Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9695 |
| ensemblid | ENSG00000134109.11 |
| hgncid | 18967 |
| symbol | EDEM1 |
| name | ER degradation enhancing alpha-mannosidase like protein 1 |
| refseq_nuc | NM_014674.3 |
| refseq_prot | NP_055489.1 |
| ensembl_nuc | ENST00000256497.9 |
| ensembl_prot | ENSP00000256497.4 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 5187707 |
| end | 5219958 |
| strand | + |
| ver | v1.2 |
| region | chr3:5187707-5219958 |
| region5000 | chr3:5182707-5224958 |
| regionname0 | EDEM1_chr3_5187707_5219958 |
| regionname5000 | EDEM1_chr3_5182707_5224958 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 657 | 361 | 92 | 66 | 149 | 14 | 38 | 119 | EDEM1_chr3_5182707_5224958 | EDEM1 | MQWRA others(652): Show |
chr3 | 5182707 | 5224958 |
| a0002 | 0/0 | 657 | 8 | 0 | 0 | 8 | 0 | 0 | 6 | EDEM1_chr3_5182707_5224958 | EDEM1 | MQWRA others(652): Show |
chr3 | 5182707 | 5224958 |
| a0003 | 0/0 | 657 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | MQWRA others(652): Show |
chr3 | 5182707 | 5224958 |
| a0004 | 0/0 | 657 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | MQWRA others(652): Show |
chr3 | 5182707 | 5224958 |
| a0005 | 0/0 | 657 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | MQWRA others(652): Show |
chr3 | 5182707 | 5224958 |
| a0006 | 0/0 | 657 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | MQWRA others(652): Show |
chr3 | 5182707 | 5224958 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1971 | 315 | 75 | 64 | 133 | 14 | 28 | EDEM1_chr3_5182707_5224958 | EDEM1 | ATGCA others(1966): Show |
chr3 | 5182707 | 5224958 | ||
| a0001c0002 | 1/0 | 1971 | 30 | 8 | 1 | 14 | 0 | 6 | EDEM1_chr3_5182707_5224958 | EDEM1 | ATGCA others(1966): Show |
chr3 | 5182707 | 5224958 | ||
| a0001c0004 | 0/0 | 1971 | 5 | 5 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | ATGCA others(1966): Show |
chr3 | 5182707 | 5224958 | ||
| a0001c0005 | 0/0 | 1971 | 3 | 1 | 1 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | ATGCA others(1966): Show |
chr3 | 5182707 | 5224958 | ||
| a0001c0006 | 0/0 | 1971 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | ATGCA others(1966): Show |
chr3 | 5182707 | 5224958 | ||
| a0001c0007 | 0/0 | 1971 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | ATGCA others(1966): Show |
chr3 | 5182707 | 5224958 | ||
| a0001c0008 | 0/0 | 1971 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | ATGCA others(1966): Show |
chr3 | 5182707 | 5224958 | ||
| a0001c0012 | 0/0 | 1971 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | ATGCA others(1966): Show |
chr3 | 5182707 | 5224958 | ||
| a0001c0013 | 0/0 | 1971 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | ATGCA others(1966): Show |
chr3 | 5182707 | 5224958 | ||
| a0001c0014 | 0/0 | 1971 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | ATGCA others(1966): Show |
chr3 | 5182707 | 5224958 | ||
| a0001c0016 | 0/0 | 1971 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | ATGCA others(1966): Show |
chr3 | 5182707 | 5224958 | ||
| a0001c0018 | 0/0 | 1971 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | ATGCA others(1966): Show |
chr3 | 5182707 | 5224958 | ||
| a0002c0003 | 0/0 | 1971 | 8 | 0 | 0 | 8 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | ATGCA others(1966): Show |
chr3 | 5182707 | 5224958 | ||
| a0003c0010 | 0/0 | 1971 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | ATGCA others(1966): Show |
chr3 | 5182707 | 5224958 | ||
| a0003c0011 | 0/0 | 1971 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | ATGCA others(1966): Show |
chr3 | 5182707 | 5224958 | ||
| a0004c0009 | 0/0 | 1971 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | ATGCA others(1966): Show |
chr3 | 5182707 | 5224958 | ||
| a0005c0017 | 0/0 | 1971 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | ATGCA others(1966): Show |
chr3 | 5182707 | 5224958 | ||
| a0006c0015 | 0/0 | 1971 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | ATGCA others(1966): Show |
chr3 | 5182707 | 5224958 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6113 | 76 | 7 | 25 | 37 | 2 | 5 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0002 | 0/0 | 6113 | 59 | 5 | 14 | 29 | 8 | 3 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0003 | 0/0 | 6113 | 34 | 0 | 6 | 25 | 0 | 3 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0004 | 0/0 | 6113 | 36 | 11 | 0 | 22 | 1 | 2 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0005 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6106): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0006 | 0/0 | 6113 | 14 | 7 | 1 | 4 | 0 | 2 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0007 | 0/0 | 6113 | 11 | 6 | 0 | 3 | 0 | 2 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0008 | 0/0 | 6113 | 6 | 0 | 2 | 3 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0009 | 0/0 | 6113 | 8 | 5 | 3 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0010 | 0/0 | 6113 | 6 | 0 | 6 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0011 | 0/0 | 6114 | 5 | 5 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6109): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0012 | 0/0 | 6111 | 5 | 5 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6106): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0013 | 0/0 | 6113 | 5 | 1 | 2 | 0 | 0 | 2 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0015 | 0/0 | 6112 | 4 | 1 | 0 | 1 | 1 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6107): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0016 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6106): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0017 | 0/0 | 6112 | 3 | 3 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6107): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0018 | 0/0 | 6113 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0019 | 0/0 | 6113 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0020 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6106): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0021 | 0/0 | 6113 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0022 | 0/0 | 6114 | 2 | 0 | 0 | 0 | 0 | 2 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6109): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0023 | 0/0 | 6114 | 2 | 0 | 1 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6109): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0024 | 0/0 | 6113 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0025 | 0/0 | 6113 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0027 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0030 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6106): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0032 | 0/0 | 6113 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0033 | 0/0 | 6113 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0035 | 0/0 | 6114 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6109): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0036 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0038 | 0/0 | 6112 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6107): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0039 | 0/0 | 6114 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6109): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0040 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0041 | 0/0 | 6112 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6107): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0042 | 0/0 | 6112 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6107): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0043 | 0/0 | 6112 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6107): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0044 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0045 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0046 | 0/0 | 6113 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0047 | 0/0 | 6114 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6109): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0048 | 0/0 | 6111 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6106): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0050 | 0/0 | 6111 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6106): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0052 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6106): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0056 | 0/0 | 6113 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0057 | 0/0 | 6113 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0059 | 0/0 | 6113 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0060 | 0/1 | 6113 | 1 | 0 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0061 | 0/0 | 6113 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0062 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0001t0063 | 0/0 | 6113 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0002t0001 | 0/0 | 6113 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0002t0005 | 0/0 | 6111 | 17 | 4 | 1 | 10 | 0 | 2 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6106): Show |
chr3 | 5182707 | 5224958 |
| a0001c0002t0016 | 0/0 | 6111 | 3 | 0 | 0 | 0 | 0 | 3 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6106): Show |
chr3 | 5182707 | 5224958 |
| a0001c0002t0018 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0002t0020 | 0/0 | 6111 | 2 | 1 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6106): Show |
chr3 | 5182707 | 5224958 |
| a0001c0002t0026 | 0/0 | 6113 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0002t0051 | 0/0 | 6111 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6106): Show |
chr3 | 5182707 | 5224958 |
| a0001c0002t0053 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6106): Show |
chr3 | 5182707 | 5224958 |
| a0001c0002t0054 | 0/0 | 6111 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6106): Show |
chr3 | 5182707 | 5224958 |
| a0001c0002t0055 | 1/0 | 6113 | 1 | 0 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0004t0014 | 0/0 | 6112 | 4 | 4 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6107): Show |
chr3 | 5182707 | 5224958 |
| a0001c0004t0029 | 0/0 | 6112 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6107): Show |
chr3 | 5182707 | 5224958 |
| a0001c0005t0001 | 0/0 | 6113 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0005t0004 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0005t0008 | 0/0 | 6113 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0006t0002 | 0/0 | 6113 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0007t0028 | 0/0 | 6113 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0008t0049 | 0/0 | 6111 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6106): Show |
chr3 | 5182707 | 5224958 |
| a0001c0012t0058 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0013t0008 | 0/0 | 6113 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0014t0037 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0016t0034 | 0/0 | 6113 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0001c0018t0031 | 0/0 | 6113 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0002c0003t0001 | 0/0 | 6113 | 3 | 0 | 0 | 3 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0002c0003t0003 | 0/0 | 6113 | 5 | 0 | 0 | 5 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0003c0010t0001 | 0/0 | 6113 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0003c0011t0002 | 0/0 | 6113 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0004c0009t0019 | 0/0 | 6113 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0005c0017t0001 | 0/0 | 6113 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| a0006c0015t0001 | 0/0 | 6113 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | AAAGG others(6108): Show |
chr3 | 5182707 | 5224958 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 17 | 1 | 5 | 10 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0001 | 0/0 | 6 | 2 | 0 | 4 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0002 | 0/0 | 8 | 0 | 2 | 2 | 3 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0003g0003 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0003g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0003g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0003g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0041 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0004g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0005g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0006g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0006g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0006g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0006g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0006g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0006g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0006g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0006g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0007g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0007g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0007g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0007g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0007g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0007g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0007g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0007g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0007g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0007g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0007g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0008g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0008g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0008g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0008g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0008g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0008g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0009g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0009g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0009g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0009g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0009g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0009g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0010g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0010g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0010g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0011g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0011g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0011g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0011g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0011g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0012g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0012g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0012g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0012g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0013g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0013g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0013g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0013g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0013g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0015g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0015g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0015g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0015g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0016g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0017g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0017g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0018g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0018g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0019g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0019g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0020g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0021g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0021g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0022g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0023g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0023g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0024g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0025g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0025g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0027g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0030g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0032g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0033g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0035g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0036g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0038g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0039g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0040g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0041g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0042g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0043g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0044g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0045g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0046g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0047g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0048g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0050g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0052g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0056g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0057g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0059g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0060g0049 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0061g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0062g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0001t0063g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0005g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0005g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0005g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0005g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0005g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0005g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0005g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0005g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0005g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0005g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0016g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0016g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0016g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0018g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0020g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0020g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0026g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0026g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0051g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0053g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0054g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0002t0055g0069 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0004t0014g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0004t0014g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0004t0029g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0005t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0005t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0005t0008g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0006t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0007t0028g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0008t0049g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0012t0058g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0013t0008g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0014t0037g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0016t0034g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0001c0018t0031g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0002c0003t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0002c0003t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0002c0003t0003g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0002c0003t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0003c0010t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0003c0011t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0004c0009t0019g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0005c0017t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| a0006c0015t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0027 | EUR | GBR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0174 | EUR | GBR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0171 | EUR | FIN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG00280 | hp2 | a0001 | c0001 | t0023 | g0009 | EUR | FIN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG00408 | hp1 | a0001 | c0001 | t0004 | g0236 | EAS | CHS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG00423 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | CHS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG00423 | hp2 | a0001 | c0001 | t0006 | g0008 | EAS | CHS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG00438 | hp1 | a0002 | c0003 | t0003 | g0002 | EAS | CHS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0252 | EAS | CHS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG00558 | hp1 | a0001 | c0002 | t0005 | g0228 | EAS | CHS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG00558 | hp2 | a0003 | c0011 | t0002 | g0027 | EAS | CHS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG00639 | hp2 | a0001 | c0001 | t0056 | g0045 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG00735 | hp2 | a0001 | c0001 | t0010 | g0046 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG00738 | hp2 | a0001 | c0001 | t0023 | g0246 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0176 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01069 | hp1 | a0001 | c0001 | t0009 | g0022 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01070 | hp1 | a0001 | c0001 | t0010 | g0006 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0036 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01071 | hp1 | a0001 | c0001 | t0009 | g0022 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0036 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01074 | hp2 | a0001 | c0001 | t0013 | g0006 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01106 | hp1 | a0001 | c0001 | t0048 | g0090 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01109 | hp1 | a0001 | c0002 | t0005 | g0083 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0201 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0198 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01169 | hp2 | a0001 | c0001 | t0013 | g0130 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01175 | hp1 | a0001 | c0001 | t0010 | g0006 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0037 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01192 | hp1 | a0001 | c0001 | t0006 | g0225 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01243 | hp1 | a0001 | c0001 | t0038 | g0062 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01243 | hp2 | a0001 | c0001 | t0009 | g0053 | AMR | PUR | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01255 | hp2 | a0001 | c0001 | t0010 | g0021 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01256 | hp2 | a0001 | c0005 | t0008 | g0113 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01258 | hp1 | a0001 | c0001 | t0008 | g0005 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01346 | hp1 | a0001 | c0001 | t0010 | g0006 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01433 | hp1 | a0001 | c0001 | t0057 | g0050 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01433 | hp2 | a0001 | c0001 | t0010 | g0006 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01496 | hp2 | a0001 | c0001 | t0008 | g0249 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01515 | hp1 | a0001 | c0001 | t0015 | g0028 | EUR | IBS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01515 | hp2 | a0001 | c0001 | t0042 | g0204 | EUR | IBS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | IBS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01891 | hp1 | a0001 | c0001 | t0019 | g0218 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01891 | hp2 | a0001 | c0001 | t0036 | g0155 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0248 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0175 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0243 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02027 | hp1 | a0001 | c0001 | t0025 | g0211 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02040 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0237 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02055 | hp1 | a0001 | c0001 | t0011 | g0061 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02055 | hp2 | a0001 | c0001 | t0021 | g0093 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02071 | hp1 | a0002 | c0003 | t0003 | g0034 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02080 | hp2 | a0001 | c0001 | t0006 | g0008 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02083 | hp2 | a0001 | c0001 | t0015 | g0165 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02129 | hp1 | a0001 | c0002 | t0005 | g0233 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02135 | hp1 | a0001 | c0002 | t0005 | g0013 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0135 | EAS | CDX | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0219 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0039 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02258 | hp1 | a0001 | c0001 | t0027 | g0092 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02258 | hp2 | a0001 | c0001 | t0052 | g0019 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02280 | hp1 | a0001 | c0012 | t0058 | g0110 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0039 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0087 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02451 | hp2 | a0001 | c0005 | t0004 | g0112 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02523 | hp2 | a0001 | c0001 | t0007 | g0202 | EAS | KHV | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02572 | hp1 | a0001 | c0004 | t0029 | g0064 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02572 | hp2 | a0001 | c0001 | t0011 | g0240 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02602 | hp1 | a0001 | c0002 | t0005 | g0077 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02602 | hp2 | a0001 | c0001 | t0006 | g0191 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02615 | hp1 | a0001 | c0001 | t0009 | g0056 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02615 | hp2 | a0001 | c0001 | t0009 | g0054 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02622 | hp1 | a0001 | c0001 | t0045 | g0212 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02622 | hp2 | a0001 | c0001 | t0021 | g0094 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02630 | hp1 | a0001 | c0001 | t0062 | g0085 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02630 | hp2 | a0001 | c0001 | t0012 | g0231 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02647 | hp1 | a0001 | c0002 | t0005 | g0042 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02647 | hp2 | a0001 | c0001 | t0024 | g0005 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02698 | hp1 | a0001 | c0001 | t0006 | g0222 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0190 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02717 | hp2 | a0001 | c0001 | t0012 | g0019 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02735 | hp2 | a0001 | c0001 | t0015 | g0247 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02738 | hp1 | a0001 | c0001 | t0022 | g0043 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02738 | hp2 | a0001 | c0005 | t0001 | g0164 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0153 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02809 | hp2 | a0001 | c0001 | t0024 | g0005 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02818 | hp1 | a0001 | c0001 | t0007 | g0216 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02818 | hp2 | a0001 | c0001 | t0016 | g0058 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02886 | hp2 | a0001 | c0001 | t0017 | g0066 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02895 | hp1 | a0001 | c0001 | t0012 | g0230 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02895 | hp2 | a0001 | c0002 | t0020 | g0042 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0213 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02897 | hp2 | a0001 | c0001 | t0012 | g0229 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02922 | hp1 | a0001 | c0001 | t0017 | g0023 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0189 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02965 | hp1 | a0001 | c0001 | t0012 | g0019 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0221 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02976 | hp1 | a0001 | c0001 | t0015 | g0016 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02976 | hp2 | a0001 | c0004 | t0014 | g0012 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03017 | hp1 | a0001 | c0008 | t0049 | g0181 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03041 | hp1 | a0001 | c0001 | t0018 | g0091 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0203 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03098 | hp1 | a0001 | c0001 | t0011 | g0059 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0226 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0220 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03195 | hp1 | a0001 | c0002 | t0054 | g0025 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0018 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03209 | hp1 | a0001 | c0004 | t0014 | g0012 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0217 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03225 | hp1 | a0001 | c0002 | t0005 | g0026 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0063 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03239 | hp2 | a0001 | c0001 | t0007 | g0208 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03453 | hp1 | a0001 | c0001 | t0013 | g0052 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0018 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03486 | hp1 | a0001 | c0001 | t0009 | g0044 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03486 | hp2 | a0001 | c0002 | t0005 | g0026 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03490 | hp1 | a0003 | c0010 | t0001 | g0001 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03490 | hp2 | a0001 | c0001 | t0004 | g0205 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03516 | hp1 | a0001 | c0004 | t0014 | g0012 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03516 | hp2 | a0001 | c0001 | t0009 | g0055 | AFR | ESN | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0156 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03540 | hp2 | a0001 | c0001 | t0011 | g0242 | AFR | GWD | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03579 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03579 | hp2 | a0001 | c0001 | t0006 | g0088 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03669 | hp2 | a0001 | c0002 | t0016 | g0025 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03688 | hp1 | a0001 | c0001 | t0008 | g0146 | SAS | STU | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03688 | hp2 | a0001 | c0002 | t0016 | g0013 | SAS | STU | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03704 | hp2 | a0001 | c0002 | t0016 | g0071 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03710 | hp1 | a0001 | c0001 | t0032 | g0001 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03710 | hp2 | a0001 | c0001 | t0013 | g0159 | SAS | PJL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03831 | hp1 | a0001 | c0002 | t0020 | g0081 | SAS | BEB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03831 | hp2 | a0001 | c0016 | t0034 | g0002 | SAS | BEB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03834 | hp1 | a0001 | c0001 | t0059 | g0048 | SAS | BEB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03834 | hp2 | a0001 | c0001 | t0033 | g0005 | SAS | BEB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03927 | hp1 | a0001 | c0001 | t0046 | g0223 | SAS | BEB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03942 | hp1 | a0001 | c0007 | t0028 | g0150 | SAS | BEB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0177 | SAS | BEB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0161 | SAS | STU | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG04115 | hp2 | a0001 | c0001 | t0022 | g0043 | SAS | STU | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0173 | SAS | BEB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG04204 | hp1 | a0001 | c0001 | t0007 | g0235 | SAS | STU | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG04204 | hp2 | a0004 | c0009 | t0019 | g0001 | SAS | STU | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG04228 | hp1 | a0001 | c0001 | t0004 | g0209 | SAS | STU | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG04228 | hp2 | a0001 | c0002 | t0005 | g0084 | SAS | STU | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18522 | hp1 | a0001 | c0001 | t0007 | g0234 | AFR | YRI | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0017 | AFR | YRI | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | CHB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18747 | hp2 | a0005 | c0017 | t0001 | g0001 | EAS | CHB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18906 | hp1 | a0001 | c0002 | t0005 | g0079 | AFR | YRI | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0254 | AFR | YRI | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18940 | hp1 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18941 | hp1 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18942 | hp2 | a0001 | c0001 | t0007 | g0183 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18943 | hp1 | a0001 | c0002 | t0005 | g0024 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18943 | hp2 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18945 | hp1 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18945 | hp2 | a0001 | c0001 | t0008 | g0007 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18950 | hp2 | a0001 | c0001 | t0025 | g0210 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18952 | hp1 | a0001 | c0002 | t0005 | g0013 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18957 | hp2 | a0001 | c0001 | t0008 | g0096 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18961 | hp2 | a0001 | c0001 | t0063 | g0003 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18962 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18965 | hp1 | a0001 | c0006 | t0002 | g0162 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18966 | hp2 | a0001 | c0001 | t0043 | g0008 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18969 | hp1 | a0001 | c0002 | t0026 | g0082 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0123 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18975 | hp2 | a0002 | c0003 | t0001 | g0035 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0122 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18982 | hp1 | a0001 | c0001 | t0004 | g0251 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18986 | hp1 | a0001 | c0001 | t0061 | g0001 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18986 | hp2 | a0001 | c0002 | t0005 | g0076 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18988 | hp1 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18989 | hp2 | a0001 | c0001 | t0041 | g0124 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18992 | hp1 | a0001 | c0002 | t0005 | g0074 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18993 | hp2 | a0001 | c0002 | t0051 | g0024 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18994 | hp1 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18998 | hp1 | a0001 | c0001 | t0004 | g0115 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19000 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19002 | hp2 | a0002 | c0003 | t0001 | g0035 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19004 | hp1 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19004 | hp2 | a0006 | c0015 | t0001 | g0127 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19010 | hp2 | a0001 | c0001 | t0006 | g0008 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19011 | hp1 | a0002 | c0003 | t0003 | g0002 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0031 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19012 | hp1 | a0001 | c0002 | t0005 | g0080 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19030 | hp1 | a0001 | c0004 | t0014 | g0065 | AFR | LWK | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19030 | hp2 | a0001 | c0001 | t0030 | g0241 | AFR | LWK | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0017 | AFR | LWK | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19043 | hp2 | a0001 | c0001 | t0039 | g0239 | AFR | LWK | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19055 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19055 | hp2 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0207 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19056 | hp2 | a0001 | c0001 | t0008 | g0141 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19057 | hp2 | a0001 | c0002 | t0026 | g0078 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19058 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19062 | hp2 | a0001 | c0001 | t0004 | g0121 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19063 | hp1 | a0001 | c0001 | t0007 | g0031 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19063 | hp2 | a0001 | c0002 | t0005 | g0072 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0030 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19075 | hp1 | a0001 | c0002 | t0005 | g0075 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19075 | hp2 | a0001 | c0001 | t0005 | g0120 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19076 | hp2 | a0001 | c0001 | t0004 | g0116 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19077 | hp1 | a0001 | c0001 | t0035 | g0111 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19077 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19081 | hp1 | a0001 | c0013 | t0008 | g0007 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19081 | hp2 | a0001 | c0001 | t0020 | g0011 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA19240 | hp2 | a0001 | c0001 | t0004 | g0215 | AFR | YRI | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA20129 | hp1 | a0001 | c0001 | t0019 | g0224 | AFR | ASW | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA20129 | hp2 | a0001 | c0001 | t0011 | g0060 | AFR | ASW | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA20752 | hp1 | a0001 | c0001 | t0004 | g0041 | EUR | TSI | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | TSI | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0144 | EUR | TSI | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0172 | EUR | TSI | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA20905 | hp1 | a0001 | c0001 | t0013 | g0021 | SAS | GIH | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA20905 | hp2 | a0001 | c0001 | t0050 | g0147 | SAS | GIH | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02109 | hp1 | a0001 | c0001 | t0047 | g0086 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02109 | hp2 | a0001 | c0014 | t0037 | g0067 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02486 | hp2 | a0001 | c0001 | t0018 | g0089 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02559 | hp1 | a0001 | c0001 | t0040 | g0214 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG02559 | hp2 | a0001 | c0018 | t0031 | g0057 | AFR | ACB | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0197 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG03471 | hp2 | a0001 | c0001 | t0044 | g0145 | AFR | MSL | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG06807 | hp1 | a0001 | c0002 | t0018 | g0070 | AFR | USA | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| HG06807 | hp2 | a0001 | c0001 | t0017 | g0023 | AFR | USA | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | USA | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | USA | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA21309 | hp1 | a0001 | c0001 | t0009 | g0051 | AFR | LWK | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| NA21309 | hp2 | a0001 | c0002 | t0053 | g0073 | AFR | LWK | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0060 | g0049 | REF | REF | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0055 | g0069 | REF | REF | EDEM1_chr3_5182707_5224958 | EDEM1 | chr3 | 5182707 | 5224958 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:5187938 | C | T | 1 | a0005 | 1 | NA18747.hp2 | missense_variant | MODERATE | c.133C>T | p.Arg45Cys | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/12 | 232/6113 | 133/1974 | 45/657 | chr3 | 5187938 | |||
| chr3:5195222 | A | G | 1 | a0006 | 1 | NA19004.hp2 | missense_variant | MODERATE | c.523A>G | p.Ile175Val | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/12 | 622/6113 | 523/1974 | 175/657 | chr3 | 5195222 | |||
| chr3:5202993 | G | A | 1 | a0002 | 8 | HG00438.hp1 HG02071.hp1 NA18943.hp2 others(5): Show |
missense_variant | MODERATE | c.886G>A | p.Asp296Asn | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/12 | 985/6113 | 886/1974 | 296/657 | chr3 | 5202993 | |||
| chr3:5207202 | G | A | 1 | a0004 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.1267G>A | p.Val423Met | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 7/12 | 1366/6113 | 1267/1974 | 423/657 | chr3 | 5207202 | |||
| chr3:5213410 | G | A | 1 | a0003 | 1 | HG03490.hp1 | missense_variant | MODERATE | c.1772G>A | p.Arg591Gln | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/12 | 1871/6113 | 1772/1974 | 591/657 | chr3 | 5213410 | |||
| chr3:5213410 | G | C | 1 | a0003 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.1772G>C | p.Arg591Pro | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/12 | 1871/6113 | 1772/1974 | 591/657 | chr3 | 5213410 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:5187922 | C | G | 1 | a0001c0018 | 1 | HG02559.hp2 | synonymous_variant | LOW | c.117C>G | p.Leu39Leu | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/12 | 216/6113 | 117/1974 | 39/657 | chr3 | 5187922 | |||
| chr3:5187958 | C | T | 1 | a0001c0005 | 3 | HG01256.hp2 HG02451.hp2 HG02738.hp2 |
synonymous_variant | LOW | c.153C>T | p.Gly51Gly | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/12 | 252/6113 | 153/1974 | 51/657 | chr3 | 5187958 | |||
| chr3:5187967 | G | A | 1 | a0001c0006 | 1 | NA18965.hp1 | synonymous_variant | LOW | c.162G>A | p.Ser54Ser | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/12 | 261/6113 | 162/1974 | 54/657 | chr3 | 5187967 | |||
| chr3:5188138 | G | A | 1 | a0001c0007 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.333G>A | p.Pro111Pro | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/12 | 432/6113 | 333/1974 | 111/657 | chr3 | 5188138 | |||
| chr3:5188222 | C | T | 1 | a0001c0016 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.417C>T | p.Val139Val | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/12 | 516/6113 | 417/1974 | 139/657 | chr3 | 5188222 | |||
| chr3:5199618 | G | A | 1 | a0001c0008 | 1 | HG03017.hp1 | synonymous_variant | LOW | c.609G>A | p.Gln203Gln | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/12 | 708/6113 | 609/1974 | 203/657 | chr3 | 5199618 | |||
| chr3:5199624 | C | A | 17 | a0001c0001 a0001c0004 a0001c0005 others(14): Show |
343 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(340): Show |
synonymous_variant | LOW | c.615C>A | p.Ala205Ala | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/12 | 714/6113 | 615/1974 | 205/657 | chr3 | 5199624 | |||
| chr3:5201870 | G | A | 1 | a0001c0004 | 5 | HG02572.hp1 HG02976.hp2 HG03209.hp1 others(2): Show |
synonymous_variant | LOW | c.804G>A | p.Ala268Ala | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 4/12 | 903/6113 | 804/1974 | 268/657 | chr3 | 5201870 | |||
| chr3:5211129 | C | T | 3 | a0001c0004 a0001c0014 a0001c0018 |
7 | HG02109.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
synonymous_variant | LOW | c.1593C>T | p.Tyr531Tyr | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/12 | 1692/6113 | 1593/1974 | 531/657 | chr3 | 5211129 | |||
| chr3:5213492 | T | C | 1 | a0001c0012 | 1 | HG02280.hp1 | synonymous_variant | LOW | c.1854T>C | p.His618His | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/12 | 1953/6113 | 1854/1974 | 618/657 | chr3 | 5213492 | |||
| chr3:5213522 | C | T | 1 | a0001c0013 | 1 | NA19081.hp1 | splice_region_variant&synonymous_variant | LOW | c.1884C>T | p.Asn628Asn | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/12 | 1983/6113 | 1884/1974 | 628/657 | chr3 | 5213522 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:5187738 | C | A | 2 | a0001c0001t0021 a0001c0001t0027 |
3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
5_prime_UTR_variant | MODIFIER | c.-68C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/12 | 68 | chr3 | 5187738 | ||||||
| chr3:5187746 | G | A | 2 | a0001c0001t0021 a0001c0001t0027 |
3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
5_prime_UTR_variant | MODIFIER | c.-60G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/12 | 60 | chr3 | 5187746 | ||||||
| chr3:5187749 | G | A | 1 | a0001c0007t0028 | 1 | HG03942.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-57G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/12 | chr3 | 5187749 | |||||||
| chr3:5187764 | G | T | 1 | a0001c0001t0063 | 1 | NA18961.hp2 | 5_prime_UTR_variant | MODIFIER | c.-42G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/12 | 42 | chr3 | 5187764 | ||||||
| chr3:5187771 | C | T | 1 | a0001c0001t0062 | 1 | HG02630.hp1 | 5_prime_UTR_variant | MODIFIER | c.-35C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/12 | 35 | chr3 | 5187771 | ||||||
| chr3:5216059 | G | A | 2 | a0001c0004t0014 a0001c0004t0029 |
5 | HG02572.hp1 HG02976.hp2 HG03209.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*141G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 141 | chr3 | 5216059 | ||||||
| chr3:5216108 | T | C | 1 | a0001c0001t0030 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*190T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 190 | chr3 | 5216108 | ||||||
| chr3:5216163 | T | C | 1 | a0001c0018t0031 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*245T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 245 | chr3 | 5216163 | ||||||
| chr3:5216224 | A | G | 1 | a0001c0001t0061 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*306A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 306 | chr3 | 5216224 | ||||||
| chr3:5216283 | T | C | 1 | a0001c0001t0032 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*365T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 365 | chr3 | 5216283 | ||||||
| chr3:5216286 | C | T | 7 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0013 others(4): Show |
23 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*368C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 368 | chr3 | 5216286 | ||||||
| chr3:5216290 | A | T | 7 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0013 others(4): Show |
23 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*372A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 372 | chr3 | 5216290 | ||||||
| chr3:5216296 | T | A | 7 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0013 others(4): Show |
23 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*378T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 378 | chr3 | 5216296 | ||||||
| chr3:5216393 | G | A | 26 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(23): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
3_prime_UTR_variant | MODIFIER | c.*475G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 475 | chr3 | 5216393 | ||||||
| chr3:5216505 | T | G | 3 | a0001c0004t0014 a0001c0004t0029 a0001c0014t0037 |
6 | HG02109.hp2 HG02572.hp1 HG02976.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*587T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 587 | chr3 | 5216505 | ||||||
| chr3:5216551 | G | C | 14 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0013 others(11): Show |
35 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*633G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 633 | chr3 | 5216551 | ||||||
| chr3:5216571 | C | T | 1 | a0001c0001t0036 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*653C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 653 | chr3 | 5216571 | ||||||
| chr3:5216595 | A | G | 7 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0013 others(4): Show |
23 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*677A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 677 | chr3 | 5216595 | ||||||
| chr3:5216746 | G | A | 56 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(53): Show |
310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
3_prime_UTR_variant | MODIFIER | c.*828G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 828 | chr3 | 5216746 | ||||||
| chr3:5216879 | T | C | 1 | a0001c0001t0048 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*961T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 961 | chr3 | 5216879 | ||||||
| chr3:5216887 | C | A | 3 | a0001c0001t0018 a0001c0001t0062 a0001c0002t0018 |
4 | HG02486.hp2 HG02630.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*969C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 969 | chr3 | 5216887 | ||||||
| chr3:5217061 | A | G | 3 | a0001c0004t0014 a0001c0004t0029 a0001c0014t0037 |
6 | HG02109.hp2 HG02572.hp1 HG02976.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1143A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 1143 | chr3 | 5217061 | ||||||
| chr3:5217078 | A | T | 3 | a0001c0004t0014 a0001c0004t0029 a0001c0014t0037 |
6 | HG02109.hp2 HG02572.hp1 HG02976.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1160A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 1160 | chr3 | 5217078 | ||||||
| chr3:5217300 | T | C | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(52): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
3_prime_UTR_variant | MODIFIER | c.*1382T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 1382 | chr3 | 5217300 | ||||||
| chr3:5217513 | A | G | 1 | a0001c0001t0059 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1595A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 1595 | chr3 | 5217513 | ||||||
| chr3:5217549 | A | G | 2 | a0001c0001t0021 a0001c0001t0027 |
3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1631A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 1631 | chr3 | 5217549 | ||||||
| chr3:5217737 | T | C | 1 | a0001c0001t0017 | 3 | HG02886.hp2 HG02922.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1819T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 1819 | chr3 | 5217737 | ||||||
| chr3:5217782 | T | C | 1 | a0001c0001t0040 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1864T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 1864 | chr3 | 5217782 | ||||||
| chr3:5217795 | T | A | 7 | a0001c0001t0009 a0001c0001t0010 a0001c0001t0013 others(4): Show |
23 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1877T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 1877 | chr3 | 5217795 | ||||||
| chr3:5217878 | T | C | 2 | a0001c0004t0014 a0001c0004t0029 |
5 | HG02572.hp1 HG02976.hp2 HG03209.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1960T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 1960 | chr3 | 5217878 | ||||||
| chr3:5217908 | G | A | 13 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0016 others(10): Show |
37 | HG00558.hp1 HG01106.hp1 HG01109.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1990G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 1990 | chr3 | 5217908 | ||||||
| chr3:5217939 | C | T | 1 | a0001c0014t0037 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2021C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2021 | chr3 | 5217939 | ||||||
| chr3:5218123 | A | C | 14 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0016 others(11): Show |
38 | HG00558.hp1 HG01106.hp1 HG01109.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2205A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2205 | chr3 | 5218123 | ||||||
| chr3:5218270 | C | A | 1 | a0001c0012t0058 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2352C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2352 | chr3 | 5218270 | ||||||
| chr3:5218271 | G | A | 1 | a0001c0004t0014 | 4 | HG02976.hp2 HG03209.hp1 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2353G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2353 | chr3 | 5218271 | ||||||
| chr3:5218323 | G | T | 1 | a0001c0001t0057 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2405G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2405 | chr3 | 5218323 | ||||||
| chr3:5218353 | G | GT | 4 | a0001c0001t0011 a0001c0001t0035 a0001c0001t0039 others(1): Show |
8 | HG02055.hp1 HG02109.hp1 HG02572.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2453dupT | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2454 | INFO_REALIGN_3_PRIME | chr3 | 5218353 | |||||
| chr3:5218353 | GT | G | 8 | a0001c0001t0015 a0001c0001t0017 a0001c0001t0038 others(5): Show |
16 | HG01243.hp1 HG01515.hp1 HG01515.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2453delT | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2453 | INFO_REALIGN_3_PRIME | chr3 | 5218353 | |||||
| chr3:5218353 | GTT | G | 15 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0016 others(12): Show |
38 | HG00558.hp1 HG01106.hp1 HG01109.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2452_*2453delTT | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2452 | INFO_REALIGN_3_PRIME | chr3 | 5218353 | |||||
| chr3:5218368 | T | C | 1 | a0001c0001t0025 | 2 | HG02027.hp1 NA18950.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2450T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2450 | chr3 | 5218368 | ||||||
| chr3:5218371 | T | TA | 2 | a0001c0001t0022 a0001c0001t0023 |
4 | HG00280.hp2 HG00738.hp2 HG02738.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2456dupA | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2457 | INFO_REALIGN_3_PRIME | chr3 | 5218371 | |||||
| chr3:5218427 | T | C | 1 | a0001c0002t0051 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2509T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2509 | chr3 | 5218427 | ||||||
| chr3:5218445 | A | C | 53 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(50): Show |
317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
3_prime_UTR_variant | MODIFIER | c.*2527A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2527 | chr3 | 5218445 | ||||||
| chr3:5218446 | C | A | 13 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0016 others(10): Show |
37 | HG00558.hp1 HG01106.hp1 HG01109.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2528C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2528 | chr3 | 5218446 | ||||||
| chr3:5218614 | G | A | 40 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0005 others(37): Show |
200 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*2696G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2696 | chr3 | 5218614 | ||||||
| chr3:5218658 | A | G | 1 | a0001c0001t0038 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2740A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2740 | chr3 | 5218658 | ||||||
| chr3:5218713 | T | A | 2 | a0001c0001t0021 a0001c0001t0044 |
3 | HG02055.hp2 HG02622.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2795T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2795 | chr3 | 5218713 | ||||||
| chr3:5218714 | A | G | 2 | a0001c0001t0021 a0001c0001t0044 |
3 | HG02055.hp2 HG02622.hp2 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2796A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2796 | chr3 | 5218714 | ||||||
| chr3:5218759 | T | G | 19 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0008 others(16): Show |
79 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*2841T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2841 | chr3 | 5218759 | ||||||
| chr3:5218760 | C | A | 19 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0008 others(16): Show |
79 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*2842C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 2842 | chr3 | 5218760 | ||||||
| chr3:5218965 | A | G | 1 | a0001c0001t0050 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3047A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 3047 | chr3 | 5218965 | ||||||
| chr3:5219095 | C | T | 1 | a0001c0016t0034 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3177C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 3177 | chr3 | 5219095 | ||||||
| chr3:5219291 | A | G | 1 | a0001c0001t0045 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3373A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 3373 | chr3 | 5219291 | ||||||
| chr3:5219424 | C | T | 1 | a0001c0001t0024 | 2 | HG02647.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3506C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 3506 | chr3 | 5219424 | ||||||
| chr3:5219495 | G | A | 1 | a0001c0001t0046 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3577G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 3577 | chr3 | 5219495 | ||||||
| chr3:5219654 | C | A | 1 | a0001c0012t0058 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3736C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 3736 | chr3 | 5219654 | ||||||
| chr3:5219684 | A | T | 1 | a0001c0012t0058 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3766A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 3766 | chr3 | 5219684 | ||||||
| chr3:5219700 | A | T | 1 | a0001c0001t0052 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3782A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 3782 | chr3 | 5219700 | ||||||
| chr3:5219701 | C | A | 2 | a0001c0001t0012 a0001c0001t0052 |
6 | HG02258.hp2 HG02630.hp2 HG02717.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3783C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 3783 | chr3 | 5219701 | ||||||
| chr3:5219709 | A | T | 1 | a0001c0001t0033 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3791A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 12/12 | 3791 | chr3 | 5219709 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:5188447 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0003g0020 |
2 | NA18966.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.509+133G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5188447 | |||||||
| chr3:5188573 | A | T | 1 | a0001c0001t0004g0254 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.509+259A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5188573 | |||||||
| chr3:5188658 | C | G | 238 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(235): Show |
310 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(307): Show |
intron_variant | MODIFIER | c.509+344C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5188658 | |||||||
| chr3:5188763 | C | G | 228 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(225): Show |
300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.509+449C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5188763 | |||||||
| chr3:5188857 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.509+543C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5188857 | |||||||
| chr3:5188980 | A | C | 3 | a0001c0001t0004g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 |
3 | HG00544.hp2 NA18962.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.509+666A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5188980 | |||||||
| chr3:5189012 | C | T | 1 | a0001c0001t0008g0249 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.509+698C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189012 | |||||||
| chr3:5189038 | C | T | 1 | a0001c0001t0002g0248 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.509+724C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189038 | |||||||
| chr3:5189044 | G | T | 1 | a0001c0002t0005g0084 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.509+730G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189044 | |||||||
| chr3:5189072 | C | T | 1 | a0001c0001t0015g0247 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.509+758C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189072 | |||||||
| chr3:5189114 | A | G | 8 | a0001c0001t0001g0009 a0001c0001t0001g0245 a0001c0001t0002g0009 others(5): Show |
11 | HG00280.hp2 HG00738.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.509+800A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189114 | |||||||
| chr3:5189182 | C | T | 1 | a0001c0001t0011g0242 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.509+868C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189182 | |||||||
| chr3:5189352 | G | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(165): Show |
233 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.509+1038G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189352 | |||||||
| chr3:5189421 | C | G | 7 | a0001c0001t0001g0009 a0001c0001t0001g0245 a0001c0001t0002g0009 others(4): Show |
10 | HG00280.hp2 HG00738.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.509+1107C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189421 | |||||||
| chr3:5189692 | T | C | 266 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(263): Show |
345 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.509+1378T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189692 | |||||||
| chr3:5189749 | T | C | 19 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0028 others(16): Show |
24 | HG00140.hp1 HG00558.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.509+1435T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189749 | |||||||
| chr3:5189793 | G | A | 56 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0206 others(53): Show |
61 | HG00544.hp2 HG00558.hp1 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.509+1479G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189793 | |||||||
| chr3:5189802 | G | C | 1 | a0001c0001t0004g0197 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.509+1488G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189802 | |||||||
| chr3:5189942 | A | C | 1 | a0001c0001t0007g0234 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.509+1628A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189942 | |||||||
| chr3:5189999 | T | G | 191 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(188): Show |
262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.509+1685T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5189999 | |||||||
| chr3:5189999 | TG | T | 50 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0206 others(47): Show |
55 | HG00544.hp2 HG00558.hp1 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.509+1695delG | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 5189999 | ||||||
| chr3:5190001 | G | A | 1 | a0001c0018t0031g0057 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.509+1687G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190001 | |||||||
| chr3:5190002 | G | GT | 191 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(188): Show |
262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.509+1688_509+1689i others(3): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190002 | |||||||
| chr3:5190086 | ACAT | A | 100 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0206 others(97): Show |
110 | HG00544.hp2 HG00558.hp1 HG00738.hp1 others(107): Show |
intron_variant | MODIFIER | c.509+1776_509+1778d others(5): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 5190086 | ||||||
| chr3:5190141 | T | C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(188): Show |
262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.509+1827T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190141 | |||||||
| chr3:5190290 | T | G | 1 | a0001c0001t0062g0085 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.509+1976T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190290 | |||||||
| chr3:5190389 | A | C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(188): Show |
262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.509+2075A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190389 | |||||||
| chr3:5190395 | C | T | 191 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(188): Show |
262 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.509+2081C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190395 | |||||||
| chr3:5190464 | C | T | 1 | a0001c0001t0001g0104 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.509+2150C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190464 | |||||||
| chr3:5190496 | G | A | 7 | a0001c0001t0002g0109 a0001c0001t0003g0010 a0001c0001t0003g0015 others(4): Show |
12 | NA18939.hp1 NA18940.hp2 NA18941.hp2 others(9): Show |
intron_variant | MODIFIER | c.509+2182G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190496 | |||||||
| chr3:5190545 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.509+2231C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190545 | |||||||
| chr3:5190568 | C | T | 1 | a0001c0001t0009g0056 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.509+2254C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190568 | |||||||
| chr3:5190771 | T | G | 5 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0003g0198 others(2): Show |
5 | HG01168.hp2 HG01169.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.509+2457T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190771 | |||||||
| chr3:5190804 | C | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
263 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(260): Show |
intron_variant | MODIFIER | c.509+2490C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190804 | |||||||
| chr3:5190836 | C | G | 2 | a0001c0001t0001g0038 a0001c0001t0002g0038 |
2 | HG01257.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.509+2522C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190836 | |||||||
| chr3:5190867 | T | A | 2 | a0001c0001t0002g0095 a0001c0001t0016g0058 |
2 | HG02818.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.509+2553T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190867 | |||||||
| chr3:5190878 | T | A | 1 | a0001c0001t0008g0249 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.509+2564T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190878 | |||||||
| chr3:5190879 | A | T | 1 | a0001c0001t0001g0195 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.509+2565A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5190879 | |||||||
| chr3:5191224 | TTTTG | T | 6 | a0001c0001t0011g0059 a0001c0001t0011g0060 a0001c0001t0011g0061 others(3): Show |
6 | HG02055.hp1 HG02572.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.509+2922_509+2925d others(6): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 5191224 | ||||||
| chr3:5191277 | G | T | 1 | a0001c0014t0037g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.509+2963G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191277 | |||||||
| chr3:5191390 | AT | A | 6 | a0001c0001t0003g0198 a0001c0001t0004g0203 a0001c0001t0008g0096 others(3): Show |
6 | HG01169.hp1 HG01256.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.509+3090delT | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | 5191390 | ||||||
| chr3:5191404 | T | A | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.509+3090T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191404 | |||||||
| chr3:5191429 | T | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.509+3115T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191429 | |||||||
| chr3:5191494 | A | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.509+3180A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191494 | |||||||
| chr3:5191597 | G | C | 1 | a0001c0001t0001g0114 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.509+3283G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191597 | |||||||
| chr3:5191680 | C | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.509+3366C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191680 | |||||||
| chr3:5191689 | T | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.509+3375T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191689 | |||||||
| chr3:5191725 | G | T | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.509+3411G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191725 | |||||||
| chr3:5191734 | A | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG00639.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.509+3420A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191734 | |||||||
| chr3:5191777 | G | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-3432G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191777 | |||||||
| chr3:5191824 | T | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-3385T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191824 | |||||||
| chr3:5191935 | A | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-3274A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191935 | |||||||
| chr3:5191973 | A | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-3236A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191973 | |||||||
| chr3:5191978 | A | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-3231A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191978 | |||||||
| chr3:5191991 | T | G | 2 | a0001c0001t0001g0199 a0001c0001t0001g0200 |
2 | HG01516.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.510-3218T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5191991 | |||||||
| chr3:5192009 | G | A | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-3200G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192009 | |||||||
| chr3:5192102 | C | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-3107C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192102 | |||||||
| chr3:5192112 | C | T | 1 | a0001c0001t0002g0192 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.510-3097C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192112 | |||||||
| chr3:5192115 | G | C | 1 | a0001c0001t0042g0204 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.510-3094G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192115 | |||||||
| chr3:5192118 | A | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-3091A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192118 | |||||||
| chr3:5192157 | C | T | 1 | a0001c0018t0031g0057 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.510-3052C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192157 | |||||||
| chr3:5192231 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.510-2978G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192231 | |||||||
| chr3:5192355 | C | A | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-2854C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192355 | |||||||
| chr3:5192395 | A | T | 2 | a0001c0001t0030g0241 a0001c0001t0039g0239 |
2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.510-2814A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192395 | |||||||
| chr3:5192416 | A | C | 6 | a0001c0001t0017g0023 a0001c0001t0017g0066 a0001c0004t0014g0012 others(3): Show |
9 | HG02559.hp2 HG02572.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.510-2793A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192416 | |||||||
| chr3:5192746 | T | C | 2 | a0001c0001t0004g0115 a0001c0001t0004g0116 |
2 | NA18998.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.510-2463T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192746 | |||||||
| chr3:5192812 | A | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-2397A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192812 | |||||||
| chr3:5192870 | G | A | 1 | a0001c0001t0009g0044 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.510-2339G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192870 | |||||||
| chr3:5192870 | G | T | 2 | a0001c0001t0030g0241 a0001c0001t0039g0239 |
2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.510-2339G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192870 | |||||||
| chr3:5192906 | A | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-2303A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192906 | |||||||
| chr3:5192919 | A | G | 3 | a0001c0001t0021g0093 a0001c0001t0021g0094 a0001c0001t0027g0092 |
3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.510-2290A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5192919 | |||||||
| chr3:5193001 | A | G | 1 | a0001c0001t0006g0191 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.510-2208A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193001 | |||||||
| chr3:5193041 | A | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(264): Show |
346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.510-2168A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193041 | |||||||
| chr3:5193211 | T | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-1998T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193211 | |||||||
| chr3:5193231 | C | G | 1 | a0001c0001t0002g0192 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.510-1978C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193231 | |||||||
| chr3:5193247 | G | A | 2 | a0001c0001t0030g0241 a0001c0001t0039g0239 |
2 | NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.510-1962G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193247 | |||||||
| chr3:5193310 | G | A | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-1899G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193310 | |||||||
| chr3:5193342 | C | G | 1 | a0001c0001t0004g0232 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.510-1867C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193342 | |||||||
| chr3:5193567 | T | A | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-1642T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193567 | |||||||
| chr3:5193616 | A | G | 3 | a0001c0001t0001g0188 a0001c0001t0002g0189 a0001c0001t0002g0190 |
3 | HG02717.hp1 HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.510-1593A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193616 | |||||||
| chr3:5193618 | A | T | 1 | a0001c0001t0001g0103 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.510-1591A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193618 | |||||||
| chr3:5193675 | G | A | 1 | a0001c0001t0003g0105 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.510-1534G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193675 | |||||||
| chr3:5193759 | A | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-1450A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193759 | |||||||
| chr3:5193788 | G | A | 19 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0206 others(16): Show |
21 | HG00544.hp2 HG00738.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.510-1421G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193788 | |||||||
| chr3:5193822 | T | A | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-1387T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193822 | |||||||
| chr3:5193919 | T | G | 1 | a0001c0014t0037g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.510-1290T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5193919 | |||||||
| chr3:5194112 | G | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-1097G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5194112 | |||||||
| chr3:5194285 | T | A | 1 | a0001c0001t0038g0062 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.510-924T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5194285 | |||||||
| chr3:5194313 | T | A | 1 | a0001c0001t0004g0063 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.510-896T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5194313 | |||||||
| chr3:5194435 | G | C | 3 | a0001c0001t0021g0093 a0001c0001t0021g0094 a0001c0001t0027g0092 |
3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.510-774G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5194435 | |||||||
| chr3:5194435 | G | T | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-774G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5194435 | |||||||
| chr3:5194574 | A | T | 1 | a0001c0001t0001g0187 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.510-635A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5194574 | |||||||
| chr3:5194590 | T | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-619T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5194590 | |||||||
| chr3:5194630 | A | G | 1 | a0001c0005t0008g0113 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.510-579A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5194630 | |||||||
| chr3:5194655 | C | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-554C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5194655 | |||||||
| chr3:5194764 | C | T | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-445C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5194764 | |||||||
| chr3:5194791 | G | A | 1 | a0001c0001t0002g0117 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.510-418G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5194791 | |||||||
| chr3:5194836 | A | C | 3 | a0001c0001t0030g0241 a0001c0001t0038g0062 a0001c0001t0039g0239 |
3 | HG01243.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.510-373A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5194836 | |||||||
| chr3:5194845 | T | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-364T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5194845 | |||||||
| chr3:5195028 | A | G | 3 | a0001c0001t0021g0093 a0001c0001t0021g0094 a0001c0001t0027g0092 |
3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.510-181A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5195028 | |||||||
| chr3:5195054 | G | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.510-155G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5195054 | |||||||
| chr3:5195054 | G | T | 1 | a0001c0001t0023g0246 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.510-155G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5195054 | |||||||
| chr3:5195122 | C | T | 5 | a0001c0001t0009g0044 a0001c0001t0009g0053 a0001c0001t0009g0054 others(2): Show |
5 | HG01243.hp2 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-87C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5195122 | |||||||
| chr3:5195155 | T | C | 1 | a0001c0002t0018g0070 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.510-54T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 1/11 | chr3 | 5195155 | |||||||
| chr3:5195293 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.582+12C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195293 | |||||||
| chr3:5195301 | T | A | 6 | a0001c0001t0017g0023 a0001c0001t0017g0066 a0001c0004t0014g0012 others(3): Show |
9 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.582+20T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195301 | |||||||
| chr3:5195305 | A | G | 1 | a0001c0014t0037g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.582+24A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195305 | |||||||
| chr3:5195500 | G | A | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+219G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195500 | |||||||
| chr3:5195564 | G | T | 8 | a0001c0001t0002g0003 a0001c0001t0002g0184 a0001c0001t0002g0185 others(5): Show |
14 | HG02056.hp1 HG02083.hp1 HG03704.hp1 others(11): Show |
intron_variant | MODIFIER | c.582+283G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195564 | |||||||
| chr3:5195599 | T | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+318T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195599 | |||||||
| chr3:5195710 | A | G | 4 | a0001c0001t0021g0093 a0001c0001t0021g0094 a0001c0001t0027g0092 others(1): Show |
4 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.582+429A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195710 | |||||||
| chr3:5195753 | C | T | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+472C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195753 | |||||||
| chr3:5195793 | C | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+512C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195793 | |||||||
| chr3:5195833 | C | T | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+552C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195833 | |||||||
| chr3:5195844 | G | C | 1 | a0001c0001t0001g0118 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.582+563G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195844 | |||||||
| chr3:5195849 | C | T | 1 | a0001c0001t0002g0182 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.582+568C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195849 | |||||||
| chr3:5195891 | G | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+610G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195891 | |||||||
| chr3:5195976 | T | G | 1 | a0001c0001t0004g0063 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.582+695T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5195976 | |||||||
| chr3:5196009 | T | A | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+728T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196009 | |||||||
| chr3:5196165 | A | T | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+884A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196165 | |||||||
| chr3:5196192 | C | T | 1 | a0001c0008t0049g0181 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.582+911C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196192 | |||||||
| chr3:5196337 | G | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+1056G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196337 | |||||||
| chr3:5196375 | T | C | 1 | a0001c0001t0003g0119 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.582+1094T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196375 | |||||||
| chr3:5196387 | T | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+1106T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196387 | |||||||
| chr3:5196426 | T | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+1145T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196426 | |||||||
| chr3:5196427 | A | T | 1 | a0001c0001t0001g0180 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.582+1146A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196427 | |||||||
| chr3:5196461 | G | GAC | 182 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(179): Show |
249 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.582+1202_582+1203d others(4): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5196461 | ||||||
| chr3:5196461 | G | GACAC | 5 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0002g0190 others(2): Show |
5 | HG00597.hp2 HG02717.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.582+1200_582+1203d others(6): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5196461 | ||||||
| chr3:5196461 | G | GACACAC | 3 | a0001c0001t0006g0008 a0001c0001t0043g0008 a0001c0004t0014g0012 |
8 | HG00423.hp2 HG02080.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.582+1198_582+1203d others(8): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5196461 | ||||||
| chr3:5196461 | G | GACGCACA others(5): Show |
1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+1182_582+1183i others(14): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5196461 | ||||||
| chr3:5196483 | C | A | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+1202C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196483 | |||||||
| chr3:5196489 | T | C | 1 | a0001c0001t0001g0126 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.582+1208T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196489 | |||||||
| chr3:5196565 | A | G | 1 | a0001c0001t0003g0119 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.582+1284A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196565 | |||||||
| chr3:5196664 | A | G | 9 | a0001c0001t0002g0037 a0001c0001t0002g0171 a0001c0001t0002g0172 others(6): Show |
9 | HG00140.hp2 HG00280.hp1 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.582+1383A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196664 | |||||||
| chr3:5196856 | CA | C | 4 | a0001c0001t0021g0093 a0001c0001t0021g0094 a0001c0001t0027g0092 others(1): Show |
4 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.582+1577delA | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5196856 | ||||||
| chr3:5196904 | A | G | 4 | a0001c0001t0021g0093 a0001c0001t0021g0094 a0001c0001t0027g0092 others(1): Show |
4 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.582+1623A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196904 | |||||||
| chr3:5196913 | GTCTTT | G | 13 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0029 others(10): Show |
18 | HG00642.hp2 HG01168.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.582+1654_582+1658d others(7): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5196913 | ||||||
| chr3:5196913 | GTCTTTTC others(3): Show |
G | 3 | a0001c0001t0012g0229 a0001c0001t0012g0230 a0001c0001t0012g0231 |
3 | HG02630.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.582+1649_582+1658d others(12): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5196913 | ||||||
| chr3:5196920 | C | CTT | 3 | a0001c0001t0021g0093 a0001c0001t0021g0094 a0001c0001t0027g0092 |
3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.582+1642_582+1643d others(4): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5196920 | ||||||
| chr3:5196930 | C | T | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+1649C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196930 | |||||||
| chr3:5196935 | C | CT | 7 | a0001c0001t0003g0010 a0001c0001t0017g0023 a0001c0001t0017g0066 others(4): Show |
8 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.582+1668dupT | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5196935 | ||||||
| chr3:5196935 | C | T | 4 | a0001c0001t0021g0093 a0001c0001t0021g0094 a0001c0001t0027g0092 others(1): Show |
4 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.582+1654C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196935 | |||||||
| chr3:5196943 | T | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+1662T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196943 | |||||||
| chr3:5196990 | G | A | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.582+1709G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5196990 | |||||||
| chr3:5197019 | C | T | 1 | a0001c0001t0002g0189 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.582+1738C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5197019 | |||||||
| chr3:5197041 | G | A | 73 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0206 others(70): Show |
81 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.582+1760G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5197041 | |||||||
| chr3:5197064 | CT | C | 240 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(237): Show |
317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.582+1801delT | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5197064 | ||||||
| chr3:5197064 | CTT | C | 6 | a0001c0001t0004g0018 a0001c0001t0004g0039 a0001c0001t0004g0254 others(3): Show |
8 | HG02257.hp2 HG02280.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.582+1800_582+1801d others(4): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5197064 | ||||||
| chr3:5197082 | T | G | 263 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(260): Show |
342 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.582+1801T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5197082 | |||||||
| chr3:5197135 | A | G | 8 | a0001c0001t0017g0023 a0001c0001t0017g0066 a0001c0001t0018g0091 others(5): Show |
11 | HG02109.hp2 HG02559.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.582+1854A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5197135 | |||||||
| chr3:5197420 | T | G | 4 | a0001c0001t0021g0093 a0001c0001t0021g0094 a0001c0001t0027g0092 others(1): Show |
4 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.582+2139T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5197420 | |||||||
| chr3:5197485 | A | G | 3 | a0001c0001t0021g0093 a0001c0001t0021g0094 a0001c0001t0027g0092 |
3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.583-2107A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5197485 | |||||||
| chr3:5197596 | T | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.583-1996T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5197596 | |||||||
| chr3:5197680 | C | T | 1 | a0001c0001t0015g0165 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.583-1912C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5197680 | |||||||
| chr3:5197739 | G | T | 1 | a0001c0001t0011g0061 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.583-1853G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5197739 | |||||||
| chr3:5197855 | C | T | 1 | a0001c0001t0004g0125 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.583-1737C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5197855 | |||||||
| chr3:5197890 | G | A | 1 | a0001c0001t0007g0234 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.583-1702G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5197890 | |||||||
| chr3:5197924 | A | G | 3 | a0001c0001t0021g0093 a0001c0001t0021g0094 a0001c0001t0027g0092 |
3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.583-1668A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5197924 | |||||||
| chr3:5197943 | A | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.583-1649A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5197943 | |||||||
| chr3:5198015 | C | T | 2 | a0001c0005t0001g0164 a0001c0005t0004g0112 |
2 | HG02451.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.583-1577C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198015 | |||||||
| chr3:5198052 | CT | C | 14 | a0001c0001t0004g0063 a0001c0001t0006g0087 a0001c0001t0006g0088 others(11): Show |
14 | HG01106.hp1 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.583-1530delT | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5198052 | ||||||
| chr3:5198139 | A | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(239): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.583-1453A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198139 | |||||||
| chr3:5198204 | C | T | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.583-1388C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198204 | |||||||
| chr3:5198236 | A | G | 1 | a0001c0001t0039g0239 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.583-1356A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198236 | |||||||
| chr3:5198295 | C | G | 1 | a0001c0001t0001g0163 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.583-1297C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198295 | |||||||
| chr3:5198347 | C | T | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.583-1245C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198347 | |||||||
| chr3:5198373 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.583-1219C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198373 | |||||||
| chr3:5198654 | G | A | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.583-938G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198654 | |||||||
| chr3:5198662 | CT | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
265 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.583-908delT | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5198662 | ||||||
| chr3:5198662 | CTT | C | 57 | a0001c0001t0001g0016 a0001c0001t0001g0129 a0001c0001t0001g0166 others(54): Show |
63 | HG00544.hp2 HG00738.hp1 HG01168.hp2 others(60): Show |
intron_variant | MODIFIER | c.583-909_583-908del others(2): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5198662 | ||||||
| chr3:5198662 | CTTT | C | 6 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0003g0173 others(3): Show |
6 | HG00280.hp1 HG02896.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.583-910_583-908del others(3): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr3 | 5198662 | ||||||
| chr3:5198683 | T | C | 1 | a0001c0001t0030g0241 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.583-909T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198683 | |||||||
| chr3:5198719 | G | A | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.583-873G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198719 | |||||||
| chr3:5198747 | T | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.583-845T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198747 | |||||||
| chr3:5198804 | A | T | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.583-788A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198804 | |||||||
| chr3:5198816 | C | A | 1 | a0001c0001t0001g0032 | 2 | NA18961.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.583-776C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198816 | |||||||
| chr3:5198884 | G | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.583-708G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198884 | |||||||
| chr3:5198946 | C | T | 3 | a0001c0001t0030g0241 a0001c0001t0038g0062 a0001c0001t0039g0239 |
3 | HG01243.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.583-646C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198946 | |||||||
| chr3:5198950 | G | A | 6 | a0001c0001t0017g0023 a0001c0001t0017g0066 a0001c0004t0014g0012 others(3): Show |
9 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.583-642G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5198950 | |||||||
| chr3:5199043 | C | T | 1 | a0001c0001t0003g0176 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.583-549C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5199043 | |||||||
| chr3:5199069 | A | G | 1 | a0001c0001t0004g0063 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.583-523A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5199069 | |||||||
| chr3:5199100 | T | A | 1 | a0001c0018t0031g0057 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.583-492T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5199100 | |||||||
| chr3:5199416 | A | T | 10 | a0001c0001t0017g0023 a0001c0001t0017g0066 a0001c0001t0021g0093 others(7): Show |
11 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.583-176A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5199416 | |||||||
| chr3:5199437 | G | T | 4 | a0001c0001t0021g0093 a0001c0001t0021g0094 a0001c0001t0027g0092 others(1): Show |
4 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.583-155G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5199437 | |||||||
| chr3:5199514 | C | T | 3 | a0001c0001t0021g0093 a0001c0001t0021g0094 a0001c0001t0027g0092 |
3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.583-78C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5199514 | |||||||
| chr3:5199538 | C | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(258): Show |
340 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(337): Show |
intron_variant | MODIFIER | c.583-54C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 2/11 | chr3 | 5199538 | |||||||
| chr3:5199783 | A | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.686+88A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5199783 | |||||||
| chr3:5199905 | C | T | 8 | a0001c0001t0004g0197 a0001c0001t0004g0203 a0001c0001t0004g0219 others(5): Show |
8 | HG01891.hp1 HG02257.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.686+210C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5199905 | |||||||
| chr3:5199910 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.686+215G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5199910 | |||||||
| chr3:5199940 | CT | C | 14 | a0001c0001t0002g0131 a0001c0001t0002g0132 a0001c0001t0003g0201 others(11): Show |
16 | HG01168.hp2 HG01256.hp2 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.686+262delT | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr3 | 5199940 | ||||||
| chr3:5200000 | A | G | 2 | a0001c0001t0002g0161 a0001c0001t0038g0062 |
2 | HG01243.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.686+305A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5200000 | |||||||
| chr3:5200060 | A | T | 4 | a0001c0001t0021g0093 a0001c0001t0021g0094 a0001c0001t0027g0092 others(1): Show |
4 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.686+365A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5200060 | |||||||
| chr3:5200125 | T | G | 62 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0206 others(59): Show |
70 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.686+430T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5200125 | |||||||
| chr3:5200151 | C | T | 1 | a0001c0001t0041g0124 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.686+456C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5200151 | |||||||
| chr3:5200174 | C | T | 1 | a0001c0001t0002g0160 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.686+479C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5200174 | |||||||
| chr3:5200240 | G | A | 16 | a0001c0001t0001g0004 a0001c0001t0002g0004 a0001c0001t0002g0020 others(13): Show |
20 | HG00597.hp1 HG01257.hp1 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.686+545G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5200240 | |||||||
| chr3:5200297 | T | A | 1 | a0001c0001t0038g0062 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.686+602T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5200297 | |||||||
| chr3:5200316 | T | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.686+621T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5200316 | |||||||
| chr3:5200459 | C | T | 1 | a0001c0002t0026g0082 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.686+764C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5200459 | |||||||
| chr3:5200534 | T | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.686+839T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5200534 | |||||||
| chr3:5200719 | A | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.686+1024A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5200719 | |||||||
| chr3:5200852 | G | A | 1 | a0001c0001t0038g0062 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.687-901G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5200852 | |||||||
| chr3:5200891 | A | C | 1 | a0001c0001t0002g0109 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.687-862A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5200891 | |||||||
| chr3:5201011 | C | T | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.687-742C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201011 | |||||||
| chr3:5201071 | T | C | 1 | a0001c0001t0004g0125 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.687-682T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201071 | |||||||
| chr3:5201103 | G | A | 4 | a0001c0001t0021g0093 a0001c0001t0021g0094 a0001c0001t0027g0092 others(1): Show |
4 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.687-650G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201103 | |||||||
| chr3:5201199 | A | C | 268 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(265): Show |
347 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.687-554A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201199 | |||||||
| chr3:5201225 | G | A | 3 | a0001c0001t0021g0093 a0001c0001t0021g0094 a0001c0001t0027g0092 |
3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.687-528G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201225 | |||||||
| chr3:5201250 | A | G | 1 | a0001c0001t0002g0136 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.687-503A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201250 | |||||||
| chr3:5201258 | G | A | 6 | a0001c0001t0017g0023 a0001c0001t0017g0066 a0001c0004t0014g0012 others(3): Show |
9 | HG02109.hp2 HG02572.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.687-495G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201258 | |||||||
| chr3:5201313 | G | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.687-440G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201313 | |||||||
| chr3:5201316 | G | C | 1 | a0001c0001t0001g0014 | 3 | HG02071.hp2 NA18944.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.687-437G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201316 | |||||||
| chr3:5201381 | C | T | 1 | a0001c0001t0035g0111 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.687-372C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201381 | |||||||
| chr3:5201393 | G | C | 1 | a0001c0005t0001g0164 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.687-360G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201393 | |||||||
| chr3:5201430 | G | A | 267 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(264): Show |
346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.687-323G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201430 | |||||||
| chr3:5201481 | A | G | 3 | a0001c0001t0030g0241 a0001c0001t0038g0062 a0001c0001t0039g0239 |
3 | HG01243.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.687-272A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201481 | |||||||
| chr3:5201497 | C | A | 4 | a0001c0001t0021g0093 a0001c0001t0021g0094 a0001c0001t0027g0092 others(1): Show |
4 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.687-256C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201497 | |||||||
| chr3:5201594 | A | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.687-159A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201594 | |||||||
| chr3:5201721 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0015g0016 |
3 | HG02976.hp1 HG03139.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.687-32T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 3/11 | chr3 | 5201721 | |||||||
| chr3:5202120 | A | G | 1 | a0001c0004t0029g0064 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.858+196A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 4/11 | chr3 | 5202120 | |||||||
| chr3:5202171 | G | A | 2 | a0001c0002t0005g0042 a0001c0002t0020g0042 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.858+247G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 4/11 | chr3 | 5202171 | |||||||
| chr3:5202227 | C | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.858+303C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 4/11 | chr3 | 5202227 | |||||||
| chr3:5202396 | G | A | 1 | a0001c0001t0003g0137 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.858+472G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 4/11 | chr3 | 5202396 | |||||||
| chr3:5202400 | G | C | 1 | a0001c0002t0018g0070 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.858+476G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 4/11 | chr3 | 5202400 | |||||||
| chr3:5202559 | T | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.859-407T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 4/11 | chr3 | 5202559 | |||||||
| chr3:5202587 | G | A | 5 | a0001c0001t0017g0023 a0001c0001t0017g0066 a0001c0004t0014g0012 others(2): Show |
8 | HG02572.hp1 HG02886.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.859-379G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 4/11 | chr3 | 5202587 | |||||||
| chr3:5202700 | G | C | 1 | a0001c0001t0001g0138 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.859-266G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 4/11 | chr3 | 5202700 | |||||||
| chr3:5202729 | C | G | 3 | a0001c0004t0014g0012 a0001c0004t0014g0065 a0001c0004t0029g0064 |
5 | HG02572.hp1 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.859-237C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 4/11 | chr3 | 5202729 | |||||||
| chr3:5202737 | T | C | 3 | a0001c0001t0017g0023 a0001c0001t0017g0066 a0001c0018t0031g0057 |
4 | HG02559.hp2 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.859-229T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 4/11 | chr3 | 5202737 | |||||||
| chr3:5202861 | G | A | 8 | a0001c0001t0004g0197 a0001c0001t0004g0203 a0001c0001t0004g0219 others(5): Show |
8 | HG01891.hp1 HG02257.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.859-105G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 4/11 | chr3 | 5202861 | |||||||
| chr3:5202906 | C | G | 1 | a0001c0001t0006g0225 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.859-60C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 4/11 | chr3 | 5202906 | |||||||
| chr3:5203170 | A | G | 1 | a0001c0018t0031g0057 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1042+21A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5203170 | |||||||
| chr3:5203224 | C | T | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1042+75C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5203224 | |||||||
| chr3:5203254 | A | G | 4 | a0001c0001t0002g0109 a0001c0001t0003g0010 a0001c0001t0003g0105 others(1): Show |
7 | NA18940.hp2 NA18956.hp1 NA18980.hp1 others(4): Show |
intron_variant | MODIFIER | c.1042+105A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5203254 | |||||||
| chr3:5203418 | C | T | 3 | a0001c0001t0007g0221 a0001c0001t0007g0226 a0001c0012t0058g0110 |
3 | HG02280.hp1 HG02965.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1042+269C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5203418 | |||||||
| chr3:5203461 | T | G | 75 | a0001c0001t0001g0004 a0001c0001t0001g0032 a0001c0001t0001g0038 others(72): Show |
105 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.1042+312T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5203461 | |||||||
| chr3:5203564 | G | A | 11 | a0001c0001t0017g0023 a0001c0001t0017g0066 a0001c0001t0030g0241 others(8): Show |
14 | HG01243.hp1 HG02109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1042+415G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5203564 | |||||||
| chr3:5203618 | T | C | 2 | a0001c0001t0050g0147 a0001c0008t0049g0181 |
2 | HG03017.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1042+469T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5203618 | |||||||
| chr3:5203775 | T | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1042+626T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5203775 | |||||||
| chr3:5203844 | A | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1042+695A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5203844 | |||||||
| chr3:5203951 | C | G | 1 | a0001c0001t0001g0032 | 2 | NA18961.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.1042+802C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5203951 | |||||||
| chr3:5204072 | A | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1042+923A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204072 | |||||||
| chr3:5204200 | C | T | 1 | a0001c0001t0011g0060 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1043-867C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204200 | |||||||
| chr3:5204298 | G | A | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1043-769G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204298 | |||||||
| chr3:5204306 | C | T | 1 | a0001c0002t0020g0081 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1043-761C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204306 | |||||||
| chr3:5204341 | T | C | 1 | a0001c0002t0053g0073 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1043-726T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204341 | |||||||
| chr3:5204373 | CT | C | 8 | a0001c0001t0017g0023 a0001c0001t0017g0066 a0001c0001t0038g0062 others(5): Show |
11 | HG01243.hp1 HG02109.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1043-683delT | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr3 | 5204373 | ||||||
| chr3:5204386 | T | G | 1 | a0001c0001t0002g0171 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1043-681T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204386 | |||||||
| chr3:5204410 | A | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1043-657A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204410 | |||||||
| chr3:5204474 | A | G | 1 | a0001c0001t0003g0036 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1043-593A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204474 | |||||||
| chr3:5204481 | C | T | 73 | a0001c0001t0001g0199 a0001c0001t0001g0200 a0001c0001t0001g0206 others(70): Show |
81 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1043-586C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204481 | |||||||
| chr3:5204607 | G | C | 1 | a0001c0001t0002g0139 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1043-460G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204607 | |||||||
| chr3:5204612 | G | A | 4 | a0001c0004t0014g0012 a0001c0004t0014g0065 a0001c0004t0029g0064 others(1): Show |
6 | HG02109.hp2 HG02572.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1043-455G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204612 | |||||||
| chr3:5204681 | C | T | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1043-386C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204681 | |||||||
| chr3:5204775 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1043-292G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204775 | |||||||
| chr3:5204844 | A | T | 1 | a0001c0001t0030g0241 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1043-223A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204844 | |||||||
| chr3:5204861 | A | G | 1 | a0001c0002t0005g0080 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1043-206A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204861 | |||||||
| chr3:5204942 | C | G | 1 | a0001c0001t0001g0101 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1043-125C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5204942 | |||||||
| chr3:5205011 | T | C | 14 | a0001c0001t0017g0023 a0001c0001t0017g0066 a0001c0001t0021g0093 others(11): Show |
17 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1043-56T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5205011 | |||||||
| chr3:5205027 | G | GT | 3 | a0001c0001t0017g0023 a0001c0001t0017g0066 a0001c0018t0031g0057 |
4 | HG02559.hp2 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1043-40_1043-39ins others(1): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 5/11 | chr3 | 5205027 | |||||||
| chr3:5205426 | A | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1217+185A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5205426 | |||||||
| chr3:5205531 | C | T | 2 | a0001c0001t0006g0213 a0001c0001t0006g0217 |
2 | HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1217+290C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5205531 | |||||||
| chr3:5205543 | T | G | 3 | a0001c0001t0021g0093 a0001c0001t0021g0094 a0001c0001t0027g0092 |
3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1217+302T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5205543 | |||||||
| chr3:5205586 | A | G | 3 | a0001c0001t0021g0093 a0001c0001t0021g0094 a0001c0001t0027g0092 |
3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1217+345A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5205586 | |||||||
| chr3:5205647 | T | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1217+406T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5205647 | |||||||
| chr3:5205703 | T | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1217+462T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5205703 | |||||||
| chr3:5205848 | A | G | 1 | a0001c0001t0059g0048 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1217+607A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5205848 | |||||||
| chr3:5205855 | G | A | 1 | a0001c0001t0038g0062 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1217+614G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5205855 | |||||||
| chr3:5205875 | C | G | 4 | a0001c0001t0021g0093 a0001c0001t0021g0094 a0001c0001t0027g0092 others(1): Show |
4 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1217+634C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5205875 | |||||||
| chr3:5205876 | G | A | 1 | a0001c0001t0004g0205 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1217+635G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5205876 | |||||||
| chr3:5205877 | T | A | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1217+636T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5205877 | |||||||
| chr3:5205881 | G | A | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1217+640G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5205881 | |||||||
| chr3:5205890 | G | A | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1217+649G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5205890 | |||||||
| chr3:5206020 | A | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1217+779A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206020 | |||||||
| chr3:5206028 | C | T | 4 | a0001c0001t0021g0093 a0001c0001t0021g0094 a0001c0001t0027g0092 others(1): Show |
4 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1217+787C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206028 | |||||||
| chr3:5206071 | A | G | 1 | a0001c0001t0038g0062 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1217+830A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206071 | |||||||
| chr3:5206129 | T | G | 14 | a0001c0001t0017g0023 a0001c0001t0017g0066 a0001c0001t0021g0093 others(11): Show |
17 | HG01243.hp1 HG02055.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1217+888T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206129 | |||||||
| chr3:5206162 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1217+921G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206162 | |||||||
| chr3:5206220 | T | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1218-933T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206220 | |||||||
| chr3:5206221 | T | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1218-932T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206221 | |||||||
| chr3:5206311 | G | A | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1218-842G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206311 | |||||||
| chr3:5206311 | G | C | 1 | a0001c0001t0003g0176 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1218-842G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206311 | |||||||
| chr3:5206318 | C | T | 1 | a0001c0001t0003g0036 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1218-835C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206318 | |||||||
| chr3:5206357 | A | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1218-796A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206357 | |||||||
| chr3:5206458 | G | A | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1218-695G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206458 | |||||||
| chr3:5206594 | G | A | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1218-559G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206594 | |||||||
| chr3:5206681 | T | G | 1 | a0001c0001t0005g0120 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1218-472T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206681 | |||||||
| chr3:5206682 | G | C | 1 | a0001c0001t0005g0120 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1218-471G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206682 | |||||||
| chr3:5206683 | C | T | 1 | a0001c0001t0005g0120 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1218-470C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206683 | |||||||
| chr3:5206706 | T | G | 1 | a0001c0001t0006g0225 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1218-447T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206706 | |||||||
| chr3:5206719 | C | A | 3 | a0001c0001t0017g0023 a0001c0001t0017g0066 a0001c0018t0031g0057 |
4 | HG02559.hp2 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218-434C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206719 | |||||||
| chr3:5206801 | C | A | 1 | a0001c0001t0002g0033 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1218-352C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206801 | |||||||
| chr3:5206878 | A | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1218-275A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206878 | |||||||
| chr3:5206932 | A | G | 3 | a0001c0001t0017g0023 a0001c0001t0017g0066 a0001c0018t0031g0057 |
4 | HG02559.hp2 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1218-221A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206932 | |||||||
| chr3:5206962 | A | T | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1218-191A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206962 | |||||||
| chr3:5206969 | T | C | 1 | a0001c0018t0031g0057 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1218-184T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206969 | |||||||
| chr3:5206991 | T | G | 1 | a0001c0001t0006g0017 | 3 | HG03579.hp1 NA18522.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1218-162T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5206991 | |||||||
| chr3:5207014 | T | G | 2 | a0001c0001t0017g0023 a0001c0001t0017g0066 |
3 | HG02886.hp2 HG02922.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1218-139T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5207014 | |||||||
| chr3:5207039 | G | A | 1 | a0001c0001t0004g0121 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1218-114G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5207039 | |||||||
| chr3:5207040 | A | G | 1 | a0001c0001t0004g0121 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1218-113A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5207040 | |||||||
| chr3:5207041 | G | A | 1 | a0001c0001t0004g0121 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1218-112G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5207041 | |||||||
| chr3:5207062 | G | A | 12 | a0001c0001t0002g0189 a0001c0001t0017g0023 a0001c0001t0017g0066 others(9): Show |
15 | HG01243.hp1 HG02109.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.1218-91G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5207062 | |||||||
| chr3:5207144 | G | A | 5 | a0001c0001t0004g0018 a0001c0001t0004g0039 a0001c0001t0004g0254 others(2): Show |
7 | HG02257.hp2 HG02280.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1218-9G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 6/11 | chr3 | 5207144 | |||||||
| chr3:5207355 | G | A | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1338+82G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 7/11 | chr3 | 5207355 | |||||||
| chr3:5207551 | G | T | 1 | a0001c0002t0005g0083 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1338+278G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 7/11 | chr3 | 5207551 | |||||||
| chr3:5207665 | T | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1338+392T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 7/11 | chr3 | 5207665 | |||||||
| chr3:5207696 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG00642.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.1339-397C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 7/11 | chr3 | 5207696 | |||||||
| chr3:5207705 | A | C | 32 | a0001c0001t0006g0191 a0001c0001t0009g0055 a0001c0001t0021g0093 others(29): Show |
34 | HG00558.hp1 HG01109.hp1 HG02055.hp2 others(31): Show |
intron_variant | MODIFIER | c.1339-388A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 7/11 | chr3 | 5207705 | |||||||
| chr3:5207713 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1339-380G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 7/11 | chr3 | 5207713 | |||||||
| chr3:5207826 | A | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1339-267A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 7/11 | chr3 | 5207826 | |||||||
| chr3:5207855 | C | T | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1339-238C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 7/11 | chr3 | 5207855 | |||||||
| chr3:5207905 | A | G | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG00639.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1339-188A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 7/11 | chr3 | 5207905 | |||||||
| chr3:5208052 | G | A | 2 | a0001c0002t0005g0074 a0001c0002t0005g0075 |
2 | NA18992.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1339-41G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 7/11 | chr3 | 5208052 | |||||||
| chr3:5208060 | A | G | 1 | a0001c0001t0002g0109 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1339-33A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 7/11 | chr3 | 5208060 | |||||||
| chr3:5208277 | GT | G | 10 | a0001c0001t0017g0023 a0001c0001t0017g0066 a0001c0001t0030g0241 others(7): Show |
13 | HG01243.hp1 HG02109.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1509+27delT | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 5208277 | ||||||
| chr3:5208280 | T | G | 1 | a0001c0018t0031g0057 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1509+17T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5208280 | |||||||
| chr3:5208600 | T | C | 1 | a0001c0001t0005g0120 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1509+337T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5208600 | |||||||
| chr3:5208665 | A | C | 1 | a0001c0001t0005g0120 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1509+402A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5208665 | |||||||
| chr3:5208743 | T | G | 3 | a0001c0001t0001g0028 a0001c0001t0015g0028 a0001c0012t0058g0110 |
3 | HG01515.hp1 HG01517.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1509+480T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5208743 | |||||||
| chr3:5208743 | T | TTG | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0004g0252 |
3 | HG00544.hp2 HG00597.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1509+496_1509+497d others(4): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 5208743 | ||||||
| chr3:5208757 | G | GTA | 3 | a0001c0004t0014g0012 a0001c0004t0014g0065 a0001c0014t0037g0067 |
5 | HG02109.hp2 HG02976.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1509+495_1509+496i others(4): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 5208757 | ||||||
| chr3:5208759 | G | A | 5 | a0001c0001t0030g0241 a0001c0001t0039g0239 a0001c0004t0014g0012 others(2): Show |
7 | HG02109.hp2 HG02976.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.1509+496G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5208759 | |||||||
| chr3:5208768 | T | TAC | 6 | a0001c0001t0012g0019 a0001c0001t0012g0229 a0001c0001t0012g0230 others(3): Show |
7 | HG02055.hp2 HG02258.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.1509+506_1509+507i others(4): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 5208768 | ||||||
| chr3:5208770 | T | C | 8 | a0001c0001t0012g0019 a0001c0001t0012g0229 a0001c0001t0012g0230 others(5): Show |
9 | HG02055.hp2 HG02258.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1509+507T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5208770 | |||||||
| chr3:5208770 | T | TAC | 8 | a0001c0001t0004g0236 a0001c0001t0009g0055 a0001c0001t0017g0023 others(5): Show |
9 | HG00408.hp1 HG01433.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1509+525_1509+526d others(4): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 5208770 | ||||||
| chr3:5208770 | TAC | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0029 a0001c0001t0001g0098 others(2): Show |
8 | HG00642.hp2 HG01168.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.1509+525_1509+526d others(4): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr3 | 5208770 | ||||||
| chr3:5208772 | C | T | 5 | a0001c0001t0038g0062 a0001c0004t0014g0012 a0001c0004t0014g0065 others(2): Show |
7 | HG01243.hp1 HG02109.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1509+509C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5208772 | |||||||
| chr3:5208790 | T | C | 1 | a0001c0001t0009g0051 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1509+527T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5208790 | |||||||
| chr3:5209039 | C | T | 4 | a0001c0001t0004g0250 a0001c0001t0004g0251 a0001c0001t0004g0252 others(1): Show |
4 | HG00544.hp2 HG02523.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.1509+776C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5209039 | |||||||
| chr3:5209040 | T | C | 2 | a0001c0001t0002g0244 a0001c0001t0003g0105 |
2 | NA18984.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.1509+777T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5209040 | |||||||
| chr3:5209429 | G | T | 1 | a0001c0001t0004g0252 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1510-746G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5209429 | |||||||
| chr3:5209617 | G | A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0140 a0001c0001t0001g0168 others(2): Show |
6 | HG00544.hp1 HG02129.hp2 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.1510-558G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5209617 | |||||||
| chr3:5209676 | G | A | 8 | a0001c0001t0017g0023 a0001c0001t0017g0066 a0001c0001t0038g0062 others(5): Show |
11 | HG01243.hp1 HG02109.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1510-499G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5209676 | |||||||
| chr3:5209755 | C | T | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1510-420C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5209755 | |||||||
| chr3:5209779 | C | T | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1510-396C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5209779 | |||||||
| chr3:5209799 | T | C | 10 | a0001c0001t0017g0023 a0001c0001t0017g0066 a0001c0001t0030g0241 others(7): Show |
13 | HG01243.hp1 HG02109.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1510-376T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5209799 | |||||||
| chr3:5209882 | A | G | 1 | a0001c0001t0008g0096 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1510-293A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5209882 | |||||||
| chr3:5209930 | A | G | 1 | a0001c0004t0014g0065 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1510-245A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5209930 | |||||||
| chr3:5209972 | A | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1510-203A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5209972 | |||||||
| chr3:5210098 | C | T | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1510-77C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 8/11 | chr3 | 5210098 | |||||||
| chr3:5210394 | G | A | 1 | a0001c0001t0023g0246 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1583+146G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210394 | |||||||
| chr3:5210428 | C | G | 1 | a0001c0001t0056g0045 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1583+180C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210428 | |||||||
| chr3:5210463 | G | T | 2 | a0001c0001t0025g0210 a0001c0001t0025g0211 |
2 | HG02027.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.1583+215G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210463 | |||||||
| chr3:5210491 | T | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1583+243T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210491 | |||||||
| chr3:5210505 | C | T | 5 | a0001c0004t0014g0012 a0001c0004t0014g0065 a0001c0004t0029g0064 others(2): Show |
7 | HG02109.hp2 HG02559.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1583+257C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210505 | |||||||
| chr3:5210634 | A | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1583+386A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210634 | |||||||
| chr3:5210655 | A | G | 1 | a0001c0001t0008g0146 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1583+407A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210655 | |||||||
| chr3:5210673 | A | G | 1 | a0001c0002t0005g0083 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1583+425A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210673 | |||||||
| chr3:5210714 | GT | G | 10 | a0001c0001t0017g0023 a0001c0001t0017g0066 a0001c0001t0030g0241 others(7): Show |
13 | HG01243.hp1 HG02280.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1584-395delT | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr3 | 5210714 | ||||||
| chr3:5210725 | T | A | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1584-395T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210725 | |||||||
| chr3:5210750 | A | G | 1 | a0001c0001t0002g0238 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1584-370A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210750 | |||||||
| chr3:5210831 | C | A | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1584-289C>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210831 | |||||||
| chr3:5210842 | G | A | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1584-278G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210842 | |||||||
| chr3:5210904 | C | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1584-216C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210904 | |||||||
| chr3:5210996 | A | T | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1584-124A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5210996 | |||||||
| chr3:5211006 | A | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1584-114A>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5211006 | |||||||
| chr3:5211103 | A | G | 11 | a0001c0001t0017g0023 a0001c0001t0017g0066 a0001c0001t0030g0241 others(8): Show |
14 | HG01243.hp1 HG02109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1584-17A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 9/11 | chr3 | 5211103 | |||||||
| chr3:5211251 | A | T | 1 | a0001c0005t0001g0164 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1680+35A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211251 | |||||||
| chr3:5211295 | G | A | 11 | a0001c0001t0017g0023 a0001c0001t0017g0066 a0001c0001t0030g0241 others(8): Show |
14 | HG01243.hp1 HG02109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1680+79G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211295 | |||||||
| chr3:5211315 | T | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1680+99T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211315 | |||||||
| chr3:5211349 | G | A | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1680+133G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211349 | |||||||
| chr3:5211350 | C | G | 1 | a0001c0001t0002g0047 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1680+134C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211350 | |||||||
| chr3:5211388 | T | G | 1 | a0001c0001t0062g0085 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1680+172T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211388 | |||||||
| chr3:5211472 | T | A | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1680+256T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211472 | |||||||
| chr3:5211651 | TGA | T | 6 | a0001c0001t0030g0241 a0001c0001t0038g0062 a0001c0004t0014g0012 others(3): Show |
8 | HG01243.hp1 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1680+437_1680+438d others(4): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr3 | 5211651 | ||||||
| chr3:5211653 | A | AGT | 25 | a0001c0001t0004g0197 a0001c0001t0005g0120 a0001c0001t0006g0191 others(22): Show |
27 | HG00558.hp1 HG01109.hp1 HG01515.hp2 others(24): Show |
intron_variant | MODIFIER | c.1680+472_1680+473d others(4): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr3 | 5211653 | ||||||
| chr3:5211653 | A | T | 1 | a0001c0002t0005g0042 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1680+437A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211653 | |||||||
| chr3:5211653 | AGT | A | 187 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(184): Show |
255 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1680+472_1680+473d others(4): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr3 | 5211653 | ||||||
| chr3:5211653 | AGTGT | A | 3 | a0001c0001t0002g0189 a0001c0001t0017g0023 a0001c0001t0017g0066 |
4 | HG02886.hp2 HG02922.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1680+470_1680+473d others(6): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr3 | 5211653 | ||||||
| chr3:5211676 | G | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(152): Show |
219 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1680+460G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211676 | |||||||
| chr3:5211721 | C | G | 1 | a0001c0001t0002g0186 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1680+505C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211721 | |||||||
| chr3:5211794 | G | A | 3 | a0001c0001t0021g0093 a0001c0001t0021g0094 a0001c0001t0027g0092 |
3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1680+578G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211794 | |||||||
| chr3:5211869 | C | T | 1 | a0001c0001t0005g0120 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1680+653C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211869 | |||||||
| chr3:5211876 | T | C | 260 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(257): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.1680+660T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211876 | |||||||
| chr3:5211884 | C | T | 1 | a0001c0002t0005g0079 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1680+668C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211884 | |||||||
| chr3:5211890 | C | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1680+674C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211890 | |||||||
| chr3:5211901 | A | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1680+685A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211901 | |||||||
| chr3:5211985 | G | A | 14 | a0001c0001t0001g0004 a0001c0001t0002g0004 a0001c0001t0002g0020 others(11): Show |
18 | HG00597.hp1 HG01257.hp1 HG01258.hp2 others(15): Show |
intron_variant | MODIFIER | c.1680+769G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5211985 | |||||||
| chr3:5212146 | G | A | 5 | a0001c0001t0002g0109 a0001c0001t0003g0010 a0001c0001t0003g0015 others(2): Show |
10 | NA18939.hp1 NA18940.hp2 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.1680+930G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5212146 | |||||||
| chr3:5212239 | C | T | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1680+1023C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5212239 | |||||||
| chr3:5212308 | C | T | 1 | a0001c0001t0009g0022 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1681-1011C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5212308 | |||||||
| chr3:5212362 | T | A | 1 | a0001c0001t0015g0165 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1681-957T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5212362 | |||||||
| chr3:5212470 | A | G | 10 | a0001c0001t0017g0023 a0001c0001t0017g0066 a0001c0001t0030g0241 others(7): Show |
13 | HG01243.hp1 HG02109.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1681-849A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5212470 | |||||||
| chr3:5212639 | A | G | 1 | a0001c0001t0006g0213 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1681-680A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5212639 | |||||||
| chr3:5212708 | G | C | 3 | a0001c0001t0021g0093 a0001c0001t0021g0094 a0001c0001t0027g0092 |
3 | HG02055.hp2 HG02258.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1681-611G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5212708 | |||||||
| chr3:5212708 | G | T | 1 | a0001c0001t0013g0052 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1681-611G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5212708 | |||||||
| chr3:5212770 | T | A | 8 | a0001c0001t0004g0197 a0001c0001t0004g0203 a0001c0001t0004g0219 others(5): Show |
8 | HG01891.hp1 HG02257.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1681-549T>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5212770 | |||||||
| chr3:5212818 | C | T | 10 | a0001c0001t0017g0023 a0001c0001t0017g0066 a0001c0001t0030g0241 others(7): Show |
13 | HG01243.hp1 HG02109.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.1681-501C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5212818 | |||||||
| chr3:5213000 | A | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(246): Show |
325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.1681-319A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5213000 | |||||||
| chr3:5213051 | T | C | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1681-268T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5213051 | |||||||
| chr3:5213054 | A | G | 11 | a0001c0001t0017g0023 a0001c0001t0017g0066 a0001c0001t0030g0241 others(8): Show |
14 | HG01243.hp1 HG02109.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1681-265A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5213054 | |||||||
| chr3:5213084 | G | A | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1681-235G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5213084 | |||||||
| chr3:5213164 | C | T | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1681-155C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5213164 | |||||||
| chr3:5213195 | G | C | 1 | a0001c0001t0004g0122 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1681-124G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 10/11 | chr3 | 5213195 | |||||||
| chr3:5213659 | C | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1884+137C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5213659 | |||||||
| chr3:5213684 | A | G | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1884+162A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5213684 | |||||||
| chr3:5213768 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1884+246G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5213768 | |||||||
| chr3:5213768 | G | C | 5 | a0001c0001t0001g0195 a0001c0001t0006g0213 a0001c0001t0006g0217 others(2): Show |
7 | HG00408.hp2 HG02896.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1884+246G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5213768 | |||||||
| chr3:5213809 | C | T | 2 | a0001c0001t0001g0143 a0001c0001t0002g0144 |
2 | HG01358.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1884+287C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5213809 | |||||||
| chr3:5214033 | G | T | 5 | a0001c0001t0004g0040 a0001c0001t0004g0041 a0001c0001t0004g0236 others(2): Show |
7 | HG00408.hp1 HG00423.hp1 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.1884+511G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214033 | |||||||
| chr3:5214107 | T | G | 1 | a0001c0018t0031g0057 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1884+585T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214107 | |||||||
| chr3:5214164 | G | A | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1884+642G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214164 | |||||||
| chr3:5214216 | T | C | 2 | a0001c0001t0001g0151 a0001c0001t0015g0165 |
2 | HG02083.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1884+694T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214216 | |||||||
| chr3:5214238 | T | C | 6 | a0001c0001t0011g0059 a0001c0001t0011g0060 a0001c0001t0011g0061 others(3): Show |
6 | HG02055.hp1 HG02572.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1884+716T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214238 | |||||||
| chr3:5214305 | C | T | 2 | a0001c0001t0004g0209 a0001c0001t0004g0252 |
2 | HG00544.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1884+783C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214305 | |||||||
| chr3:5214484 | G | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(160): Show |
229 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.1884+962G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214484 | |||||||
| chr3:5214509 | C | T | 1 | a0001c0001t0022g0043 | 2 | HG02738.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1884+987C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214509 | |||||||
| chr3:5214555 | C | T | 3 | a0001c0001t0030g0241 a0001c0001t0038g0062 a0001c0001t0039g0239 |
3 | HG01243.hp1 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1884+1033C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214555 | |||||||
| chr3:5214655 | T | G | 7 | a0001c0001t0017g0023 a0001c0001t0017g0066 a0001c0004t0014g0012 others(4): Show |
10 | HG02280.hp1 HG02559.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1884+1133T>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214655 | |||||||
| chr3:5214710 | G | C | 6 | a0001c0001t0009g0051 a0001c0002t0005g0024 a0001c0002t0005g0076 others(3): Show |
6 | NA18943.hp1 NA18969.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.1885-1119G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214710 | |||||||
| chr3:5214719 | G | T | 1 | a0001c0001t0002g0132 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1885-1110G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214719 | |||||||
| chr3:5214850 | C | T | 1 | a0001c0001t0010g0046 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1885-979C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214850 | |||||||
| chr3:5214900 | C | T | 1 | a0001c0001t0019g0224 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1885-929C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214900 | |||||||
| chr3:5214995 | C | T | 4 | a0001c0001t0006g0087 a0001c0001t0006g0088 a0001c0002t0005g0026 others(1): Show |
5 | HG02280.hp1 HG02451.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1885-834C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5214995 | |||||||
| chr3:5215014 | G | C | 16 | a0001c0001t0006g0213 a0001c0001t0006g0217 a0001c0001t0011g0059 others(13): Show |
16 | HG01106.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1885-815G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215014 | |||||||
| chr3:5215033 | C | G | 1 | a0001c0001t0003g0176 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1885-796C>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215033 | |||||||
| chr3:5215034 | A | T | 1 | a0001c0001t0002g0047 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1885-795A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215034 | |||||||
| chr3:5215078 | G | A | 1 | a0001c0001t0030g0241 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1885-751G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215078 | |||||||
| chr3:5215080 | G | T | 3 | a0001c0001t0001g0138 a0001c0001t0001g0157 a0001c0001t0001g0180 |
3 | HG01952.hp1 HG01978.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1885-749G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215080 | |||||||
| chr3:5215097 | A | T | 242 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(239): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.1885-732A>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215097 | |||||||
| chr3:5215099 | G | T | 1 | a0001c0001t0005g0120 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1885-730G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215099 | |||||||
| chr3:5215107 | C | T | 3 | a0001c0001t0002g0117 a0001c0001t0003g0137 a0002c0003t0001g0035 |
4 | NA18964.hp2 NA18975.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1885-722C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215107 | |||||||
| chr3:5215171 | G | A | 270 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(267): Show |
347 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.1885-658G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215171 | |||||||
| chr3:5215223 | A | G | 1 | a0001c0001t0040g0214 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1885-606A>G | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215223 | |||||||
| chr3:5215271 | G | C | 2 | a0001c0001t0062g0085 a0001c0002t0018g0070 |
2 | HG02630.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1885-558G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215271 | |||||||
| chr3:5215294 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1885-535G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215294 | |||||||
| chr3:5215299 | G | A | 2 | a0001c0004t0029g0064 a0001c0012t0058g0110 |
2 | HG02280.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1885-530G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215299 | |||||||
| chr3:5215312 | T | TA | 27 | a0001c0001t0001g0029 a0001c0001t0001g0100 a0001c0001t0001g0103 others(24): Show |
29 | HG00408.hp2 HG00642.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.1885-514dupA | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr3 | 5215312 | ||||||
| chr3:5215316 | G | A | 27 | a0001c0001t0001g0029 a0001c0001t0001g0100 a0001c0001t0001g0103 others(24): Show |
29 | HG00408.hp2 HG00642.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.1885-513G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215316 | |||||||
| chr3:5215341 | T | C | 1 | a0001c0001t0003g0108 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1885-488T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215341 | |||||||
| chr3:5215341 | TAGTG | T | 8 | a0001c0001t0004g0197 a0001c0001t0004g0203 a0001c0001t0004g0219 others(5): Show |
8 | HG01243.hp1 HG02257.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1885-484_1885-481d others(6): Show |
EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr3 | 5215341 | ||||||
| chr3:5215345 | G | T | 7 | a0001c0001t0002g0002 a0001c0001t0021g0094 a0001c0001t0027g0092 others(4): Show |
9 | HG00642.hp1 HG01433.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.1885-484G>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215345 | |||||||
| chr3:5215393 | G | A | 91 | a0001c0001t0001g0005 a0001c0001t0001g0114 a0001c0001t0001g0140 others(88): Show |
107 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.1885-436G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215393 | |||||||
| chr3:5215422 | C | T | 2 | a0001c0001t0006g0213 a0001c0001t0006g0217 |
2 | HG02896.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1885-407C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215422 | |||||||
| chr3:5215430 | G | C | 16 | a0001c0001t0001g0097 a0001c0001t0009g0022 a0001c0001t0009g0044 others(13): Show |
20 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.1885-399G>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215430 | |||||||
| chr3:5215463 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1885-366C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215463 | |||||||
| chr3:5215464 | G | A | 1 | a0001c0001t0004g0250 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1885-365G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215464 | |||||||
| chr3:5215477 | C | T | 2 | a0001c0001t0038g0062 a0001c0012t0058g0110 |
2 | HG01243.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.1885-352C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215477 | |||||||
| chr3:5215482 | C | T | 1 | a0001c0012t0058g0110 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1885-347C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215482 | |||||||
| chr3:5215491 | T | C | 1 | a0001c0001t0038g0062 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1885-338T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215491 | |||||||
| chr3:5215493 | C | T | 1 | a0001c0001t0038g0062 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1885-336C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215493 | |||||||
| chr3:5215528 | G | A | 1 | a0001c0001t0038g0062 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1885-301G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215528 | |||||||
| chr3:5215530 | T | C | 1 | a0001c0001t0039g0239 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1885-299T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215530 | |||||||
| chr3:5215690 | G | A | 12 | a0001c0001t0017g0023 a0001c0001t0017g0066 a0001c0001t0021g0093 others(9): Show |
15 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1885-139G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215690 | |||||||
| chr3:5215700 | C | T | 2 | a0001c0001t0004g0115 a0001c0001t0004g0116 |
2 | NA18998.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1885-129C>T | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215700 | |||||||
| chr3:5215729 | T | C | 1 | a0001c0002t0026g0082 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1885-100T>C | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215729 | |||||||
| chr3:5215813 | G | A | 2 | a0001c0001t0003g0173 a0001c0001t0003g0177 |
2 | HG03942.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.1885-16G>A | EDEM1 | ENSG00000134109.11 | transcript | ENST00000256497.9 | protein_coding | 11/11 | chr3 | 5215813 |