 | G | A | 1 | a0002c0002t0004 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*22G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 21/21 | 22 | chr14 | 105470237 | ||||||
| chr14:105470384 | T | G | 1 | a0003c0006t0005 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*169T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 21/21 | 169 | chr14 | 105470384 | ||||||
| chr14:105470616 | C | T | 1 | a0001c0001t0002 | 6 | HG01255.hp2 HG01891.hp2 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*401C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 21/21 | 401 | chr14 | 105470616 | ||||||
| chr14:105470656 | CCTTGTCT others(12): Show |
C | 1 | a0001c0001t0007 | 1 | HG02132.hp2 | 3_prime_UTR_variant | MODIFIER | c.*442_*460delCTTGTC others(13): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 21/21 | 442 | chr14 | 105470656 | ||||||
| chr14:105470697 | G | T | 1 | a0008c0018t0006 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*482G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 21/21 | 482 | chr14 | 105470697 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:105420107 | G | GCCCCCAC others(18): Show |
4 | a0001c0001t0001g0021 a0003c0008t0001g0018 a0003c0008t0001g0019 others(1): Show |
4 | HG02300.hp2 HG03098.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.28+50_28+74dupACCC others(21): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105420107 | ||||||
| chr14:105420182 | G | C | 2 | a0001c0001t0001g0023 a0001c0001t0007g0022 |
2 | HG02132.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.28+119G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105420182 | |||||||
| chr14:105420298 | C | G | 1 | a0001c0001t0001g0274 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.28+235C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105420298 | |||||||
| chr14:105420344 | G | T | 1 | a0001c0001t0001g0273 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.28+281G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105420344 | |||||||
| chr14:105420576 | C | A | 1 | a0001c0001t0001g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.28+513C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105420576 | |||||||
| chr14:105420627 | A | G | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG02451.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.28+564A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105420627 | |||||||
| chr14:105420753 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.28+690C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105420753 | |||||||
| chr14:105420950 | C | T | 1 | a0002c0002t0001g0269 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.28+887C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105420950 | |||||||
| chr14:105421051 | C | T | 227 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(224): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.28+988C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105421051 | |||||||
| chr14:105421115 | T | TGG | 24 | a0001c0001t0001g0017 a0001c0001t0001g0248 a0001c0001t0001g0249 others(21): Show |
25 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(22): Show |
intron_variant | MODIFIER | c.28+1054_28+1055dup others(2): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105421115 | ||||||
| chr14:105421175 | C | G | 1 | a0001c0001t0002g0245 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.28+1112C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105421175 | |||||||
| chr14:105421180 | C | G | 1 | a0003c0008t0001g0020 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.28+1117C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105421180 | |||||||
| chr14:105421310 | C | T | 1 | a0003c0004t0001g0006 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.28+1247C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105421310 | |||||||
| chr14:105421430 | G | C | 1 | a0002c0002t0001g0066 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.28+1367G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105421430 | |||||||
| chr14:105421597 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.28+1534C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105421597 | |||||||
| chr14:105421685 | G | T | 1 | a0001c0001t0001g0243 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.28+1622G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105421685 | |||||||
| chr14:105421801 | A | G | 23 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0053 others(20): Show |
23 | HG00639.hp2 HG01167.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.28+1738A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105421801 | |||||||
| chr14:105421825 | G | A | 1 | a0002c0002t0001g0067 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.28+1762G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105421825 | |||||||
| chr14:105421836 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.28+1773C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105421836 | |||||||
| chr14:105422081 | C | T | 2 | a0001c0001t0001g0046 a0001c0012t0001g0242 |
2 | HG00639.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.28+2018C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105422081 | |||||||
| chr14:105422096 | C | T | 1 | a0002c0002t0001g0240 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.28+2033C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105422096 | |||||||
| chr14:105422120 | C | T | 12 | a0003c0004t0001g0003 a0003c0004t0001g0064 a0003c0007t0001g0003 others(9): Show |
12 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.28+2057C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105422120 | |||||||
| chr14:105422235 | C | T | 4 | a0001c0001t0001g0053 a0003c0004t0001g0054 a0003c0004t0001g0055 others(1): Show |
4 | HG03130.hp2 HG03579.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.28+2172C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105422235 | |||||||
| chr14:105422261 | C | T | 1 | a0003c0008t0001g0052 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.28+2198C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105422261 | |||||||
| chr14:105422322 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.28+2259C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105422322 | |||||||
| chr14:105422439 | C | G | 1 | a0001c0012t0001g0043 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.28+2376C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105422439 | |||||||
| chr14:105422890 | G | T | 2 | a0003c0004t0001g0055 a0003c0004t0001g0056 |
2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.28+2827G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105422890 | |||||||
| chr14:105422903 | T | G | 2 | a0001c0001t0001g0047 a0001c0001t0001g0053 |
2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.28+2840T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105422903 | |||||||
| chr14:105423006 | C | T | 17 | a0001c0017t0001g0050 a0002c0002t0001g0051 a0003c0004t0001g0003 others(14): Show |
17 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.28+2943C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423006 | |||||||
| chr14:105423049 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.28+2986T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423049 | |||||||
| chr14:105423090 | C | T | 243 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(240): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.28+3027C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423090 | |||||||
| chr14:105423204 | T | G | 18 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0012t0001g0242 others(15): Show |
18 | HG00639.hp2 HG01167.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.28+3141T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423204 | |||||||
| chr14:105423208 | T | C | 1 | a0005c0005t0001g0069 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.28+3145T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423208 | |||||||
| chr14:105423215 | A | AT | 20 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0045 others(17): Show |
20 | HG00621.hp1 HG00621.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.28+3174dupT | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105423215 | ||||||
| chr14:105423215 | A | ATT | 13 | a0001c0001t0001g0047 a0001c0001t0001g0239 a0001c0012t0001g0242 others(10): Show |
13 | HG00639.hp2 HG01167.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.28+3173_28+3174dup others(2): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105423215 | ||||||
| chr14:105423215 | AT | A | 13 | a0001c0001t0001g0071 a0001c0001t0001g0074 a0001c0001t0001g0270 others(10): Show |
13 | HG00323.hp2 HG01175.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.28+3174delT | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105423215 | ||||||
| chr14:105423224 | T | G | 1 | a0002c0002t0001g0070 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.28+3161T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423224 | |||||||
| chr14:105423241 | A | G | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.28+3178A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423241 | |||||||
| chr14:105423333 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0238 |
3 | HG01884.hp1 HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.28+3270C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423333 | |||||||
| chr14:105423448 | C | T | 1 | a0003c0008t0001g0052 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.28+3385C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423448 | |||||||
| chr14:105423464 | G | T | 12 | a0003c0004t0001g0003 a0003c0004t0001g0064 a0003c0007t0001g0003 others(9): Show |
12 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.28+3401G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423464 | |||||||
| chr14:105423571 | CA | C | 9 | a0001c0001t0001g0021 a0001c0001t0001g0223 a0001c0001t0001g0224 others(6): Show |
10 | HG00099.hp2 HG00323.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.28+3520delA | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105423571 | ||||||
| chr14:105423583 | A | T | 1 | a0001c0001t0001g0228 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.28+3520A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423583 | |||||||
| chr14:105423648 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.28+3585G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423648 | |||||||
| chr14:105423727 | G | A | 1 | a0003c0004t0001g0054 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.28+3664G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423727 | |||||||
| chr14:105423736 | C | T | 1 | a0001c0001t0001g0237 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.28+3673C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423736 | |||||||
| chr14:105423936 | C | T | 1 | a0001c0001t0001g0220 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.28+3873C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105423936 | |||||||
| chr14:105424124 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.28+4061C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105424124 | |||||||
| chr14:105424146 | A | T | 1 | a0003c0008t0001g0052 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.28+4083A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105424146 | |||||||
| chr14:105424217 | C | T | 1 | a0001c0012t0001g0043 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.28+4154C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105424217 | |||||||
| chr14:105424322 | T | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0053 |
2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.28+4259T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105424322 | |||||||
| chr14:105424344 | C | T | 4 | a0001c0012t0001g0043 a0003c0004t0001g0054 a0003c0004t0001g0055 others(1): Show |
4 | HG03130.hp2 HG03579.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.28+4281C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105424344 | |||||||
| chr14:105424370 | A | AT | 9 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0044 others(6): Show |
9 | HG01928.hp2 HG02280.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.28+4320dupT | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105424370 | ||||||
| chr14:105424473 | T | G | 1 | a0001c0001t0001g0071 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.28+4410T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105424473 | |||||||
| chr14:105424480 | C | T | 1 | a0001c0012t0001g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.28+4417C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105424480 | |||||||
| chr14:105424565 | G | A | 1 | a0003c0008t0001g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.28+4502G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105424565 | |||||||
| chr14:105424702 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.28+4639G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105424702 | |||||||
| chr14:105424727 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0001g0045 |
2 | HG03225.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.28+4664C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105424727 | |||||||
| chr14:105424793 | G | A | 1 | a0002c0002t0001g0070 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.28+4730G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105424793 | |||||||
| chr14:105424902 | C | T | 2 | a0002c0002t0001g0218 a0002c0002t0001g0227 |
2 | HG00099.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.28+4839C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105424902 | |||||||
| chr14:105424903 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.28+4840G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105424903 | |||||||
| chr14:105425014 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0238 |
3 | HG01884.hp1 HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.28+4951C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105425014 | |||||||
| chr14:105425120 | T | G | 2 | a0001c0001t0001g0047 a0001c0001t0001g0053 |
2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.28+5057T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105425120 | |||||||
| chr14:105425124 | T | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0053 |
2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.28+5061T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105425124 | |||||||
| chr14:105425154 | G | A | 1 | a0002c0002t0001g0221 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.28+5091G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105425154 | |||||||
| chr14:105425174 | C | G | 2 | a0003c0004t0001g0055 a0003c0004t0001g0056 |
2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.28+5111C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105425174 | |||||||
| chr14:105425205 | A | G | 1 | a0001c0012t0001g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.28+5142A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105425205 | |||||||
| chr14:105425306 | G | A | 2 | a0001c0017t0001g0050 a0002c0002t0001g0051 |
2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.28+5243G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105425306 | |||||||
| chr14:105425784 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.28+5721C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105425784 | |||||||
| chr14:105425806 | G | C | 9 | a0001c0001t0001g0004 a0001c0001t0001g0079 a0001c0001t0001g0080 others(6): Show |
11 | HG00639.hp1 HG00642.hp1 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.28+5743G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105425806 | |||||||
| chr14:105425839 | A | G | 1 | a0007c0013t0001g0038 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.28+5776A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105425839 | |||||||
| chr14:105425849 | G | C | 216 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(213): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.28+5786G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105425849 | |||||||
| chr14:105425956 | G | A | 1 | a0001c0017t0001g0050 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.28+5893G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105425956 | |||||||
| chr14:105426089 | G | A | 2 | a0001c0017t0001g0050 a0002c0002t0001g0051 |
2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.28+6026G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105426089 | |||||||
| chr14:105426183 | A | C | 20 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0012t0001g0242 others(17): Show |
20 | HG00639.hp2 HG01167.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.28+6120A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105426183 | |||||||
| chr14:105426233 | G | A | 1 | a0001c0001t0001g0189 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.28+6170G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105426233 | |||||||
| chr14:105426262 | G | A | 3 | a0001c0017t0001g0050 a0002c0002t0001g0051 a0002c0002t0001g0188 |
3 | HG03704.hp2 NA18951.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.28+6199G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105426262 | |||||||
| chr14:105426374 | A | AC | 12 | a0003c0004t0001g0003 a0003c0004t0001g0064 a0003c0007t0001g0003 others(9): Show |
12 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.28+6312dupC | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105426374 | ||||||
| chr14:105426375 | C | CA | 204 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(201): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.28+6333dupA | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105426375 | ||||||
| chr14:105426375 | C | CAA | 16 | a0001c0001t0001g0044 a0001c0001t0001g0084 a0001c0001t0001g0086 others(13): Show |
16 | HG00673.hp1 HG00735.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.28+6332_28+6333dup others(2): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105426375 | ||||||
| chr14:105426505 | C | T | 3 | a0003c0004t0001g0054 a0003c0004t0001g0055 a0003c0004t0001g0056 |
3 | HG03130.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.28+6442C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105426505 | |||||||
| chr14:105426569 | C | A | 1 | a0001c0001t0001g0241 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.28+6506C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105426569 | |||||||
| chr14:105426634 | CGTCT | C | 3 | a0003c0004t0001g0054 a0003c0004t0001g0055 a0003c0004t0001g0056 |
3 | HG03130.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.28+6577_28+6580del others(4): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105426634 | ||||||
| chr14:105426745 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.28+6682C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105426745 | |||||||
| chr14:105426778 | C | T | 2 | a0001c0017t0001g0050 a0002c0002t0001g0051 |
2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.28+6715C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105426778 | |||||||
| chr14:105426895 | G | T | 1 | a0002c0002t0001g0234 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.28+6832G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105426895 | |||||||
| chr14:105427071 | C | T | 2 | a0003c0004t0001g0006 a0003c0004t0001g0032 |
3 | HG01167.hp2 HG01169.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.28+7008C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105427071 | |||||||
| chr14:105427074 | A | G | 259 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(256): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.28+7011A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105427074 | |||||||
| chr14:105427241 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.28+7178G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105427241 | |||||||
| chr14:105427402 | C | T | 9 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0166 others(6): Show |
10 | HG00544.hp2 HG00558.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.28+7339C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105427402 | |||||||
| chr14:105427527 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.28+7464T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105427527 | |||||||
| chr14:105427532 | C | T | 1 | a0001c0001t0001g0192 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.28+7469C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105427532 | |||||||
| chr14:105427588 | A | G | 5 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(2): Show |
5 | HG00323.hp2 HG00733.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.28+7525A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105427588 | |||||||
| chr14:105427611 | T | G | 12 | a0003c0004t0001g0003 a0003c0004t0001g0064 a0003c0007t0001g0003 others(9): Show |
12 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.28+7548T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105427611 | |||||||
| chr14:105427756 | A | C | 12 | a0003c0004t0001g0003 a0003c0004t0001g0064 a0003c0007t0001g0003 others(9): Show |
12 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.28+7693A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105427756 | |||||||
| chr14:105427924 | A | ACGCAAG | 18 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0012t0001g0242 others(15): Show |
18 | HG00639.hp2 HG01167.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.28+7861_28+7862ins others(6): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105427924 | |||||||
| chr14:105427949 | CAG | C | 10 | a0003c0006t0001g0002 a0003c0006t0001g0028 a0003c0006t0001g0029 others(7): Show |
13 | HG00735.hp2 HG01891.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.28+7889_28+7890del others(2): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105427949 | ||||||
| chr14:105428015 | C | CA | 20 | a0001c0001t0001g0077 a0001c0001t0001g0263 a0001c0001t0001g0270 others(17): Show |
23 | HG00323.hp1 HG00735.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.28+7971dupA | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105428015 | ||||||
| chr14:105428015 | C | CAA | 225 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(222): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.28+7970_28+7971dup others(2): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105428015 | ||||||
| chr14:105428015 | C | CAAA | 11 | a0001c0001t0001g0024 a0001c0001t0001g0047 a0001c0001t0001g0093 others(8): Show |
11 | HG00639.hp1 HG00639.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.28+7969_28+7971dup others(3): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105428015 | ||||||
| chr14:105428015 | C | CAAAA | 14 | a0001c0017t0001g0050 a0002c0002t0001g0051 a0003c0004t0001g0003 others(11): Show |
14 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.28+7968_28+7971dup others(4): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105428015 | ||||||
| chr14:105428015 | CAAAAAAA others(3): Show |
C | 1 | a0003c0008t0001g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.28+7962_28+7971del others(10): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105428015 | ||||||
| chr14:105428173 | CAGCCCCC others(1231): Show |
C | 1 | a0003c0008t0001g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.28+8113_29-9259del | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105428173 | ||||||
| chr14:105428190 | C | T | 1 | a0001c0012t0001g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.28+8127C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105428190 | |||||||
| chr14:105428401 | C | T | 1 | a0002c0002t0001g0240 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.28+8338C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105428401 | |||||||
| chr14:105428410 | C | T | 1 | a0003c0004t0001g0006 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.28+8347C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105428410 | |||||||
| chr14:105428487 | C | T | 1 | a0001c0001t0001g0012 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.28+8424C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105428487 | |||||||
| chr14:105428519 | C | T | 1 | a0001c0012t0001g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.28+8456C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105428519 | |||||||
| chr14:105428704 | A | G | 4 | a0001c0012t0001g0043 a0003c0004t0001g0054 a0003c0004t0001g0055 others(1): Show |
4 | HG03130.hp2 HG03579.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.28+8641A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105428704 | |||||||
| chr14:105428710 | A | G | 1 | a0001c0001t0001g0077 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.28+8647A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105428710 | |||||||
| chr14:105428717 | CT | C | 270 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(267): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.28+8666delT | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105428717 | ||||||
| chr14:105428744 | A | G | 259 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(256): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.28+8681A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105428744 | |||||||
| chr14:105428850 | G | A | 4 | a0001c0012t0001g0043 a0003c0004t0001g0054 a0003c0004t0001g0055 others(1): Show |
4 | HG03130.hp2 HG03579.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.28+8787G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105428850 | |||||||
| chr14:105428873 | C | T | 1 | a0003c0008t0001g0052 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.28+8810C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105428873 | |||||||
| chr14:105428913 | T | C | 1 | a0005c0005t0001g0159 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.28+8850T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105428913 | |||||||
| chr14:105428958 | C | G | 1 | a0001c0001t0001g0129 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.28+8895C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105428958 | |||||||
| chr14:105428994 | G | A | 144 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(141): Show |
155 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.28+8931G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105428994 | |||||||
| chr14:105429041 | G | A | 13 | a0003c0004t0001g0003 a0003c0004t0001g0064 a0003c0007t0001g0003 others(10): Show |
13 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.28+8978G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429041 | |||||||
| chr14:105429075 | G | A | 18 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0012t0001g0242 others(15): Show |
18 | HG00639.hp2 HG01167.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.28+9012G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429075 | |||||||
| chr14:105429188 | A | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0238 |
3 | HG01884.hp1 HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.28+9125A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429188 | |||||||
| chr14:105429204 | T | G | 2 | a0003c0004t0001g0006 a0003c0004t0001g0032 |
3 | HG01167.hp2 HG01169.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.28+9141T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429204 | |||||||
| chr14:105429279 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.28+9216C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429279 | |||||||
| chr14:105429312 | G | C | 5 | a0002c0002t0001g0091 a0002c0002t0001g0233 a0002c0015t0001g0131 others(2): Show |
5 | HG00621.hp2 NA18942.hp1 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.28+9249G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429312 | |||||||
| chr14:105429354 | C | T | 2 | a0001c0001t0001g0017 a0004c0003t0001g0260 |
2 | HG02109.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.28+9291C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429354 | |||||||
| chr14:105429372 | G | A | 1 | a0002c0002t0001g0133 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.29-9300G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429372 | |||||||
| chr14:105429452 | A | AT | 7 | a0001c0001t0001g0162 a0001c0001t0001g0192 a0001c0001t0001g0217 others(4): Show |
7 | HG01981.hp2 HG02486.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.29-9203dupT | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105429452 | ||||||
| chr14:105429521 | G | A | 8 | a0001c0001t0001g0049 a0001c0001t0002g0073 a0001c0001t0002g0095 others(5): Show |
8 | HG01255.hp2 HG01891.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.29-9151G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429521 | |||||||
| chr14:105429542 | C | G | 8 | a0001c0001t0001g0021 a0001c0001t0001g0092 a0001c0001t0001g0224 others(5): Show |
9 | HG00099.hp2 HG00323.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.29-9130C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429542 | |||||||
| chr14:105429576 | C | T | 1 | a0004c0003t0001g0186 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.29-9096C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429576 | |||||||
| chr14:105429663 | C | T | 2 | a0005c0005t0001g0222 a0009c0016t0001g0090 |
2 | NA18989.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.29-9009C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429663 | |||||||
| chr14:105429743 | G | A | 143 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(140): Show |
154 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.29-8929G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429743 | |||||||
| chr14:105429752 | C | CTTT | 21 | a0001c0001t0001g0024 a0001c0001t0001g0047 a0001c0001t0001g0053 others(18): Show |
21 | HG01167.hp1 HG01993.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.29-8901_29-8899dup others(3): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105429752 | ||||||
| chr14:105429752 | C | CTTTT | 192 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(189): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.29-8902_29-8899dup others(4): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105429752 | ||||||
| chr14:105429752 | C | CTTTTT | 42 | a0001c0001t0001g0049 a0001c0001t0001g0074 a0001c0001t0001g0082 others(39): Show |
42 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.29-8903_29-8899dup others(5): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105429752 | ||||||
| chr14:105429752 | C | CTTTTTT | 13 | a0001c0001t0002g0245 a0003c0004t0001g0054 a0003c0004t0001g0055 others(10): Show |
16 | HG00735.hp2 HG01891.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.29-8904_29-8899dup others(6): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105429752 | ||||||
| chr14:105429820 | G | A | 237 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(234): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.29-8852G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105429820 | |||||||
| chr14:105430053 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.29-8619G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105430053 | |||||||
| chr14:105430385 | C | G | 3 | a0002c0002t0001g0015 a0002c0002t0001g0225 a0002c0002t0001g0227 |
4 | HG00099.hp2 HG01243.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-8287C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105430385 | |||||||
| chr14:105430484 | C | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0003c0008t0001g0052 |
3 | HG03041.hp2 HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.29-8188C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105430484 | |||||||
| chr14:105430520 | A | G | 259 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(256): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.29-8152A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105430520 | |||||||
| chr14:105430537 | C | T | 5 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0017t0001g0050 others(2): Show |
5 | HG03041.hp2 HG03471.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.29-8135C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105430537 | |||||||
| chr14:105430564 | T | A | 237 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(234): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.29-8108T>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105430564 | |||||||
| chr14:105430571 | G | A | 237 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(234): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.29-8101G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105430571 | |||||||
| chr14:105430582 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.29-8090C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105430582 | |||||||
| chr14:105430658 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.29-8014G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105430658 | |||||||
| chr14:105430847 | T | G | 1 | a0003c0004t0001g0120 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.29-7825T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105430847 | |||||||
| chr14:105430961 | A | G | 1 | a0003c0014t0001g0031 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.29-7711A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105430961 | |||||||
| chr14:105430978 | T | C | 259 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(256): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.29-7694T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105430978 | |||||||
| chr14:105431261 | C | G | 1 | a0001c0012t0001g0043 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.29-7411C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105431261 | |||||||
| chr14:105431542 | T | TA | 2 | a0003c0004t0001g0006 a0003c0004t0001g0032 |
3 | HG01167.hp2 HG01169.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.29-7127dupA | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105431542 | ||||||
| chr14:105431638 | C | G | 1 | a0001c0012t0001g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.29-7034C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105431638 | |||||||
| chr14:105431647 | G | C | 1 | a0002c0002t0001g0124 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.29-7025G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105431647 | |||||||
| chr14:105431686 | C | T | 10 | a0003c0006t0001g0002 a0003c0006t0001g0028 a0003c0006t0001g0029 others(7): Show |
13 | HG00735.hp2 HG01891.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.29-6986C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105431686 | |||||||
| chr14:105431696 | G | A | 1 | a0003c0008t0001g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.29-6976G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105431696 | |||||||
| chr14:105431718 | C | T | 7 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0012t0001g0043 others(4): Show |
7 | HG03041.hp2 HG03130.hp2 HG03471.hp2 others(4): Show |
intron_variant | MODIFIER | c.29-6954C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105431718 | |||||||
| chr14:105431777 | C | T | 2 | a0001c0001t0001g0040 a0004c0003t0001g0039 |
2 | HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.29-6895C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105431777 | |||||||
| chr14:105431801 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.29-6871T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105431801 | |||||||
| chr14:105431853 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.29-6819T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105431853 | |||||||
| chr14:105431911 | G | C | 1 | a0003c0008t0001g0052 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.29-6761G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105431911 | |||||||
| chr14:105431915 | T | C | 1 | a0003c0008t0001g0052 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.29-6757T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105431915 | |||||||
| chr14:105431927 | G | A | 1 | a0002c0002t0001g0173 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.29-6745G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105431927 | |||||||
| chr14:105432034 | A | C | 19 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0118 others(16): Show |
19 | HG00639.hp2 HG01167.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.29-6638A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105432034 | |||||||
| chr14:105432036 | C | T | 1 | a0001c0001t0001g0118 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.29-6636C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105432036 | |||||||
| chr14:105432237 | TTTTA | T | 3 | a0001c0001t0001g0211 a0001c0001t0001g0217 a0002c0002t0001g0225 |
3 | HG01243.hp1 NA18941.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.29-6419_29-6416del others(4): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105432237 | ||||||
| chr14:105432295 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0053 |
2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.29-6377C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105432295 | |||||||
| chr14:105432378 | T | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0099 a0001c0001t0001g0100 others(1): Show |
5 | HG00733.hp1 HG03516.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.29-6294T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105432378 | |||||||
| chr14:105432383 | G | GGT | 4 | a0001c0001t0001g0007 a0001c0001t0001g0099 a0001c0001t0001g0100 others(1): Show |
5 | HG00733.hp1 HG03516.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.29-6288_29-6287ins others(2): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105432383 | ||||||
| chr14:105432396 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.29-6276A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105432396 | |||||||
| chr14:105432401 | C | T | 5 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0017t0001g0050 others(2): Show |
5 | HG03041.hp2 HG03471.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.29-6271C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105432401 | |||||||
| chr14:105432605 | A | T | 16 | a0001c0012t0001g0043 a0001c0012t0001g0242 a0003c0004t0001g0003 others(13): Show |
16 | HG00639.hp2 HG01167.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.29-6067A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105432605 | |||||||
| chr14:105432786 | T | C | 5 | a0003c0004t0001g0064 a0003c0007t0001g0058 a0003c0007t0001g0059 others(2): Show |
5 | HG02109.hp1 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.29-5886T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105432786 | |||||||
| chr14:105432976 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.29-5696C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105432976 | |||||||
| chr14:105432980 | T | C | 1 | a0001c0001t0001g0270 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.29-5692T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105432980 | |||||||
| chr14:105432998 | C | T | 1 | a0001c0011t0001g0210 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.29-5674C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105432998 | |||||||
| chr14:105433007 | A | G | 259 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(256): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.29-5665A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105433007 | |||||||
| chr14:105433238 | A | G | 240 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(237): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.29-5434A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105433238 | |||||||
| chr14:105433329 | C | T | 1 | a0003c0008t0001g0052 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.29-5343C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105433329 | |||||||
| chr14:105433330 | G | A | 141 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(138): Show |
151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.29-5342G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105433330 | |||||||
| chr14:105433397 | C | T | 7 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0012t0001g0043 others(4): Show |
7 | HG00639.hp2 HG03041.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.29-5275C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105433397 | |||||||
| chr14:105433455 | C | T | 1 | a0003c0008t0001g0052 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.29-5217C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105433455 | |||||||
| chr14:105433472 | A | G | 10 | a0003c0006t0001g0002 a0003c0006t0001g0028 a0003c0006t0001g0029 others(7): Show |
13 | HG00735.hp2 HG01891.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.29-5200A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105433472 | |||||||
| chr14:105433481 | G | C | 141 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(138): Show |
151 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.29-5191G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105433481 | |||||||
| chr14:105433543 | G | A | 1 | a0002c0002t0001g0226 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.29-5129G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105433543 | |||||||
| chr14:105433756 | G | A | 259 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(256): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.29-4916G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105433756 | |||||||
| chr14:105433765 | T | A | 259 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(256): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.29-4907T>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105433765 | |||||||
| chr14:105433834 | A | T | 22 | a0001c0001t0001g0053 a0001c0012t0001g0043 a0001c0012t0001g0242 others(19): Show |
22 | HG00639.hp2 HG01167.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.29-4838A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105433834 | |||||||
| chr14:105434209 | C | T | 238 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(235): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.29-4463C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105434209 | |||||||
| chr14:105434220 | G | T | 4 | a0001c0012t0001g0043 a0001c0017t0001g0050 a0002c0002t0001g0051 others(1): Show |
4 | HG03130.hp2 HG03704.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.29-4452G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105434220 | |||||||
| chr14:105434224 | A | C | 1 | a0001c0001t0001g0209 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.29-4448A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105434224 | |||||||
| chr14:105434281 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0012t0001g0242 |
3 | HG00639.hp2 HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.29-4391G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105434281 | |||||||
| chr14:105434379 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.29-4293A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105434379 | |||||||
| chr14:105434478 | G | A | 1 | a0002c0002t0001g0194 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.29-4194G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105434478 | |||||||
| chr14:105434490 | CT | C | 8 | a0001c0001t0001g0118 a0001c0001t0001g0191 a0001c0001t0001g0209 others(5): Show |
8 | HG00597.hp2 HG00735.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.29-4161delT | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105434490 | ||||||
| chr14:105434490 | CTT | C | 226 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(223): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.29-4162_29-4161del others(2): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105434490 | ||||||
| chr14:105434490 | CTTT | C | 25 | a0001c0001t0001g0068 a0001c0001t0001g0079 a0001c0001t0001g0122 others(22): Show |
25 | HG00323.hp2 HG01069.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.29-4163_29-4161del others(3): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105434490 | ||||||
| chr14:105434591 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.29-4081C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105434591 | |||||||
| chr14:105434735 | A | G | 1 | a0001c0001t0001g0182 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.29-3937A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105434735 | |||||||
| chr14:105434742 | C | G | 1 | a0004c0003t0001g0117 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.29-3930C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105434742 | |||||||
| chr14:105434748 | G | A | 8 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0044 others(5): Show |
8 | HG01074.hp2 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.29-3924G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105434748 | |||||||
| chr14:105434848 | CTTACTCA others(4): Show |
C | 1 | a0001c0001t0001g0270 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.29-3821_29-3811del others(11): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105434848 | ||||||
| chr14:105434919 | G | A | 4 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0168 others(1): Show |
4 | HG00544.hp2 HG02165.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-3753G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105434919 | |||||||
| chr14:105435031 | A | G | 2 | a0001c0001t0001g0151 a0002c0002t0001g0152 |
2 | HG00597.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.29-3641A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105435031 | |||||||
| chr14:105435118 | A | C | 271 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(268): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.29-3554A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105435118 | |||||||
| chr14:105435289 | TTTAAG | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0012t0001g0242 |
3 | HG00639.hp2 HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.29-3379_29-3375del others(5): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105435289 | ||||||
| chr14:105435389 | G | A | 6 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0044 others(3): Show |
6 | HG02280.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.29-3283G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105435389 | |||||||
| chr14:105435413 | C | A | 236 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(233): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.29-3259C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105435413 | |||||||
| chr14:105435733 | G | A | 13 | a0003c0004t0001g0003 a0003c0004t0001g0048 a0003c0004t0001g0064 others(10): Show |
13 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.29-2939G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105435733 | |||||||
| chr14:105435936 | C | G | 1 | a0001c0001t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.29-2736C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105435936 | |||||||
| chr14:105435969 | G | A | 1 | a0001c0012t0001g0043 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.29-2703G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105435969 | |||||||
| chr14:105436117 | A | T | 1 | a0004c0003t0001g0260 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.29-2555A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105436117 | |||||||
| chr14:105436176 | G | A | 1 | a0001c0012t0001g0043 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.29-2496G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105436176 | |||||||
| chr14:105436224 | G | A | 2 | a0003c0004t0001g0055 a0003c0004t0001g0056 |
2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.29-2448G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105436224 | |||||||
| chr14:105436269 | A | T | 14 | a0001c0001t0001g0004 a0001c0001t0001g0079 a0001c0001t0001g0080 others(11): Show |
16 | HG00639.hp1 HG00642.hp1 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.29-2403A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105436269 | |||||||
| chr14:105436350 | T | C | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.29-2322T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105436350 | |||||||
| chr14:105436382 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.29-2290G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105436382 | |||||||
| chr14:105436423 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.29-2249C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105436423 | |||||||
| chr14:105436576 | G | A | 4 | a0003c0006t0001g0028 a0003c0006t0001g0029 a0003c0006t0001g0033 others(1): Show |
4 | HG02572.hp2 HG02615.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.29-2096G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105436576 | |||||||
| chr14:105436609 | C | T | 13 | a0003c0004t0001g0003 a0003c0004t0001g0048 a0003c0004t0001g0064 others(10): Show |
13 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.29-2063C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105436609 | |||||||
| chr14:105436725 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.29-1947C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105436725 | |||||||
| chr14:105436749 | G | A | 14 | a0003c0004t0001g0003 a0003c0004t0001g0048 a0003c0004t0001g0064 others(11): Show |
14 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.29-1923G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105436749 | |||||||
| chr14:105436799 | C | T | 1 | a0001c0012t0001g0043 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.29-1873C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105436799 | |||||||
| chr14:105436949 | C | T | 1 | a0001c0011t0001g0203 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.29-1723C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105436949 | |||||||
| chr14:105437044 | C | T | 87 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(84): Show |
100 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.29-1628C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437044 | |||||||
| chr14:105437232 | CGGGCGTG others(63): Show |
C | 1 | a0001c0001t0001g0172 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.29-1420_29-1351del others(70): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105437232 | ||||||
| chr14:105437237 | GTGTGCCT others(35): Show |
G | 235 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(232): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.29-1420_29-1379del others(42): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105437237 | ||||||
| chr14:105437266 | TGTCCTCA others(21): Show |
T | 1 | a0003c0008t0001g0052 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.29-1393_29-1366del others(28): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105437266 | ||||||
| chr14:105437279 | A | G | 34 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0012t0001g0043 others(31): Show |
38 | HG00639.hp2 HG00735.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.29-1393A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437279 | |||||||
| chr14:105437295 | G | A | 1 | a0001c0012t0001g0043 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.29-1377G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437295 | |||||||
| chr14:105437323 | G | A | 12 | a0003c0004t0001g0006 a0003c0004t0001g0032 a0003c0006t0001g0002 others(9): Show |
16 | HG00735.hp2 HG01167.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.29-1349G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437323 | |||||||
| chr14:105437354 | G | C | 245 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(242): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.29-1318G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437354 | |||||||
| chr14:105437387 | G | A | 239 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(236): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.29-1285G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437387 | |||||||
| chr14:105437442 | C | CGGGCATG others(77): Show |
1 | a0002c0002t0001g0101 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.29-1210_29-1127dup others(84): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr14 | 105437442 | ||||||
| chr14:105437517 | G | A | 1 | a0002c0002t0001g0123 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.29-1155G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437517 | |||||||
| chr14:105437557 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.29-1115C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437557 | |||||||
| chr14:105437603 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.29-1069C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437603 | |||||||
| chr14:105437827 | G | A | 1 | a0001c0012t0001g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.29-845G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437827 | |||||||
| chr14:105437914 | G | A | 6 | a0001c0001t0002g0073 a0001c0001t0002g0095 a0001c0001t0002g0096 others(3): Show |
6 | HG01255.hp2 HG01891.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.29-758G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437914 | |||||||
| chr14:105437919 | G | T | 1 | a0003c0004t0001g0006 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.29-753G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437919 | |||||||
| chr14:105437930 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.29-742C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437930 | |||||||
| chr14:105437994 | G | A | 24 | a0001c0001t0001g0125 a0001c0001t0001g0182 a0002c0002t0001g0067 others(21): Show |
24 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(21): Show |
intron_variant | MODIFIER | c.29-678G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105437994 | |||||||
| chr14:105438336 | C | T | 1 | a0003c0008t0001g0052 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.29-336C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105438336 | |||||||
| chr14:105438493 | C | T | 233 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(230): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.29-179C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 1/20 | chr14 | 105438493 | |||||||
| chr14:105438772 | G | A | 1 | a0001c0012t0001g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.96+33G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105438772 | |||||||
| chr14:105438789 | C | T | 250 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(247): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.96+50C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105438789 | |||||||
| chr14:105438815 | A | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0100 |
3 | HG00733.hp1 NA18522.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.96+76A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105438815 | |||||||
| chr14:105438835 | G | A | 4 | a0002c0002t0001g0088 a0002c0002t0001g0130 a0002c0002t0001g0164 others(1): Show |
4 | HG00673.hp1 NA18943.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+96G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105438835 | |||||||
| chr14:105438899 | C | T | 1 | a0002c0002t0001g0148 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.96+160C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105438899 | |||||||
| chr14:105439001 | G | C | 1 | a0002c0015t0001g0131 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.96+262G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105439001 | |||||||
| chr14:105439155 | C | CCCACCCC others(73): Show |
1 | a0003c0007t0001g0059 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.96+435_96+436insGT others(78): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105439155 | ||||||
| chr14:105439155 | C | CCCACCCC others(73): Show |
269 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(266): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.96+435_96+436insGT others(78): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105439155 | ||||||
| chr14:105439155 | C | CCCACCCC others(73): Show |
1 | a0003c0008t0001g0052 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.96+435_96+436insGT others(78): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105439155 | ||||||
| chr14:105439208 | A | C | 2 | a0001c0001t0001g0129 a0001c0001t0001g0232 |
2 | HG01243.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.96+469A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105439208 | |||||||
| chr14:105439215 | C | T | 1 | a0003c0008t0001g0052 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.96+476C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105439215 | |||||||
| chr14:105439566 | G | A | 2 | a0001c0017t0001g0050 a0002c0002t0001g0051 |
2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.96+827G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105439566 | |||||||
| chr14:105439581 | G | A | 3 | a0001c0017t0001g0050 a0002c0002t0001g0051 a0003c0004t0001g0054 |
3 | HG03130.hp2 HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.96+842G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105439581 | |||||||
| chr14:105439687 | G | C | 1 | a0003c0006t0001g0002 | 4 | HG02922.hp2 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.96+948G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105439687 | |||||||
| chr14:105439736 | C | T | 147 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(144): Show |
157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.96+997C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105439736 | |||||||
| chr14:105439759 | G | A | 1 | a0001c0012t0001g0043 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.96+1020G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105439759 | |||||||
| chr14:105440010 | C | T | 6 | a0001c0012t0001g0043 a0001c0017t0001g0050 a0002c0002t0001g0051 others(3): Show |
6 | HG03130.hp2 HG03579.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+1271C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105440010 | |||||||
| chr14:105440065 | G | T | 1 | a0002c0002t0001g0105 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.96+1326G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105440065 | |||||||
| chr14:105440185 | A | C | 8 | a0001c0001t0001g0008 a0001c0001t0001g0086 a0001c0001t0001g0094 others(5): Show |
9 | HG00140.hp1 HG00642.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.96+1446A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105440185 | |||||||
| chr14:105440243 | C | T | 13 | a0003c0004t0001g0003 a0003c0004t0001g0048 a0003c0004t0001g0064 others(10): Show |
13 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.96+1504C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105440243 | |||||||
| chr14:105440244 | G | A | 9 | a0003c0006t0001g0002 a0003c0006t0001g0028 a0003c0006t0001g0029 others(6): Show |
12 | HG00735.hp2 HG02559.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.96+1505G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105440244 | |||||||
| chr14:105440359 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.96+1620T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105440359 | |||||||
| chr14:105440454 | C | T | 4 | a0001c0012t0001g0043 a0003c0004t0001g0054 a0003c0004t0001g0055 others(1): Show |
4 | HG03130.hp2 HG03579.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+1715C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105440454 | |||||||
| chr14:105440460 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.96+1721C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105440460 | |||||||
| chr14:105440504 | G | A | 6 | a0001c0001t0002g0073 a0001c0001t0002g0095 a0001c0001t0002g0096 others(3): Show |
6 | HG01255.hp2 HG01891.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.96+1765G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105440504 | |||||||
| chr14:105440696 | C | T | 1 | a0001c0011t0001g0203 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.96+1957C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105440696 | |||||||
| chr14:105440822 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.96+2083C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105440822 | |||||||
| chr14:105440969 | C | T | 1 | a0003c0008t0001g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.96+2230C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105440969 | |||||||
| chr14:105440999 | G | A | 4 | a0002c0002t0001g0088 a0002c0002t0001g0130 a0002c0002t0001g0164 others(1): Show |
4 | HG00673.hp1 NA18943.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+2260G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105440999 | |||||||
| chr14:105441096 | C | T | 35 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0230 others(32): Show |
38 | HG00639.hp2 HG00735.hp2 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.96+2357C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441096 | |||||||
| chr14:105441098 | C | T | 8 | a0001c0001t0001g0007 a0001c0001t0001g0042 a0001c0001t0001g0044 others(5): Show |
9 | HG00733.hp1 HG02055.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+2359C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441098 | |||||||
| chr14:105441111 | TG | T | 15 | a0001c0001t0001g0230 a0001c0012t0001g0242 a0003c0004t0001g0003 others(12): Show |
15 | HG00639.hp2 HG01167.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.96+2378delG | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105441111 | ||||||
| chr14:105441126 | T | A | 5 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0012t0001g0043 others(2): Show |
5 | HG00639.hp2 HG03041.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.96+2387T>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441126 | |||||||
| chr14:105441232 | G | A | 1 | a0001c0001t0001g0272 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.96+2493G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441232 | |||||||
| chr14:105441260 | G | GC | 13 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0230 others(10): Show |
13 | HG00597.hp2 HG00642.hp1 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.96+2528dupC | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105441260 | ||||||
| chr14:105441260 | GC | G | 12 | a0001c0001t0001g0047 a0001c0001t0001g0116 a0003c0006t0001g0002 others(9): Show |
15 | HG00735.hp2 HG02559.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.96+2528delC | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105441260 | ||||||
| chr14:105441268 | GC | G | 6 | a0003c0004t0001g0048 a0003c0004t0001g0064 a0003c0007t0001g0058 others(3): Show |
6 | HG02109.hp1 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+2533delC | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105441268 | ||||||
| chr14:105441269 | C | G | 18 | a0001c0001t0001g0046 a0001c0001t0001g0116 a0001c0001t0001g0172 others(15): Show |
19 | HG00323.hp2 HG01167.hp2 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.96+2530C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441269 | |||||||
| chr14:105441305 | C | T | 215 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(212): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.96+2566C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441305 | |||||||
| chr14:105441404 | C | T | 1 | a0001c0012t0001g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.96+2665C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441404 | |||||||
| chr14:105441447 | T | C | 9 | a0001c0001t0001g0100 a0003c0004t0001g0003 a0003c0006t0001g0033 others(6): Show |
9 | HG01167.hp1 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+2708T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441447 | |||||||
| chr14:105441450 | G | A | 1 | a0004c0003t0001g0186 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.96+2711G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441450 | |||||||
| chr14:105441516 | T | C | 54 | a0001c0001t0001g0036 a0001c0001t0001g0040 a0001c0001t0001g0046 others(51): Show |
58 | HG00639.hp2 HG01099.hp1 HG01167.hp2 others(55): Show |
intron_variant | MODIFIER | c.96+2777T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441516 | |||||||
| chr14:105441519 | A | G | 15 | a0001c0001t0001g0046 a0001c0012t0001g0043 a0003c0004t0001g0110 others(12): Show |
18 | HG00735.hp2 HG01167.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.96+2780A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441519 | |||||||
| chr14:105441523 | A | G | 19 | a0001c0001t0001g0046 a0001c0001t0001g0232 a0001c0012t0001g0043 others(16): Show |
22 | HG00639.hp2 HG00735.hp2 HG01167.hp1 others(19): Show |
intron_variant | MODIFIER | c.96+2784A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441523 | |||||||
| chr14:105441525 | G | T | 13 | a0001c0012t0001g0043 a0003c0006t0001g0002 a0003c0006t0001g0028 others(10): Show |
16 | HG00735.hp2 HG01167.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.96+2786G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441525 | |||||||
| chr14:105441538 | G | T | 14 | a0001c0001t0001g0044 a0001c0012t0001g0043 a0003c0006t0001g0002 others(11): Show |
17 | HG00735.hp2 HG01167.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.96+2799G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441538 | |||||||
| chr14:105441554 | A | G | 6 | a0003c0004t0001g0032 a0003c0004t0001g0055 a0003c0004t0001g0056 others(3): Show |
6 | HG02615.hp1 HG03225.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.96+2815A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441554 | |||||||
| chr14:105441561 | G | C | 270 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(267): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.96+2822G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441561 | |||||||
| chr14:105441566 | G | A | 271 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(268): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.96+2827G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441566 | |||||||
| chr14:105441569 | C | T | 1 | a0001c0017t0001g0050 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.96+2830C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441569 | |||||||
| chr14:105441570 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.96+2831G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441570 | |||||||
| chr14:105441580 | A | G | 5 | a0002c0002t0001g0101 a0002c0002t0001g0179 a0002c0002t0001g0180 others(2): Show |
5 | HG02056.hp2 NA18955.hp1 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.96+2841A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441580 | |||||||
| chr14:105441606 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.96+2867A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441606 | |||||||
| chr14:105441619 | T | C | 2 | a0001c0001t0001g0084 a0001c0001t0001g0093 |
2 | HG01106.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.96+2880T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441619 | |||||||
| chr14:105441621 | C | T | 1 | a0005c0005t0001g0069 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.96+2882C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441621 | |||||||
| chr14:105441641 | A | C | 1 | a0003c0004t0001g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.96+2902A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441641 | |||||||
| chr14:105441650 | C | G | 1 | a0001c0012t0001g0043 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.96+2911C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441650 | |||||||
| chr14:105441650 | C | T | 1 | a0002c0002t0001g0173 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.96+2911C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441650 | |||||||
| chr14:105441654 | C | T | 3 | a0001c0012t0001g0242 a0001c0017t0001g0050 a0002c0002t0001g0051 |
3 | HG00639.hp2 HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.96+2915C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441654 | |||||||
| chr14:105441655 | G | T | 1 | a0002c0002t0001g0173 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.96+2916G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441655 | |||||||
| chr14:105441656 | T | A | 3 | a0001c0001t0001g0036 a0007c0013t0001g0037 a0007c0013t0001g0038 |
3 | HG01496.hp1 HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.96+2917T>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441656 | |||||||
| chr14:105441656 | T | C | 3 | a0003c0004t0001g0054 a0003c0004t0001g0055 a0003c0004t0001g0056 |
3 | HG03130.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.96+2917T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441656 | |||||||
| chr14:105441657 | G | A | 1 | a0001c0001t0001g0005 | 3 | HG03491.hp1 HG03492.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.96+2918G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441657 | |||||||
| chr14:105441662 | C | T | 1 | a0006c0010t0001g0165 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.96+2923C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441662 | |||||||
| chr14:105441663 | G | A | 2 | a0001c0001t0001g0021 a0002c0002t0001g0221 |
2 | HG00323.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.96+2924G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441663 | |||||||
| chr14:105441666 | C | T | 2 | a0001c0001t0001g0021 a0002c0002t0001g0221 |
2 | HG00323.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.96+2927C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441666 | |||||||
| chr14:105441673 | G | A | 3 | a0001c0001t0001g0021 a0001c0012t0001g0043 a0002c0002t0001g0221 |
3 | HG00323.hp1 HG02300.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.96+2934G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441673 | |||||||
| chr14:105441674 | A | G | 3 | a0001c0001t0001g0021 a0001c0012t0001g0043 a0002c0002t0001g0221 |
3 | HG00323.hp1 HG02300.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.96+2935A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441674 | |||||||
| chr14:105441686 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.96+2947C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441686 | |||||||
| chr14:105441699 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.96+2960C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441699 | |||||||
| chr14:105441712 | T | G | 1 | a0001c0001t0001g0197 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.96+2973T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441712 | |||||||
| chr14:105441719 | G | A | 240 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(237): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.96+2980G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441719 | |||||||
| chr14:105441725 | T | C | 6 | a0001c0001t0001g0150 a0002c0002t0001g0196 a0003c0004t0001g0006 others(3): Show |
7 | HG00639.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.96+2986T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441725 | |||||||
| chr14:105441726 | G | A | 1 | a0002c0002t0001g0196 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.96+2987G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441726 | |||||||
| chr14:105441733 | G | C | 6 | a0001c0001t0001g0092 a0001c0001t0001g0224 a0002c0002t0001g0015 others(3): Show |
7 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+2994G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441733 | |||||||
| chr14:105441742 | C | A | 1 | a0001c0001t0001g0264 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.96+3003C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441742 | |||||||
| chr14:105441743 | G | A | 28 | a0001c0001t0001g0047 a0001c0017t0001g0050 a0002c0002t0001g0051 others(25): Show |
31 | HG00735.hp2 HG01167.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.96+3004G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441743 | |||||||
| chr14:105441748 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.96+3009C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441748 | |||||||
| chr14:105441749 | C | A | 267 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(264): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.96+3010C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441749 | |||||||
| chr14:105441749 | C | G | 2 | a0001c0001t0001g0239 a0002c0002t0001g0196 |
2 | HG01261.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.96+3010C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441749 | |||||||
| chr14:105441750 | C | T | 2 | a0002c0002t0001g0178 a0002c0002t0001g0184 |
2 | HG00438.hp2 HG00558.hp2 |
intron_variant | MODIFIER | c.96+3011C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441750 | |||||||
| chr14:105441754 | A | G | 6 | a0001c0001t0001g0092 a0001c0001t0001g0224 a0002c0002t0001g0015 others(3): Show |
7 | HG00099.hp2 HG01109.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.96+3015A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441754 | |||||||
| chr14:105441757 | A | G | 13 | a0001c0001t0001g0092 a0001c0001t0001g0149 a0001c0001t0001g0224 others(10): Show |
14 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.96+3018A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441757 | |||||||
| chr14:105441763 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.96+3024C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441763 | |||||||
| chr14:105441772 | C | T | 1 | a0005c0005t0001g0161 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.96+3033C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441772 | |||||||
| chr14:105441781 | G | A | 1 | a0004c0003t0001g0112 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.96+3042G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441781 | |||||||
| chr14:105441788 | T | C | 11 | a0001c0001t0001g0047 a0003c0006t0001g0002 a0003c0006t0001g0028 others(8): Show |
14 | HG00735.hp2 HG01891.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.96+3049T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441788 | |||||||
| chr14:105441814 | A | C | 12 | a0003c0004t0001g0003 a0003c0004t0001g0064 a0003c0007t0001g0003 others(9): Show |
12 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.96+3075A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441814 | |||||||
| chr14:105441840 | AG | A | 3 | a0001c0012t0001g0043 a0003c0004t0001g0032 a0003c0008t0001g0052 |
3 | HG03471.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.96+3104delG | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105441840 | ||||||
| chr14:105441875 | G | A | 21 | a0001c0012t0001g0043 a0001c0012t0001g0242 a0001c0017t0001g0050 others(18): Show |
21 | HG00639.hp2 HG01167.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.96+3136G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441875 | |||||||
| chr14:105441887 | T | A | 270 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(267): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.96+3148T>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105441887 | |||||||
| chr14:105442057 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0238 |
3 | HG01884.hp1 HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.96+3318C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442057 | |||||||
| chr14:105442102 | G | A | 1 | a0003c0004t0001g0032 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.97-3316G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442102 | |||||||
| chr14:105442149 | A | G | 1 | a0003c0004t0001g0032 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.97-3269A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442149 | |||||||
| chr14:105442235 | C | T | 1 | a0001c0001t0001g0232 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.97-3183C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442235 | |||||||
| chr14:105442249 | G | T | 2 | a0002c0002t0001g0075 a0002c0002t0001g0146 |
2 | HG00738.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.97-3169G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442249 | |||||||
| chr14:105442259 | G | A | 247 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(244): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.97-3159G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442259 | |||||||
| chr14:105442333 | G | A | 1 | a0003c0004t0001g0006 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.97-3085G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442333 | |||||||
| chr14:105442443 | G | A | 270 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(267): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.97-2975G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442443 | |||||||
| chr14:105442546 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.97-2872G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442546 | |||||||
| chr14:105442555 | T | C | 264 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(261): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.97-2863T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442555 | |||||||
| chr14:105442606 | G | A | 4 | a0001c0001t0001g0198 a0001c0001t0001g0211 a0001c0001t0001g0217 others(1): Show |
4 | NA18941.hp1 NA18942.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.97-2812G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442606 | |||||||
| chr14:105442642 | T | TCAGAACA others(46): Show |
23 | a0001c0001t0001g0010 a0001c0001t0001g0040 a0001c0001t0001g0042 others(20): Show |
24 | HG01069.hp2 HG01099.hp1 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.97-2728_97-2676dup others(53): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442642 | ||||||
| chr14:105442645 | G | GAACAGAC others(1404): Show |
1 | a0003c0004t0001g0032 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.97-2694_97-2693ins others(1411): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442645 | ||||||
| chr14:105442645 | G | GAACAGAC others(152): Show |
1 | a0001c0001t0001g0249 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.97-2676_97-2675ins others(159): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442645 | ||||||
| chr14:105442725 | G | A | 3 | a0001c0001t0001g0046 a0001c0012t0001g0043 a0003c0004t0001g0032 |
3 | HG02451.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.97-2693G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442725 | |||||||
| chr14:105442743 | G | A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0125 a0001c0001t0001g0238 others(5): Show |
9 | HG01175.hp1 HG01361.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.97-2675G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442743 | |||||||
| chr14:105442743 | GCAGAACA others(46): Show |
G | 1 | a0001c0012t0001g0043 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.97-2672_97-2620del others(53): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442743 | ||||||
| chr14:105442746 | G | C | 10 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0001t0001g0125 others(7): Show |
11 | HG01175.hp1 HG01361.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.97-2672G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442746 | |||||||
| chr14:105442751 | C | G | 10 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0001t0001g0125 others(7): Show |
11 | HG01175.hp1 HG01361.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.97-2667C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442751 | |||||||
| chr14:105442778 | G | GCTGTGTG others(205): Show |
13 | a0001c0001t0001g0008 a0001c0001t0001g0086 a0001c0001t0001g0094 others(10): Show |
14 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.97-2623_97-2622ins others(212): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442778 | ||||||
| chr14:105442778 | G | GCTGTGTG others(311): Show |
1 | a0001c0001t0001g0252 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.97-2623_97-2622ins others(318): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442778 | ||||||
| chr14:105442778 | GCTGTGTG others(46): Show |
G | 1 | a0001c0001t0001g0046 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.97-2622_97-2570del others(53): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442778 | ||||||
| chr14:105442782 | T | C | 12 | a0003c0004t0001g0003 a0003c0004t0001g0064 a0003c0007t0001g0003 others(9): Show |
12 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.97-2636T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442782 | |||||||
| chr14:105442796 | A | ACACAACA others(205): Show |
1 | a0001c0001t0001g0013 | 2 | HG00408.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.97-2588_97-2587ins others(212): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442796 | ||||||
| chr14:105442796 | A | ACACAACA others(152): Show |
128 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0014 others(125): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.97-2588_97-2587ins others(159): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442796 | ||||||
| chr14:105442796 | A | ACACAACA others(311): Show |
4 | a0002c0002t0001g0067 a0002c0002t0001g0174 a0002c0002t0001g0235 others(1): Show |
4 | HG00609.hp1 HG00621.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-2588_97-2587ins others(318): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442796 | ||||||
| chr14:105442796 | A | ACACAACA others(152): Show |
3 | a0001c0001t0001g0016 a0001c0001t0001g0238 a0002c0002t0001g0185 |
4 | HG01884.hp1 HG02258.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-2588_97-2587ins others(159): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442796 | ||||||
| chr14:105442796 | A | ACACAACA others(470): Show |
1 | a0001c0001t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.97-2588_97-2587ins others(477): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442796 | ||||||
| chr14:105442796 | A | ACACAACA others(258): Show |
20 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0074 others(17): Show |
21 | HG00544.hp2 HG00558.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.97-2588_97-2587ins others(265): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442796 | ||||||
| chr14:105442796 | A | ACACAACA others(364): Show |
2 | a0001c0001t0001g0093 a0001c0001t0001g0229 |
2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.97-2588_97-2587ins others(371): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442796 | ||||||
| chr14:105442796 | A | ACACAACA others(470): Show |
1 | a0001c0001t0001g0084 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.97-2588_97-2587ins others(477): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442796 | ||||||
| chr14:105442796 | A | ACACAACA others(311): Show |
1 | a0001c0001t0001g0113 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.97-2588_97-2587ins others(318): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442796 | ||||||
| chr14:105442796 | A | ACACAACA others(152): Show |
3 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0003g0247 |
3 | HG00323.hp2 HG02486.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.97-2605_97-2604ins others(159): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442796 | ||||||
| chr14:105442796 | A | G | 14 | a0001c0001t0001g0008 a0001c0001t0001g0086 a0001c0001t0001g0094 others(11): Show |
15 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.97-2622A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442796 | |||||||
| chr14:105442831 | A | ACTGTGTG others(46): Show |
1 | a0001c0001t0001g0249 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.97-2567_97-2566ins others(53): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442831 | ||||||
| chr14:105442831 | A | ACTGTGTG others(46): Show |
89 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0010 others(86): Show |
99 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.97-2567_97-2566ins others(53): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442831 | ||||||
| chr14:105442831 | A | ACTGTGTG others(629): Show |
1 | a0004c0003t0001g0205 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.97-2567_97-2566ins others(636): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105442831 | ||||||
| chr14:105442831 | A | G | 180 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(177): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.97-2587A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105442831 | |||||||
| chr14:105443000 | G | T | 264 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(261): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.97-2418G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105443000 | |||||||
| chr14:105443043 | A | T | 266 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(263): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.97-2375A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105443043 | |||||||
| chr14:105443099 | C | T | 239 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(236): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.97-2319C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105443099 | |||||||
| chr14:105443153 | G | A | 2 | a0003c0004t0001g0006 a0003c0004t0001g0032 |
3 | HG01167.hp2 HG01169.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.97-2265G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105443153 | |||||||
| chr14:105443190 | A | G | 266 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(263): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.97-2228A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105443190 | |||||||
| chr14:105443313 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.97-2105C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105443313 | |||||||
| chr14:105443635 | A | C | 255 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(252): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.97-1783A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105443635 | |||||||
| chr14:105443690 | T | C | 2 | a0001c0012t0001g0043 a0003c0004t0001g0054 |
2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-1728T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105443690 | |||||||
| chr14:105443730 | G | T | 272 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(269): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.97-1688G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105443730 | |||||||
| chr14:105443816 | T | C | 267 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(264): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.97-1602T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105443816 | |||||||
| chr14:105443856 | T | C | 267 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(264): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.97-1562T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105443856 | |||||||
| chr14:105443901 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.97-1517C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105443901 | |||||||
| chr14:105443946 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0118 |
2 | NA18939.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.97-1472G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105443946 | |||||||
| chr14:105444112 | G | T | 1 | a0003c0004t0001g0054 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.97-1306G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444112 | |||||||
| chr14:105444122 | C | G | 2 | a0001c0017t0001g0050 a0002c0002t0001g0051 |
2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.97-1296C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444122 | |||||||
| chr14:105444231 | C | T | 2 | a0001c0001t0001g0137 a0002c0002t0001g0154 |
2 | HG01099.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.97-1187C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444231 | |||||||
| chr14:105444252 | G | A | 1 | a0003c0009t0001g0025 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.97-1166G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444252 | |||||||
| chr14:105444272 | G | A | 2 | a0001c0001t0001g0047 a0001c0001t0001g0053 |
2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.97-1146G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444272 | |||||||
| chr14:105444343 | C | G | 2 | a0003c0009t0001g0026 a0003c0009t0001g0030 |
2 | HG00735.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.97-1075C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444343 | |||||||
| chr14:105444353 | C | T | 1 | a0002c0002t0001g0070 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.97-1065C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444353 | |||||||
| chr14:105444399 | A | T | 253 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(250): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.97-1019A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444399 | |||||||
| chr14:105444444 | C | A | 2 | a0001c0012t0001g0043 a0003c0004t0001g0054 |
2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.97-974C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444444 | |||||||
| chr14:105444461 | G | A | 31 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0016 others(28): Show |
34 | HG00733.hp1 HG01069.hp2 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.97-957G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444461 | |||||||
| chr14:105444514 | C | G | 1 | a0002c0002t0004g0145 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.97-904C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444514 | |||||||
| chr14:105444675 | C | T | 1 | a0002c0002t0001g0160 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.97-743C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444675 | |||||||
| chr14:105444789 | TTA | T | 12 | a0003c0004t0001g0003 a0003c0004t0001g0064 a0003c0007t0001g0003 others(9): Show |
12 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.97-628_97-627delTA | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444789 | |||||||
| chr14:105444790 | T | TA | 21 | a0001c0001t0001g0007 a0001c0001t0001g0040 a0001c0001t0001g0042 others(18): Show |
25 | HG00733.hp1 HG00735.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.97-611dupA | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105444790 | ||||||
| chr14:105444790 | TA | T | 22 | a0001c0001t0001g0005 a0001c0001t0001g0046 a0001c0001t0001g0047 others(19): Show |
22 | HG00558.hp1 HG01168.hp2 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.97-611delA | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | INFO_REALIGN_3_PRIME | chr14 | 105444790 | ||||||
| chr14:105444856 | C | T | 12 | a0003c0004t0001g0003 a0003c0004t0001g0064 a0003c0007t0001g0003 others(9): Show |
12 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.97-562C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444856 | |||||||
| chr14:105444937 | C | T | 1 | a0001c0012t0001g0043 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.97-481C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444937 | |||||||
| chr14:105444938 | G | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0099 a0001c0001t0001g0100 others(1): Show |
5 | HG00733.hp1 HG03516.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.97-480G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444938 | |||||||
| chr14:105444992 | C | T | 2 | a0001c0001t0001g0047 a0001c0001t0001g0053 |
2 | HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.97-426C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105444992 | |||||||
| chr14:105445101 | C | G | 1 | a0003c0008t0001g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.97-317C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105445101 | |||||||
| chr14:105445111 | G | A | 1 | a0002c0002t0001g0139 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.97-307G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105445111 | |||||||
| chr14:105445141 | T | C | 1 | a0001c0012t0001g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.97-277T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105445141 | |||||||
| chr14:105445225 | T | C | 273 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(270): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.97-193T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105445225 | |||||||
| chr14:105445245 | T | C | 1 | a0002c0002t0001g0155 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.97-173T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105445245 | |||||||
| chr14:105445302 | G | A | 269 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(266): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.97-116G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105445302 | |||||||
| chr14:105445330 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.97-88G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105445330 | |||||||
| chr14:105445372 | C | G | 1 | a0001c0001t0001g0086 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.97-46C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 2/20 | chr14 | 105445372 | |||||||
| chr14:105445546 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.190+35G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105445546 | |||||||
| chr14:105445554 | C | T | 12 | a0003c0004t0001g0003 a0003c0004t0001g0064 a0003c0007t0001g0003 others(9): Show |
12 | HG01167.hp1 HG02109.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.190+43C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105445554 | |||||||
| chr14:105445555 | G | A | 2 | a0001c0017t0001g0050 a0002c0002t0001g0051 |
2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190+44G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105445555 | |||||||
| chr14:105445573 | G | A | 1 | a0001c0001t0001g0012 | 2 | NA18960.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.190+62G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105445573 | |||||||
| chr14:105445720 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.190+209C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105445720 | |||||||
| chr14:105446126 | C | T | 1 | a0002c0002t0001g0105 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.190+615C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105446126 | |||||||
| chr14:105446127 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.190+616G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105446127 | |||||||
| chr14:105446353 | G | A | 1 | a0003c0004t0001g0054 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.190+842G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105446353 | |||||||
| chr14:105446353 | G | C | 2 | a0001c0001t0001g0008 a0004c0003t0001g0085 |
3 | HG00140.hp1 HG03704.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.190+842G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105446353 | |||||||
| chr14:105446440 | C | T | 2 | a0001c0001t0001g0021 a0002c0002t0001g0221 |
2 | HG00323.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.190+929C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105446440 | |||||||
| chr14:105446517 | C | G | 2 | a0001c0001t0001g0192 a0001c0001t0001g0220 |
2 | NA19003.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.190+1006C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105446517 | |||||||
| chr14:105446525 | C | T | 2 | a0003c0008t0001g0019 a0003c0008t0001g0020 |
2 | HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.190+1014C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105446525 | |||||||
| chr14:105446774 | C | T | 6 | a0001c0001t0001g0047 a0001c0001t0001g0053 a0001c0001t0001g0189 others(3): Show |
6 | HG03041.hp2 NA19003.hp1 NA19030.hp2 others(3): Show |
intron_variant | MODIFIER | c.190+1263C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105446774 | |||||||
| chr14:105446812 | G | C | 1 | a0001c0012t0001g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.190+1301G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105446812 | |||||||
| chr14:105446818 | C | T | 2 | a0001c0017t0001g0050 a0002c0002t0001g0051 |
2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190+1307C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105446818 | |||||||
| chr14:105446828 | G | T | 1 | a0001c0012t0001g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.190+1317G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105446828 | |||||||
| chr14:105446876 | G | A | 1 | a0005c0005t0001g0132 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.190+1365G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105446876 | |||||||
| chr14:105447002 | G | A | 1 | a0002c0002t0001g0156 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.190+1491G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447002 | |||||||
| chr14:105447111 | G | A | 2 | a0001c0017t0001g0050 a0002c0002t0001g0051 |
2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.190+1600G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447111 | |||||||
| chr14:105447183 | C | T | 265 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(262): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.190+1672C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447183 | |||||||
| chr14:105447276 | G | C | 6 | a0001c0001t0001g0004 a0001c0001t0001g0079 a0001c0001t0001g0080 others(3): Show |
8 | HG00642.hp1 HG00738.hp2 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.190+1765G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447276 | |||||||
| chr14:105447287 | C | T | 1 | a0003c0004t0001g0006 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.190+1776C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447287 | |||||||
| chr14:105447299 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.190+1788G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447299 | |||||||
| chr14:105447437 | C | G | 1 | a0001c0001t0001g0172 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.191-1922C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447437 | |||||||
| chr14:105447554 | A | T | 2 | a0001c0017t0001g0050 a0002c0002t0001g0051 |
2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.191-1805A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447554 | |||||||
| chr14:105447557 | G | T | 1 | a0003c0008t0001g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.191-1802G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447557 | |||||||
| chr14:105447604 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.191-1755G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447604 | |||||||
| chr14:105447680 | G | A | 2 | a0001c0017t0001g0050 a0002c0002t0001g0051 |
2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.191-1679G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447680 | |||||||
| chr14:105447686 | C | T | 1 | a0002c0002t0001g0181 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.191-1673C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447686 | |||||||
| chr14:105447822 | C | A | 1 | a0001c0001t0001g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.191-1537C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447822 | |||||||
| chr14:105447824 | C | A | 2 | a0001c0017t0001g0050 a0002c0002t0001g0051 |
2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.191-1535C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447824 | |||||||
| chr14:105447844 | C | G | 2 | a0001c0017t0001g0050 a0002c0002t0001g0051 |
2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.191-1515C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105447844 | |||||||
| chr14:105448122 | C | A | 2 | a0001c0017t0001g0050 a0002c0002t0001g0051 |
2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.191-1237C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105448122 | |||||||
| chr14:105448200 | C | T | 2 | a0001c0017t0001g0050 a0002c0002t0001g0051 |
2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.191-1159C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105448200 | |||||||
| chr14:105448240 | T | A | 1 | a0001c0001t0001g0255 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.191-1119T>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105448240 | |||||||
| chr14:105448264 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.191-1095C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105448264 | |||||||
| chr14:105448276 | C | T | 2 | a0001c0001t0001g0267 a0001c0001t0003g0247 |
2 | HG00323.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.191-1083C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105448276 | |||||||
| chr14:105448518 | C | A | 2 | a0001c0017t0001g0050 a0002c0002t0001g0051 |
2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.191-841C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105448518 | |||||||
| chr14:105448601 | A | C | 2 | a0001c0017t0001g0050 a0002c0002t0001g0051 |
2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.191-758A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105448601 | |||||||
| chr14:105448611 | G | A | 1 | a0003c0004t0001g0006 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.191-748G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105448611 | |||||||
| chr14:105448712 | A | AAC | 239 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(236): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.191-645_191-644dup others(2): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr14 | 105448712 | ||||||
| chr14:105448834 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.191-525G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105448834 | |||||||
| chr14:105448857 | T | C | 272 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(269): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.191-502T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105448857 | |||||||
| chr14:105448871 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.191-488C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105448871 | |||||||
| chr14:105448907 | G | A | 1 | a0003c0014t0001g0031 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.191-452G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105448907 | |||||||
| chr14:105448951 | C | T | 265 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(262): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.191-408C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105448951 | |||||||
| chr14:105449091 | T | C | 1 | a0001c0001t0001g0255 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.191-268T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105449091 | |||||||
| chr14:105449185 | C | T | 1 | a0002c0015t0001g0131 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.191-174C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105449185 | |||||||
| chr14:105449223 | C | T | 1 | a0004c0003t0001g0106 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.191-136C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 3/20 | chr14 | 105449223 | |||||||
| chr14:105449531 | C | T | 1 | a0002c0002t0001g0226 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.241+122C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449531 | |||||||
| chr14:105449572 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.241+163G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449572 | |||||||
| chr14:105449720 | C | T | 1 | a0005c0005t0001g0159 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.241+311C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449720 | |||||||
| chr14:105449872 | G | T | 2 | a0001c0017t0001g0050 a0002c0002t0001g0051 |
2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.242-186G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449872 | |||||||
| chr14:105449890 | C | A | 1 | a0005c0005t0001g0222 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.242-168C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449890 | |||||||
| chr14:105449901 | T | G | 1 | a0005c0005t0001g0222 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.242-157T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449901 | |||||||
| chr14:105449902 | A | G | 1 | a0005c0005t0001g0222 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.242-156A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449902 | |||||||
| chr14:105449906 | T | G | 1 | a0005c0005t0001g0222 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.242-152T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449906 | |||||||
| chr14:105449908 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.242-150G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449908 | |||||||
| chr14:105449914 | T | G | 1 | a0005c0005t0001g0222 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.242-144T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449914 | |||||||
| chr14:105449920 | A | AGGGGGGG others(4): Show |
1 | a0005c0005t0001g0222 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.242-137_242-136ins others(11): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr14 | 105449920 | ||||||
| chr14:105449922 | T | G | 1 | a0005c0005t0001g0222 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.242-136T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449922 | |||||||
| chr14:105449924 | T | C | 1 | a0005c0005t0001g0222 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.242-134T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449924 | |||||||
| chr14:105449925 | C | G | 1 | a0005c0005t0001g0222 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.242-133C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449925 | |||||||
| chr14:105449926 | C | G | 1 | a0005c0005t0001g0222 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.242-132C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449926 | |||||||
| chr14:105449926 | C | T | 1 | a0003c0004t0001g0032 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.242-132C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449926 | |||||||
| chr14:105449968 | C | T | 1 | a0005c0005t0001g0102 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.242-90C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449968 | |||||||
| chr14:105449977 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0190 |
3 | NA18612.hp2 NA18947.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.242-81G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449977 | |||||||
| chr14:105449977 | G | T | 3 | a0003c0009t0001g0025 a0003c0009t0001g0026 a0003c0009t0001g0030 |
3 | HG00735.hp2 HG02895.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.242-81G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105449977 | |||||||
| chr14:105450028 | C | T | 2 | a0001c0017t0001g0050 a0002c0002t0001g0051 |
2 | HG03704.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.242-30C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 4/20 | chr14 | 105450028 | |||||||
| chr14:105450327 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19030.hp2 | splice_region_variant&intron_variant | LOW | c.432+3G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450327 | |||||||
| chr14:105450345 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.432+21G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450345 | |||||||
| chr14:105450364 | G | A | 1 | a0003c0014t0001g0031 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.432+40G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450364 | |||||||
| chr14:105450432 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0093 a0001c0001t0001g0229 |
3 | HG01175.hp2 HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.432+108C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450432 | |||||||
| chr14:105450460 | G | A | 185 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(182): Show |
204 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.432+136G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450460 | |||||||
| chr14:105450503 | G | A | 1 | a0003c0004t0001g0006 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.432+179G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450503 | |||||||
| chr14:105450520 | G | A | 1 | a0003c0004t0001g0006 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.432+196G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450520 | |||||||
| chr14:105450680 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.432+356C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450680 | |||||||
| chr14:105450730 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.432+406G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450730 | |||||||
| chr14:105450878 | G | A | 1 | a0003c0009t0001g0025 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.432+554G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450878 | |||||||
| chr14:105450888 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.432+564G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450888 | |||||||
| chr14:105450907 | G | A | 2 | a0001c0001t0001g0255 a0001c0001t0001g0263 |
2 | HG00099.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.432+583G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450907 | |||||||
| chr14:105450911 | G | A | 1 | a0005c0005t0001g0161 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.432+587G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450911 | |||||||
| chr14:105450929 | G | A | 1 | a0003c0004t0001g0006 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.432+605G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450929 | |||||||
| chr14:105450959 | T | C | 259 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(256): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.432+635T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450959 | |||||||
| chr14:105450969 | C | T | 1 | a0003c0004t0001g0032 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.432+645C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105450969 | |||||||
| chr14:105451096 | G | A | 2 | a0001c0001t0001g0253 a0004c0003t0001g0251 |
2 | HG01358.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.432+772G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105451096 | |||||||
| chr14:105451160 | G | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0100 a0001c0001t0001g0129 others(2): Show |
6 | HG00733.hp1 HG01243.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.432+836G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105451160 | |||||||
| chr14:105451360 | G | A | 1 | a0002c0002t0001g0225 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.432+1036G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105451360 | |||||||
| chr14:105451479 | G | C | 60 | a0001c0001t0001g0021 a0001c0001t0001g0076 a0001c0001t0001g0092 others(57): Show |
70 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(67): Show |
intron_variant | MODIFIER | c.432+1155G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105451479 | |||||||
| chr14:105451482 | C | T | 8 | a0001c0001t0001g0047 a0001c0012t0001g0242 a0003c0004t0001g0064 others(5): Show |
8 | HG00639.hp2 HG01167.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.432+1158C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105451482 | |||||||
| chr14:105451747 | A | T | 1 | a0003c0004t0001g0006 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.432+1423A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105451747 | |||||||
| chr14:105451775 | CTTTTTTT others(2): Show |
C | 17 | a0001c0001t0001g0013 a0001c0001t0001g0153 a0001c0001t0001g0198 others(14): Show |
18 | HG00408.hp2 HG00609.hp1 HG00609.hp2 others(15): Show |
intron_variant | MODIFIER | c.432+1459_432+1467d others(11): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr14 | 105451775 | ||||||
| chr14:105451775 | CTTTTTTT others(3): Show |
C | 163 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(160): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.432+1459_432+1468d others(12): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr14 | 105451775 | ||||||
| chr14:105451775 | CTTTTTTT others(4): Show |
C | 9 | a0001c0001t0001g0190 a0001c0001t0001g0200 a0001c0001t0002g0095 others(6): Show |
9 | HG00099.hp2 HG01257.hp1 HG02273.hp1 others(6): Show |
intron_variant | MODIFIER | c.432+1459_432+1469d others(13): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr14 | 105451775 | ||||||
| chr14:105451783 | G | GT | 8 | a0001c0001t0001g0016 a0001c0001t0001g0150 a0001c0001t0001g0252 others(5): Show |
8 | HG01175.hp1 HG01261.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.432+1483dupT | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr14 | 105451783 | ||||||
| chr14:105451783 | G | T | 1 | a0001c0001t0001g0010 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.432+1459G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105451783 | |||||||
| chr14:105451783 | GT | G | 12 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0068 others(9): Show |
15 | HG01069.hp2 HG01358.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.432+1483delT | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr14 | 105451783 | ||||||
| chr14:105451786 | T | TG | 4 | a0001c0012t0001g0242 a0001c0017t0001g0050 a0002c0002t0001g0051 others(1): Show |
4 | HG00639.hp2 HG02818.hp2 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.432+1462_432+1463i others(3): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105451786 | |||||||
| chr14:105451787 | T | G | 5 | a0001c0001t0001g0053 a0001c0012t0001g0043 a0003c0004t0001g0006 others(2): Show |
6 | HG01167.hp2 HG01169.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.432+1463T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105451787 | |||||||
| chr14:105451791 | T | C | 3 | a0001c0001t0001g0107 a0001c0001t0001g0244 a0001c0011t0001g0203 |
3 | HG00673.hp2 HG02015.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.432+1467T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105451791 | |||||||
| chr14:105451883 | C | T | 225 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(222): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.432+1559C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105451883 | |||||||
| chr14:105452212 | G | A | 1 | a0003c0006t0001g0034 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.432+1888G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105452212 | |||||||
| chr14:105452473 | A | C | 1 | a0001c0017t0001g0050 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.433-1720A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105452473 | |||||||
| chr14:105452661 | G | T | 1 | a0001c0001t0001g0074 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.433-1532G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105452661 | |||||||
| chr14:105452768 | C | T | 1 | a0001c0012t0001g0043 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.433-1425C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105452768 | |||||||
| chr14:105452869 | T | G | 2 | a0001c0001t0001g0053 a0001c0012t0001g0242 |
2 | HG00639.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.433-1324T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105452869 | |||||||
| chr14:105452912 | C | G | 1 | a0002c0002t0001g0070 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.433-1281C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105452912 | |||||||
| chr14:105452940 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.433-1253C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105452940 | |||||||
| chr14:105452977 | A | G | 7 | a0003c0004t0001g0006 a0003c0006t0001g0002 a0003c0006t0001g0028 others(4): Show |
11 | HG01167.hp2 HG01169.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.433-1216A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105452977 | |||||||
| chr14:105453036 | C | G | 2 | a0001c0001t0001g0170 a0001c0001t0007g0022 |
2 | HG02132.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.433-1157C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105453036 | |||||||
| chr14:105453088 | C | T | 258 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(255): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.433-1105C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105453088 | |||||||
| chr14:105453132 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.433-1061C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105453132 | |||||||
| chr14:105453185 | C | T | 16 | a0001c0001t0001g0047 a0003c0004t0001g0003 a0003c0004t0001g0064 others(13): Show |
16 | HG00735.hp2 HG01167.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.433-1008C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105453185 | |||||||
| chr14:105453207 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.433-986G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105453207 | |||||||
| chr14:105453222 | C | T | 15 | a0003c0004t0001g0003 a0003c0004t0001g0064 a0003c0007t0001g0003 others(12): Show |
15 | HG00735.hp2 HG01167.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.433-971C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105453222 | |||||||
| chr14:105453301 | G | A | 1 | a0004c0003t0001g0186 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.433-892G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105453301 | |||||||
| chr14:105453321 | A | G | 2 | a0003c0004t0001g0055 a0003c0004t0001g0056 |
2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.433-872A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105453321 | |||||||
| chr14:105453538 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.433-655A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105453538 | |||||||
| chr14:105453580 | C | T | 1 | a0002c0002t0001g0051 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.433-613C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105453580 | |||||||
| chr14:105453953 | C | T | 1 | a0001c0017t0001g0050 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.433-240C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105453953 | |||||||
| chr14:105454023 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.433-170T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105454023 | |||||||
| chr14:105454114 | C | T | 1 | a0001c0017t0001g0050 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.433-79C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105454114 | |||||||
| chr14:105454115 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.433-78G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105454115 | |||||||
| chr14:105454118 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.433-75C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 6/20 | chr14 | 105454118 | |||||||
| chr14:105454534 | T | C | 262 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(259): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.550+224T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105454534 | |||||||
| chr14:105454602 | T | C | 2 | a0001c0001t0001g0153 a0004c0003t0001g0128 |
2 | NA18955.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.550+292T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105454602 | |||||||
| chr14:105454629 | C | T | 1 | a0002c0002t0001g0183 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.550+319C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105454629 | |||||||
| chr14:105454661 | C | T | 2 | a0003c0009t0001g0026 a0003c0009t0001g0030 |
2 | HG00735.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.550+351C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105454661 | |||||||
| chr14:105454670 | G | A | 2 | a0001c0012t0001g0043 a0001c0017t0001g0050 |
2 | HG03704.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.550+360G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105454670 | |||||||
| chr14:105454731 | C | T | 6 | a0003c0004t0001g0003 a0003c0007t0001g0003 a0003c0007t0001g0057 others(3): Show |
6 | HG02280.hp2 HG02572.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.550+421C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105454731 | |||||||
| chr14:105454799 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.550+489G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105454799 | |||||||
| chr14:105454806 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.550+496C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105454806 | |||||||
| chr14:105454845 | C | T | 1 | a0003c0006t0001g0034 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.550+535C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105454845 | |||||||
| chr14:105454862 | T | A | 1 | a0001c0001t0001g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.550+552T>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105454862 | |||||||
| chr14:105455064 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.550+754C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105455064 | |||||||
| chr14:105455098 | G | T | 1 | a0003c0008t0001g0052 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.550+788G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105455098 | |||||||
| chr14:105455117 | G | C | 1 | a0001c0001t0001g0086 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.550+807G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105455117 | |||||||
| chr14:105455157 | C | T | 4 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0045 others(1): Show |
4 | HG02280.hp1 HG03225.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.550+847C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105455157 | |||||||
| chr14:105455262 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.550+952C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105455262 | |||||||
| chr14:105455312 | G | A | 1 | a0002c0002t0004g0145 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.550+1002G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105455312 | |||||||
| chr14:105455345 | T | A | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(238): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.550+1035T>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105455345 | |||||||
| chr14:105455609 | A | G | 247 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(244): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.550+1299A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105455609 | |||||||
| chr14:105455755 | C | T | 3 | a0002c0002t0001g0175 a0002c0002t0001g0176 a0002c0002t0001g0177 |
3 | NA18943.hp2 NA18973.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.550+1445C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105455755 | |||||||
| chr14:105455894 | C | T | 238 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(235): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.550+1584C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105455894 | |||||||
| chr14:105455954 | ACTGTGCT others(31): Show |
A | 1 | a0001c0017t0001g0050 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.550+1682_550+1719d others(40): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr14 | 105455954 | ||||||
| chr14:105455980 | T | TGTGGGGA others(202): Show |
1 | a0003c0008t0001g0052 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.550+1674_550+1675i others(211): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr14 | 105455980 | ||||||
| chr14:105455985 | A | G | 1 | a0003c0008t0001g0052 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.550+1675A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105455985 | |||||||
| chr14:105455991 | C | T | 2 | a0001c0001t0001g0107 a0001c0001t0001g0244 |
2 | HG00673.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.550+1681C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105455991 | |||||||
| chr14:105455992 | G | A | 1 | a0003c0008t0001g0052 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.550+1682G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105455992 | |||||||
| chr14:105456023 | A | G | 3 | a0003c0004t0001g0055 a0003c0004t0001g0056 a0003c0008t0001g0052 |
3 | HG03471.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.550+1713A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105456023 | |||||||
| chr14:105456039 | G | C | 239 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(236): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.550+1729G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105456039 | |||||||
| chr14:105456203 | G | A | 1 | a0002c0002t0001g0103 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.550+1893G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105456203 | |||||||
| chr14:105456210 | C | T | 1 | a0003c0008t0001g0052 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.550+1900C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105456210 | |||||||
| chr14:105456436 | G | A | 1 | a0001c0001t0001g0118 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.551-1834G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105456436 | |||||||
| chr14:105456537 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.551-1733C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105456537 | |||||||
| chr14:105456585 | C | T | 3 | a0001c0001t0002g0073 a0001c0001t0002g0095 a0001c0001t0002g0098 |
3 | HG02895.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.551-1685C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105456585 | |||||||
| chr14:105456726 | C | G | 243 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(240): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.551-1544C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105456726 | |||||||
| chr14:105457083 | A | G | 1 | a0001c0017t0001g0050 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.551-1187A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105457083 | |||||||
| chr14:105457548 | C | T | 1 | a0001c0001t0001g0182 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.551-722C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105457548 | |||||||
| chr14:105457563 | G | T | 1 | a0003c0004t0001g0032 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.551-707G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105457563 | |||||||
| chr14:105457604 | A | C | 240 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(237): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.551-666A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105457604 | |||||||
| chr14:105457634 | A | G | 1 | a0003c0004t0001g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.551-636A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105457634 | |||||||
| chr14:105457751 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.551-519C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105457751 | |||||||
| chr14:105457795 | G | A | 3 | a0001c0001t0001g0248 a0001c0001t0001g0254 a0001c0001t0001g0261 |
3 | HG01261.hp2 HG02145.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.551-475G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105457795 | |||||||
| chr14:105457928 | A | AAAT | 3 | a0001c0001t0001g0053 a0001c0001t0001g0265 a0003c0006t0001g0028 |
3 | HG00733.hp2 HG02615.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.551-319_551-317dup others(3): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr14 | 105457928 | ||||||
| chr14:105458156 | C | A | 1 | a0001c0001t0001g0099 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.551-114C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105458156 | |||||||
| chr14:105458201 | G | A | 240 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(237): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.551-69G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105458201 | |||||||
| chr14:105458214 | G | A | 1 | a0001c0017t0001g0050 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.551-56G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105458214 | |||||||
| chr14:105458225 | C | T | 26 | a0001c0001t0001g0053 a0003c0004t0001g0003 a0003c0004t0001g0006 others(23): Show |
30 | HG00735.hp2 HG01167.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.551-45C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105458225 | |||||||
| chr14:105458266 | G | T | 1 | a0001c0001t0001g0264 | 1 | HG01358.hp1 | splice_region_variant&intron_variant | LOW | c.551-4G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 7/20 | chr14 | 105458266 | |||||||
| chr14:105458375 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG02965.hp2 | splice_region_variant&intron_variant | LOW | c.653+3G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105458375 | |||||||
| chr14:105458449 | G | A | 237 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(234): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.653+77G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105458449 | |||||||
| chr14:105458587 | G | A | 2 | a0003c0004t0001g0055 a0003c0004t0001g0056 |
2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.653+215G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105458587 | |||||||
| chr14:105458828 | C | T | 25 | a0001c0001t0001g0011 a0001c0001t0001g0023 a0001c0001t0001g0074 others(22): Show |
26 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.653+456C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105458828 | |||||||
| chr14:105458868 | C | T | 241 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(238): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.653+496C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105458868 | |||||||
| chr14:105458888 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.653+516G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105458888 | |||||||
| chr14:105458898 | C | G | 2 | a0005c0005t0001g0222 a0009c0016t0001g0090 |
2 | NA18989.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.653+526C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105458898 | |||||||
| chr14:105458928 | C | A | 240 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(237): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.653+556C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105458928 | |||||||
| chr14:105458963 | T | C | 8 | a0001c0001t0001g0008 a0001c0001t0001g0086 a0001c0001t0001g0094 others(5): Show |
9 | HG00140.hp1 HG00642.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.653+591T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105458963 | |||||||
| chr14:105459008 | G | T | 2 | a0001c0001t0001g0125 a0002c0002t0001g0138 |
2 | HG01361.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.653+636G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459008 | |||||||
| chr14:105459019 | CGCTGCCC others(288): Show |
C | 1 | a0001c0017t0001g0050 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.653+733_654-959del | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459019 | ||||||
| chr14:105459050 | GGGGAGCT others(111): Show |
G | 2 | a0003c0004t0001g0055 a0003c0004t0001g0056 |
2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.653+733_653+850del | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459050 | ||||||
| chr14:105459105 | A | G | 2 | a0001c0012t0001g0043 a0001c0012t0001g0242 |
2 | HG00639.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.653+733A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459105 | |||||||
| chr14:105459130 | G | C | 2 | a0001c0012t0001g0043 a0001c0012t0001g0242 |
2 | HG00639.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.653+758G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459130 | |||||||
| chr14:105459136 | G | A | 3 | a0001c0001t0001g0068 a0001c0001t0001g0214 a0001c0001t0001g0215 |
3 | HG01069.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.653+764G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459136 | |||||||
| chr14:105459137 | C | T | 2 | a0001c0012t0001g0043 a0001c0012t0001g0242 |
2 | HG00639.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.653+765C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459137 | |||||||
| chr14:105459145 | G | A | 2 | a0001c0012t0001g0043 a0001c0012t0001g0242 |
2 | HG00639.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.653+773G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459145 | |||||||
| chr14:105459145 | GTGGCCCC others(111): Show |
G | 3 | a0001c0001t0001g0192 a0001c0001t0001g0223 a0002c0002t0001g0226 |
3 | HG01168.hp2 HG01975.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.653+796_653+913del | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459145 | ||||||
| chr14:105459164 | CCCTAGGG others(406): Show |
C | 235 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(232): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.653+796_654-778del | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459164 | ||||||
| chr14:105459164 | CCCTAGGG others(524): Show |
C | 1 | a0005c0005t0001g0143 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.653+796_654-660del | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459164 | ||||||
| chr14:105459168 | A | G | 5 | a0001c0001t0001g0053 a0001c0001t0001g0266 a0001c0012t0001g0043 others(2): Show |
5 | HG00639.hp2 HG03471.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.653+796A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459168 | |||||||
| chr14:105459196 | T | C | 1 | a0001c0001t0001g0266 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.653+824T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459196 | |||||||
| chr14:105459204 | A | G | 2 | a0001c0001t0001g0266 a0001c0012t0001g0043 |
2 | HG03654.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.653+832A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459204 | |||||||
| chr14:105459222 | C | T | 2 | a0001c0001t0001g0266 a0001c0012t0001g0043 |
2 | HG03654.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.653+850C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459222 | |||||||
| chr14:105459223 | G | C | 2 | a0001c0001t0001g0266 a0001c0012t0001g0043 |
2 | HG03654.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.653+851G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459223 | |||||||
| chr14:105459248 | C | G | 3 | a0001c0001t0001g0266 a0001c0012t0001g0043 a0001c0012t0001g0242 |
3 | HG00639.hp2 HG03654.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.653+876C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459248 | |||||||
| chr14:105459281 | T | C | 2 | a0001c0001t0001g0266 a0001c0012t0001g0043 |
2 | HG03654.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.653+909T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459281 | |||||||
| chr14:105459282 | C | G | 2 | a0001c0001t0001g0266 a0001c0012t0001g0043 |
2 | HG03654.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.653+910C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459282 | |||||||
| chr14:105459313 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.653+941G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459313 | |||||||
| chr14:105459314 | T | C | 3 | a0001c0001t0001g0192 a0001c0001t0001g0223 a0002c0002t0001g0226 |
3 | HG01168.hp2 HG01975.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.653+942T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459314 | |||||||
| chr14:105459322 | G | A | 3 | a0001c0001t0001g0266 a0001c0012t0001g0043 a0001c0012t0001g0242 |
3 | HG00639.hp2 HG03654.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.653+950G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459322 | |||||||
| chr14:105459340 | T | C | 1 | a0001c0012t0001g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.653+968T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459340 | |||||||
| chr14:105459341 | C | G | 1 | a0001c0012t0001g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.653+969C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459341 | |||||||
| chr14:105459366 | G | A | 1 | a0001c0012t0001g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.654-992G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459366 | |||||||
| chr14:105459373 | T | C | 1 | a0001c0001t0001g0266 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.654-985T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459373 | |||||||
| chr14:105459400 | G | A | 1 | a0001c0012t0001g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.654-958G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459400 | |||||||
| chr14:105459425 | G | A | 1 | a0001c0012t0001g0043 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.654-933G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459425 | |||||||
| chr14:105459431 | G | A | 4 | a0001c0001t0001g0192 a0001c0001t0001g0223 a0001c0001t0001g0266 others(1): Show |
4 | HG01168.hp2 HG01975.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.654-927G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459431 | |||||||
| chr14:105459432 | T | C | 1 | a0001c0012t0001g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.654-926T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459432 | |||||||
| chr14:105459440 | A | G | 1 | a0001c0012t0001g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.654-918A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459440 | |||||||
| chr14:105459458 | T | C | 1 | a0001c0012t0001g0043 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.654-900T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459458 | |||||||
| chr14:105459459 | C | A | 1 | a0001c0012t0001g0043 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.654-899C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459459 | |||||||
| chr14:105459459 | CCCTGGGG others(465): Show |
C | 1 | a0001c0001t0001g0266 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.654-874_654-403del | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459459 | ||||||
| chr14:105459491 | T | C | 5 | a0001c0001t0001g0192 a0001c0001t0001g0223 a0001c0012t0001g0043 others(2): Show |
5 | HG01168.hp2 HG01975.hp2 HG03704.hp2 others(2): Show |
intron_variant | MODIFIER | c.654-867T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459491 | |||||||
| chr14:105459499 | G | A | 3 | a0001c0012t0001g0242 a0003c0004t0001g0055 a0003c0004t0001g0056 |
3 | HG00639.hp2 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.654-859G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459499 | |||||||
| chr14:105459517 | C | T | 1 | a0001c0012t0001g0043 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.654-841C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459517 | |||||||
| chr14:105459518 | G | A | 1 | a0001c0017t0001g0050 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.654-840G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459518 | |||||||
| chr14:105459518 | G | C | 1 | a0001c0012t0001g0043 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.654-840G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459518 | |||||||
| chr14:105459518 | GCCTGGGG others(465): Show |
G | 1 | a0002c0002t0001g0226 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.654-815_654-344del | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459518 | ||||||
| chr14:105459536 | CTGGGGGC others(524): Show |
C | 2 | a0001c0001t0001g0192 a0001c0001t0001g0223 |
2 | HG01975.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.654-815_654-285del | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459536 | ||||||
| chr14:105459543 | C | A | 28 | a0001c0001t0001g0053 a0003c0004t0001g0003 a0003c0004t0001g0006 others(25): Show |
32 | HG00735.hp2 HG01167.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.654-815C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459543 | |||||||
| chr14:105459543 | C | G | 2 | a0001c0012t0001g0043 a0001c0017t0001g0050 |
2 | HG03704.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.654-815C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459543 | |||||||
| chr14:105459550 | T | C | 1 | a0001c0017t0001g0050 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.654-808T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459550 | |||||||
| chr14:105459558 | A | G | 1 | a0001c0017t0001g0050 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.654-800A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459558 | |||||||
| chr14:105459576 | C | T | 1 | a0001c0012t0001g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.654-782C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459576 | |||||||
| chr14:105459577 | A | C | 1 | a0001c0012t0001g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.654-781A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459577 | |||||||
| chr14:105459577 | A | G | 1 | a0001c0012t0001g0043 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.654-781A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459577 | |||||||
| chr14:105459602 | G | C | 1 | a0001c0012t0001g0043 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.654-756G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459602 | |||||||
| chr14:105459609 | C | T | 2 | a0001c0012t0001g0043 a0001c0012t0001g0242 |
2 | HG00639.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.654-749C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459609 | |||||||
| chr14:105459617 | G | A | 3 | a0001c0012t0001g0043 a0003c0004t0001g0055 a0003c0004t0001g0056 |
3 | HG03579.hp1 NA19030.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.654-741G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459617 | |||||||
| chr14:105459636 | CCCTGGGG others(229): Show |
C | 2 | a0003c0004t0001g0055 a0003c0004t0001g0056 |
2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.654-682_654-447del | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459636 | ||||||
| chr14:105459661 | GAGTCCGT others(52): Show |
G | 1 | a0001c0012t0001g0043 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.654-664_654-606del others(59): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459661 | ||||||
| chr14:105459695 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.654-663G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459695 | |||||||
| chr14:105459695 | G | T | 1 | a0002c0002t0001g0105 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.654-663G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459695 | |||||||
| chr14:105459713 | CTGGGGGC others(112): Show |
C | 1 | a0001c0001t0001g0169 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.654-644_654-526del | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459713 | |||||||
| chr14:105459720 | C | G | 237 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(234): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.654-638C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459720 | |||||||
| chr14:105459726 | G | A | 233 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(230): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.654-632G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459726 | |||||||
| chr14:105459726 | G | C | 1 | a0004c0003t0001g0260 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.654-632G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459726 | |||||||
| chr14:105459727 | T | C | 1 | a0005c0005t0001g0143 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.654-631T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459727 | |||||||
| chr14:105459735 | A | G | 3 | a0001c0012t0001g0043 a0003c0008t0001g0052 a0005c0005t0001g0143 |
3 | HG03471.hp2 HG04204.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.654-623A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459735 | |||||||
| chr14:105459747 | CCCTGGTC others(118): Show |
C | 1 | a0001c0001t0001g0150 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.654-605_654-481del | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459747 | ||||||
| chr14:105459754 | CCCTGGGG others(111): Show |
C | 234 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(231): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.654-546_654-429del | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459754 | ||||||
| chr14:105459786 | T | C | 2 | a0001c0001t0001g0004 a0001c0017t0001g0050 |
2 | HG02273.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.654-572T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459786 | |||||||
| chr14:105459794 | G | A | 17 | a0001c0012t0001g0043 a0003c0004t0001g0003 a0003c0004t0001g0032 others(14): Show |
17 | HG00735.hp2 HG01167.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.654-564G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459794 | |||||||
| chr14:105459812 | T | C | 2 | a0001c0012t0001g0043 a0005c0005t0001g0143 |
2 | HG04204.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.654-546T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459812 | |||||||
| chr14:105459813 | C | G | 2 | a0001c0012t0001g0043 a0005c0005t0001g0143 |
2 | HG04204.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.654-545C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459813 | |||||||
| chr14:105459813 | CCCTGGGG others(52): Show |
C | 2 | a0001c0001t0001g0004 a0001c0017t0001g0050 |
2 | HG02273.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.654-505_654-447del others(59): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459813 | ||||||
| chr14:105459844 | G | A | 2 | a0001c0001t0001g0169 a0005c0005t0001g0143 |
2 | HG00558.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.654-514G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459844 | |||||||
| chr14:105459871 | C | T | 3 | a0001c0001t0001g0169 a0001c0012t0001g0043 a0005c0005t0001g0143 |
3 | HG00558.hp1 HG04204.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.654-487C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459871 | |||||||
| chr14:105459872 | G | C | 3 | a0001c0001t0001g0169 a0001c0012t0001g0043 a0005c0005t0001g0143 |
3 | HG00558.hp1 HG04204.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.654-486G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459872 | |||||||
| chr14:105459872 | G | GCCTGGGG others(52): Show |
2 | a0001c0001t0001g0053 a0003c0008t0001g0052 |
2 | HG03471.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.654-447_654-446ins others(59): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | INFO_REALIGN_3_PRIME | chr14 | 105459872 | ||||||
| chr14:105459897 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.654-461G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459897 | |||||||
| chr14:105459904 | T | C | 237 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(234): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.654-454T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459904 | |||||||
| chr14:105459971 | A | G | 4 | a0001c0001t0001g0047 a0001c0012t0001g0043 a0001c0012t0001g0242 others(1): Show |
4 | HG00639.hp2 HG02109.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.654-387A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105459971 | |||||||
| chr14:105460030 | A | G | 17 | a0003c0004t0001g0003 a0003c0004t0001g0032 a0003c0004t0001g0064 others(14): Show |
17 | HG00735.hp2 HG01167.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.654-328A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105460030 | |||||||
| chr14:105460059 | C | T | 1 | a0001c0017t0001g0050 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.654-299C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105460059 | |||||||
| chr14:105460060 | G | T | 2 | a0001c0012t0001g0043 a0001c0012t0001g0242 |
2 | HG00639.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.654-298G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105460060 | |||||||
| chr14:105460067 | G | C | 269 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(266): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.654-291G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105460067 | |||||||
| chr14:105460177 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.654-181T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105460177 | |||||||
| chr14:105460197 | C | T | 4 | a0001c0012t0001g0043 a0001c0012t0001g0242 a0003c0004t0001g0055 others(1): Show |
4 | HG00639.hp2 HG03579.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.654-161C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105460197 | |||||||
| chr14:105460264 | C | T | 4 | a0002c0002t0001g0088 a0002c0002t0001g0130 a0002c0002t0001g0164 others(1): Show |
4 | HG00673.hp1 NA18943.hp1 NA18947.hp1 others(1): Show |
intron_variant | MODIFIER | c.654-94C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105460264 | |||||||
| chr14:105460272 | G | C | 1 | a0001c0017t0001g0050 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.654-86G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 8/20 | chr14 | 105460272 | |||||||
| chr14:105460482 | G | C | 1 | a0001c0017t0001g0050 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.753+25G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 9/20 | chr14 | 105460482 | |||||||
| chr14:105460972 | G | A | 1 | a0003c0007t0001g0057 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.942+19G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105460972 | |||||||
| chr14:105461014 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.942+61G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105461014 | |||||||
| chr14:105461096 | T | C | 41 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0017 others(38): Show |
44 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.942+143T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105461096 | |||||||
| chr14:105461134 | A | G | 19 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0024 others(16): Show |
21 | HG01069.hp2 HG01099.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.942+181A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105461134 | |||||||
| chr14:105461213 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.942+260T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105461213 | |||||||
| chr14:105461273 | C | T | 22 | a0001c0001t0001g0009 a0001c0001t0001g0077 a0001c0001t0001g0127 others(19): Show |
22 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(19): Show |
intron_variant | MODIFIER | c.942+320C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105461273 | |||||||
| chr14:105461346 | G | A | 1 | a0002c0002t0001g0152 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.942+393G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105461346 | |||||||
| chr14:105461439 | G | GGACCCCC others(21): Show |
1 | a0009c0016t0001g0090 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.942+487_942+514dup others(28): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr14 | 105461439 | ||||||
| chr14:105461599 | C | T | 240 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(237): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.942+646C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105461599 | |||||||
| chr14:105461684 | C | A | 1 | a0001c0001t0001g0024 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.942+731C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105461684 | |||||||
| chr14:105461710 | A | T | 1 | a0001c0001t0001g0047 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.942+757A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105461710 | |||||||
| chr14:105461768 | C | T | 2 | a0003c0004t0001g0055 a0003c0004t0001g0056 |
2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.942+815C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105461768 | |||||||
| chr14:105462110 | A | ACGGTCTC others(33): Show |
270 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(267): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.943-1045_943-1044i others(42): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr14 | 105462110 | ||||||
| chr14:105462110 | A | ACGGTCTC others(35): Show |
1 | a0005c0005t0001g0222 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.943-1061_943-1060i others(44): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr14 | 105462110 | ||||||
| chr14:105462110 | A | ACGGTCTT others(33): Show |
1 | a0001c0001t0001g0172 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.943-1068_943-1067i others(42): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr14 | 105462110 | ||||||
| chr14:105462110 | A | ATGGTCTC others(33): Show |
1 | a0003c0004t0001g0054 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.943-1074_943-1073i others(42): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462110 | |||||||
| chr14:105462110 | A | G | 1 | a0005c0005t0001g0159 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.943-1074A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462110 | |||||||
| chr14:105462337 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.943-847G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462337 | |||||||
| chr14:105462395 | G | C | 1 | a0001c0017t0001g0050 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.943-789G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462395 | |||||||
| chr14:105462459 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.943-725C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462459 | |||||||
| chr14:105462548 | C | T | 27 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0024 others(24): Show |
29 | HG01069.hp2 HG01099.hp1 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.943-636C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462548 | |||||||
| chr14:105462560 | ACT | A | 8 | a0003c0004t0001g0006 a0003c0006t0001g0002 a0003c0006t0001g0028 others(5): Show |
12 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.943-621_943-620del others(2): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr14 | 105462560 | ||||||
| chr14:105462594 | C | T | 1 | a0003c0008t0001g0018 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.943-590C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462594 | |||||||
| chr14:105462672 | C | T | 2 | a0002c0002t0001g0233 a0005c0005t0001g0161 |
2 | HG00597.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.943-512C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462672 | |||||||
| chr14:105462673 | G | A | 1 | a0001c0001t0001g0005 | 3 | HG03491.hp1 HG03492.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.943-511G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462673 | |||||||
| chr14:105462726 | G | A | 1 | a0005c0005t0001g0161 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.943-458G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462726 | |||||||
| chr14:105462784 | G | C | 1 | a0003c0004t0001g0048 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.943-400G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462784 | |||||||
| chr14:105462796 | G | A | 1 | a0001c0017t0001g0050 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.943-388G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462796 | |||||||
| chr14:105462856 | G | A | 2 | a0003c0006t0001g0034 a0003c0014t0001g0031 |
2 | HG01891.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.943-328G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462856 | |||||||
| chr14:105462863 | C | CGTCTCAA others(4): Show |
8 | a0001c0001t0001g0021 a0001c0001t0001g0092 a0001c0001t0001g0224 others(5): Show |
9 | HG00099.hp2 HG00323.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.943-312_943-311ins others(11): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr14 | 105462863 | ||||||
| chr14:105462998 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.943-186C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105462998 | |||||||
| chr14:105463050 | C | T | 1 | a0001c0017t0001g0050 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.943-134C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105463050 | |||||||
| chr14:105463068 | C | T | 1 | a0001c0001t0001g0199 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.943-116C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105463068 | |||||||
| chr14:105463085 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.943-99C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105463085 | |||||||
| chr14:105463104 | G | GCTGCAGC others(11): Show |
1 | a0002c0015t0001g0131 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.943-79_943-78insTG others(16): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr14 | 105463104 | ||||||
| chr14:105463106 | C | T | 231 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(228): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.943-78C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105463106 | |||||||
| chr14:105463168 | G | A | 15 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0040 others(12): Show |
17 | HG00323.hp2 HG01069.hp2 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.943-16G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 10/20 | chr14 | 105463168 | |||||||
| chr14:105463284 | C | T | 1 | a0002c0002t0001g0188 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1017+26C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 11/20 | chr14 | 105463284 | |||||||
| chr14:105463292 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1017+34G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 11/20 | chr14 | 105463292 | |||||||
| chr14:105463320 | C | T | 1 | a0001c0012t0001g0242 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1017+62C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 11/20 | chr14 | 105463320 | |||||||
| chr14:105463408 | C | T | 31 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0040 others(28): Show |
33 | HG00099.hp2 HG01069.hp2 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.1018-85C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 11/20 | chr14 | 105463408 | |||||||
| chr14:105463560 | G | T | 1 | a0001c0001t0001g0168 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1076+9G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 12/20 | chr14 | 105463560 | |||||||
| chr14:105463562 | C | T | 2 | a0001c0001t0001g0270 a0001c0017t0001g0050 |
2 | HG03704.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1076+11C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 12/20 | chr14 | 105463562 | |||||||
| chr14:105463628 | C | CG | 3 | a0003c0006t0001g0029 a0003c0009t0001g0030 a0004c0003t0001g0205 |
3 | HG00735.hp2 HG02572.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.1076+80dupG | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr14 | 105463628 | ||||||
| chr14:105463634 | C | T | 1 | a0003c0014t0001g0031 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1076+83C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 12/20 | chr14 | 105463634 | |||||||
| chr14:105463693 | A | T | 1 | a0001c0012t0001g0043 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1076+142A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 12/20 | chr14 | 105463693 | |||||||
| chr14:105463719 | G | A | 3 | a0001c0001t0001g0036 a0007c0013t0001g0037 a0007c0013t0001g0038 |
3 | HG01496.hp1 HG02717.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1076+168G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 12/20 | chr14 | 105463719 | |||||||
| chr14:105463726 | C | T | 1 | a0003c0004t0001g0032 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1076+175C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 12/20 | chr14 | 105463726 | |||||||
| chr14:105463824 | G | C | 1 | a0001c0017t0001g0050 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1077-208G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 12/20 | chr14 | 105463824 | |||||||
| chr14:105463832 | C | T | 1 | a0001c0017t0001g0050 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1077-200C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 12/20 | chr14 | 105463832 | |||||||
| chr14:105463833 | G | A | 7 | a0001c0001t0001g0207 a0001c0001t0002g0073 a0001c0001t0002g0095 others(4): Show |
7 | HG01255.hp2 HG01891.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1077-199G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 12/20 | chr14 | 105463833 | |||||||
| chr14:105463869 | T | C | 1 | a0001c0001t0001g0270 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1077-163T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 12/20 | chr14 | 105463869 | |||||||
| chr14:105463907 | G | A | 1 | a0001c0019t0001g0206 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1077-125G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 12/20 | chr14 | 105463907 | |||||||
| chr14:105463927 | C | T | 1 | a0003c0008t0001g0052 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1077-105C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 12/20 | chr14 | 105463927 | |||||||
| chr14:105464190 | G | A | 1 | a0004c0003t0001g0205 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1192+43G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 13/20 | chr14 | 105464190 | |||||||
| chr14:105464269 | C | T | 1 | a0001c0001t0001g0250 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1192+122C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 13/20 | chr14 | 105464269 | |||||||
| chr14:105464280 | T | C | 1 | a0002c0002t0001g0075 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1192+133T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 13/20 | chr14 | 105464280 | |||||||
| chr14:105464573 | G | C | 2 | a0001c0001t0001g0047 a0001c0001t0001g0270 |
2 | HG03041.hp2 NA21309.hp1 |
splice_region_variant&intron_variant | LOW | c.1344+6G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 14/20 | chr14 | 105464573 | |||||||
| chr14:105464573 | G | T | 2 | a0003c0004t0001g0055 a0003c0004t0001g0056 |
2 | HG03579.hp1 NA20300.hp2 |
splice_region_variant&intron_variant | LOW | c.1344+6G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 14/20 | chr14 | 105464573 | |||||||
| chr14:105464586 | G | A | 207 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(204): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1344+19G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 14/20 | chr14 | 105464586 | |||||||
| chr14:105464616 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1344+49C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 14/20 | chr14 | 105464616 | |||||||
| chr14:105464632 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1345-42G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 14/20 | chr14 | 105464632 | |||||||
| chr14:105464641 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1345-33G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 14/20 | chr14 | 105464641 | |||||||
| chr14:105464978 | GTCC | G | 17 | a0001c0001t0001g0017 a0001c0001t0001g0248 a0001c0001t0001g0250 others(14): Show |
18 | HG00099.hp1 HG00323.hp2 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.1535-110_1535-108d others(5): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr14 | 105464978 | ||||||
| chr14:105465044 | C | T | 1 | a0002c0002t0001g0158 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1535-50C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 15/20 | chr14 | 105465044 | |||||||
| chr14:105465225 | C | G | 3 | a0001c0001t0001g0254 a0001c0001t0001g0261 a0001c0001t0001g0268 |
3 | HG01261.hp2 HG01981.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1624+42C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105465225 | |||||||
| chr14:105465247 | C | T | 1 | a0002c0002t0001g0181 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1624+64C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105465247 | |||||||
| chr14:105465248 | A | G | 263 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(260): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.1624+65A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105465248 | |||||||
| chr14:105465296 | C | T | 1 | a0003c0004t0001g0032 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1624+113C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105465296 | |||||||
| chr14:105465572 | A | C | 3 | a0001c0001t0002g0073 a0001c0001t0002g0095 a0001c0001t0002g0098 |
3 | HG02895.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1624+389A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105465572 | |||||||
| chr14:105465684 | G | C | 1 | a0001c0001t0001g0049 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1624+501G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105465684 | |||||||
| chr14:105465736 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1624+553G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105465736 | |||||||
| chr14:105466069 | G | C | 1 | a0003c0004t0001g0032 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1625-357G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105466069 | |||||||
| chr14:105466119 | G | A | 169 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(166): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1625-307G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105466119 | |||||||
| chr14:105466207 | G | A | 129 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(126): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.1625-219G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105466207 | |||||||
| chr14:105466215 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1625-211C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105466215 | |||||||
| chr14:105466217 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1625-209C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105466217 | |||||||
| chr14:105466225 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1625-201C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105466225 | |||||||
| chr14:105466299 | C | CAG | 75 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0012 others(72): Show |
83 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1625-127_1625-126i others(4): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 16/20 | chr14 | 105466299 | |||||||
| chr14:105466589 | CCCCCGCC others(16): Show |
C | 1 | a0002c0002t0001g0141 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1777+27_1777+49del others(23): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr14 | 105466589 | ||||||
| chr14:105466597 | C | T | 1 | a0001c0017t0001g0050 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1777+19C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 17/20 | chr14 | 105466597 | |||||||
| chr14:105466757 | C | T | 27 | a0001c0001t0001g0047 a0003c0004t0001g0003 a0003c0004t0001g0006 others(24): Show |
31 | HG00735.hp2 HG01167.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.1813+15C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105466757 | |||||||
| chr14:105466764 | G | A | 3 | a0002c0002t0001g0134 a0002c0002t0001g0155 a0002c0002t0001g0188 |
3 | NA18951.hp1 NA18975.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1813+22G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105466764 | |||||||
| chr14:105466772 | C | T | 1 | a0003c0008t0001g0052 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1813+30C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105466772 | |||||||
| chr14:105466786 | G | A | 1 | a0002c0002t0001g0142 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1813+44G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105466786 | |||||||
| chr14:105466822 | C | T | 1 | a0001c0001t0001g0010 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1813+80C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105466822 | |||||||
| chr14:105466954 | T | C | 2 | a0001c0012t0001g0043 a0001c0012t0001g0242 |
2 | HG00639.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1813+212T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105466954 | |||||||
| chr14:105467159 | A | G | 2 | a0001c0012t0001g0043 a0001c0012t0001g0242 |
2 | HG00639.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1813+417A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105467159 | |||||||
| chr14:105467216 | C | T | 4 | a0001c0001t0001g0007 a0001c0001t0001g0099 a0001c0001t0001g0100 others(1): Show |
5 | HG00733.hp1 HG03516.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.1813+474C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105467216 | |||||||
| chr14:105467525 | C | T | 2 | a0003c0004t0001g0055 a0003c0004t0001g0056 |
2 | HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1813+783C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105467525 | |||||||
| chr14:105467619 | C | T | 2 | a0001c0012t0001g0043 a0001c0012t0001g0242 |
2 | HG00639.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1813+877C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105467619 | |||||||
| chr14:105467804 | C | G | 2 | a0001c0012t0001g0043 a0001c0012t0001g0242 |
2 | HG00639.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1813+1062C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105467804 | |||||||
| chr14:105468051 | G | T | 20 | a0003c0004t0001g0003 a0003c0004t0001g0032 a0003c0004t0001g0048 others(17): Show |
20 | HG00735.hp2 HG01167.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1813+1309G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468051 | |||||||
| chr14:105468121 | C | T | 6 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0044 others(3): Show |
6 | HG02280.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1814-1346C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468121 | |||||||
| chr14:105468260 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1814-1207G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468260 | |||||||
| chr14:105468265 | C | T | 3 | a0001c0001t0001g0108 a0001c0001t0001g0231 a0001c0001t0001g0271 |
3 | HG02451.hp2 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1814-1202C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468265 | |||||||
| chr14:105468398 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1069T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468398 | |||||||
| chr14:105468399 | T | A | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1068T>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468399 | |||||||
| chr14:105468406 | G | C | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1061G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468406 | |||||||
| chr14:105468407 | G | C | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1060G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468407 | |||||||
| chr14:105468413 | T | A | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1054T>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468413 | |||||||
| chr14:105468414 | G | C | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1053G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468414 | |||||||
| chr14:105468416 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1051G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468416 | |||||||
| chr14:105468418 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1049T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468418 | |||||||
| chr14:105468420 | T | A | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1047T>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468420 | |||||||
| chr14:105468444 | G | A | 1 | a0001c0001t0001g0011 | 2 | NA18971.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.1814-1023G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468444 | |||||||
| chr14:105468444 | G | C | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1023G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468444 | |||||||
| chr14:105468448 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1019A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468448 | |||||||
| chr14:105468449 | T | G | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1018T>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468449 | |||||||
| chr14:105468451 | A | T | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1016A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468451 | |||||||
| chr14:105468455 | A | C | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1012A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468455 | |||||||
| chr14:105468457 | C | G | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1010C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468457 | |||||||
| chr14:105468459 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1008G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468459 | |||||||
| chr14:105468461 | G | C | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1006G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468461 | |||||||
| chr14:105468462 | C | A | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1005C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468462 | |||||||
| chr14:105468464 | C | A | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1003C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468464 | |||||||
| chr14:105468465 | C | A | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1002C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468465 | |||||||
| chr14:105468466 | C | A | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-1001C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468466 | |||||||
| chr14:105468468 | C | A | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-999C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468468 | |||||||
| chr14:105468473 | C | A | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-994C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468473 | |||||||
| chr14:105468475 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-992C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468475 | |||||||
| chr14:105468477 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-990G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468477 | |||||||
| chr14:105468488 | C | G | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-979C>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468488 | |||||||
| chr14:105468494 | A | T | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-973A>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468494 | |||||||
| chr14:105468495 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-972A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468495 | |||||||
| chr14:105468496 | A | C | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-971A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468496 | |||||||
| chr14:105468499 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-968G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468499 | |||||||
| chr14:105468500 | G | C | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-967G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468500 | |||||||
| chr14:105468507 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-960A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468507 | |||||||
| chr14:105468508 | A | C | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-959A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468508 | |||||||
| chr14:105468514 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-953A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468514 | |||||||
| chr14:105468515 | C | A | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-952C>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468515 | |||||||
| chr14:105468543 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-924C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468543 | |||||||
| chr14:105468544 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-923C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468544 | |||||||
| chr14:105468548 | G | T | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-919G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468548 | |||||||
| chr14:105468549 | G | C | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-918G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468549 | |||||||
| chr14:105468559 | A | C | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-908A>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468559 | |||||||
| chr14:105468561 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-906T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468561 | |||||||
| chr14:105468564 | G | T | 1 | a0001c0001t0001g0244 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1814-903G>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468564 | |||||||
| chr14:105468611 | T | A | 1 | a0004c0003t0001g0186 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1814-856T>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468611 | |||||||
| chr14:105468704 | A | G | 238 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(235): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.1814-763A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468704 | |||||||
| chr14:105468786 | A | G | 272 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(269): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1814-681A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468786 | |||||||
| chr14:105468859 | G | C | 4 | a0001c0001t0001g0189 a0001c0001t0001g0192 a0001c0001t0001g0207 others(1): Show |
4 | NA19003.hp1 NA19064.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.1814-608G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468859 | |||||||
| chr14:105468870 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1814-597G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105468870 | |||||||
| chr14:105469075 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1814-392G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105469075 | |||||||
| chr14:105469112 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1814-355G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105469112 | |||||||
| chr14:105469167 | GGGTGGAC others(25): Show |
G | 1 | a0005c0005t0001g0216 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1814-298_1814-267d others(34): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr14 | 105469167 | ||||||
| chr14:105469187 | T | C | 1 | a0004c0003t0001g0262 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1814-280T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105469187 | |||||||
| chr14:105469259 | C | T | 1 | a0002c0002t0001g0176 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1814-208C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105469259 | |||||||
| chr14:105469287 | C | T | 2 | a0007c0013t0001g0037 a0007c0013t0001g0038 |
2 | HG01496.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1814-180C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105469287 | |||||||
| chr14:105469384 | A | G | 271 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(268): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1814-83A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105469384 | |||||||
| chr14:105469416 | T | C | 1 | a0001c0001t0001g0053 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1814-51T>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 18/20 | chr14 | 105469416 | |||||||
| chr14:105469523 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1845+25G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 19/20 | chr14 | 105469523 | |||||||
| chr14:105469670 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1846-171C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 19/20 | chr14 | 105469670 | |||||||
| chr14:105469714 | G | C | 7 | a0001c0001t0001g0023 a0001c0001t0001g0166 a0001c0001t0001g0167 others(4): Show |
7 | HG00544.hp2 HG02132.hp2 HG02165.hp1 others(4): Show |
intron_variant | MODIFIER | c.1846-127G>C | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 19/20 | chr14 | 105469714 | |||||||
| chr14:105469727 | A | G | 272 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(269): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1846-114A>G | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 19/20 | chr14 | 105469727 | |||||||
| chr14:105469763 | A | ACCTTGGC others(8): Show |
242 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(239): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1846-75_1846-74ins others(15): Show |
MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr14 | 105469763 | ||||||
| chr14:105469817 | C | T | 8 | a0003c0004t0001g0006 a0003c0006t0001g0002 a0003c0006t0001g0028 others(5): Show |
12 | HG01167.hp2 HG01169.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1846-24C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 19/20 | chr14 | 105469817 | |||||||
| chr14:105470015 | G | A | 1 | a0002c0002t0001g0157 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1997+23G>A | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 20/20 | chr14 | 105470015 | |||||||
| chr14:105470036 | C | T | 4 | a0001c0001t0001g0172 a0001c0001t0001g0272 a0006c0010t0001g0126 others(1): Show |
4 | HG02896.hp1 HG02897.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1998-29C>T | MTA1 | ENSG00000182979.18 | transcript | ENST00000331320.12 | protein_coding | 20/20 | chr14 | 105470036 |