Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57222 |
| ensemblid | ENSG00000113719.17 |
| hgncid | 29205 |
| symbol | ERGIC1 |
| name | endoplasmic reticulum-golgi intermediate compartment 1 |
| refseq_nuc | NM_001031711.3 |
| refseq_prot | NP_001026881.1 |
| ensembl_nuc | ENST00000393784.8 |
| ensembl_prot | ENSP00000377374.3 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 172834251 |
| end | 172952683 |
| strand | + |
| ver | v1.2 |
| region | chr5:172834251-172952683 |
| region5000 | chr5:172829251-172957683 |
| regionname0 | ERGIC1_chr5_172834251_172952683 |
| regionname5000 | ERGIC1_chr5_172829251_172957683 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 290 | 332 | 87 | 70 | 123 | 10 | 40 | 86 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | MPFDF others(285): Show |
chr5 | 172829251 | 172957683 |
| a0002 | 0/0 | 290 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | MPFDF others(285): Show |
chr5 | 172829251 | 172957683 |
| a0003 | 0/0 | 290 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | MPFDF others(285): Show |
chr5 | 172829251 | 172957683 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 870 | 330 | 86 | 70 | 122 | 10 | 40 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ATGCC others(865): Show |
chr5 | 172829251 | 172957683 | ||
| a0001c0002 | 0/0 | 870 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ATGCC others(865): Show |
chr5 | 172829251 | 172957683 | ||
| a0001c0005 | 0/0 | 870 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ATGCC others(865): Show |
chr5 | 172829251 | 172957683 | ||
| a0002c0003 | 0/0 | 870 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ATGCC others(865): Show |
chr5 | 172829251 | 172957683 | ||
| a0003c0004 | 0/0 | 870 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ATGCC others(865): Show |
chr5 | 172829251 | 172957683 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2905 | 177 | 15 | 40 | 96 | 6 | 20 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2900): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0002 | 1/0 | 2903 | 63 | 7 | 24 | 13 | 4 | 14 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2898): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0003 | 0/0 | 2908 | 28 | 23 | 2 | 1 | 0 | 2 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2903): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0004 | 0/0 | 2904 | 10 | 1 | 0 | 9 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2899): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0005 | 0/0 | 2907 | 10 | 9 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2902): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0006 | 0/0 | 2907 | 8 | 7 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2902): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0007 | 0/0 | 2903 | 3 | 3 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2898): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0008 | 0/0 | 2908 | 3 | 3 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2903): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0009 | 0/0 | 2915 | 2 | 2 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2910): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0010 | 0/0 | 2903 | 2 | 2 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2898): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0011 | 0/0 | 2903 | 2 | 0 | 0 | 0 | 0 | 2 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2898): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0012 | 0/0 | 2910 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2905): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0013 | 0/0 | 2907 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2902): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0014 | 0/0 | 2907 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2902): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0015 | 0/0 | 2903 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2898): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0016 | 0/0 | 2907 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2902): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0017 | 0/0 | 2905 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2900): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0019 | 0/0 | 2905 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2900): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0020 | 0/0 | 2905 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2900): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0021 | 0/1 | 2903 | 1 | 0 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2898): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0022 | 0/0 | 2905 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2900): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0023 | 0/0 | 2903 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2898): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0024 | 0/0 | 2905 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2900): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0025 | 0/0 | 2905 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2900): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0026 | 0/0 | 2905 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2900): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0027 | 0/0 | 2908 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2903): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0028 | 0/0 | 2905 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2900): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0029 | 0/0 | 2903 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2898): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0030 | 0/0 | 2907 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2902): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0031 | 0/0 | 2906 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2901): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0032 | 0/0 | 2902 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2897): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0033 | 0/0 | 2907 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2902): Show |
chr5 | 172829251 | 172957683 |
| a0001c0001t0034 | 0/0 | 2902 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2897): Show |
chr5 | 172829251 | 172957683 |
| a0001c0002t0001 | 0/0 | 2905 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2900): Show |
chr5 | 172829251 | 172957683 |
| a0001c0005t0018 | 0/0 | 2903 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2898): Show |
chr5 | 172829251 | 172957683 |
| a0002c0003t0002 | 0/0 | 2903 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2898): Show |
chr5 | 172829251 | 172957683 |
| a0003c0004t0003 | 0/0 | 2908 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | ACTTC others(2903): Show |
chr5 | 172829251 | 172957683 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0300 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0003g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0004g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0005g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0005g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0005g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0005g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0005g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0005g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0006g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0006g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0006g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0006g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0006g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0006g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0006g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0007g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0007g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0007g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0008g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0008g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0008g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0009g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0009g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0010g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0010g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0011g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0011g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0012g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0013g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0014g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0015g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0016g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0017g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0019g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0020g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0021g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0022g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0023g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0024g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0025g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0026g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0027g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0028g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0029g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0030g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0031g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0032g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0033g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0001t0034g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0001c0005t0018g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0002c0003t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| a0003c0004t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0138 | EUR | GBR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | GBR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0093 | EUR | FIN | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0115 | EUR | FIN | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0139 | EUR | FIN | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0216 | EUR | FIN | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | CHS | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00438 | hp1 | a0002 | c0003 | t0002 | g0012 | EAS | CHS | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | CHS | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | CHS | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0101 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0319 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0278 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01109 | hp2 | a0001 | c0001 | t0005 | g0105 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0287 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01175 | hp2 | a0001 | c0001 | t0020 | g0078 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0055 | AMR | PUR | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | CLM | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | CLM | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | CLM | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | CLM | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0239 | AMR | CLM | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01261 | hp2 | a0001 | c0001 | t0028 | g0088 | AMR | CLM | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | CLM | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0064 | EUR | IBS | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | ACB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01884 | hp2 | a0001 | c0001 | t0030 | g0089 | AFR | ACB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0285 | AMR | PEL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0280 | AMR | PEL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0095 | AMR | PEL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0275 | AMR | PEL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0284 | AFR | ACB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02055 | hp2 | a0001 | c0001 | t0032 | g0084 | AFR | ACB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | KHV | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0180 | EAS | KHV | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | ACB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0293 | AFR | ACB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CDX | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CDX | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | CDX | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CDX | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02280 | hp1 | a0001 | c0001 | t0005 | g0162 | AFR | ACB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02280 | hp2 | a0001 | c0001 | t0009 | g0330 | AFR | ACB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0253 | AMR | PEL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PEL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PEL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | ACB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02451 | hp2 | a0001 | c0001 | t0009 | g0329 | AFR | ACB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02523 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | KHV | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02572 | hp1 | a0001 | c0001 | t0012 | g0331 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0277 | SAS | PJL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0145 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0156 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0270 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0274 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02630 | hp2 | a0001 | c0001 | t0007 | g0281 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0272 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0297 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0098 | SAS | PJL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02717 | hp1 | a0001 | c0001 | t0007 | g0282 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02717 | hp2 | a0001 | c0001 | t0003 | g0271 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0004 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0269 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0229 | SAS | PJL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02809 | hp1 | a0001 | c0001 | t0027 | g0091 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0273 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0198 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0155 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02886 | hp1 | a0001 | c0001 | t0034 | g0086 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02895 | hp1 | a0001 | c0001 | t0014 | g0173 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02896 | hp1 | a0001 | c0001 | t0008 | g0150 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0309 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02897 | hp1 | a0001 | c0001 | t0010 | g0189 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02897 | hp2 | a0001 | c0001 | t0008 | g0187 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0308 | AFR | ESN | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0311 | AFR | ESN | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0206 | AFR | ESN | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | ESN | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02970 | hp2 | a0001 | c0005 | t0018 | g0161 | AFR | ESN | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0154 | AFR | ESN | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0333 | AFR | ESN | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03041 | hp1 | a0001 | c0001 | t0008 | g0205 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0316 | AFR | MSL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03098 | hp2 | a0001 | c0001 | t0033 | g0085 | AFR | MSL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03130 | hp1 | a0001 | c0001 | t0007 | g0314 | AFR | ESN | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0326 | AFR | ESN | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03139 | hp1 | a0001 | c0001 | t0022 | g0315 | AFR | ESN | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03139 | hp2 | a0001 | c0001 | t0013 | g0291 | AFR | ESN | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03195 | hp2 | a0001 | c0001 | t0006 | g0184 | AFR | ESN | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | MSL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03209 | hp2 | a0001 | c0001 | t0005 | g0266 | AFR | MSL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0294 | AFR | MSL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0106 | AFR | MSL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0283 | AFR | MSL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03453 | hp2 | a0001 | c0001 | t0029 | g0131 | AFR | MSL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0301 | AFR | MSL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | MSL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0028 | SAS | PJL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0061 | AFR | ESN | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03516 | hp2 | a0001 | c0001 | t0010 | g0058 | AFR | ESN | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0318 | SAS | PJL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0034 | SAS | PJL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03669 | hp1 | a0001 | c0001 | t0017 | g0234 | SAS | PJL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | STU | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | STU | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0212 | SAS | PJL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03831 | hp1 | a0001 | c0001 | t0011 | g0099 | SAS | BEB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0324 | SAS | BEB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03942 | hp2 | a0001 | c0001 | t0011 | g0117 | SAS | BEB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG04115 | hp1 | a0001 | c0001 | t0024 | g0323 | SAS | STU | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | STU | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | BEB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | STU | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG04199 | hp2 | a0001 | c0001 | t0003 | g0035 | SAS | STU | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0147 | SAS | STU | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | STU | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | STU | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | STU | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0296 | AFR | YRI | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | YRI | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18612 | hp1 | a0001 | c0001 | t0004 | g0178 | EAS | CHB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | CHB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0298 | AFR | YRI | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0292 | AFR | YRI | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18939 | hp1 | a0001 | c0001 | t0004 | g0108 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18951 | hp2 | a0001 | c0001 | t0025 | g0045 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18953 | hp2 | a0001 | c0001 | t0004 | g0176 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18954 | hp1 | a0001 | c0001 | t0004 | g0247 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0251 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18966 | hp1 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18966 | hp2 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18970 | hp1 | a0001 | c0001 | t0004 | g0166 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18971 | hp2 | a0001 | c0001 | t0026 | g0215 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0299 | AFR | LWK | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19030 | hp2 | a0001 | c0001 | t0031 | g0083 | AFR | LWK | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19057 | hp1 | a0001 | c0001 | t0004 | g0023 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0328 | AFR | YRI | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | YRI | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0334 | AFR | ASW | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA20129 | hp2 | a0001 | c0001 | t0016 | g0197 | AFR | ASW | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0146 | EUR | TSI | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | TSI | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | GIH | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0135 | SAS | GIH | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | CLM | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG01123 | hp2 | a0001 | c0001 | t0019 | g0068 | AMR | CLM | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | ACB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | ACB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0107 | AFR | ACB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0210 | AFR | ACB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0192 | AFR | ACB | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0267 | AFR | MSL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG03471 | hp2 | a0001 | c0001 | t0006 | g0310 | AFR | MSL | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | USA | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| HG06807 | hp2 | a0003 | c0004 | t0003 | g0312 | AFR | USA | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | USA | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA20300 | hp2 | a0001 | c0001 | t0023 | g0332 | AFR | USA | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0053 | AFR | LWK | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| NA21309 | hp2 | a0001 | c0001 | t0015 | g0199 | AFR | LWK | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0021 | g0076 | REF | REF | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0300 | REF | REF | ERGIC1_chr5_172829251_172957683 | ERGIC1 | chr5 | 172829251 | 172957683 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:172914785 | C | T | 1 | a0003 | 1 | HG06807.hp2 | missense_variant | MODERATE | c.322C>T | p.Pro108Ser | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/10 | 485/2903 | 322/873 | 108/290 | chr5 | 172914785 | |||
| chr5:172914797 | G | T | 1 | a0002 | 1 | HG00438.hp1 | missense_variant | MODERATE | c.334G>T | p.Gly112Trp | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/10 | 497/2903 | 334/873 | 112/290 | chr5 | 172914797 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:172909685 | C | T | 1 | a0001c0005 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.174C>T | p.Val58Val | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/10 | 337/2903 | 174/873 | 58/290 | chr5 | 172909685 | |||
| chr5:172924010 | C | T | 1 | a0001c0002 | 1 | NA18959.hp2 | synonymous_variant | LOW | c.381C>T | p.Pro127Pro | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/10 | 544/2903 | 381/873 | 127/290 | chr5 | 172924010 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:172834267 | A | AGGCGAGT | 2 | a0001c0001t0009 a0001c0001t0012 |
3 | HG02280.hp2 HG02451.hp2 HG02572.hp1 |
5_prime_UTR_variant | MODIFIER | c.-124_-118dupGCGAGT others(1): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/10 | 117 | INFO_REALIGN_3_PRIME | chr5 | 172834267 | |||||
| chr5:172834298 | CA | C | 4 | a0001c0001t0031 a0001c0001t0032 a0001c0001t0033 others(1): Show |
4 | HG02055.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-115delA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/10 | 115 | chr5 | 172834298 | ||||||
| chr5:172834401 | C | T | 4 | a0001c0001t0027 a0001c0001t0028 a0001c0001t0029 others(1): Show |
4 | HG01261.hp2 HG01884.hp2 HG02809.hp1 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-13C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/10 | chr5 | 172834401 | |||||||
| chr5:172950873 | G | T | 1 | a0001c0001t0008 | 3 | HG02896.hp1 HG02897.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*57G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 10/10 | 57 | chr5 | 172950873 | ||||||
| chr5:172951116 | G | A | 1 | a0001c0001t0013 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*300G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 10/10 | 300 | chr5 | 172951116 | ||||||
| chr5:172951181 | A | G | 1 | a0001c0001t0013 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*365A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 10/10 | 365 | chr5 | 172951181 | ||||||
| chr5:172951627 | A | C | 1 | a0001c0001t0026 | 1 | NA18971.hp2 | 3_prime_UTR_variant | MODIFIER | c.*811A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 10/10 | 811 | chr5 | 172951627 | ||||||
| chr5:172951643 | A | G | 1 | a0001c0001t0025 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*827A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 10/10 | 827 | chr5 | 172951643 | ||||||
| chr5:172951785 | C | A | 4 | a0001c0001t0010 a0001c0001t0014 a0001c0001t0031 others(1): Show |
5 | HG02055.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*969C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 10/10 | 969 | chr5 | 172951785 | ||||||
| chr5:172951786 | C | T | 1 | a0001c0001t0024 | 1 | HG04115.hp1 | 3_prime_UTR_variant | MODIFIER | c.*970C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 10/10 | 970 | chr5 | 172951786 | ||||||
| chr5:172951817 | T | C | 1 | a0001c0001t0015 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1001T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 10/10 | 1001 | chr5 | 172951817 | ||||||
| chr5:172951853 | G | T | 3 | a0001c0001t0005 a0001c0001t0023 a0001c0001t0030 |
12 | HG01109.hp2 HG01884.hp2 HG02280.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1037G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 10/10 | 1037 | chr5 | 172951853 | ||||||
| chr5:172951854 | T | C | 19 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(16): Show |
68 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*1038T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 10/10 | 1038 | chr5 | 172951854 | ||||||
| chr5:172951857 | G | C | 1 | a0001c0001t0017 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1041G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 10/10 | 1041 | chr5 | 172951857 | ||||||
| chr5:172951866 | T | C | 1 | a0001c0005t0018 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1050T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 10/10 | 1050 | chr5 | 172951866 | ||||||
| chr5:172951915 | C | T | 1 | a0001c0001t0022 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1099C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 10/10 | 1099 | chr5 | 172951915 | ||||||
| chr5:172952019 | G | T | 1 | a0001c0001t0011 | 2 | HG03831.hp1 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1203G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 10/10 | 1203 | chr5 | 172952019 | ||||||
| chr5:172952279 | G | A | 2 | a0001c0001t0016 a0001c0001t0019 |
2 | HG01123.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1463G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 10/10 | 1463 | chr5 | 172952279 | ||||||
| chr5:172952520 | G | GA | 1 | a0001c0001t0004 | 10 | HG02074.hp2 HG03130.hp2 NA18612.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1717dupA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 10/10 | 1718 | INFO_REALIGN_3_PRIME | chr5 | 172952520 | |||||
| chr5:172952520 | G | GAA | 10 | a0001c0001t0001 a0001c0001t0017 a0001c0001t0019 others(7): Show |
186 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(183): Show |
3_prime_UTR_variant | MODIFIER | c.*1716_*1717dupAA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 10/10 | 1718 | INFO_REALIGN_3_PRIME | chr5 | 172952520 | |||||
| chr5:172952533 | A | AAAAAC | 6 | a0001c0001t0003 a0001c0001t0008 a0001c0001t0009 others(3): Show |
36 | HG00408.hp2 HG00639.hp2 HG01243.hp2 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*1717_*1718insAAAA others(1): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 10/10 | 1718 | chr5 | 172952533 | ||||||
| chr5:172952533 | A | AAAAC | 7 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0013 others(4): Show |
23 | HG01109.hp2 HG01884.hp2 HG02280.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*1717_*1718insAAAC | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 10/10 | 1718 | chr5 | 172952533 | ||||||
| chr5:172952534 | C | A | 1 | a0001c0001t0020 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1718C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 10/10 | 1718 | chr5 | 172952534 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:172834459 | G | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(77): Show |
80 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.20+26G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172834459 | |||||||
| chr5:172834486 | C | A | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(82): Show |
85 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.20+53C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172834486 | |||||||
| chr5:172834535 | C | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(81): Show |
84 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.20+102C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172834535 | |||||||
| chr5:172834540 | C | T | 1 | a0001c0001t0003g0334 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.20+107C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172834540 | |||||||
| chr5:172834580 | G | GC | 79 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0126 others(76): Show |
79 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.20+156dupC | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172834580 | ||||||
| chr5:172834580 | G | GCC | 35 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0096 others(32): Show |
35 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.20+155_20+156dupCC | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172834580 | ||||||
| chr5:172834580 | GC | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(90): Show |
93 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.20+156delC | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172834580 | ||||||
| chr5:172834589 | CT | C | 82 | a0001c0001t0001g0081 a0001c0001t0001g0201 a0001c0001t0001g0202 others(79): Show |
82 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.20+157delT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172834589 | |||||||
| chr5:172834590 | T | C | 139 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0096 others(136): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.20+157T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172834590 | |||||||
| chr5:172834695 | C | T | 89 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(86): Show |
89 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.20+262C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172834695 | |||||||
| chr5:172834939 | G | A | 9 | a0001c0001t0001g0325 a0001c0001t0001g0327 a0001c0001t0002g0122 others(6): Show |
9 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.20+506G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172834939 | |||||||
| chr5:172834994 | G | T | 1 | a0001c0001t0001g0121 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.20+561G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172834994 | |||||||
| chr5:172835165 | C | T | 10 | a0001c0001t0001g0325 a0001c0001t0001g0327 a0001c0001t0002g0122 others(7): Show |
10 | HG02055.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.20+732C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172835165 | |||||||
| chr5:172835201 | A | G | 4 | a0001c0001t0031g0083 a0001c0001t0032g0084 a0001c0001t0033g0085 others(1): Show |
4 | HG02055.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.20+768A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172835201 | |||||||
| chr5:172835247 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.20+814A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172835247 | |||||||
| chr5:172835479 | T | TA | 43 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0096 others(40): Show |
43 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.20+1047dupA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172835479 | ||||||
| chr5:172835482 | C | G | 2 | a0001c0001t0001g0079 a0001c0001t0020g0078 |
2 | HG01175.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.20+1049C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172835482 | |||||||
| chr5:172835520 | T | G | 4 | a0001c0001t0001g0325 a0001c0001t0004g0326 a0001c0001t0007g0281 others(1): Show |
4 | HG02109.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.20+1087T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172835520 | |||||||
| chr5:172835650 | C | A | 1 | a0001c0001t0001g0201 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.20+1217C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172835650 | |||||||
| chr5:172835670 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(83): Show |
86 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.20+1237C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172835670 | |||||||
| chr5:172835688 | C | T | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.20+1255C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172835688 | |||||||
| chr5:172835738 | C | G | 115 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0193 others(112): Show |
115 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.20+1305C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172835738 | |||||||
| chr5:172835839 | A | T | 89 | a0001c0001t0001g0200 a0001c0001t0001g0201 a0001c0001t0001g0202 others(86): Show |
89 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.20+1406A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172835839 | |||||||
| chr5:172835864 | C | G | 122 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0193 others(119): Show |
122 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.20+1431C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172835864 | |||||||
| chr5:172835875 | G | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(209): Show |
212 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.20+1442G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172835875 | |||||||
| chr5:172835990 | A | G | 107 | a0001c0001t0001g0090 a0001c0001t0001g0092 a0001c0001t0001g0096 others(104): Show |
107 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.20+1557A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172835990 | |||||||
| chr5:172836004 | C | T | 1 | a0001c0001t0003g0101 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.20+1571C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172836004 | |||||||
| chr5:172836012 | G | T | 1 | a0001c0001t0002g0280 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.20+1579G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172836012 | |||||||
| chr5:172836013 | C | T | 1 | a0001c0001t0003g0328 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.20+1580C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172836013 | |||||||
| chr5:172836254 | G | C | 4 | a0001c0001t0001g0325 a0001c0001t0004g0326 a0001c0001t0007g0281 others(1): Show |
4 | HG02109.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.20+1821G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172836254 | |||||||
| chr5:172836275 | G | A | 1 | a0001c0001t0002g0317 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.20+1842G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172836275 | |||||||
| chr5:172836446 | T | C | 4 | a0001c0001t0001g0325 a0001c0001t0004g0326 a0001c0001t0007g0281 others(1): Show |
4 | HG02109.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.20+2013T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172836446 | |||||||
| chr5:172836523 | G | A | 112 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0193 others(109): Show |
112 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.20+2090G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172836523 | |||||||
| chr5:172836602 | C | T | 2 | a0001c0001t0001g0118 a0001c0001t0001g0303 |
2 | NA18979.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.20+2169C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172836602 | |||||||
| chr5:172836610 | A | G | 116 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0193 others(113): Show |
116 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.20+2177A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172836610 | |||||||
| chr5:172836780 | C | T | 1 | a0001c0001t0001g0279 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.20+2347C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172836780 | |||||||
| chr5:172836781 | G | A | 1 | a0001c0001t0002g0082 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.20+2348G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172836781 | |||||||
| chr5:172836786 | C | G | 13 | a0001c0001t0001g0268 a0001c0001t0001g0276 a0001c0001t0001g0277 others(10): Show |
13 | HG01071.hp1 HG01993.hp2 HG02602.hp2 others(10): Show |
intron_variant | MODIFIER | c.20+2353C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172836786 | |||||||
| chr5:172836789 | G | C | 1 | a0001c0001t0001g0202 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.20+2356G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172836789 | |||||||
| chr5:172836830 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.20+2397G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172836830 | |||||||
| chr5:172836855 | G | T | 1 | a0001c0001t0003g0328 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.20+2422G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172836855 | |||||||
| chr5:172836919 | C | G | 112 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0193 others(109): Show |
112 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(109): Show |
intron_variant | MODIFIER | c.20+2486C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172836919 | |||||||
| chr5:172837181 | G | T | 23 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0193 others(20): Show |
23 | HG00544.hp2 HG01884.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.20+2748G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172837181 | |||||||
| chr5:172837230 | T | C | 1 | a0001c0001t0001g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.20+2797T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172837230 | |||||||
| chr5:172837286 | C | T | 3 | a0001c0001t0009g0329 a0001c0001t0009g0330 a0001c0001t0012g0331 |
3 | HG02280.hp2 HG02451.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.20+2853C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172837286 | |||||||
| chr5:172837412 | A | T | 1 | a0001c0001t0001g0100 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.20+2979A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172837412 | |||||||
| chr5:172837459 | T | A | 1 | a0001c0001t0001g0123 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.20+3026T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172837459 | |||||||
| chr5:172837719 | G | A | 3 | a0001c0001t0001g0327 a0001c0001t0002g0333 a0001c0001t0003g0328 |
3 | HG02451.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.20+3286G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172837719 | |||||||
| chr5:172837833 | C | CGT | 4 | a0001c0001t0031g0083 a0001c0001t0032g0084 a0001c0001t0033g0085 others(1): Show |
4 | HG02055.hp2 HG02886.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.20+3407_20+3408dup others(2): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172837833 | ||||||
| chr5:172838232 | G | C | 181 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(178): Show |
181 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(178): Show |
intron_variant | MODIFIER | c.20+3799G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172838232 | |||||||
| chr5:172838284 | T | A | 1 | a0001c0001t0002g0318 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.20+3851T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172838284 | |||||||
| chr5:172838337 | A | G | 91 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(88): Show |
91 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.20+3904A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172838337 | |||||||
| chr5:172838397 | G | A | 79 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(76): Show |
79 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.20+3964G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172838397 | |||||||
| chr5:172838684 | G | C | 1 | a0001c0001t0001g0123 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.20+4251G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172838684 | |||||||
| chr5:172838866 | A | C | 2 | a0001c0001t0002g0191 a0001c0001t0011g0117 |
2 | HG03942.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.20+4433A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172838866 | |||||||
| chr5:172838949 | A | T | 3 | a0001c0001t0001g0327 a0001c0001t0002g0333 a0001c0001t0003g0328 |
3 | HG02451.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.20+4516A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172838949 | |||||||
| chr5:172839240 | C | CA | 7 | a0001c0001t0001g0124 a0001c0001t0001g0149 a0001c0001t0001g0288 others(4): Show |
7 | HG01167.hp2 HG01192.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.20+4827dupA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172839240 | ||||||
| chr5:172839240 | CA | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0190 others(103): Show |
106 | HG00323.hp2 HG00408.hp2 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.20+4827delA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172839240 | ||||||
| chr5:172839261 | G | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0005g0005 others(2): Show |
5 | HG02523.hp2 HG02723.hp1 NA19065.hp2 others(2): Show |
intron_variant | MODIFIER | c.20+4828G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172839261 | |||||||
| chr5:172839261 | G | GTA | 75 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(72): Show |
75 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.20+4838_20+4839dup others(2): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172839261 | ||||||
| chr5:172839261 | G | GTATA | 3 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0002g0008 |
3 | HG01346.hp1 HG01346.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.20+4836_20+4839dup others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172839261 | ||||||
| chr5:172839322 | A | G | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(208): Show |
211 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(208): Show |
intron_variant | MODIFIER | c.20+4889A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172839322 | |||||||
| chr5:172839378 | GCAAGACC | G | 3 | a0001c0001t0001g0327 a0001c0001t0002g0333 a0001c0001t0003g0328 |
3 | HG02451.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.20+4947_20+4953del others(7): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172839378 | ||||||
| chr5:172839380 | AAGACCCC | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(205): Show |
208 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.20+4956_20+4962del others(7): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172839380 | ||||||
| chr5:172839387 | C | G | 3 | a0001c0001t0001g0327 a0001c0001t0002g0333 a0001c0001t0003g0328 |
3 | HG02451.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.20+4954C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172839387 | |||||||
| chr5:172839457 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.20+5024G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172839457 | |||||||
| chr5:172839496 | G | A | 2 | a0001c0001t0002g0010 a0001c0001t0002g0011 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.20+5063G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172839496 | |||||||
| chr5:172839600 | CACACAT | C | 4 | a0001c0001t0001g0325 a0001c0001t0004g0326 a0001c0001t0007g0281 others(1): Show |
4 | HG02109.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.20+5181_20+5186del others(6): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172839600 | ||||||
| chr5:172839685 | C | T | 3 | a0001c0001t0001g0327 a0001c0001t0002g0333 a0001c0001t0003g0328 |
3 | HG02451.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.20+5252C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172839685 | |||||||
| chr5:172839855 | G | A | 3 | a0001c0001t0001g0327 a0001c0001t0002g0333 a0001c0001t0003g0328 |
3 | HG02451.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.20+5422G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172839855 | |||||||
| chr5:172839871 | T | A | 1 | a0001c0001t0001g0123 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.20+5438T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172839871 | |||||||
| chr5:172840035 | G | A | 1 | a0001c0001t0009g0329 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.20+5602G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172840035 | |||||||
| chr5:172840136 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.20+5703C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172840136 | |||||||
| chr5:172840154 | CACGCTG | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0200 others(83): Show |
86 | HG00323.hp2 HG00408.hp2 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.20+5724_20+5729del others(6): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172840154 | ||||||
| chr5:172840199 | C | T | 13 | a0001c0001t0001g0202 a0001c0001t0001g0204 a0001c0001t0001g0252 others(10): Show |
13 | HG01433.hp2 HG01975.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.20+5766C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172840199 | |||||||
| chr5:172840207 | G | A | 84 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(81): Show |
84 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.20+5774G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172840207 | |||||||
| chr5:172840381 | C | T | 4 | a0001c0001t0001g0325 a0001c0001t0004g0326 a0001c0001t0007g0281 others(1): Show |
4 | HG02109.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.20+5948C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172840381 | |||||||
| chr5:172840567 | G | A | 3 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0005g0206 |
3 | HG01257.hp2 HG01258.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.20+6134G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172840567 | |||||||
| chr5:172840619 | G | T | 6 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(3): Show |
6 | HG02015.hp2 NA18953.hp1 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.20+6186G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172840619 | |||||||
| chr5:172841000 | A | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(206): Show |
209 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.20+6567A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172841000 | |||||||
| chr5:172841020 | C | T | 3 | a0001c0001t0003g0328 a0001c0001t0003g0334 a0001c0001t0023g0332 |
3 | NA19240.hp1 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.20+6587C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172841020 | |||||||
| chr5:172841038 | T | C | 2 | a0001c0001t0001g0327 a0001c0001t0002g0333 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.20+6605T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172841038 | |||||||
| chr5:172841053 | G | A | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(316): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.20+6620G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172841053 | |||||||
| chr5:172841085 | G | C | 3 | a0001c0001t0001g0268 a0001c0001t0003g0267 a0001c0001t0005g0266 |
3 | HG03209.hp2 HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.20+6652G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172841085 | |||||||
| chr5:172841240 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.20+6807A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172841240 | |||||||
| chr5:172841253 | C | T | 2 | a0001c0001t0001g0202 a0001c0001t0001g0260 |
2 | NA18969.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.20+6820C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172841253 | |||||||
| chr5:172841254 | G | A | 3 | a0001c0001t0003g0328 a0001c0001t0003g0334 a0001c0001t0023g0332 |
3 | NA19240.hp1 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.20+6821G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172841254 | |||||||
| chr5:172841558 | G | C | 2 | a0001c0001t0008g0150 a0001c0001t0008g0187 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.20+7125G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172841558 | |||||||
| chr5:172841627 | G | A | 92 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(89): Show |
92 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.20+7194G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172841627 | |||||||
| chr5:172841646 | G | A | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(210): Show |
213 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.20+7213G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172841646 | |||||||
| chr5:172841733 | C | T | 4 | a0001c0001t0001g0144 a0001c0001t0002g0146 a0001c0001t0002g0287 others(1): Show |
4 | HG01175.hp1 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.20+7300C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172841733 | |||||||
| chr5:172841809 | C | G | 1 | a0001c0001t0001g0069 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.20+7376C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172841809 | |||||||
| chr5:172842116 | G | T | 119 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0119 others(116): Show |
119 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.20+7683G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172842116 | |||||||
| chr5:172842325 | G | A | 3 | a0001c0001t0003g0328 a0001c0001t0003g0334 a0001c0001t0023g0332 |
3 | NA19240.hp1 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.20+7892G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172842325 | |||||||
| chr5:172842338 | A | G | 1 | a0001c0001t0001g0250 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.20+7905A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172842338 | |||||||
| chr5:172842393 | A | T | 2 | a0001c0001t0001g0143 a0001c0001t0002g0142 |
2 | HG01074.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.20+7960A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172842393 | |||||||
| chr5:172842401 | A | G | 4 | a0001c0001t0001g0325 a0001c0001t0004g0326 a0001c0001t0007g0281 others(1): Show |
4 | HG02109.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.20+7968A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172842401 | |||||||
| chr5:172842521 | T | A | 3 | a0001c0001t0003g0328 a0001c0001t0003g0334 a0001c0001t0023g0332 |
3 | NA19240.hp1 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.20+8088T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172842521 | |||||||
| chr5:172842545 | C | T | 4 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0075 others(1): Show |
4 | HG02015.hp2 NA18953.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.20+8112C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172842545 | |||||||
| chr5:172842592 | C | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0119 others(119): Show |
122 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.20+8159C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172842592 | |||||||
| chr5:172842690 | T | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0119 others(119): Show |
122 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.20+8257T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172842690 | |||||||
| chr5:172842817 | A | C | 1 | a0001c0001t0024g0323 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.20+8384A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172842817 | |||||||
| chr5:172842852 | G | A | 4 | a0001c0001t0001g0103 a0001c0001t0001g0148 a0001c0001t0001g0151 others(1): Show |
4 | HG02165.hp2 NA18977.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.20+8419G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172842852 | |||||||
| chr5:172842868 | G | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(90): Show |
93 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.20+8435G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172842868 | |||||||
| chr5:172842999 | C | G | 1 | a0001c0001t0003g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.20+8566C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172842999 | |||||||
| chr5:172843169 | A | G | 122 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0119 others(119): Show |
122 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.20+8736A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172843169 | |||||||
| chr5:172843198 | G | A | 1 | a0001c0001t0001g0002 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.20+8765G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172843198 | |||||||
| chr5:172843241 | G | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0186 others(87): Show |
90 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(87): Show |
intron_variant | MODIFIER | c.20+8808G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172843241 | |||||||
| chr5:172843250 | T | C | 3 | a0001c0001t0009g0329 a0001c0001t0009g0330 a0001c0001t0012g0331 |
3 | HG02280.hp2 HG02451.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.20+8817T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172843250 | |||||||
| chr5:172843252 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0119 others(116): Show |
119 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(116): Show |
intron_variant | MODIFIER | c.20+8819T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172843252 | |||||||
| chr5:172843284 | C | T | 9 | a0001c0001t0001g0325 a0001c0001t0001g0327 a0001c0001t0002g0333 others(6): Show |
9 | HG02109.hp2 HG02451.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.20+8851C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172843284 | |||||||
| chr5:172843330 | A | G | 1 | a0001c0001t0011g0099 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.20+8897A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172843330 | |||||||
| chr5:172843393 | T | C | 1 | a0001c0001t0002g0125 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.20+8960T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172843393 | |||||||
| chr5:172843681 | C | G | 6 | a0001c0001t0001g0325 a0001c0001t0001g0327 a0001c0001t0002g0333 others(3): Show |
6 | HG02109.hp2 HG02451.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.20+9248C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172843681 | |||||||
| chr5:172843760 | C | T | 1 | a0001c0001t0002g0082 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.20+9327C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172843760 | |||||||
| chr5:172843876 | A | T | 2 | a0001c0001t0001g0079 a0001c0001t0020g0078 |
2 | HG01175.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.20+9443A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172843876 | |||||||
| chr5:172843906 | G | A | 2 | a0001c0001t0001g0327 a0001c0001t0002g0333 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.20+9473G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172843906 | |||||||
| chr5:172843948 | C | T | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0265 |
3 | HG01168.hp2 HG01169.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.20+9515C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172843948 | |||||||
| chr5:172844004 | A | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0186 others(95): Show |
98 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.20+9571A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172844004 | |||||||
| chr5:172844048 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.20+9615A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172844048 | |||||||
| chr5:172844049 | C | T | 11 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(8): Show |
11 | HG00733.hp1 HG01074.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.20+9616C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172844049 | |||||||
| chr5:172844310 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.20+9877A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172844310 | |||||||
| chr5:172844533 | G | A | 5 | a0001c0001t0002g0082 a0001c0001t0031g0083 a0001c0001t0032g0084 others(2): Show |
5 | HG02055.hp2 HG02886.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.20+10100G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172844533 | |||||||
| chr5:172844772 | A | T | 1 | a0001c0001t0001g0200 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.20+10339A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172844772 | |||||||
| chr5:172844819 | T | C | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(316): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.20+10386T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172844819 | |||||||
| chr5:172844832 | C | T | 1 | a0001c0001t0002g0125 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.20+10399C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172844832 | |||||||
| chr5:172844839 | C | T | 100 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0115 others(97): Show |
100 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.20+10406C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172844839 | |||||||
| chr5:172844845 | C | G | 100 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0115 others(97): Show |
100 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.20+10412C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172844845 | |||||||
| chr5:172844978 | G | C | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(316): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.20+10545G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172844978 | |||||||
| chr5:172845039 | TATA | T | 156 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0015 others(153): Show |
156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.20+10607_20+10609d others(5): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172845039 | |||||||
| chr5:172845042 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.20+10609A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172845042 | |||||||
| chr5:172845043 | T | G | 260 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0013 others(257): Show |
260 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.20+10610T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172845043 | |||||||
| chr5:172845044 | A | G | 157 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0015 others(154): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.20+10611A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172845044 | |||||||
| chr5:172845204 | T | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(206): Show |
209 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.20+10771T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172845204 | |||||||
| chr5:172845286 | C | G | 1 | a0001c0001t0034g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.20+10853C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172845286 | |||||||
| chr5:172845445 | G | A | 4 | a0001c0001t0001g0325 a0001c0001t0004g0326 a0001c0001t0007g0281 others(1): Show |
4 | HG02109.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.20+11012G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172845445 | |||||||
| chr5:172845549 | G | A | 8 | a0001c0001t0001g0325 a0001c0001t0001g0327 a0001c0001t0002g0333 others(5): Show |
8 | HG02109.hp2 HG02451.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.20+11116G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172845549 | |||||||
| chr5:172845551 | T | G | 6 | a0001c0001t0001g0325 a0001c0001t0001g0327 a0001c0001t0002g0333 others(3): Show |
6 | HG02109.hp2 HG02451.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.20+11118T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172845551 | |||||||
| chr5:172845568 | G | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0115 others(92): Show |
95 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.20+11135G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172845568 | |||||||
| chr5:172845727 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.20+11294A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172845727 | |||||||
| chr5:172845872 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.20+11439G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172845872 | |||||||
| chr5:172846060 | G | A | 24 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0057 others(21): Show |
24 | HG00639.hp2 HG00738.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.20+11627G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172846060 | |||||||
| chr5:172846061 | G | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(114): Show |
117 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.20+11628G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172846061 | |||||||
| chr5:172846084 | G | A | 2 | a0001c0001t0003g0328 a0001c0001t0003g0334 |
2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.20+11651G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172846084 | |||||||
| chr5:172846089 | TCTC | T | 3 | a0001c0001t0003g0061 a0001c0001t0009g0329 a0001c0001t0009g0330 |
3 | HG02280.hp2 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.20+11657_20+11659d others(5): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172846089 | |||||||
| chr5:172846108 | G | A | 1 | a0001c0001t0034g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.20+11675G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172846108 | |||||||
| chr5:172846183 | G | A | 2 | a0001c0001t0001g0327 a0001c0001t0002g0333 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.20+11750G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172846183 | |||||||
| chr5:172846401 | G | T | 1 | a0001c0001t0001g0097 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.20+11968G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172846401 | |||||||
| chr5:172846690 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(115): Show |
118 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.20+12257A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172846690 | |||||||
| chr5:172846743 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.20+12310T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172846743 | |||||||
| chr5:172846811 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0121 others(83): Show |
86 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.20+12378G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172846811 | |||||||
| chr5:172847110 | T | C | 3 | a0001c0001t0001g0143 a0001c0001t0002g0087 a0001c0001t0002g0142 |
3 | HG01074.hp1 HG01192.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.20+12677T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172847110 | |||||||
| chr5:172847380 | C | T | 4 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | NA18942.hp2 NA18960.hp1 NA18985.hp1 others(1): Show |
intron_variant | MODIFIER | c.20+12947C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172847380 | |||||||
| chr5:172847513 | T | A | 1 | a0001c0001t0001g0304 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.20+13080T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172847513 | |||||||
| chr5:172847566 | T | C | 7 | a0001c0001t0001g0100 a0001c0001t0001g0104 a0001c0001t0001g0126 others(4): Show |
7 | HG02155.hp1 HG03239.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.20+13133T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172847566 | |||||||
| chr5:172847587 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0047 a0001c0001t0002g0046 |
3 | HG01346.hp1 HG01361.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.20+13154C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172847587 | |||||||
| chr5:172847618 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.20+13185A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172847618 | |||||||
| chr5:172847662 | G | A | 167 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(164): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.20+13229G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172847662 | |||||||
| chr5:172847760 | G | A | 1 | a0001c0001t0001g0126 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.20+13327G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172847760 | |||||||
| chr5:172847792 | C | T | 4 | a0001c0001t0001g0325 a0001c0001t0004g0326 a0001c0001t0007g0281 others(1): Show |
4 | HG02109.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.20+13359C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172847792 | |||||||
| chr5:172847803 | A | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(147): Show |
150 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.20+13370A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172847803 | |||||||
| chr5:172847809 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0121 others(83): Show |
86 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.20+13376G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172847809 | |||||||
| chr5:172847970 | A | T | 1 | a0001c0001t0001g0070 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.20+13537A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172847970 | |||||||
| chr5:172847971 | C | T | 21 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0057 others(18): Show |
21 | HG00639.hp2 HG00738.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.20+13538C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172847971 | |||||||
| chr5:172848020 | T | C | 11 | a0001c0001t0001g0052 a0001c0001t0001g0119 a0001c0001t0001g0120 others(8): Show |
11 | HG00544.hp2 HG02145.hp1 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.20+13587T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172848020 | |||||||
| chr5:172848096 | A | G | 2 | a0001c0001t0001g0327 a0001c0001t0002g0333 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.20+13663A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172848096 | |||||||
| chr5:172848149 | G | A | 1 | a0001c0001t0001g0319 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.20+13716G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172848149 | |||||||
| chr5:172848160 | A | C | 3 | a0001c0001t0002g0122 a0001c0001t0023g0332 a0001c0001t0034g0086 |
3 | HG02886.hp1 HG02970.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.20+13727A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172848160 | |||||||
| chr5:172848260 | G | A | 29 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0057 others(26): Show |
29 | HG00639.hp2 HG00738.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.20+13827G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172848260 | |||||||
| chr5:172848336 | G | A | 4 | a0001c0001t0006g0053 a0001c0001t0031g0083 a0001c0001t0032g0084 others(1): Show |
4 | HG02055.hp2 HG03098.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.20+13903G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172848336 | |||||||
| chr5:172848368 | C | T | 11 | a0001c0001t0002g0082 a0001c0001t0003g0061 a0001c0001t0003g0198 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.20+13935C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172848368 | |||||||
| chr5:172848369 | G | A | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.20+13936G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172848369 | |||||||
| chr5:172848371 | TAGAG | T | 4 | a0001c0001t0001g0325 a0001c0001t0004g0326 a0001c0001t0007g0281 others(1): Show |
4 | HG02109.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.20+13941_20+13944d others(6): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172848371 | ||||||
| chr5:172848495 | G | A | 1 | a0001c0001t0006g0004 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.20+14062G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172848495 | |||||||
| chr5:172848516 | A | G | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.20+14083A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172848516 | |||||||
| chr5:172848671 | A | G | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(315): Show |
318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.20+14238A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172848671 | |||||||
| chr5:172848689 | G | A | 1 | a0001c0001t0005g0005 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.20+14256G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172848689 | |||||||
| chr5:172848994 | A | C | 3 | a0001c0001t0001g0096 a0001c0001t0002g0095 a0001c0001t0002g0138 |
3 | HG00140.hp1 HG01433.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.20+14561A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172848994 | |||||||
| chr5:172849272 | C | T | 1 | a0001c0001t0024g0323 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.20+14839C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172849272 | |||||||
| chr5:172849325 | G | A | 190 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(187): Show |
190 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.20+14892G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172849325 | |||||||
| chr5:172849505 | G | A | 1 | a0001c0001t0001g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.20+15072G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172849505 | |||||||
| chr5:172849611 | G | T | 54 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0021 others(51): Show |
54 | HG00408.hp1 HG00438.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.20+15178G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172849611 | |||||||
| chr5:172849901 | T | G | 1 | a0001c0001t0001g0072 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.20+15468T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172849901 | |||||||
| chr5:172849904 | G | A | 4 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0003g0292 others(1): Show |
4 | HG01243.hp1 HG02572.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.20+15471G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172849904 | |||||||
| chr5:172850016 | G | C | 4 | a0001c0001t0001g0325 a0001c0001t0004g0326 a0001c0001t0007g0281 others(1): Show |
4 | HG02109.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.20+15583G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172850016 | |||||||
| chr5:172850046 | C | T | 1 | a0001c0001t0002g0094 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.20+15613C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172850046 | |||||||
| chr5:172850130 | AGGT | A | 3 | a0001c0001t0003g0198 a0001c0001t0015g0199 a0001c0001t0016g0197 |
3 | HG02818.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.20+15700_20+15702d others(5): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172850130 | ||||||
| chr5:172850141 | G | A | 3 | a0001c0001t0003g0198 a0001c0001t0015g0199 a0001c0001t0016g0197 |
3 | HG02818.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.20+15708G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172850141 | |||||||
| chr5:172850213 | C | T | 2 | a0001c0001t0002g0093 a0001c0001t0002g0137 |
2 | HG00280.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.20+15780C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172850213 | |||||||
| chr5:172850282 | G | A | 1 | a0001c0001t0003g0210 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.20+15849G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172850282 | |||||||
| chr5:172850289 | C | G | 2 | a0001c0001t0001g0325 a0001c0001t0004g0326 |
2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.20+15856C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172850289 | |||||||
| chr5:172850374 | C | T | 1 | a0001c0001t0003g0101 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.20+15941C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172850374 | |||||||
| chr5:172850376 | G | A | 2 | a0001c0001t0001g0327 a0001c0001t0002g0333 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.20+15943G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172850376 | |||||||
| chr5:172850503 | G | T | 2 | a0001c0001t0003g0328 a0001c0001t0003g0334 |
2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.20+16070G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172850503 | |||||||
| chr5:172850672 | T | C | 21 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0057 others(18): Show |
21 | HG00639.hp2 HG00738.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.20+16239T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172850672 | |||||||
| chr5:172850774 | T | C | 1 | a0001c0001t0001g0070 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.20+16341T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172850774 | |||||||
| chr5:172850781 | C | T | 1 | a0001c0001t0015g0199 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.20+16348C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172850781 | |||||||
| chr5:172850800 | G | T | 1 | a0001c0001t0001g0051 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.20+16367G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172850800 | |||||||
| chr5:172851062 | A | G | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(315): Show |
318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.20+16629A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172851062 | |||||||
| chr5:172851149 | C | T | 21 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0057 others(18): Show |
21 | HG00639.hp2 HG00738.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.20+16716C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172851149 | |||||||
| chr5:172851200 | C | CA | 6 | a0001c0001t0001g0103 a0001c0001t0002g0122 a0001c0001t0003g0293 others(3): Show |
6 | HG02145.hp2 HG02559.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.20+16787dupA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172851200 | ||||||
| chr5:172851200 | CA | C | 29 | a0001c0001t0001g0020 a0001c0001t0001g0043 a0001c0001t0001g0100 others(26): Show |
29 | HG01070.hp2 HG01169.hp2 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.20+16787delA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172851200 | ||||||
| chr5:172851200 | CAA | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0121 others(80): Show |
83 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.20+16786_20+16787d others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172851200 | ||||||
| chr5:172851200 | CAAA | C | 21 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0057 others(18): Show |
21 | HG00639.hp2 HG00738.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.20+16785_20+16787d others(5): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172851200 | ||||||
| chr5:172851216 | A | T | 1 | a0001c0001t0001g0092 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.20+16783A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172851216 | |||||||
| chr5:172851221 | T | A | 3 | a0001c0001t0001g0092 a0001c0001t0002g0098 a0001c0001t0002g0130 |
3 | HG01123.hp1 HG02683.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.20+16788T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172851221 | |||||||
| chr5:172851372 | G | A | 1 | a0001c0001t0003g0101 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.20+16939G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172851372 | |||||||
| chr5:172851423 | C | A | 1 | a0001c0001t0002g0318 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.20+16990C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172851423 | |||||||
| chr5:172851424 | G | A | 1 | a0001c0001t0002g0142 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.20+16991G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172851424 | |||||||
| chr5:172851435 | G | A | 2 | a0001c0001t0001g0327 a0001c0001t0002g0333 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.20+17002G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172851435 | |||||||
| chr5:172851450 | A | G | 2 | a0001c0001t0001g0112 a0001c0001t0001g0175 |
2 | HG01261.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.20+17017A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172851450 | |||||||
| chr5:172851465 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.20+17032C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172851465 | |||||||
| chr5:172851489 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.20+17056A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172851489 | |||||||
| chr5:172851495 | C | T | 1 | a0001c0001t0001g0264 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.20+17062C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172851495 | |||||||
| chr5:172851704 | C | T | 2 | a0001c0001t0003g0328 a0001c0001t0003g0334 |
2 | NA19240.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.20+17271C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172851704 | |||||||
| chr5:172851717 | T | C | 6 | a0001c0001t0003g0061 a0001c0001t0003g0198 a0001c0001t0009g0329 others(3): Show |
6 | HG02280.hp2 HG02451.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.20+17284T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172851717 | |||||||
| chr5:172851720 | G | A | 2 | a0001c0001t0001g0325 a0001c0001t0004g0326 |
2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.20+17287G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172851720 | |||||||
| chr5:172851754 | C | T | 2 | a0001c0001t0007g0281 a0001c0001t0007g0282 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.20+17321C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172851754 | |||||||
| chr5:172851877 | G | A | 21 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0057 others(18): Show |
21 | HG00639.hp2 HG00738.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.20+17444G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172851877 | |||||||
| chr5:172851955 | C | G | 6 | a0001c0001t0001g0019 a0001c0001t0001g0111 a0001c0001t0001g0112 others(3): Show |
6 | HG00140.hp2 HG00733.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.20+17522C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172851955 | |||||||
| chr5:172852020 | C | G | 2 | a0001c0001t0001g0325 a0001c0001t0004g0326 |
2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.20+17587C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172852020 | |||||||
| chr5:172852061 | A | G | 88 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0052 others(85): Show |
88 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.20+17628A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172852061 | |||||||
| chr5:172852168 | C | G | 4 | a0001c0001t0001g0327 a0001c0001t0002g0333 a0001c0001t0007g0281 others(1): Show |
4 | HG02451.hp1 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.20+17735C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172852168 | |||||||
| chr5:172852278 | C | T | 21 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0057 others(18): Show |
21 | HG00639.hp2 HG00738.hp2 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.20+17845C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172852278 | |||||||
| chr5:172852544 | T | C | 2 | a0001c0001t0001g0327 a0001c0001t0002g0333 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.20+18111T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172852544 | |||||||
| chr5:172852667 | G | A | 2 | a0001c0001t0002g0010 a0001c0001t0002g0011 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.20+18234G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172852667 | |||||||
| chr5:172852729 | G | C | 14 | a0001c0001t0001g0121 a0001c0001t0001g0268 a0001c0001t0001g0276 others(11): Show |
14 | HG00639.hp1 HG01071.hp1 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.20+18296G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172852729 | |||||||
| chr5:172853101 | CTG | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0121 others(83): Show |
86 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.20+18674_20+18675d others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172853101 | ||||||
| chr5:172853159 | C | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0121 others(83): Show |
86 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.20+18726C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172853159 | |||||||
| chr5:172853175 | G | A | 3 | a0001c0001t0003g0061 a0001c0001t0009g0329 a0001c0001t0009g0330 |
3 | HG02280.hp2 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.20+18742G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172853175 | |||||||
| chr5:172853244 | T | A | 2 | a0001c0001t0003g0154 a0001c0001t0005g0105 |
2 | HG01109.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.20+18811T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172853244 | |||||||
| chr5:172853403 | A | T | 1 | a0001c0001t0001g0209 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.20+18970A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172853403 | |||||||
| chr5:172853478 | G | A | 2 | a0001c0001t0001g0327 a0001c0001t0002g0333 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.20+19045G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172853478 | |||||||
| chr5:172853533 | C | G | 2 | a0001c0001t0001g0327 a0001c0001t0002g0333 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.20+19100C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172853533 | |||||||
| chr5:172853873 | C | T | 1 | a0001c0001t0003g0101 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.20+19440C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172853873 | |||||||
| chr5:172854108 | A | C | 15 | a0001c0001t0001g0327 a0001c0001t0002g0082 a0001c0001t0002g0333 others(12): Show |
15 | HG02055.hp2 HG02280.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.20+19675A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172854108 | |||||||
| chr5:172854217 | C | CAA | 11 | a0001c0001t0002g0082 a0001c0001t0003g0061 a0001c0001t0003g0198 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.20+19798_20+19799d others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172854217 | ||||||
| chr5:172854285 | G | A | 2 | a0001c0001t0003g0155 a0001c0001t0005g0156 |
2 | HG02622.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.20+19852G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172854285 | |||||||
| chr5:172854287 | C | T | 1 | a0001c0001t0001g0264 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.20+19854C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172854287 | |||||||
| chr5:172854288 | G | A | 1 | a0001c0001t0006g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.20+19855G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172854288 | |||||||
| chr5:172854323 | A | G | 2 | a0001c0001t0001g0255 a0001c0001t0002g0324 |
2 | HG02129.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.20+19890A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172854323 | |||||||
| chr5:172854413 | T | C | 11 | a0001c0001t0002g0082 a0001c0001t0003g0061 a0001c0001t0003g0198 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.20+19980T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172854413 | |||||||
| chr5:172854413 | T | G | 2 | a0001c0001t0001g0327 a0001c0001t0002g0333 |
2 | HG02451.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.20+19980T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172854413 | |||||||
| chr5:172854461 | T | C | 11 | a0001c0001t0002g0082 a0001c0001t0003g0061 a0001c0001t0003g0198 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.20+20028T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172854461 | |||||||
| chr5:172854462 | G | A | 1 | a0001c0001t0002g0082 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.20+20029G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172854462 | |||||||
| chr5:172854780 | C | T | 9 | a0001c0001t0002g0082 a0001c0001t0003g0061 a0001c0001t0006g0053 others(6): Show |
9 | HG02055.hp2 HG02280.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.20+20347C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172854780 | |||||||
| chr5:172855218 | G | T | 6 | a0001c0001t0001g0307 a0001c0001t0001g0313 a0001c0001t0003g0316 others(3): Show |
6 | HG01884.hp1 HG03098.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.20+20785G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172855218 | |||||||
| chr5:172855238 | G | T | 66 | a0001c0001t0001g0042 a0001c0001t0001g0115 a0001c0001t0001g0123 others(63): Show |
66 | HG00280.hp2 HG00408.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.20+20805G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172855238 | |||||||
| chr5:172855313 | C | T | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.20+20880C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172855313 | |||||||
| chr5:172855387 | C | T | 3 | a0001c0001t0001g0020 a0001c0001t0002g0146 a0001c0001t0003g0145 |
3 | HG01070.hp2 HG02615.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.20+20954C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172855387 | |||||||
| chr5:172855562 | A | G | 1 | a0001c0001t0001g0041 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.20+21129A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172855562 | |||||||
| chr5:172855677 | G | T | 1 | a0001c0001t0002g0146 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.20+21244G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172855677 | |||||||
| chr5:172855700 | C | T | 128 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(125): Show |
128 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.20+21267C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172855700 | |||||||
| chr5:172855882 | G | A | 14 | a0001c0001t0001g0304 a0001c0001t0001g0307 a0001c0001t0001g0313 others(11): Show |
14 | HG01884.hp1 HG02280.hp2 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.20+21449G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172855882 | |||||||
| chr5:172855942 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.20+21509C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172855942 | |||||||
| chr5:172856417 | CA | C | 100 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0018 others(97): Show |
100 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.20+21985delA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172856417 | |||||||
| chr5:172856422 | T | G | 278 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(275): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.20+21989T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172856422 | |||||||
| chr5:172856502 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.20+22069C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172856502 | |||||||
| chr5:172856569 | C | A | 317 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(314): Show |
317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.20+22136C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172856569 | |||||||
| chr5:172856616 | C | A | 4 | a0001c0001t0001g0295 a0001c0001t0002g0082 a0001c0001t0007g0281 others(1): Show |
4 | HG02615.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.20+22183C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172856616 | |||||||
| chr5:172856785 | G | A | 3 | a0001c0001t0001g0096 a0001c0001t0002g0095 a0001c0001t0002g0138 |
3 | HG00140.hp1 HG01433.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.20+22352G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172856785 | |||||||
| chr5:172856927 | A | G | 30 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(27): Show |
30 | HG00738.hp2 HG01071.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.20+22494A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172856927 | |||||||
| chr5:172857102 | T | A | 4 | a0001c0001t0001g0325 a0001c0001t0003g0198 a0001c0001t0004g0326 others(1): Show |
4 | HG02109.hp2 HG02818.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.20+22669T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172857102 | |||||||
| chr5:172857159 | G | A | 80 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(77): Show |
80 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(77): Show |
intron_variant | MODIFIER | c.20+22726G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172857159 | |||||||
| chr5:172857168 | G | A | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(316): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.20+22735G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172857168 | |||||||
| chr5:172857288 | A | G | 4 | a0001c0001t0001g0128 a0001c0001t0003g0034 a0001c0001t0003g0035 others(1): Show |
4 | HG03654.hp2 HG03669.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.20+22855A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172857288 | |||||||
| chr5:172857403 | C | T | 5 | a0001c0001t0001g0033 a0001c0001t0001g0072 a0001c0001t0001g0074 others(2): Show |
5 | HG00597.hp2 HG02015.hp2 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.20+22970C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172857403 | |||||||
| chr5:172857541 | G | A | 56 | a0001c0001t0001g0042 a0001c0001t0001g0062 a0001c0001t0001g0063 others(53): Show |
56 | HG00140.hp1 HG00733.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.20+23108G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172857541 | |||||||
| chr5:172857588 | GC | G | 273 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(270): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.20+23163delC | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172857588 | ||||||
| chr5:172857600 | C | T | 18 | a0001c0001t0001g0134 a0001c0001t0001g0276 a0001c0001t0001g0277 others(15): Show |
18 | HG00741.hp1 HG01175.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.20+23167C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172857600 | |||||||
| chr5:172857645 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.20+23212C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172857645 | |||||||
| chr5:172857703 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.20+23270G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172857703 | |||||||
| chr5:172857773 | T | G | 108 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0015 others(105): Show |
108 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.20+23340T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172857773 | |||||||
| chr5:172857953 | G | A | 2 | a0001c0001t0001g0200 a0001c0001t0001g0223 |
2 | NA19011.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.20+23520G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172857953 | |||||||
| chr5:172857969 | G | A | 1 | a0001c0001t0001g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.20+23536G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172857969 | |||||||
| chr5:172858082 | C | A | 1 | a0001c0001t0003g0334 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.20+23649C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172858082 | |||||||
| chr5:172858086 | C | T | 67 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(64): Show |
67 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.20+23653C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172858086 | |||||||
| chr5:172858090 | T | C | 7 | a0001c0001t0001g0069 a0001c0001t0001g0193 a0001c0001t0001g0194 others(4): Show |
7 | HG00597.hp1 HG02155.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.20+23657T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172858090 | |||||||
| chr5:172858131 | G | C | 4 | a0001c0001t0002g0122 a0001c0001t0031g0083 a0001c0001t0032g0084 others(1): Show |
4 | HG02055.hp2 HG02970.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.20+23698G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172858131 | |||||||
| chr5:172858416 | T | G | 2 | a0001c0001t0001g0325 a0001c0001t0004g0326 |
2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.20+23983T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172858416 | |||||||
| chr5:172858484 | G | T | 312 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(309): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.20+24051G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172858484 | |||||||
| chr5:172858508 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.20+24075C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172858508 | |||||||
| chr5:172858568 | C | T | 1 | a0001c0001t0006g0270 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.20+24135C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172858568 | |||||||
| chr5:172858602 | T | C | 196 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(193): Show |
196 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.20+24169T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172858602 | |||||||
| chr5:172858640 | C | A | 3 | a0001c0001t0001g0325 a0001c0001t0001g0327 a0001c0001t0004g0326 |
3 | HG02109.hp2 HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.20+24207C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172858640 | |||||||
| chr5:172858647 | T | C | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.20+24214T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172858647 | |||||||
| chr5:172858668 | G | A | 297 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(294): Show |
297 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.20+24235G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172858668 | |||||||
| chr5:172858674 | A | C | 3 | a0001c0001t0003g0061 a0001c0001t0009g0329 a0001c0001t0009g0330 |
3 | HG02280.hp2 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.20+24241A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172858674 | |||||||
| chr5:172858692 | C | T | 3 | a0001c0001t0003g0283 a0001c0001t0003g0284 a0001c0001t0003g0328 |
3 | HG02055.hp1 HG03453.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.20+24259C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172858692 | |||||||
| chr5:172858880 | C | T | 3 | a0001c0001t0001g0325 a0001c0001t0001g0327 a0001c0001t0004g0326 |
3 | HG02109.hp2 HG02451.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.20+24447C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172858880 | |||||||
| chr5:172858894 | G | C | 1 | a0001c0001t0001g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.20+24461G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172858894 | |||||||
| chr5:172859069 | C | T | 2 | a0001c0001t0001g0325 a0001c0001t0004g0326 |
2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.20+24636C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172859069 | |||||||
| chr5:172859076 | G | T | 1 | a0001c0001t0001g0037 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.20+24643G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172859076 | |||||||
| chr5:172859147 | C | T | 9 | a0001c0001t0001g0159 a0001c0001t0001g0268 a0001c0001t0002g0160 others(6): Show |
9 | HG02559.hp2 HG02572.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.20+24714C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172859147 | |||||||
| chr5:172859152 | C | G | 2 | a0001c0001t0001g0302 a0001c0001t0011g0099 |
2 | HG03688.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.20+24719C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172859152 | |||||||
| chr5:172859175 | G | T | 1 | a0001c0001t0001g0071 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.20+24742G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172859175 | |||||||
| chr5:172859229 | C | G | 296 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(293): Show |
296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.20+24796C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172859229 | |||||||
| chr5:172859350 | G | A | 9 | a0001c0001t0001g0159 a0001c0001t0001g0268 a0001c0001t0002g0160 others(6): Show |
9 | HG02559.hp2 HG02572.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.20+24917G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172859350 | |||||||
| chr5:172859361 | G | A | 2 | a0001c0001t0001g0325 a0001c0001t0004g0326 |
2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.20+24928G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172859361 | |||||||
| chr5:172859376 | C | G | 189 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(186): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.20+24943C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172859376 | |||||||
| chr5:172859388 | T | C | 2 | a0001c0001t0002g0207 a0001c0001t0002g0208 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.20+24955T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172859388 | |||||||
| chr5:172859410 | C | G | 1 | a0001c0001t0002g0278 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.20+24977C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172859410 | |||||||
| chr5:172859476 | G | T | 1 | a0001c0001t0001g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.20+25043G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172859476 | |||||||
| chr5:172859489 | G | GA | 71 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(68): Show |
71 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.20+25065dupA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172859489 | ||||||
| chr5:172859490 | A | G | 93 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0030 others(90): Show |
93 | HG00408.hp1 HG00609.hp2 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.20+25057A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172859490 | |||||||
| chr5:172859505 | G | A | 296 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(293): Show |
296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.20+25072G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172859505 | |||||||
| chr5:172859639 | G | T | 4 | a0001c0001t0001g0002 a0001c0001t0008g0150 a0001c0001t0008g0187 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.20+25206G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172859639 | |||||||
| chr5:172859737 | T | A | 1 | a0001c0001t0001g0006 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.20+25304T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172859737 | |||||||
| chr5:172859783 | G | C | 3 | a0001c0001t0001g0001 a0001c0001t0003g0296 a0001c0001t0005g0106 |
3 | HG02886.hp2 HG03225.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.20+25350G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172859783 | |||||||
| chr5:172859970 | T | C | 4 | a0001c0001t0001g0017 a0001c0001t0001g0129 a0001c0001t0001g0261 others(1): Show |
4 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(1): Show |
intron_variant | MODIFIER | c.20+25537T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172859970 | |||||||
| chr5:172860153 | AG | A | 185 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(182): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.20+25721delG | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172860153 | |||||||
| chr5:172860426 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.20+25993G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172860426 | |||||||
| chr5:172860449 | C | T | 1 | a0001c0001t0003g0311 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.20+26016C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172860449 | |||||||
| chr5:172860450 | G | A | 2 | a0001c0001t0001g0062 a0001c0001t0002g0229 |
2 | HG00733.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.20+26017G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172860450 | |||||||
| chr5:172860454 | C | T | 2 | a0001c0001t0003g0273 a0001c0001t0003g0274 |
2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.20+26021C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172860454 | |||||||
| chr5:172860521 | C | G | 1 | a0001c0001t0003g0334 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.20+26088C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172860521 | |||||||
| chr5:172860569 | C | T | 1 | a0001c0001t0034g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.20+26136C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172860569 | |||||||
| chr5:172860614 | T | G | 301 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(298): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.20+26181T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172860614 | |||||||
| chr5:172860746 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.20+26313G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172860746 | |||||||
| chr5:172860777 | G | A | 9 | a0001c0001t0001g0159 a0001c0001t0001g0268 a0001c0001t0002g0160 others(6): Show |
9 | HG02559.hp2 HG02572.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.20+26344G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172860777 | |||||||
| chr5:172860807 | C | T | 2 | a0001c0001t0001g0007 a0001c0001t0001g0047 |
2 | HG01346.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.20+26374C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172860807 | |||||||
| chr5:172860878 | G | C | 1 | a0001c0001t0001g0211 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.20+26445G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172860878 | |||||||
| chr5:172860916 | G | A | 2 | a0001c0001t0001g0325 a0001c0001t0004g0326 |
2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.20+26483G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172860916 | |||||||
| chr5:172861099 | G | A | 8 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0305 others(5): Show |
8 | HG01243.hp1 HG02145.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.20+26666G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172861099 | |||||||
| chr5:172861113 | G | A | 3 | a0001c0001t0001g0124 a0001c0001t0001g0127 a0001c0001t0017g0234 |
3 | HG03239.hp2 HG03669.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.20+26680G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172861113 | |||||||
| chr5:172861130 | C | T | 1 | a0001c0001t0002g0280 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.20+26697C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172861130 | |||||||
| chr5:172861148 | G | A | 9 | a0001c0001t0001g0159 a0001c0001t0001g0268 a0001c0001t0002g0160 others(6): Show |
9 | HG02559.hp2 HG02572.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.20+26715G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172861148 | |||||||
| chr5:172861160 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.20+26727G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172861160 | |||||||
| chr5:172861323 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.20+26890C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172861323 | |||||||
| chr5:172861443 | G | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0129 |
2 | HG00423.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.20+27010G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172861443 | |||||||
| chr5:172861694 | C | A | 290 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(287): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.21-27005C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172861694 | |||||||
| chr5:172861802 | T | A | 312 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(309): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.21-26897T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172861802 | |||||||
| chr5:172861904 | A | C | 290 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(287): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.21-26795A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172861904 | |||||||
| chr5:172861948 | G | T | 312 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(309): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.21-26751G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172861948 | |||||||
| chr5:172861956 | T | G | 1 | a0001c0001t0001g0193 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.21-26743T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172861956 | |||||||
| chr5:172861988 | T | A | 1 | a0001c0001t0001g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.21-26711T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172861988 | |||||||
| chr5:172862061 | G | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0129 a0001c0001t0001g0151 others(2): Show |
5 | HG00423.hp1 HG00558.hp1 HG00609.hp1 others(2): Show |
intron_variant | MODIFIER | c.21-26638G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172862061 | |||||||
| chr5:172862084 | C | T | 72 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(69): Show |
72 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.21-26615C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172862084 | |||||||
| chr5:172862146 | T | G | 1 | a0001c0001t0001g0241 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.21-26553T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172862146 | |||||||
| chr5:172862307 | C | CA | 23 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0021 others(20): Show |
23 | HG01169.hp1 HG01192.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.21-26367dupA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172862307 | ||||||
| chr5:172862307 | C | CAA | 173 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(170): Show |
173 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.21-26368_21-26367d others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172862307 | ||||||
| chr5:172862307 | C | CAAA | 24 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0043 others(21): Show |
24 | HG00140.hp2 HG00741.hp2 HG01175.hp2 others(21): Show |
intron_variant | MODIFIER | c.21-26369_21-26367d others(5): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172862307 | ||||||
| chr5:172862307 | C | CAAAAA | 6 | a0001c0001t0001g0031 a0001c0001t0001g0050 a0001c0001t0001g0196 others(3): Show |
6 | NA18944.hp1 NA18954.hp1 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.21-26371_21-26367d others(7): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172862307 | ||||||
| chr5:172862307 | C | CAAAAAA | 59 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0039 others(56): Show |
59 | HG00408.hp1 HG00609.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.21-26372_21-26367d others(8): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172862307 | ||||||
| chr5:172862307 | C | CAAAAAAA | 13 | a0001c0001t0001g0051 a0001c0001t0001g0074 a0001c0001t0001g0116 others(10): Show |
13 | HG01433.hp2 HG02074.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.21-26373_21-26367d others(9): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172862307 | ||||||
| chr5:172862307 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0128 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.21-26376_21-26367d others(12): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172862307 | ||||||
| chr5:172862412 | C | T | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.21-26287C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172862412 | |||||||
| chr5:172862453 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0019g0068 |
2 | HG01074.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.21-26246G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172862453 | |||||||
| chr5:172862467 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.21-26232G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172862467 | |||||||
| chr5:172862639 | C | G | 1 | a0001c0001t0003g0334 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.21-26060C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172862639 | |||||||
| chr5:172862661 | A | G | 1 | a0001c0001t0015g0199 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.21-26038A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172862661 | |||||||
| chr5:172862873 | C | G | 1 | a0001c0001t0003g0334 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.21-25826C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172862873 | |||||||
| chr5:172862926 | C | T | 315 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(312): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.21-25773C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172862926 | |||||||
| chr5:172862963 | C | T | 283 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(280): Show |
283 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.21-25736C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172862963 | |||||||
| chr5:172862989 | A | G | 3 | a0001c0001t0003g0061 a0001c0001t0009g0329 a0001c0001t0009g0330 |
3 | HG02280.hp2 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.21-25710A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172862989 | |||||||
| chr5:172863009 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.21-25690T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172863009 | |||||||
| chr5:172863331 | G | A | 1 | a0001c0001t0003g0334 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.21-25368G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172863331 | |||||||
| chr5:172863410 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.21-25289G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172863410 | |||||||
| chr5:172863434 | A | G | 1 | a0001c0001t0001g0077 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.21-25265A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172863434 | |||||||
| chr5:172863588 | A | G | 292 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(289): Show |
292 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(289): Show |
intron_variant | MODIFIER | c.21-25111A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172863588 | |||||||
| chr5:172863631 | G | A | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.21-25068G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172863631 | |||||||
| chr5:172863682 | GA | G | 11 | a0001c0001t0001g0134 a0001c0001t0001g0276 a0001c0001t0001g0277 others(8): Show |
11 | HG00741.hp1 HG01175.hp1 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.21-25010delA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172863682 | ||||||
| chr5:172863709 | T | A | 288 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(285): Show |
288 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(285): Show |
intron_variant | MODIFIER | c.21-24990T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172863709 | |||||||
| chr5:172863825 | G | A | 206 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(203): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.21-24874G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172863825 | |||||||
| chr5:172863982 | G | A | 1 | a0001c0001t0003g0283 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.21-24717G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172863982 | |||||||
| chr5:172864104 | G | C | 204 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(201): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.21-24595G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172864104 | |||||||
| chr5:172864246 | A | G | 81 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(78): Show |
81 | HG00408.hp1 HG00609.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.21-24453A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172864246 | |||||||
| chr5:172864268 | C | CT | 6 | a0001c0001t0001g0196 a0001c0001t0001g0209 a0001c0001t0001g0305 others(3): Show |
6 | HG02145.hp1 HG02451.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.21-24409dupT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172864268 | ||||||
| chr5:172864268 | C | CTT | 14 | a0001c0001t0001g0288 a0001c0001t0001g0307 a0001c0001t0001g0313 others(11): Show |
14 | HG01167.hp2 HG01884.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.21-24410_21-24409d others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172864268 | ||||||
| chr5:172864268 | C | CTTTT | 8 | a0001c0001t0001g0159 a0001c0001t0001g0268 a0001c0001t0002g0160 others(5): Show |
8 | HG02559.hp2 HG02572.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.21-24412_21-24409d others(6): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172864268 | ||||||
| chr5:172864268 | CT | C | 191 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(188): Show |
191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.21-24409delT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172864268 | ||||||
| chr5:172864268 | CTT | C | 9 | a0001c0001t0001g0165 a0001c0001t0001g0325 a0001c0001t0002g0073 others(6): Show |
9 | HG02109.hp2 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.21-24410_21-24409d others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172864268 | ||||||
| chr5:172864313 | C | G | 290 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(287): Show |
290 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.21-24386C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172864313 | |||||||
| chr5:172864409 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.21-24290C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172864409 | |||||||
| chr5:172864503 | C | A | 78 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(75): Show |
78 | HG00408.hp1 HG00609.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.21-24196C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172864503 | |||||||
| chr5:172864579 | CA | C | 3 | a0001c0001t0003g0061 a0001c0001t0009g0329 a0001c0001t0009g0330 |
3 | HG02280.hp2 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.21-24116delA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172864579 | ||||||
| chr5:172864773 | T | C | 1 | a0001c0001t0034g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.21-23926T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172864773 | |||||||
| chr5:172865051 | C | CT | 78 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(75): Show |
78 | HG00408.hp1 HG00609.hp2 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.21-23625dupT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172865051 | ||||||
| chr5:172865051 | C | CTT | 7 | a0001c0001t0001g0090 a0001c0001t0001g0133 a0001c0001t0001g0209 others(4): Show |
7 | HG01192.hp2 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.21-23626_21-23625d others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172865051 | ||||||
| chr5:172865051 | CTT | C | 19 | a0001c0001t0001g0017 a0001c0001t0001g0021 a0001c0001t0001g0070 others(16): Show |
19 | HG00423.hp1 HG00741.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.21-23626_21-23625d others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172865051 | ||||||
| chr5:172865051 | CTTT | C | 176 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(173): Show |
176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.21-23627_21-23625d others(5): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172865051 | ||||||
| chr5:172865051 | CTTTT | C | 10 | a0001c0001t0001g0144 a0001c0001t0001g0223 a0001c0001t0001g0238 others(7): Show |
10 | HG02055.hp2 HG02165.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.21-23628_21-23625d others(6): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172865051 | ||||||
| chr5:172865203 | C | T | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.21-23496C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172865203 | |||||||
| chr5:172865230 | A | G | 1 | a0001c0001t0034g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.21-23469A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172865230 | |||||||
| chr5:172865248 | G | C | 1 | a0001c0001t0003g0334 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.21-23451G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172865248 | |||||||
| chr5:172865303 | G | A | 1 | a0001c0001t0002g0130 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.21-23396G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172865303 | |||||||
| chr5:172865495 | A | T | 2 | a0001c0001t0001g0110 a0001c0001t0001g0182 |
2 | HG03927.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.21-23204A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172865495 | |||||||
| chr5:172865543 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.21-23156C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172865543 | |||||||
| chr5:172865620 | G | A | 1 | a0001c0001t0003g0334 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.21-23079G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172865620 | |||||||
| chr5:172865691 | A | G | 11 | a0001c0001t0001g0288 a0001c0001t0001g0307 a0001c0001t0001g0313 others(8): Show |
11 | HG01167.hp2 HG01884.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.21-23008A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172865691 | |||||||
| chr5:172865817 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.21-22882C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172865817 | |||||||
| chr5:172865906 | G | A | 326 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(323): Show |
326 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.21-22793G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172865906 | |||||||
| chr5:172866051 | C | A | 2 | a0001c0001t0001g0244 a0001c0001t0004g0247 |
2 | NA18954.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.21-22648C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172866051 | |||||||
| chr5:172866332 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(164): Show |
167 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.21-22367C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172866332 | |||||||
| chr5:172866459 | G | A | 2 | a0001c0001t0002g0269 a0001c0001t0006g0270 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.21-22240G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172866459 | |||||||
| chr5:172866508 | C | A | 3 | a0001c0001t0003g0061 a0001c0001t0009g0329 a0001c0001t0009g0330 |
3 | HG02280.hp2 HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.21-22191C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172866508 | |||||||
| chr5:172866593 | G | A | 2 | a0001c0001t0001g0209 a0001c0001t0001g0214 |
2 | NA18968.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.21-22106G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172866593 | |||||||
| chr5:172866618 | G | A | 5 | a0001c0001t0001g0149 a0001c0001t0001g0169 a0001c0001t0001g0170 others(2): Show |
5 | HG01106.hp1 HG01943.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.21-22081G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172866618 | |||||||
| chr5:172866622 | T | C | 2 | a0001c0001t0001g0325 a0001c0001t0004g0326 |
2 | HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.21-22077T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172866622 | |||||||
| chr5:172866649 | T | C | 1 | a0001c0001t0005g0106 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.21-22050T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172866649 | |||||||
| chr5:172866747 | T | C | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(301): Show |
304 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(301): Show |
intron_variant | MODIFIER | c.21-21952T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172866747 | |||||||
| chr5:172866962 | A | C | 161 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0015 others(158): Show |
161 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.21-21737A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172866962 | |||||||
| chr5:172867001 | A | AGATGATG others(11): Show |
3 | a0001c0001t0001g0295 a0001c0001t0001g0325 a0001c0001t0004g0326 |
3 | HG02109.hp2 HG02615.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.21-21675_21-21658d others(20): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172867001 | ||||||
| chr5:172867019 | TGATGATG others(8): Show |
T | 2 | a0001c0001t0003g0273 a0001c0001t0003g0274 |
2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.21-21647_21-21633d others(17): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172867019 | ||||||
| chr5:172867103 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.21-21596G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172867103 | |||||||
| chr5:172867190 | C | T | 10 | a0001c0001t0001g0103 a0001c0001t0001g0179 a0001c0001t0001g0241 others(7): Show |
10 | HG00609.hp2 NA18943.hp1 NA18952.hp2 others(7): Show |
intron_variant | MODIFIER | c.21-21509C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172867190 | |||||||
| chr5:172867191 | G | T | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(208): Show |
211 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.21-21508G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172867191 | |||||||
| chr5:172867510 | G | A | 74 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(71): Show |
74 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(71): Show |
intron_variant | MODIFIER | c.21-21189G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172867510 | |||||||
| chr5:172867633 | A | T | 7 | a0001c0001t0001g0265 a0001c0001t0002g0207 a0001c0001t0002g0208 others(4): Show |
7 | HG01257.hp2 HG01258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.21-21066A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172867633 | |||||||
| chr5:172867634 | C | A | 1 | a0001c0001t0019g0068 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.21-21065C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172867634 | |||||||
| chr5:172867783 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.21-20916G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172867783 | |||||||
| chr5:172867913 | G | A | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(209): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.21-20786G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172867913 | |||||||
| chr5:172867964 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0002g0060 |
2 | HG03492.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.21-20735C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172867964 | |||||||
| chr5:172867997 | C | T | 2 | a0001c0001t0003g0293 a0001c0001t0010g0058 |
2 | HG02145.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.21-20702C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172867997 | |||||||
| chr5:172867998 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.21-20701G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172867998 | |||||||
| chr5:172868007 | G | C | 213 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(210): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.21-20692G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172868007 | |||||||
| chr5:172868020 | C | G | 1 | a0001c0001t0003g0328 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.21-20679C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172868020 | |||||||
| chr5:172868124 | C | T | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(296): Show |
299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.21-20575C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172868124 | |||||||
| chr5:172868148 | C | T | 79 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(76): Show |
79 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.21-20551C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172868148 | |||||||
| chr5:172868317 | G | A | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(292): Show |
295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.21-20382G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172868317 | |||||||
| chr5:172868496 | A | G | 1 | a0001c0001t0003g0154 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.21-20203A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172868496 | |||||||
| chr5:172868598 | C | T | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.21-20101C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172868598 | |||||||
| chr5:172868711 | G | C | 3 | a0001c0001t0001g0295 a0001c0001t0001g0325 a0001c0001t0004g0326 |
3 | HG02109.hp2 HG02615.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.21-19988G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172868711 | |||||||
| chr5:172868725 | C | A | 1 | a0001c0001t0002g0153 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.21-19974C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172868725 | |||||||
| chr5:172868747 | A | T | 88 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0031 others(85): Show |
88 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.21-19952A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172868747 | |||||||
| chr5:172868823 | T | C | 1 | a0001c0001t0002g0087 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.21-19876T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172868823 | |||||||
| chr5:172868833 | A | G | 2 | a0001c0001t0003g0273 a0001c0001t0003g0274 |
2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.21-19866A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172868833 | |||||||
| chr5:172868927 | G | C | 6 | a0001c0001t0001g0069 a0001c0001t0001g0193 a0001c0001t0001g0194 others(3): Show |
6 | HG00597.hp1 HG02155.hp2 NA18956.hp1 others(3): Show |
intron_variant | MODIFIER | c.21-19772G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172868927 | |||||||
| chr5:172869149 | G | A | 2 | a0001c0001t0007g0281 a0001c0001t0007g0282 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.21-19550G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172869149 | |||||||
| chr5:172869203 | A | G | 3 | a0001c0001t0001g0295 a0001c0001t0001g0325 a0001c0001t0004g0326 |
3 | HG02109.hp2 HG02615.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.21-19496A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172869203 | |||||||
| chr5:172869235 | C | T | 2 | a0001c0001t0002g0087 a0001c0001t0016g0197 |
2 | HG01192.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.21-19464C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172869235 | |||||||
| chr5:172869261 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.21-19438G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172869261 | |||||||
| chr5:172869322 | A | C | 1 | a0001c0001t0003g0198 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.21-19377A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172869322 | |||||||
| chr5:172869501 | G | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(205): Show |
208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.21-19198G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172869501 | |||||||
| chr5:172869650 | A | G | 1 | a0001c0001t0001g0043 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.21-19049A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172869650 | |||||||
| chr5:172869670 | T | C | 1 | a0001c0001t0001g0279 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.21-19029T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172869670 | |||||||
| chr5:172869777 | C | T | 1 | a0001c0001t0002g0087 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.21-18922C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172869777 | |||||||
| chr5:172869851 | C | G | 4 | a0001c0001t0002g0026 a0001c0001t0002g0177 a0001c0001t0002g0221 others(1): Show |
4 | NA18747.hp2 NA18944.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.21-18848C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172869851 | |||||||
| chr5:172870155 | T | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0009 others(189): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.21-18544T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172870155 | |||||||
| chr5:172870475 | T | G | 1 | a0001c0001t0001g0258 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.21-18224T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172870475 | |||||||
| chr5:172870575 | T | A | 1 | a0001c0001t0001g0258 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.21-18124T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172870575 | |||||||
| chr5:172870603 | A | G | 1 | a0001c0001t0001g0258 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.21-18096A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172870603 | |||||||
| chr5:172870604 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.21-18095G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172870604 | |||||||
| chr5:172870617 | A | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0265 a0001c0001t0001g0289 others(7): Show |
10 | HG01243.hp1 HG02109.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.21-18082A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172870617 | |||||||
| chr5:172870792 | C | G | 1 | a0001c0001t0001g0126 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.21-17907C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172870792 | |||||||
| chr5:172870793 | A | G | 19 | a0001c0001t0001g0001 a0001c0001t0001g0265 a0001c0001t0001g0289 others(16): Show |
19 | HG01192.hp1 HG01243.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.21-17906A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172870793 | |||||||
| chr5:172870850 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.21-17849C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172870850 | |||||||
| chr5:172870934 | G | T | 1 | a0001c0001t0001g0037 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.21-17765G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172870934 | |||||||
| chr5:172870937 | C | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0265 a0001c0001t0001g0289 others(7): Show |
10 | HG01243.hp1 HG02109.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.21-17762C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172870937 | |||||||
| chr5:172870982 | C | T | 4 | a0001c0001t0001g0304 a0001c0001t0003g0198 a0001c0001t0003g0272 others(1): Show |
4 | HG02647.hp1 HG02818.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.21-17717C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172870982 | |||||||
| chr5:172871033 | C | G | 1 | a0001c0001t0002g0098 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.21-17666C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172871033 | |||||||
| chr5:172871038 | A | G | 9 | a0001c0001t0001g0295 a0001c0001t0002g0087 a0001c0001t0003g0273 others(6): Show |
9 | HG01192.hp1 HG02615.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.21-17661A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172871038 | |||||||
| chr5:172871070 | G | T | 72 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(69): Show |
72 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.21-17629G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172871070 | |||||||
| chr5:172871178 | C | T | 2 | a0001c0001t0001g0295 a0001c0001t0023g0332 |
2 | HG02615.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.21-17521C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172871178 | |||||||
| chr5:172871201 | G | T | 1 | a0001c0001t0034g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.21-17498G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172871201 | |||||||
| chr5:172871314 | C | T | 2 | a0001c0001t0005g0005 a0001c0001t0015g0199 |
2 | NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.21-17385C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172871314 | |||||||
| chr5:172871319 | C | T | 2 | a0001c0001t0005g0005 a0001c0001t0015g0199 |
2 | NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.21-17380C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172871319 | |||||||
| chr5:172871433 | C | T | 2 | a0001c0001t0005g0005 a0001c0001t0015g0199 |
2 | NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.21-17266C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172871433 | |||||||
| chr5:172871584 | G | T | 5 | a0001c0001t0001g0149 a0001c0001t0001g0169 a0001c0001t0001g0170 others(2): Show |
5 | HG01106.hp1 HG01943.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.21-17115G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172871584 | |||||||
| chr5:172871626 | C | T | 1 | a0001c0001t0034g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.21-17073C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172871626 | |||||||
| chr5:172871768 | G | T | 2 | a0001c0001t0003g0273 a0001c0001t0003g0274 |
2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.21-16931G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172871768 | |||||||
| chr5:172871891 | G | A | 2 | a0001c0001t0002g0087 a0001c0001t0016g0197 |
2 | HG01192.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.21-16808G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172871891 | |||||||
| chr5:172871961 | A | G | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(313): Show |
316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.21-16738A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172871961 | |||||||
| chr5:172871994 | A | G | 194 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(191): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.21-16705A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172871994 | |||||||
| chr5:172872065 | C | T | 2 | a0001c0001t0002g0087 a0001c0001t0016g0197 |
2 | HG01192.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.21-16634C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172872065 | |||||||
| chr5:172872160 | G | A | 1 | a0001c0001t0025g0045 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.21-16539G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172872160 | |||||||
| chr5:172872278 | C | T | 3 | a0001c0001t0001g0295 a0001c0001t0023g0332 a0001c0005t0018g0161 |
3 | HG02615.hp2 HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.21-16421C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172872278 | |||||||
| chr5:172872298 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.21-16401A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172872298 | |||||||
| chr5:172872717 | A | AG | 3 | a0001c0001t0001g0295 a0001c0001t0023g0332 a0001c0005t0018g0161 |
3 | HG02615.hp2 HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.21-15980dupG | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172872717 | ||||||
| chr5:172872908 | G | A | 2 | a0001c0001t0002g0087 a0001c0001t0016g0197 |
2 | HG01192.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.21-15791G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172872908 | |||||||
| chr5:172873039 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.21-15660C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172873039 | |||||||
| chr5:172873079 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.21-15620C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172873079 | |||||||
| chr5:172873226 | G | C | 1 | a0001c0001t0002g0087 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.21-15473G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172873226 | |||||||
| chr5:172873245 | G | A | 1 | a0001c0001t0006g0270 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.21-15454G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172873245 | |||||||
| chr5:172873398 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(132): Show |
135 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.21-15301T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172873398 | |||||||
| chr5:172873404 | T | C | 2 | a0001c0001t0001g0009 a0001c0001t0002g0008 |
2 | HG01346.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.21-15295T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172873404 | |||||||
| chr5:172873461 | C | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0265 a0001c0001t0001g0289 others(6): Show |
9 | HG01243.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.21-15238C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172873461 | |||||||
| chr5:172873467 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(133): Show |
136 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.21-15232A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172873467 | |||||||
| chr5:172873602 | G | A | 2 | a0001c0001t0005g0005 a0001c0001t0015g0199 |
2 | NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.21-15097G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172873602 | |||||||
| chr5:172873730 | C | G | 1 | a0001c0001t0003g0055 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.21-14969C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172873730 | |||||||
| chr5:172873874 | T | G | 1 | a0001c0001t0002g0014 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.21-14825T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172873874 | |||||||
| chr5:172873880 | C | G | 4 | a0001c0001t0001g0040 a0001c0001t0001g0226 a0001c0001t0001g0260 others(1): Show |
4 | HG00673.hp1 NA18939.hp1 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.21-14819C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172873880 | |||||||
| chr5:172873938 | A | G | 5 | a0001c0001t0002g0122 a0001c0001t0007g0281 a0001c0001t0007g0282 others(2): Show |
5 | HG02055.hp2 HG02630.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.21-14761A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172873938 | |||||||
| chr5:172874084 | A | AT | 6 | a0001c0001t0001g0097 a0001c0001t0001g0295 a0001c0001t0002g0087 others(3): Show |
6 | HG01192.hp1 HG01255.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.21-14603dupT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172874084 | ||||||
| chr5:172874115 | G | T | 14 | a0001c0001t0001g0001 a0001c0001t0001g0265 a0001c0001t0001g0289 others(11): Show |
14 | HG01192.hp1 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.21-14584G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172874115 | |||||||
| chr5:172874121 | C | T | 1 | a0001c0001t0003g0267 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.21-14578C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172874121 | |||||||
| chr5:172874270 | G | A | 2 | a0001c0001t0003g0155 a0001c0001t0005g0105 |
2 | HG01109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.21-14429G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172874270 | |||||||
| chr5:172874328 | G | A | 1 | a0001c0001t0016g0197 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.21-14371G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172874328 | |||||||
| chr5:172874337 | T | C | 1 | a0001c0001t0001g0248 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.21-14362T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172874337 | |||||||
| chr5:172874338 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.21-14361C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172874338 | |||||||
| chr5:172874368 | A | G | 1 | a0001c0001t0002g0130 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.21-14331A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172874368 | |||||||
| chr5:172874427 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.21-14272C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172874427 | |||||||
| chr5:172874746 | C | A | 1 | a0001c0001t0001g0248 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.21-13953C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172874746 | |||||||
| chr5:172874756 | T | C | 1 | a0001c0001t0005g0266 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.21-13943T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172874756 | |||||||
| chr5:172874917 | T | C | 3 | a0001c0001t0001g0134 a0001c0001t0001g0276 a0001c0001t0001g0277 |
3 | HG02602.hp2 HG03017.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.21-13782T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172874917 | |||||||
| chr5:172874921 | T | TA | 8 | a0001c0001t0001g0002 a0001c0001t0001g0051 a0001c0001t0001g0214 others(5): Show |
8 | HG02145.hp1 HG03453.hp1 HG03927.hp1 others(5): Show |
intron_variant | MODIFIER | c.21-13759dupA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172874921 | ||||||
| chr5:172874921 | TA | T | 19 | a0001c0001t0001g0001 a0001c0001t0001g0041 a0001c0001t0001g0126 others(16): Show |
19 | HG01192.hp1 HG01243.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.21-13759delA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172874921 | ||||||
| chr5:172874976 | C | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0265 a0001c0001t0001g0289 others(8): Show |
11 | HG01243.hp1 HG01243.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.21-13723C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172874976 | |||||||
| chr5:172875406 | A | G | 15 | a0001c0001t0001g0001 a0001c0001t0001g0265 a0001c0001t0001g0289 others(12): Show |
15 | HG01192.hp1 HG01243.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.21-13293A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172875406 | |||||||
| chr5:172875601 | G | A | 3 | a0001c0001t0001g0295 a0001c0001t0023g0332 a0001c0005t0018g0161 |
3 | HG02615.hp2 HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.21-13098G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172875601 | |||||||
| chr5:172875860 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.21-12839G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172875860 | |||||||
| chr5:172876030 | G | A | 1 | a0001c0001t0002g0073 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.21-12669G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172876030 | |||||||
| chr5:172876100 | T | G | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(135): Show |
138 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.21-12599T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172876100 | |||||||
| chr5:172876154 | G | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(134): Show |
137 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(134): Show |
intron_variant | MODIFIER | c.21-12545G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172876154 | |||||||
| chr5:172876200 | G | T | 128 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(125): Show |
128 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(125): Show |
intron_variant | MODIFIER | c.21-12499G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172876200 | |||||||
| chr5:172876226 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(135): Show |
138 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(135): Show |
intron_variant | MODIFIER | c.21-12473G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172876226 | |||||||
| chr5:172876254 | T | C | 1 | a0001c0001t0005g0005 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.21-12445T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172876254 | |||||||
| chr5:172876340 | G | A | 7 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0005g0156 others(4): Show |
7 | HG01257.hp2 HG01258.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.21-12359G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172876340 | |||||||
| chr5:172876485 | A | G | 12 | a0001c0001t0001g0288 a0001c0001t0001g0307 a0001c0001t0001g0313 others(9): Show |
12 | HG01167.hp2 HG01884.hp1 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.21-12214A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172876485 | |||||||
| chr5:172876547 | A | G | 54 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0029 others(51): Show |
54 | HG00438.hp1 HG00609.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.21-12152A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172876547 | |||||||
| chr5:172876551 | C | T | 2 | a0001c0001t0002g0217 a0001c0001t0002g0218 |
2 | HG00741.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.21-12148C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172876551 | |||||||
| chr5:172876711 | C | G | 1 | a0001c0001t0002g0025 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.21-11988C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172876711 | |||||||
| chr5:172876840 | T | C | 1 | a0001c0001t0002g0098 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.21-11859T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172876840 | |||||||
| chr5:172876854 | A | G | 1 | a0001c0001t0002g0098 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.21-11845A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172876854 | |||||||
| chr5:172876873 | A | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0265 a0001c0001t0001g0289 others(9): Show |
12 | HG01192.hp1 HG01243.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.21-11826A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172876873 | |||||||
| chr5:172877408 | ATATG | A | 9 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0230 others(6): Show |
9 | HG00741.hp1 HG01123.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.21-11289_21-11286d others(6): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172877408 | ||||||
| chr5:172877410 | A | ATG | 14 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0001g0327 others(11): Show |
14 | HG01070.hp1 HG01071.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.21-11259_21-11258d others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172877410 | ||||||
| chr5:172877410 | A | ATGTG | 6 | a0001c0001t0001g0001 a0001c0001t0001g0265 a0001c0001t0001g0295 others(3): Show |
6 | HG01975.hp2 HG02615.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.21-11261_21-11258d others(6): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172877410 | ||||||
| chr5:172877410 | ATG | A | 77 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0013 others(74): Show |
77 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.21-11259_21-11258d others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172877410 | ||||||
| chr5:172877436 | G | A | 1 | a0001c0001t0025g0045 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.21-11263G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172877436 | |||||||
| chr5:172877438 | G | A | 10 | a0001c0001t0001g0042 a0001c0001t0001g0096 a0001c0001t0001g0169 others(7): Show |
10 | HG00323.hp1 HG01433.hp1 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.21-11261G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172877438 | |||||||
| chr5:172877438 | G | GTA | 8 | a0001c0001t0001g0040 a0001c0001t0001g0075 a0001c0001t0001g0196 others(5): Show |
8 | HG00673.hp1 HG02055.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.21-11260_21-11259i others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172877438 | ||||||
| chr5:172877440 | G | A | 196 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(193): Show |
196 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.21-11259G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172877440 | |||||||
| chr5:172877440 | G | GTA | 6 | a0001c0001t0001g0057 a0001c0001t0001g0090 a0001c0001t0001g0104 others(3): Show |
6 | HG00738.hp2 HG01192.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.21-11241_21-11240d others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172877440 | ||||||
| chr5:172877442 | A | G | 25 | a0001c0001t0001g0062 a0001c0001t0001g0288 a0001c0001t0001g0289 others(22): Show |
25 | HG00733.hp1 HG01167.hp2 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.21-11257A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172877442 | |||||||
| chr5:172877444 | A | G | 2 | a0001c0001t0002g0087 a0001c0001t0005g0297 |
2 | HG01192.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.21-11255A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172877444 | |||||||
| chr5:172877446 | A | G | 2 | a0001c0001t0002g0087 a0001c0001t0005g0266 |
2 | HG01192.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.21-11253A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172877446 | |||||||
| chr5:172877448 | A | G | 1 | a0001c0001t0002g0087 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.21-11251A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172877448 | |||||||
| chr5:172877450 | A | G | 1 | a0001c0001t0002g0087 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.21-11249A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172877450 | |||||||
| chr5:172877452 | A | G | 1 | a0001c0001t0002g0087 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.21-11247A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172877452 | |||||||
| chr5:172877455 | TATA | T | 13 | a0001c0001t0001g0016 a0001c0001t0001g0169 a0001c0001t0001g0200 others(10): Show |
13 | HG01943.hp2 HG01981.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.21-11243_21-11241d others(5): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172877455 | |||||||
| chr5:172877456 | A | T | 1 | a0001c0001t0001g0201 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.21-11243A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172877456 | |||||||
| chr5:172877456 | ATAT | A | 61 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0019 others(58): Show |
61 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.21-11241_21-11239d others(5): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172877456 | ||||||
| chr5:172877457 | TA | T | 8 | a0001c0001t0001g0048 a0001c0001t0001g0230 a0001c0001t0002g0094 others(5): Show |
8 | HG00741.hp1 HG01123.hp1 HG01175.hp1 others(5): Show |
intron_variant | MODIFIER | c.21-11241delA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172877457 | |||||||
| chr5:172877458 | A | ATATATAT others(3): Show |
3 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0013g0291 |
3 | HG01243.hp1 HG02572.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.21-11240_21-11239i others(12): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172877458 | ||||||
| chr5:172877458 | A | T | 54 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0018 others(51): Show |
54 | HG00323.hp1 HG00544.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.21-11241A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172877458 | |||||||
| chr5:172877459 | T | TA | 5 | a0001c0001t0001g0074 a0001c0001t0001g0248 a0001c0001t0004g0176 others(2): Show |
5 | HG02886.hp1 NA18953.hp1 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.21-11240_21-11239i others(3): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172877459 | |||||||
| chr5:172877460 | T | A | 121 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(118): Show |
121 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.21-11239T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172877460 | |||||||
| chr5:172877461 | T | A | 8 | a0001c0001t0001g0074 a0001c0001t0001g0248 a0001c0001t0001g0259 others(5): Show |
8 | HG01192.hp1 HG01975.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.21-11238T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172877461 | |||||||
| chr5:172877462 | T | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0020 a0001c0001t0001g0029 others(33): Show |
36 | HG00323.hp2 HG00438.hp1 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.21-11237T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172877462 | |||||||
| chr5:172877463 | T | A | 3 | a0001c0001t0002g0087 a0001c0001t0005g0297 a0001c0001t0034g0086 |
3 | HG01192.hp1 HG02647.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.21-11236T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172877463 | |||||||
| chr5:172877464 | T | A | 15 | a0001c0001t0001g0038 a0001c0001t0001g0288 a0001c0001t0001g0307 others(12): Show |
15 | HG01167.hp2 HG01884.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.21-11235T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172877464 | |||||||
| chr5:172877465 | T | A | 1 | a0001c0001t0005g0297 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.21-11234T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172877465 | |||||||
| chr5:172877506 | C | T | 1 | a0001c0005t0018g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.21-11193C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172877506 | |||||||
| chr5:172877522 | C | T | 1 | a0001c0001t0011g0117 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.21-11177C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172877522 | |||||||
| chr5:172877608 | GC | G | 111 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(108): Show |
111 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.21-11090delC | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172877608 | |||||||
| chr5:172877612 | C | T | 3 | a0001c0001t0003g0055 a0001c0001t0005g0005 a0001c0001t0015g0199 |
3 | HG01243.hp2 NA19240.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.21-11087C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172877612 | |||||||
| chr5:172877626 | C | T | 1 | a0001c0001t0004g0166 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.21-11073C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172877626 | |||||||
| chr5:172877700 | G | A | 1 | a0001c0001t0003g0328 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.21-10999G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172877700 | |||||||
| chr5:172877917 | C | T | 2 | a0001c0001t0002g0026 a0001c0001t0004g0023 |
2 | NA18944.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.21-10782C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172877917 | |||||||
| chr5:172878106 | G | A | 1 | a0001c0001t0034g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.21-10593G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172878106 | |||||||
| chr5:172878142 | G | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(78): Show |
81 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(78): Show |
intron_variant | MODIFIER | c.21-10557G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172878142 | |||||||
| chr5:172878365 | G | A | 3 | a0001c0001t0001g0134 a0001c0001t0001g0276 a0001c0001t0001g0277 |
3 | HG02602.hp2 HG03017.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.21-10334G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172878365 | |||||||
| chr5:172878477 | T | C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0265 a0001c0001t0001g0289 others(6): Show |
9 | HG01243.hp1 HG02109.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.21-10222T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172878477 | |||||||
| chr5:172878534 | G | A | 2 | a0001c0001t0001g0209 a0001c0001t0001g0214 |
2 | NA18968.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.21-10165G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172878534 | |||||||
| chr5:172878625 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.21-10074A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172878625 | |||||||
| chr5:172878747 | G | A | 1 | a0001c0001t0005g0005 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.21-9952G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172878747 | |||||||
| chr5:172878770 | G | A | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.21-9929G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172878770 | |||||||
| chr5:172878847 | G | T | 1 | a0001c0001t0001g0015 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.21-9852G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172878847 | |||||||
| chr5:172879105 | A | G | 8 | a0001c0001t0001g0295 a0001c0001t0002g0087 a0001c0001t0003g0055 others(5): Show |
8 | HG01192.hp1 HG01243.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.21-9594A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172879105 | |||||||
| chr5:172879455 | C | T | 12 | a0001c0001t0001g0288 a0001c0001t0001g0307 a0001c0001t0001g0313 others(9): Show |
12 | HG01167.hp2 HG01884.hp1 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.21-9244C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172879455 | |||||||
| chr5:172879495 | T | C | 1 | a0001c0001t0004g0166 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.21-9204T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172879495 | |||||||
| chr5:172879537 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(123): Show |
126 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.21-9162C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172879537 | |||||||
| chr5:172879581 | T | C | 1 | a0001c0001t0005g0297 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.21-9118T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172879581 | |||||||
| chr5:172879592 | G | A | 1 | a0001c0001t0001g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.21-9107G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172879592 | |||||||
| chr5:172879731 | G | C | 1 | a0001c0001t0001g0021 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.21-8968G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172879731 | |||||||
| chr5:172879877 | C | A | 2 | a0001c0001t0002g0138 a0001c0001t0002g0146 |
2 | HG00140.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.21-8822C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172879877 | |||||||
| chr5:172879925 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.21-8774C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172879925 | |||||||
| chr5:172879952 | A | C | 27 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0038 others(24): Show |
27 | HG00438.hp1 HG00609.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.21-8747A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172879952 | |||||||
| chr5:172880283 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0244 |
2 | NA18986.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.21-8416C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172880283 | |||||||
| chr5:172880662 | T | A | 1 | a0001c0001t0011g0099 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.21-8037T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172880662 | |||||||
| chr5:172880987 | G | A | 72 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0020 others(69): Show |
72 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.21-7712G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172880987 | |||||||
| chr5:172881405 | T | G | 1 | a0001c0001t0003g0055 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.21-7294T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172881405 | |||||||
| chr5:172881460 | A | G | 10 | a0001c0001t0002g0122 a0001c0001t0003g0328 a0001c0001t0005g0005 others(7): Show |
10 | HG02055.hp2 HG02630.hp2 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.21-7239A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172881460 | |||||||
| chr5:172881663 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.21-7036G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172881663 | |||||||
| chr5:172881694 | A | C | 1 | a0001c0001t0001g0104 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.21-7005A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172881694 | |||||||
| chr5:172881714 | A | G | 1 | a0001c0001t0003g0328 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.21-6985A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172881714 | |||||||
| chr5:172881731 | G | A | 2 | a0001c0001t0002g0087 a0001c0001t0005g0297 |
2 | HG01192.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.21-6968G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172881731 | |||||||
| chr5:172881923 | T | C | 1 | a0001c0001t0016g0197 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.21-6776T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172881923 | |||||||
| chr5:172882162 | G | A | 2 | a0001c0001t0002g0269 a0001c0001t0006g0270 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.21-6537G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172882162 | |||||||
| chr5:172882166 | G | C | 19 | a0001c0001t0001g0268 a0001c0001t0002g0122 a0001c0001t0003g0154 others(16): Show |
19 | HG02055.hp2 HG02559.hp2 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.21-6533G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172882166 | |||||||
| chr5:172882189 | G | A | 5 | a0001c0001t0001g0063 a0001c0001t0001g0136 a0001c0001t0002g0010 others(2): Show |
5 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.21-6510G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172882189 | |||||||
| chr5:172882336 | G | T | 1 | a0001c0001t0013g0291 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.21-6363G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172882336 | |||||||
| chr5:172882496 | G | A | 1 | a0001c0001t0003g0334 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.21-6203G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172882496 | |||||||
| chr5:172882574 | T | A | 1 | a0001c0001t0004g0166 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.21-6125T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172882574 | |||||||
| chr5:172882576 | T | C | 8 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0232 others(5): Show |
8 | HG00639.hp1 HG00741.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.21-6123T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172882576 | |||||||
| chr5:172882583 | T | G | 6 | a0001c0001t0001g0305 a0001c0001t0002g0269 a0001c0001t0003g0293 others(3): Show |
6 | HG02145.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.21-6116T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172882583 | |||||||
| chr5:172882715 | G | C | 5 | a0001c0001t0001g0305 a0001c0001t0002g0269 a0001c0001t0003g0293 others(2): Show |
5 | HG02145.hp1 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.21-5984G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172882715 | |||||||
| chr5:172882807 | C | T | 2 | a0001c0001t0023g0332 a0001c0005t0018g0161 |
2 | HG02970.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.21-5892C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172882807 | |||||||
| chr5:172882850 | A | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(108): Show |
111 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.21-5849A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172882850 | |||||||
| chr5:172882925 | A | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(117): Show |
120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.21-5774A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172882925 | |||||||
| chr5:172883009 | T | C | 8 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0232 others(5): Show |
8 | HG00639.hp1 HG00741.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.21-5690T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172883009 | |||||||
| chr5:172883124 | T | A | 1 | a0001c0001t0001g0248 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.21-5575T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172883124 | |||||||
| chr5:172883127 | A | T | 1 | a0001c0001t0001g0248 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.21-5572A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172883127 | |||||||
| chr5:172883149 | T | A | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.21-5550T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172883149 | |||||||
| chr5:172883184 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.21-5515G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172883184 | |||||||
| chr5:172883260 | T | A | 7 | a0001c0001t0003g0061 a0001c0001t0003g0155 a0001c0001t0003g0283 others(4): Show |
7 | HG01109.hp2 HG02451.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.21-5439T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172883260 | |||||||
| chr5:172883302 | G | T | 1 | a0001c0005t0018g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.21-5397G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172883302 | |||||||
| chr5:172883303 | C | T | 1 | a0001c0005t0018g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.21-5396C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172883303 | |||||||
| chr5:172883308 | G | A | 1 | a0002c0003t0002g0012 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.21-5391G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172883308 | |||||||
| chr5:172883368 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.21-5331C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172883368 | |||||||
| chr5:172883618 | C | T | 1 | a0001c0001t0003g0055 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.21-5081C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172883618 | |||||||
| chr5:172883665 | T | C | 1 | a0001c0001t0034g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.21-5034T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172883665 | |||||||
| chr5:172883694 | T | G | 1 | a0001c0001t0001g0252 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.21-5005T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172883694 | |||||||
| chr5:172883753 | G | A | 4 | a0001c0001t0001g0313 a0001c0001t0001g0325 a0001c0001t0004g0326 others(1): Show |
4 | HG01884.hp1 HG02109.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.21-4946G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172883753 | |||||||
| chr5:172883761 | C | T | 1 | a0001c0001t0005g0301 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.21-4938C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172883761 | |||||||
| chr5:172883762 | G | A | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.21-4937G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172883762 | |||||||
| chr5:172883776 | G | A | 4 | a0001c0001t0001g0313 a0001c0001t0001g0325 a0001c0001t0004g0326 others(1): Show |
4 | HG01884.hp1 HG02109.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.21-4923G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172883776 | |||||||
| chr5:172883866 | C | G | 2 | a0001c0001t0006g0004 a0001c0001t0006g0053 |
2 | HG02723.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.21-4833C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172883866 | |||||||
| chr5:172884098 | G | A | 183 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(180): Show |
183 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.21-4601G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172884098 | |||||||
| chr5:172884244 | G | GT | 23 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0001g0051 others(20): Show |
23 | HG01243.hp2 HG01257.hp2 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.21-4429dupT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172884244 | ||||||
| chr5:172884244 | G | GTT | 72 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0018 others(69): Show |
72 | HG00733.hp2 HG00738.hp2 HG00741.hp1 others(69): Show |
intron_variant | MODIFIER | c.21-4430_21-4429dup others(2): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172884244 | ||||||
| chr5:172884244 | G | GTTT | 10 | a0001c0001t0001g0038 a0001c0001t0001g0080 a0001c0001t0001g0165 others(7): Show |
10 | HG01243.hp1 HG02055.hp1 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.21-4431_21-4429dup others(3): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172884244 | ||||||
| chr5:172884244 | GT | G | 20 | a0001c0001t0001g0029 a0001c0001t0001g0097 a0001c0001t0001g0115 others(17): Show |
20 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(17): Show |
intron_variant | MODIFIER | c.21-4429delT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172884244 | ||||||
| chr5:172884255 | T | TG | 8 | a0001c0001t0001g0063 a0001c0001t0001g0136 a0001c0001t0001g0265 others(5): Show |
8 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.21-4444_21-4443ins others(1): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172884255 | |||||||
| chr5:172884256 | T | G | 18 | a0001c0001t0001g0115 a0001c0001t0001g0288 a0001c0001t0001g0305 others(15): Show |
18 | HG00280.hp2 HG01167.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.21-4443T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172884256 | |||||||
| chr5:172884256 | T | TG | 106 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0015 others(103): Show |
106 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.21-4443_21-4442ins others(1): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172884256 | |||||||
| chr5:172884257 | T | G | 2 | a0001c0001t0001g0248 a0001c0001t0004g0023 |
2 | NA18968.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.21-4442T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172884257 | |||||||
| chr5:172884265 | T | G | 10 | a0001c0001t0001g0288 a0001c0001t0001g0307 a0001c0001t0003g0267 others(7): Show |
10 | HG01167.hp2 HG02896.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.21-4434T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172884265 | |||||||
| chr5:172884266 | T | G | 1 | a0001c0005t0018g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.21-4433T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172884266 | |||||||
| chr5:172884366 | T | G | 5 | a0001c0001t0001g0063 a0001c0001t0001g0136 a0001c0001t0002g0010 others(2): Show |
5 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.21-4333T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172884366 | |||||||
| chr5:172884492 | C | T | 21 | a0001c0001t0001g0002 a0001c0001t0001g0064 a0001c0001t0001g0072 others(18): Show |
21 | HG00639.hp1 HG00741.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.21-4207C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172884492 | |||||||
| chr5:172884568 | C | T | 5 | a0001c0001t0001g0063 a0001c0001t0001g0136 a0001c0001t0002g0010 others(2): Show |
5 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.21-4131C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172884568 | |||||||
| chr5:172884677 | C | T | 10 | a0001c0001t0001g0288 a0001c0001t0001g0307 a0001c0001t0003g0267 others(7): Show |
10 | HG01167.hp2 HG02896.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.21-4022C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172884677 | |||||||
| chr5:172884794 | T | C | 1 | a0001c0001t0001g0022 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.21-3905T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172884794 | |||||||
| chr5:172884940 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.21-3759G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172884940 | |||||||
| chr5:172884994 | A | G | 1 | a0001c0001t0001g0219 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.21-3705A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172884994 | |||||||
| chr5:172885186 | T | C | 12 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0002g0229 others(9): Show |
12 | HG01257.hp2 HG01258.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.21-3513T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172885186 | |||||||
| chr5:172885305 | A | AT | 218 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(215): Show |
218 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.21-3385dupT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172885305 | ||||||
| chr5:172885305 | AT | A | 17 | a0001c0001t0001g0265 a0001c0001t0001g0288 a0001c0001t0001g0307 others(14): Show |
17 | HG01167.hp2 HG01243.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.21-3385delT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172885305 | ||||||
| chr5:172885450 | A | T | 1 | a0001c0001t0001g0070 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.21-3249A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172885450 | |||||||
| chr5:172885477 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.21-3222C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172885477 | |||||||
| chr5:172885527 | T | C | 3 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0013g0291 |
3 | HG01243.hp1 HG02572.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.21-3172T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172885527 | |||||||
| chr5:172885571 | A | G | 4 | a0001c0001t0001g0265 a0001c0001t0003g0055 a0001c0001t0003g0298 others(1): Show |
4 | HG01243.hp2 HG03195.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.21-3128A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172885571 | |||||||
| chr5:172885625 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.21-3074C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172885625 | |||||||
| chr5:172885658 | A | G | 2 | a0001c0001t0001g0265 a0001c0001t0003g0298 |
2 | HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.21-3041A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172885658 | |||||||
| chr5:172885706 | T | TCCTGCTG others(8): Show |
42 | a0001c0001t0001g0038 a0001c0001t0001g0059 a0001c0001t0001g0115 others(39): Show |
42 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.21-2985_21-2984ins others(15): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172885706 | ||||||
| chr5:172885770 | C | T | 3 | a0001c0001t0001g0313 a0001c0001t0001g0325 a0001c0001t0004g0326 |
3 | HG01884.hp1 HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.21-2929C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172885770 | |||||||
| chr5:172885872 | G | A | 1 | a0001c0001t0003g0055 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.21-2827G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172885872 | |||||||
| chr5:172885990 | A | C | 10 | a0001c0001t0001g0121 a0001c0001t0001g0144 a0001c0001t0002g0217 others(7): Show |
10 | HG00639.hp1 HG00741.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.21-2709A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172885990 | |||||||
| chr5:172886031 | G | C | 88 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0030 others(85): Show |
88 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.21-2668G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172886031 | |||||||
| chr5:172886069 | C | T | 1 | a0001c0001t0022g0315 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.21-2630C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172886069 | |||||||
| chr5:172886208 | G | A | 101 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0030 others(98): Show |
101 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.21-2491G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172886208 | |||||||
| chr5:172886229 | G | A | 2 | a0001c0001t0002g0217 a0001c0001t0002g0218 |
2 | HG00741.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.21-2470G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172886229 | |||||||
| chr5:172886246 | G | A | 2 | a0001c0001t0002g0243 a0001c0001t0004g0246 |
2 | NA18966.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.21-2453G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172886246 | |||||||
| chr5:172886277 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.21-2422C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172886277 | |||||||
| chr5:172886494 | C | T | 32 | a0001c0001t0001g0265 a0001c0001t0001g0295 a0001c0001t0001g0313 others(29): Show |
32 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.21-2205C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172886494 | |||||||
| chr5:172886549 | G | T | 4 | a0001c0001t0002g0082 a0001c0001t0003g0273 a0001c0001t0003g0274 others(1): Show |
4 | HG02630.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.21-2150G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172886549 | |||||||
| chr5:172886596 | A | G | 6 | a0001c0001t0002g0082 a0001c0001t0003g0273 a0001c0001t0003g0274 others(3): Show |
6 | HG02630.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.21-2103A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172886596 | |||||||
| chr5:172886604 | TTAATAA | T | 9 | a0001c0001t0001g0288 a0001c0001t0001g0307 a0001c0001t0003g0267 others(6): Show |
9 | HG01167.hp2 HG02896.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.21-2089_21-2084del others(6): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172886604 | ||||||
| chr5:172886812 | G | GC | 6 | a0001c0001t0002g0082 a0001c0001t0003g0273 a0001c0001t0003g0274 others(3): Show |
6 | HG02630.hp1 HG02809.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.21-1884dupC | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr5 | 172886812 | ||||||
| chr5:172887014 | G | T | 4 | a0001c0001t0002g0082 a0001c0001t0003g0273 a0001c0001t0003g0274 others(1): Show |
4 | HG02630.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.21-1685G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172887014 | |||||||
| chr5:172887035 | G | T | 24 | a0001c0001t0001g0295 a0001c0001t0001g0313 a0001c0001t0001g0325 others(21): Show |
24 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.21-1664G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172887035 | |||||||
| chr5:172887066 | C | A | 9 | a0001c0001t0001g0288 a0001c0001t0001g0307 a0001c0001t0003g0267 others(6): Show |
9 | HG01167.hp2 HG02896.hp2 HG03098.hp1 others(6): Show |
intron_variant | MODIFIER | c.21-1633C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172887066 | |||||||
| chr5:172887088 | A | G | 93 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0030 others(90): Show |
93 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.21-1611A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172887088 | |||||||
| chr5:172887211 | G | A | 13 | a0001c0001t0001g0047 a0001c0001t0001g0063 a0001c0001t0001g0151 others(10): Show |
13 | HG01081.hp2 HG01167.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.21-1488G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172887211 | |||||||
| chr5:172887327 | C | T | 18 | a0001c0001t0001g0295 a0001c0001t0003g0155 a0001c0001t0003g0283 others(15): Show |
18 | HG01109.hp2 HG01884.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.21-1372C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172887327 | |||||||
| chr5:172887369 | C | T | 1 | a0001c0001t0001g0190 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.21-1330C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172887369 | |||||||
| chr5:172887400 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.21-1299G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172887400 | |||||||
| chr5:172887460 | A | G | 89 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(86): Show |
89 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.21-1239A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172887460 | |||||||
| chr5:172887473 | C | G | 86 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(83): Show |
86 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.21-1226C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172887473 | |||||||
| chr5:172887477 | T | C | 15 | a0001c0001t0001g0006 a0001c0001t0001g0080 a0001c0001t0001g0126 others(12): Show |
15 | HG00408.hp2 HG00423.hp2 HG02056.hp2 others(12): Show |
intron_variant | MODIFIER | c.21-1222T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172887477 | |||||||
| chr5:172887548 | C | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0050 a0001c0001t0001g0238 |
3 | NA18960.hp1 NA18967.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.21-1151C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172887548 | |||||||
| chr5:172887792 | A | G | 266 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0009 others(263): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.21-907A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172887792 | |||||||
| chr5:172887884 | G | C | 1 | a0001c0001t0004g0246 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.21-815G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172887884 | |||||||
| chr5:172887944 | G | T | 3 | a0001c0001t0001g0009 a0001c0001t0002g0008 a0001c0001t0002g0087 |
3 | HG01192.hp1 HG01346.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.21-755G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172887944 | |||||||
| chr5:172888066 | A | G | 3 | a0001c0001t0001g0265 a0001c0001t0003g0298 a0001c0001t0005g0005 |
3 | HG03195.hp1 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.21-633A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172888066 | |||||||
| chr5:172888069 | C | A | 168 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0016 others(165): Show |
168 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.21-630C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172888069 | |||||||
| chr5:172888331 | A | G | 6 | a0001c0001t0001g0064 a0001c0001t0001g0097 a0001c0001t0001g0134 others(3): Show |
6 | HG01106.hp2 HG01255.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.21-368A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172888331 | |||||||
| chr5:172888368 | G | A | 3 | a0001c0001t0001g0265 a0001c0001t0003g0298 a0001c0001t0005g0005 |
3 | HG03195.hp1 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.21-331G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172888368 | |||||||
| chr5:172888466 | A | G | 1 | a0001c0001t0002g0324 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.21-233A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172888466 | |||||||
| chr5:172888528 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.21-171A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172888528 | |||||||
| chr5:172888612 | T | G | 4 | a0001c0001t0002g0082 a0001c0001t0003g0273 a0001c0001t0003g0274 others(1): Show |
4 | HG02630.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.21-87T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 1/9 | chr5 | 172888612 | |||||||
| chr5:172888787 | C | T | 1 | a0001c0001t0003g0198 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.82+27C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172888787 | |||||||
| chr5:172888869 | G | A | 82 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(79): Show |
82 | HG00323.hp2 HG00597.hp1 HG00597.hp2 others(79): Show |
intron_variant | MODIFIER | c.82+109G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172888869 | |||||||
| chr5:172888895 | G | A | 1 | a0001c0001t0003g0294 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.82+135G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172888895 | |||||||
| chr5:172888993 | G | A | 3 | a0001c0001t0003g0284 a0001c0001t0009g0330 a0001c0001t0033g0085 |
3 | HG02055.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.82+233G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172888993 | |||||||
| chr5:172889010 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.82+250C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172889010 | |||||||
| chr5:172889164 | G | A | 21 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0295 others(18): Show |
21 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.82+404G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172889164 | |||||||
| chr5:172889271 | C | T | 2 | a0001c0001t0003g0273 a0001c0001t0003g0274 |
2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.82+511C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172889271 | |||||||
| chr5:172889369 | G | T | 1 | a0001c0001t0003g0154 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.82+609G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172889369 | |||||||
| chr5:172889405 | T | TA | 10 | a0001c0001t0001g0123 a0001c0001t0001g0202 a0001c0001t0001g0268 others(7): Show |
10 | HG01070.hp1 HG01071.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.82+656dupA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172889405 | ||||||
| chr5:172889412 | A | T | 1 | a0001c0001t0005g0206 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.82+652A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172889412 | |||||||
| chr5:172889980 | G | A | 5 | a0001c0001t0001g0313 a0001c0001t0001g0325 a0001c0001t0003g0061 others(2): Show |
5 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.82+1220G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172889980 | |||||||
| chr5:172890116 | G | C | 6 | a0001c0001t0001g0265 a0001c0001t0003g0055 a0001c0001t0003g0298 others(3): Show |
6 | HG01243.hp2 HG03195.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+1356G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172890116 | |||||||
| chr5:172890133 | G | A | 1 | a0001c0001t0005g0266 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.82+1373G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172890133 | |||||||
| chr5:172890133 | G | T | 2 | a0001c0001t0003g0328 a0001c0001t0010g0058 |
2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.82+1373G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172890133 | |||||||
| chr5:172890256 | T | C | 2 | a0001c0001t0002g0132 a0001c0001t0002g0239 |
2 | HG01258.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.82+1496T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172890256 | |||||||
| chr5:172890350 | A | T | 3 | a0001c0001t0001g0265 a0001c0001t0003g0298 a0001c0001t0005g0005 |
3 | HG03195.hp1 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.82+1590A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172890350 | |||||||
| chr5:172890434 | T | G | 25 | a0001c0001t0001g0121 a0001c0001t0001g0144 a0001c0001t0001g0289 others(22): Show |
25 | HG00639.hp1 HG00741.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.82+1674T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172890434 | |||||||
| chr5:172890465 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.82+1705G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172890465 | |||||||
| chr5:172890506 | C | G | 86 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(83): Show |
86 | HG00323.hp2 HG00597.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.82+1746C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172890506 | |||||||
| chr5:172890541 | G | C | 6 | a0001c0001t0001g0313 a0001c0001t0001g0325 a0001c0001t0003g0061 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+1781G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172890541 | |||||||
| chr5:172890625 | G | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0050 a0001c0001t0001g0238 |
3 | NA18960.hp1 NA18967.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.82+1865G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172890625 | |||||||
| chr5:172890840 | AC | A | 83 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(80): Show |
83 | HG00323.hp2 HG00597.hp1 HG00597.hp2 others(80): Show |
intron_variant | MODIFIER | c.82+2081delC | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172890840 | |||||||
| chr5:172890959 | G | A | 1 | a0001c0001t0022g0315 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.82+2199G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172890959 | |||||||
| chr5:172890971 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.82+2211C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172890971 | |||||||
| chr5:172891001 | T | G | 1 | a0001c0001t0034g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.82+2241T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172891001 | |||||||
| chr5:172891478 | C | T | 4 | a0001c0001t0001g0265 a0001c0001t0003g0055 a0001c0001t0003g0298 others(1): Show |
4 | HG01243.hp2 HG03195.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.82+2718C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172891478 | |||||||
| chr5:172891524 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.82+2764T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172891524 | |||||||
| chr5:172891793 | C | T | 1 | a0001c0001t0003g0328 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.82+3033C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172891793 | |||||||
| chr5:172892060 | A | ATTTTTGT others(12): Show |
2 | a0001c0001t0001g0041 a0001c0001t0002g0142 |
2 | HG01257.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.82+3301_82+3302ins others(19): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172892060 | ||||||
| chr5:172892060 | A | ATTTTTTT others(12): Show |
49 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(46): Show |
49 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.82+3301_82+3302ins others(19): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172892060 | ||||||
| chr5:172892062 | G | GT | 17 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0241 others(14): Show |
17 | HG01258.hp2 HG01515.hp1 HG02300.hp2 others(14): Show |
intron_variant | MODIFIER | c.82+3326dupT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172892062 | ||||||
| chr5:172892062 | G | T | 1 | a0001c0001t0001g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.82+3302G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172892062 | |||||||
| chr5:172892062 | GT | G | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(139): Show |
142 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.82+3326delT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172892062 | ||||||
| chr5:172892062 | GTT | G | 52 | a0001c0001t0001g0037 a0001c0001t0001g0071 a0001c0001t0001g0100 others(49): Show |
52 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.82+3325_82+3326del others(2): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172892062 | ||||||
| chr5:172892062 | GTTT | G | 6 | a0001c0001t0001g0262 a0001c0001t0001g0295 a0001c0001t0005g0266 others(3): Show |
6 | HG02615.hp2 HG02723.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+3324_82+3326del others(3): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172892062 | ||||||
| chr5:172892070 | T | G | 1 | a0001c0001t0015g0199 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.82+3310T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172892070 | |||||||
| chr5:172892071 | T | G | 1 | a0001c0001t0006g0053 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82+3311T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172892071 | |||||||
| chr5:172892073 | T | G | 49 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(46): Show |
49 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.82+3313T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172892073 | |||||||
| chr5:172892076 | T | G | 1 | a0001c0001t0001g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.82+3316T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172892076 | |||||||
| chr5:172892337 | G | A | 6 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0048 others(3): Show |
6 | HG02074.hp1 NA18942.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+3577G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172892337 | |||||||
| chr5:172892343 | C | T | 51 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(48): Show |
51 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.82+3583C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172892343 | |||||||
| chr5:172892368 | T | G | 6 | a0001c0001t0001g0265 a0001c0001t0003g0055 a0001c0001t0003g0298 others(3): Show |
6 | HG01243.hp2 HG03195.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+3608T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172892368 | |||||||
| chr5:172892500 | C | T | 1 | a0001c0001t0003g0328 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.82+3740C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172892500 | |||||||
| chr5:172892680 | C | A | 4 | a0001c0001t0001g0265 a0001c0001t0003g0055 a0001c0001t0003g0298 others(1): Show |
4 | HG01243.hp2 HG03195.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.82+3920C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172892680 | |||||||
| chr5:172892733 | T | G | 89 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(86): Show |
89 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.82+3973T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172892733 | |||||||
| chr5:172892800 | CTG | C | 6 | a0001c0001t0001g0313 a0001c0001t0001g0325 a0001c0001t0003g0061 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.82+4041_82+4042del others(2): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172892800 | |||||||
| chr5:172892941 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.83-4061C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172892941 | |||||||
| chr5:172892942 | A | G | 6 | a0001c0001t0001g0265 a0001c0001t0003g0055 a0001c0001t0003g0298 others(3): Show |
6 | HG01243.hp2 HG03195.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-4060A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172892942 | |||||||
| chr5:172893021 | A | G | 89 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(86): Show |
89 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.83-3981A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893021 | |||||||
| chr5:172893066 | C | T | 17 | a0001c0001t0001g0295 a0001c0001t0003g0155 a0001c0001t0003g0283 others(14): Show |
17 | HG01109.hp2 HG02280.hp1 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.83-3936C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893066 | |||||||
| chr5:172893125 | T | C | 174 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0016 others(171): Show |
174 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.83-3877T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893125 | |||||||
| chr5:172893241 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.83-3761G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893241 | |||||||
| chr5:172893260 | G | C | 6 | a0001c0001t0001g0265 a0001c0001t0003g0055 a0001c0001t0003g0298 others(3): Show |
6 | HG01243.hp2 HG03195.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-3742G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893260 | |||||||
| chr5:172893302 | C | T | 3 | a0001c0001t0003g0311 a0001c0001t0007g0281 a0001c0001t0007g0282 |
3 | HG02630.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.83-3700C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893302 | |||||||
| chr5:172893443 | C | T | 1 | a0001c0001t0003g0272 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.83-3559C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893443 | |||||||
| chr5:172893498 | G | A | 2 | a0001c0001t0003g0271 a0001c0001t0003g0292 |
2 | HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.83-3504G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893498 | |||||||
| chr5:172893671 | T | C | 61 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(58): Show |
61 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.83-3331T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893671 | |||||||
| chr5:172893810 | G | A | 78 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(75): Show |
78 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.83-3192G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893810 | |||||||
| chr5:172893868 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.83-3134G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893868 | |||||||
| chr5:172893868 | G | GAT | 3 | a0001c0001t0001g0213 a0001c0001t0001g0276 a0001c0001t0001g0277 |
3 | HG02602.hp2 HG03017.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.83-3097_83-3096dup others(2): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893868 | ||||||
| chr5:172893868 | G | GATAT | 3 | a0001c0001t0006g0309 a0001c0001t0023g0332 a0001c0001t0026g0215 |
3 | HG02896.hp2 NA18971.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.83-3099_83-3096dup others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893868 | ||||||
| chr5:172893868 | G | GATATAT | 7 | a0001c0001t0001g0288 a0001c0001t0001g0307 a0001c0001t0003g0296 others(4): Show |
7 | HG01167.hp2 HG02809.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.83-3101_83-3096dup others(6): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893868 | ||||||
| chr5:172893868 | G | GATATATA others(3): Show |
1 | a0001c0001t0003g0267 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.83-3105_83-3096dup others(10): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893868 | ||||||
| chr5:172893868 | GATATATA others(1): Show |
G | 5 | a0001c0001t0001g0071 a0001c0001t0001g0100 a0001c0001t0001g0200 others(2): Show |
5 | NA18956.hp2 NA18968.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.83-3103_83-3096del others(8): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893868 | ||||||
| chr5:172893868 | GATATATA others(3): Show |
G | 1 | a0001c0001t0001g0259 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.83-3105_83-3096del others(10): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893868 | ||||||
| chr5:172893868 | GATATATA others(9): Show |
G | 1 | a0001c0001t0011g0099 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.83-3111_83-3096del others(16): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893868 | ||||||
| chr5:172893868 | GATATATA others(15): Show |
G | 4 | a0001c0001t0002g0082 a0001c0001t0002g0318 a0001c0001t0003g0273 others(1): Show |
4 | HG02630.hp1 HG02809.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-3117_83-3096del others(22): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893868 | ||||||
| chr5:172893868 | GATATATA others(63): Show |
G | 6 | a0001c0001t0001g0265 a0001c0001t0003g0055 a0001c0001t0003g0298 others(3): Show |
6 | HG01243.hp2 HG03195.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-3117_83-3048del others(70): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893868 | ||||||
| chr5:172893882 | T | C | 83 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(80): Show |
83 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.83-3120T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893882 | |||||||
| chr5:172893893 | A | G | 1 | a0001c0001t0001g0232 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.83-3109A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893893 | |||||||
| chr5:172893895 | A | G | 3 | a0001c0001t0001g0232 a0001c0001t0002g0130 a0001c0001t0009g0330 |
3 | HG01106.hp2 HG01123.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.83-3107A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893895 | |||||||
| chr5:172893896 | T | TACACACA others(31): Show |
4 | a0001c0001t0001g0121 a0001c0001t0001g0144 a0001c0001t0002g0217 others(1): Show |
4 | HG00639.hp1 HG00741.hp2 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.83-3105_83-3104ins others(38): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893896 | ||||||
| chr5:172893896 | T | TATACACA others(31): Show |
1 | a0001c0005t0018g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.83-3103_83-3102ins others(38): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893896 | ||||||
| chr5:172893896 | T | TATATACA others(31): Show |
2 | a0001c0001t0003g0061 a0001c0001t0009g0329 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.83-3101_83-3100ins others(38): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893896 | ||||||
| chr5:172893897 | A | G | 5 | a0001c0001t0001g0232 a0001c0001t0002g0130 a0001c0001t0003g0284 others(2): Show |
5 | HG01106.hp2 HG01123.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.83-3105A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893897 | |||||||
| chr5:172893898 | T | TACAC | 43 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0040 others(40): Show |
43 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.83-3103_83-3102ins others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893898 | ||||||
| chr5:172893898 | T | TACACACA others(33): Show |
1 | a0001c0001t0001g0182 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.83-3103_83-3102ins others(40): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893898 | ||||||
| chr5:172893898 | T | TACACATA others(31): Show |
25 | a0001c0001t0001g0020 a0001c0001t0001g0031 a0001c0001t0001g0033 others(22): Show |
25 | HG00323.hp2 HG00597.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.83-3103_83-3102ins others(38): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893898 | ||||||
| chr5:172893898 | T | TACACATA others(81): Show |
1 | a0001c0001t0001g0110 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.83-3103_83-3102ins others(88): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893898 | ||||||
| chr5:172893899 | A | G | 5 | a0001c0001t0001g0232 a0001c0001t0002g0130 a0001c0001t0003g0284 others(2): Show |
5 | HG01106.hp2 HG01123.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.83-3103A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893899 | |||||||
| chr5:172893900 | T | C | 3 | a0001c0001t0001g0211 a0001c0001t0001g0256 a0001c0001t0001g0327 |
3 | HG02451.hp1 NA18998.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.83-3102T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893900 | |||||||
| chr5:172893900 | T | TACATATA others(27): Show |
3 | a0001c0001t0001g0313 a0001c0001t0001g0325 a0001c0001t0004g0326 |
3 | HG01884.hp1 HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.83-3101_83-3100ins others(34): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893900 | ||||||
| chr5:172893901 | A | ATGTG | 4 | a0001c0001t0001g0268 a0001c0001t0010g0189 a0001c0001t0012g0331 others(1): Show |
4 | HG02572.hp1 HG02895.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.83-3100_83-3099ins others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893901 | ||||||
| chr5:172893901 | A | ATGTGTGT others(5): Show |
1 | a0001c0001t0001g0249 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.83-3100_83-3099ins others(12): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893901 | ||||||
| chr5:172893901 | A | ATGTGTGT others(7): Show |
1 | a0001c0001t0001g0049 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.83-3100_83-3099ins others(14): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893901 | ||||||
| chr5:172893901 | A | G | 6 | a0001c0001t0001g0232 a0001c0001t0002g0130 a0001c0001t0002g0318 others(3): Show |
6 | HG01106.hp2 HG01123.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.83-3101A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893901 | |||||||
| chr5:172893902 | T | C | 3 | a0001c0001t0001g0211 a0001c0001t0001g0256 a0001c0001t0001g0327 |
3 | HG02451.hp1 NA18998.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.83-3100T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893902 | |||||||
| chr5:172893903 | A | ATGTG | 3 | a0001c0001t0003g0311 a0001c0001t0007g0281 a0001c0001t0007g0282 |
3 | HG02630.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.83-3098_83-3097ins others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893903 | ||||||
| chr5:172893903 | A | ATGTGTGT others(5): Show |
2 | a0001c0001t0001g0051 a0001c0001t0001g0264 |
2 | NA19010.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.83-3098_83-3097ins others(12): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893903 | ||||||
| chr5:172893903 | A | G | 16 | a0001c0001t0001g0049 a0001c0001t0001g0232 a0001c0001t0001g0249 others(13): Show |
16 | HG00609.hp2 HG01106.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.83-3099A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893903 | |||||||
| chr5:172893905 | A | ATATATAT others(13): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0214 a0001c0001t0006g0270 |
3 | HG02622.hp2 HG02886.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(20): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(23): Show |
1 | a0001c0001t0002g0146 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(30): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(29): Show |
1 | a0001c0001t0001g0006 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(36): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(9): Show |
2 | a0001c0001t0001g0163 a0001c0001t0001g0226 |
2 | NA18988.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(16): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(21): Show |
1 | a0001c0001t0002g0243 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(28): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(25): Show |
1 | a0001c0001t0001g0059 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(32): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(9): Show |
1 | a0001c0001t0001g0134 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(16): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0164 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(18): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(15): Show |
1 | a0001c0001t0002g0287 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(22): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(19): Show |
1 | a0001c0001t0001g0019 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(26): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(29): Show |
1 | a0001c0001t0002g0135 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(36): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(31): Show |
1 | a0001c0001t0001g0030 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(38): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(5): Show |
1 | a0003c0004t0003g0312 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(12): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(7): Show |
2 | a0001c0001t0001g0114 a0001c0001t0001g0260 |
2 | HG02056.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(14): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(9): Show |
1 | a0001c0001t0002g0269 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(16): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(19): Show |
2 | a0001c0001t0001g0165 a0001c0001t0003g0145 |
2 | HG02615.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(26): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0149 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(34): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0257 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(10): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0190 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(14): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(9): Show |
2 | a0001c0001t0002g0024 a0002c0003t0002g0012 |
2 | HG00438.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(16): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(11): Show |
1 | a0001c0001t0002g0147 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(18): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(13): Show |
2 | a0001c0001t0002g0025 a0001c0001t0002g0275 |
2 | HG01993.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(20): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(15): Show |
1 | a0001c0001t0001g0015 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(22): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(21): Show |
2 | a0001c0001t0002g0278 a0001c0001t0002g0324 |
2 | HG01071.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(28): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(25): Show |
1 | a0001c0001t0001g0133 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(32): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(3): Show |
2 | a0001c0001t0001g0302 a0001c0001t0003g0101 |
2 | HG00639.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(10): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(5): Show |
1 | a0001c0001t0003g0035 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(12): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(9): Show |
4 | a0001c0001t0001g0123 a0001c0001t0001g0126 a0001c0001t0001g0238 others(1): Show |
4 | HG03491.hp2 NA19057.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(16): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(11): Show |
11 | a0001c0001t0001g0021 a0001c0001t0001g0050 a0001c0001t0001g0112 others(8): Show |
11 | HG00280.hp1 HG00558.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(18): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(13): Show |
7 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0079 others(4): Show |
7 | HG00408.hp1 HG00609.hp1 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(20): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(15): Show |
4 | a0001c0001t0001g0248 a0001c0001t0002g0060 a0001c0001t0003g0034 others(1): Show |
4 | HG03492.hp2 HG03654.hp2 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(22): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(17): Show |
4 | a0001c0001t0002g0027 a0001c0001t0002g0028 a0001c0001t0002g0317 others(1): Show |
4 | HG02056.hp2 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(24): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(19): Show |
6 | a0001c0001t0001g0115 a0001c0001t0001g0124 a0001c0001t0001g0127 others(3): Show |
6 | HG00280.hp2 HG00423.hp2 HG00733.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(26): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(21): Show |
2 | a0001c0001t0001g0090 a0001c0001t0001g0230 |
2 | HG01192.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(28): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(23): Show |
2 | a0001c0001t0001g0119 a0001c0001t0001g0258 |
2 | HG01981.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(30): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(25): Show |
1 | a0001c0001t0001g0109 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(32): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0141 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(34): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATAT others(29): Show |
2 | a0001c0001t0002g0010 a0001c0001t0002g0011 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(36): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATG | 3 | a0001c0001t0001g0002 a0001c0001t0001g0072 a0001c0001t0001g0262 |
3 | HG02015.hp2 NA18962.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(6): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATGT others(3): Show |
1 | a0001c0001t0001g0092 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(10): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATGT others(5): Show |
2 | a0001c0001t0002g0046 a0001c0001t0002g0280 |
2 | HG01952.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(12): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATGT others(7): Show |
4 | a0001c0001t0001g0009 a0001c0001t0002g0008 a0001c0001t0002g0026 others(1): Show |
4 | HG01192.hp1 HG01346.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(14): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATGT others(9): Show |
5 | a0001c0001t0001g0062 a0001c0001t0001g0179 a0001c0001t0001g0228 others(2): Show |
5 | HG00733.hp1 HG02738.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(16): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATGT others(11): Show |
7 | a0001c0001t0001g0111 a0001c0001t0001g0129 a0001c0001t0001g0152 others(4): Show |
7 | HG00140.hp2 HG00438.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(18): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATGT others(13): Show |
1 | a0001c0001t0001g0116 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(20): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATGT others(15): Show |
1 | a0001c0001t0001g0067 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(22): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATGT others(17): Show |
6 | a0001c0001t0001g0022 a0001c0001t0001g0203 a0001c0001t0001g0235 others(3): Show |
6 | HG01175.hp2 HG01943.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(24): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATGT others(19): Show |
3 | a0001c0001t0001g0018 a0001c0001t0001g0227 a0001c0001t0001g0245 |
3 | HG01928.hp1 HG01928.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(26): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATGT others(21): Show |
5 | a0001c0001t0001g0043 a0001c0001t0001g0074 a0001c0001t0001g0075 others(2): Show |
5 | HG02293.hp2 HG02300.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(28): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATGT others(23): Show |
1 | a0001c0001t0001g0196 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(30): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATGT others(27): Show |
1 | a0001c0001t0001g0201 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(34): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATATTG others(10): Show |
1 | a0001c0001t0001g0202 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(17): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATGTG | 3 | a0001c0001t0001g0064 a0001c0001t0001g0097 a0001c0001t0001g0128 |
3 | HG01255.hp2 HG01515.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(6): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATGTGT others(5): Show |
3 | a0001c0001t0001g0219 a0001c0001t0002g0132 a0001c0001t0002g0239 |
3 | HG01258.hp2 HG02300.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(12): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATGTGT others(7): Show |
5 | a0001c0001t0001g0052 a0001c0001t0001g0103 a0001c0001t0001g0113 others(2): Show |
5 | HG00544.hp1 HG02165.hp2 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(14): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATGTGT others(9): Show |
5 | a0001c0001t0001g0017 a0001c0001t0001g0029 a0001c0001t0001g0143 others(2): Show |
5 | HG00423.hp1 HG01074.hp1 HG04115.hp2 others(2): Show |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(16): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATGTGT others(11): Show |
5 | a0001c0001t0002g0098 a0001c0001t0002g0160 a0001c0001t0002g0221 others(2): Show |
5 | HG00408.hp2 HG02683.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(18): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATGTGT others(13): Show |
1 | a0001c0001t0001g0172 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(20): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATGTGT others(15): Show |
1 | a0001c0001t0004g0108 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(22): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATGTGT others(17): Show |
2 | a0001c0001t0001g0140 a0001c0001t0001g0233 |
2 | HG01168.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.83-3096_83-3095ins others(24): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATGTGT others(19): Show |
1 | a0001c0001t0002g0094 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(26): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATATGTGT others(23): Show |
1 | a0001c0001t0004g0180 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.83-3096_83-3095ins others(30): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATGTGTGT others(5): Show |
2 | a0001c0001t0001g0077 a0001c0001t0001g0096 |
2 | HG01433.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.83-3077_83-3066dup others(12): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATGTGTGT others(7): Show |
3 | a0001c0001t0001g0263 a0001c0001t0002g0014 a0001c0001t0004g0166 |
3 | HG00558.hp1 NA18960.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.83-3079_83-3066dup others(14): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATGTGTGT others(9): Show |
3 | a0001c0001t0001g0241 a0001c0001t0002g0177 a0001c0002t0001g0251 |
3 | NA18747.hp2 NA18959.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.83-3081_83-3066dup others(16): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | ATGTGTGT others(11): Show |
1 | a0001c0001t0001g0037 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.83-3083_83-3066dup others(18): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893905 | A | G | 38 | a0001c0001t0001g0038 a0001c0001t0001g0049 a0001c0001t0001g0051 others(35): Show |
38 | HG00609.hp2 HG01070.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.83-3097A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893905 | |||||||
| chr5:172893905 | ATGTGTGT others(3): Show |
A | 1 | a0001c0001t0001g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.83-3075_83-3066del others(10): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893905 | ||||||
| chr5:172893907 | G | A | 42 | a0001c0001t0001g0081 a0001c0001t0001g0204 a0001c0001t0001g0211 others(39): Show |
42 | HG00323.hp1 HG01109.hp2 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.83-3095G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893907 | |||||||
| chr5:172893909 | G | A | 4 | a0001c0001t0001g0211 a0001c0001t0001g0213 a0001c0001t0001g0256 others(1): Show |
4 | HG02896.hp2 NA18967.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.83-3093G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893909 | |||||||
| chr5:172893913 | G | A | 22 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0040 others(19): Show |
22 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(19): Show |
intron_variant | MODIFIER | c.83-3089G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893913 | |||||||
| chr5:172893913 | G | GTATATAT others(17): Show |
13 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0003g0334 others(10): Show |
13 | HG01243.hp1 HG01884.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.83-3088_83-3087ins others(24): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893913 | ||||||
| chr5:172893913 | G | GTATATAT others(19): Show |
8 | a0001c0001t0001g0295 a0001c0001t0003g0155 a0001c0001t0003g0283 others(5): Show |
8 | HG01109.hp2 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.83-3088_83-3087ins others(26): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893913 | ||||||
| chr5:172893914 | T | TATATATA others(11): Show |
2 | a0001c0001t0001g0193 a0001c0001t0001g0237 |
2 | NA18956.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.83-3088_83-3087ins others(18): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893914 | |||||||
| chr5:172893915 | G | A | 65 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(62): Show |
65 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(62): Show |
intron_variant | MODIFIER | c.83-3087G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893915 | |||||||
| chr5:172893916 | T | TATATATA others(9): Show |
19 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0040 others(16): Show |
19 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.83-3086_83-3085ins others(16): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893916 | |||||||
| chr5:172893917 | G | A | 35 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0040 others(32): Show |
35 | HG00544.hp2 HG00597.hp1 HG00639.hp1 others(32): Show |
intron_variant | MODIFIER | c.83-3085G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893917 | |||||||
| chr5:172893918 | T | TATATATA others(7): Show |
1 | a0001c0001t0001g0255 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.83-3084_83-3083ins others(14): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893918 | |||||||
| chr5:172893919 | G | A | 62 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(59): Show |
62 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.83-3083G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893919 | |||||||
| chr5:172893921 | G | A | 61 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(58): Show |
61 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(58): Show |
intron_variant | MODIFIER | c.83-3081G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893921 | |||||||
| chr5:172893923 | G | A | 66 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(63): Show |
66 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.83-3079G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893923 | |||||||
| chr5:172893925 | G | A | 47 | a0001c0001t0001g0020 a0001c0001t0001g0031 a0001c0001t0001g0033 others(44): Show |
47 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.83-3077G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893925 | |||||||
| chr5:172893926 | T | G | 1 | a0001c0001t0001g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.83-3076T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893926 | |||||||
| chr5:172893927 | G | A | 61 | a0001c0001t0001g0020 a0001c0001t0001g0031 a0001c0001t0001g0033 others(58): Show |
61 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.83-3075G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893927 | |||||||
| chr5:172893929 | G | A | 61 | a0001c0001t0001g0020 a0001c0001t0001g0031 a0001c0001t0001g0033 others(58): Show |
61 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.83-3073G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893929 | |||||||
| chr5:172893931 | G | A | 63 | a0001c0001t0001g0020 a0001c0001t0001g0031 a0001c0001t0001g0033 others(60): Show |
63 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.83-3071G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893931 | |||||||
| chr5:172893933 | G | A | 92 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0016 others(89): Show |
92 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.83-3069G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893933 | |||||||
| chr5:172893935 | G | A | 104 | a0001c0001t0001g0006 a0001c0001t0001g0020 a0001c0001t0001g0022 others(101): Show |
104 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.83-3067G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893935 | |||||||
| chr5:172893935 | G | GTATA | 6 | a0001c0001t0001g0123 a0001c0001t0001g0126 a0001c0001t0001g0181 others(3): Show |
6 | HG02818.hp1 HG03491.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.83-3051_83-3048dup others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893935 | ||||||
| chr5:172893935 | G | GTATATA | 6 | a0001c0001t0001g0059 a0001c0001t0002g0027 a0001c0001t0002g0028 others(3): Show |
6 | HG03491.hp1 HG03492.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.83-3053_83-3048dup others(6): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893935 | ||||||
| chr5:172893935 | G | GTGTGTGT others(13): Show |
1 | a0001c0001t0002g0095 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.83-3066_83-3065ins others(20): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893935 | ||||||
| chr5:172893935 | G | GTGTGTGT others(11): Show |
2 | a0001c0001t0001g0080 a0001c0001t0002g0139 |
2 | HG00323.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.83-3066_83-3065ins others(18): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893935 | ||||||
| chr5:172893935 | G | GTGTGTGT others(13): Show |
1 | a0001c0001t0002g0138 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.83-3066_83-3065ins others(20): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893935 | ||||||
| chr5:172893935 | G | GTGTGTGT others(17): Show |
2 | a0001c0001t0002g0054 a0001c0001t0026g0215 |
2 | HG01255.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.83-3066_83-3065ins others(24): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893935 | ||||||
| chr5:172893935 | G | GTGTGTGT others(13): Show |
1 | a0001c0001t0001g0319 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.83-3066_83-3065ins others(20): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893935 | ||||||
| chr5:172893935 | G | GTGTGTGT others(15): Show |
3 | a0001c0001t0002g0207 a0001c0001t0002g0208 a0001c0001t0028g0088 |
3 | HG01257.hp2 HG01258.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.83-3066_83-3065ins others(22): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893935 | ||||||
| chr5:172893935 | G | GTGTGTGT others(17): Show |
4 | a0001c0001t0001g0038 a0001c0001t0001g0204 a0001c0001t0002g0044 others(1): Show |
4 | HG02015.hp1 HG02165.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.83-3066_83-3065ins others(24): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893935 | ||||||
| chr5:172893935 | G | GTGTGTGT others(19): Show |
2 | a0001c0001t0002g0056 a0001c0001t0002g0137 |
2 | HG01168.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.83-3066_83-3065ins others(26): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893935 | ||||||
| chr5:172893935 | G | GTGTGTGT others(13): Show |
2 | a0001c0001t0001g0231 a0001c0001t0002g0066 |
2 | HG01081.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.83-3066_83-3065ins others(20): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893935 | ||||||
| chr5:172893935 | G | GTGTGTGT others(15): Show |
2 | a0001c0001t0002g0153 a0001c0001t0002g0333 |
2 | HG02976.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.83-3066_83-3065ins others(22): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893935 | ||||||
| chr5:172893935 | G | GTGTGTGT others(19): Show |
1 | a0001c0001t0001g0306 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.83-3066_83-3065ins others(26): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893935 | ||||||
| chr5:172893935 | G | GTGTGTGT others(17): Show |
3 | a0001c0001t0001g0321 a0001c0001t0001g0322 a0001c0001t0016g0197 |
3 | HG01070.hp1 HG01071.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.83-3066_83-3065ins others(24): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893935 | ||||||
| chr5:172893935 | G | GTGTGTGT others(19): Show |
3 | a0001c0001t0001g0304 a0001c0001t0025g0045 a0001c0001t0029g0131 |
3 | HG03209.hp1 HG03453.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.83-3066_83-3065ins others(26): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893935 | ||||||
| chr5:172893935 | G | GTGTGTGT others(19): Show |
1 | a0001c0001t0001g0057 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.83-3066_83-3065ins others(26): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893935 | ||||||
| chr5:172893935 | G | GTGTGTGT others(21): Show |
2 | a0001c0001t0001g0081 a0001c0001t0003g0272 |
2 | HG02647.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.83-3066_83-3065ins others(28): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893935 | ||||||
| chr5:172893937 | A | G | 27 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0062 others(24): Show |
27 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.83-3065A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893937 | |||||||
| chr5:172893939 | A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0148 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.83-3048_83-3047ins others(34): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893939 | ||||||
| chr5:172893939 | A | ATATATAT others(25): Show |
2 | a0001c0001t0001g0224 a0001c0001t0001g0252 |
2 | HG02074.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.83-3048_83-3047ins others(32): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893939 | ||||||
| chr5:172893939 | A | ATATATAT others(23): Show |
16 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0040 others(13): Show |
16 | HG00544.hp2 HG00597.hp1 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.83-3048_83-3047ins others(30): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893939 | ||||||
| chr5:172893939 | A | ATATATAT others(21): Show |
2 | a0001c0001t0001g0255 a0001c0001t0002g0195 |
2 | HG02129.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.83-3048_83-3047ins others(28): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893939 | ||||||
| chr5:172893939 | A | ATATATAT others(31): Show |
1 | a0001c0001t0001g0279 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.83-3048_83-3047ins others(38): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893939 | ||||||
| chr5:172893939 | A | ATATATAT others(5): Show |
2 | a0001c0001t0001g0110 a0001c0001t0001g0182 |
2 | HG03927.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.83-3052_83-3051ins others(12): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893939 | ||||||
| chr5:172893939 | A | ATATATAT others(3): Show |
20 | a0001c0001t0001g0020 a0001c0001t0001g0031 a0001c0001t0001g0033 others(17): Show |
20 | HG00323.hp2 HG00597.hp2 HG01070.hp2 others(17): Show |
intron_variant | MODIFIER | c.83-3054_83-3053ins others(10): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893939 | ||||||
| chr5:172893939 | A | ATATATAT others(1): Show |
4 | a0001c0001t0001g0070 a0001c0001t0008g0150 a0001c0001t0008g0187 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.83-3056_83-3055ins others(8): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172893939 | ||||||
| chr5:172893939 | A | G | 5 | a0001c0001t0001g0051 a0001c0001t0001g0211 a0001c0001t0001g0256 others(2): Show |
5 | HG02896.hp2 HG03471.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.83-3063A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893939 | |||||||
| chr5:172893941 | A | G | 29 | a0001c0001t0001g0121 a0001c0001t0001g0289 a0001c0001t0001g0290 others(26): Show |
29 | HG00639.hp1 HG00741.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.83-3061A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893941 | |||||||
| chr5:172893989 | CAG | C | 4 | a0001c0001t0001g0123 a0001c0001t0001g0321 a0001c0001t0001g0322 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.83-3012_83-3011del others(2): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172893989 | |||||||
| chr5:172894037 | T | C | 3 | a0001c0001t0002g0138 a0001c0001t0002g0207 a0001c0001t0002g0208 |
3 | HG00140.hp1 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.83-2965T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172894037 | |||||||
| chr5:172894046 | A | AT | 7 | a0001c0001t0001g0200 a0001c0001t0001g0265 a0001c0001t0003g0055 others(4): Show |
7 | HG01243.hp2 HG03195.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.83-2943dupT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172894046 | ||||||
| chr5:172894046 | AT | A | 6 | a0001c0001t0001g0077 a0001c0001t0001g0168 a0001c0001t0001g0216 others(3): Show |
6 | HG00323.hp2 NA18954.hp1 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.83-2943delT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172894046 | ||||||
| chr5:172894076 | A | G | 6 | a0001c0001t0001g0313 a0001c0001t0001g0325 a0001c0001t0003g0061 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-2926A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172894076 | |||||||
| chr5:172894096 | A | T | 1 | a0001c0001t0001g0190 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.83-2906A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172894096 | |||||||
| chr5:172894132 | C | CT | 75 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0022 others(72): Show |
75 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(72): Show |
intron_variant | MODIFIER | c.83-2846dupT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172894132 | ||||||
| chr5:172894132 | C | CTT | 14 | a0001c0001t0001g0119 a0001c0001t0001g0164 a0001c0001t0001g0185 others(11): Show |
14 | HG00140.hp1 HG01167.hp1 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.83-2847_83-2846dup others(2): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172894132 | ||||||
| chr5:172894132 | C | CTTTT | 18 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0295 others(15): Show |
18 | HG01243.hp1 HG02280.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.83-2849_83-2846dup others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172894132 | ||||||
| chr5:172894132 | C | CTTTTT | 8 | a0001c0001t0001g0313 a0001c0001t0001g0325 a0001c0001t0003g0061 others(5): Show |
8 | HG01109.hp2 HG01884.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.83-2850_83-2846dup others(5): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172894132 | ||||||
| chr5:172894132 | C | CTTTTTTT | 43 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.83-2852_83-2846dup others(7): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172894132 | ||||||
| chr5:172894132 | C | CTTTTTTT others(1): Show |
11 | a0001c0001t0001g0047 a0001c0001t0001g0121 a0001c0001t0001g0144 others(8): Show |
11 | HG00639.hp1 HG01361.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.83-2853_83-2846dup others(8): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172894132 | ||||||
| chr5:172894132 | CT | C | 9 | a0001c0001t0001g0050 a0001c0001t0001g0190 a0001c0001t0001g0248 others(6): Show |
9 | HG00558.hp1 HG02809.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.83-2846delT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172894132 | ||||||
| chr5:172894195 | C | CT | 150 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0018 others(147): Show |
150 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.83-2789dupT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172894195 | ||||||
| chr5:172894195 | C | CTT | 17 | a0001c0001t0001g0006 a0001c0001t0001g0144 a0001c0001t0001g0165 others(14): Show |
17 | HG01255.hp1 HG01884.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.83-2790_83-2789dup others(2): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172894195 | ||||||
| chr5:172894259 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.83-2743G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172894259 | |||||||
| chr5:172894416 | G | T | 4 | a0001c0001t0001g0123 a0001c0001t0001g0321 a0001c0001t0001g0322 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.83-2586G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172894416 | |||||||
| chr5:172894440 | C | A | 1 | a0001c0001t0011g0099 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.83-2562C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172894440 | |||||||
| chr5:172894441 | G | A | 2 | a0001c0001t0002g0243 a0001c0001t0004g0246 |
2 | NA18966.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.83-2561G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172894441 | |||||||
| chr5:172894455 | A | G | 51 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(48): Show |
51 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.83-2547A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172894455 | |||||||
| chr5:172894496 | C | T | 8 | a0001c0001t0001g0020 a0001c0001t0001g0047 a0001c0001t0001g0063 others(5): Show |
8 | HG00323.hp2 HG01070.hp2 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.83-2506C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172894496 | |||||||
| chr5:172894532 | A | G | 7 | a0001c0001t0001g0295 a0001c0001t0003g0155 a0001c0001t0003g0283 others(4): Show |
7 | HG01109.hp2 HG02615.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.83-2470A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172894532 | |||||||
| chr5:172894534 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.83-2468T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172894534 | |||||||
| chr5:172894583 | G | T | 6 | a0001c0001t0001g0265 a0001c0001t0003g0055 a0001c0001t0003g0298 others(3): Show |
6 | HG01243.hp2 HG03195.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.83-2419G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172894583 | |||||||
| chr5:172894680 | A | C | 327 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(324): Show |
327 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.83-2322A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172894680 | |||||||
| chr5:172894864 | G | A | 4 | a0001c0001t0001g0123 a0001c0001t0001g0321 a0001c0001t0001g0322 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.83-2138G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172894864 | |||||||
| chr5:172894905 | G | T | 78 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0030 others(75): Show |
78 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.83-2097G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172894905 | |||||||
| chr5:172894977 | G | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0050 a0001c0001t0001g0238 |
3 | NA18960.hp1 NA18967.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.83-2025G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172894977 | |||||||
| chr5:172895139 | T | C | 89 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(86): Show |
89 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.83-1863T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172895139 | |||||||
| chr5:172895141 | A | G | 1 | a0001c0001t0003g0210 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.83-1861A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172895141 | |||||||
| chr5:172895271 | C | T | 174 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0016 others(171): Show |
174 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(171): Show |
intron_variant | MODIFIER | c.83-1731C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172895271 | |||||||
| chr5:172895305 | C | T | 1 | a0001c0001t0003g0055 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.83-1697C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172895305 | |||||||
| chr5:172895380 | A | C | 2 | a0001c0001t0002g0025 a0001c0001t0002g0060 |
2 | HG03017.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.83-1622A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172895380 | |||||||
| chr5:172895401 | C | T | 1 | a0001c0001t0034g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.83-1601C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172895401 | |||||||
| chr5:172895423 | C | T | 21 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0295 others(18): Show |
21 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.83-1579C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172895423 | |||||||
| chr5:172895488 | GC | G | 79 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0022 others(76): Show |
79 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.83-1513delC | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172895488 | |||||||
| chr5:172895506 | A | G | 21 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0295 others(18): Show |
21 | HG01109.hp2 HG01243.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.83-1496A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172895506 | |||||||
| chr5:172895510 | T | C | 10 | a0001c0001t0001g0081 a0001c0001t0001g0115 a0001c0001t0001g0254 others(7): Show |
10 | HG00140.hp1 HG00280.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.83-1492T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172895510 | |||||||
| chr5:172895566 | C | G | 2 | a0001c0001t0001g0064 a0001c0001t0001g0097 |
2 | HG01255.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.83-1436C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172895566 | |||||||
| chr5:172895777 | G | T | 1 | a0001c0001t0003g0316 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.83-1225G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172895777 | |||||||
| chr5:172895904 | C | T | 2 | a0001c0001t0001g0286 a0001c0001t0020g0078 |
2 | HG01175.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.83-1098C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172895904 | |||||||
| chr5:172895933 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.83-1069C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172895933 | |||||||
| chr5:172896206 | C | T | 3 | a0001c0001t0001g0181 a0001c0001t0001g0202 a0001c0001t0001g0235 |
3 | NA18747.hp1 NA18963.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.83-796C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172896206 | |||||||
| chr5:172896534 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.83-468G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172896534 | |||||||
| chr5:172896540 | C | T | 1 | a0001c0001t0003g0328 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.83-462C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | chr5 | 172896540 | |||||||
| chr5:172896650 | GA | G | 3 | a0001c0001t0003g0284 a0001c0001t0009g0330 a0001c0001t0033g0085 |
3 | HG02055.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.83-349delA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr5 | 172896650 | ||||||
| chr5:172897125 | A | T | 84 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(81): Show |
84 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.155+51A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172897125 | |||||||
| chr5:172897264 | A | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0144 |
2 | HG00639.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.155+190A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172897264 | |||||||
| chr5:172897386 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.155+312G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172897386 | |||||||
| chr5:172897428 | C | CA | 17 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0019 others(14): Show |
17 | HG00140.hp2 HG01261.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.155+370dupA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172897428 | ||||||
| chr5:172897428 | CA | C | 7 | a0001c0001t0001g0152 a0001c0001t0001g0226 a0001c0001t0001g0238 others(4): Show |
7 | HG00558.hp1 HG01192.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.155+370delA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172897428 | ||||||
| chr5:172897443 | A | AAAAAAGA others(1): Show |
50 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(47): Show |
50 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(47): Show |
intron_variant | MODIFIER | c.155+370_155+371ins others(8): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172897443 | ||||||
| chr5:172897443 | A | AAAAAGAG | 32 | a0001c0001t0001g0121 a0001c0001t0001g0126 a0001c0001t0001g0144 others(29): Show |
32 | HG00639.hp1 HG00741.hp2 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.155+370_155+371ins others(7): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172897443 | ||||||
| chr5:172897443 | A | AAAG | 6 | a0001c0001t0001g0265 a0001c0001t0003g0055 a0001c0001t0003g0298 others(3): Show |
6 | HG01243.hp2 HG03195.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.155+370_155+371ins others(3): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172897443 | ||||||
| chr5:172897443 | A | G | 6 | a0001c0001t0001g0190 a0001c0001t0001g0226 a0001c0001t0002g0054 others(3): Show |
6 | HG01168.hp1 HG01255.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.155+369A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172897443 | |||||||
| chr5:172897463 | A | G | 16 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0019 others(13): Show |
16 | HG00140.hp2 HG01261.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.155+389A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172897463 | |||||||
| chr5:172897555 | G | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(156): Show |
159 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.155+481G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172897555 | |||||||
| chr5:172897576 | T | A | 1 | a0001c0001t0005g0106 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.155+502T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172897576 | |||||||
| chr5:172897770 | C | G | 6 | a0001c0001t0001g0313 a0001c0001t0001g0325 a0001c0001t0003g0061 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.155+696C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172897770 | |||||||
| chr5:172897894 | A | T | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(247): Show |
250 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.155+820A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172897894 | |||||||
| chr5:172897975 | G | A | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(246): Show |
249 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(246): Show |
intron_variant | MODIFIER | c.155+901G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172897975 | |||||||
| chr5:172898112 | C | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(247): Show |
250 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(247): Show |
intron_variant | MODIFIER | c.155+1038C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172898112 | |||||||
| chr5:172898204 | G | T | 1 | a0001c0001t0011g0117 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.155+1130G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172898204 | |||||||
| chr5:172898250 | CATT | C | 3 | a0001c0001t0003g0284 a0001c0001t0009g0330 a0001c0001t0033g0085 |
3 | HG02055.hp1 HG02280.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.155+1179_155+1181d others(5): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172898250 | ||||||
| chr5:172898341 | T | G | 1 | a0001c0001t0001g0213 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.155+1267T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172898341 | |||||||
| chr5:172898394 | A | G | 84 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(81): Show |
84 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.155+1320A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172898394 | |||||||
| chr5:172898518 | T | C | 84 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(81): Show |
84 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.155+1444T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172898518 | |||||||
| chr5:172898568 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.155+1494C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172898568 | |||||||
| chr5:172898602 | A | C | 1 | a0001c0001t0002g0278 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.155+1528A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172898602 | |||||||
| chr5:172898816 | C | G | 84 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(81): Show |
84 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.155+1742C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172898816 | |||||||
| chr5:172898949 | C | T | 6 | a0001c0001t0001g0265 a0001c0001t0003g0055 a0001c0001t0003g0298 others(3): Show |
6 | HG01243.hp2 HG03195.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.155+1875C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172898949 | |||||||
| chr5:172898969 | C | A | 1 | a0001c0005t0018g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.155+1895C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172898969 | |||||||
| chr5:172898972 | G | T | 2 | a0001c0001t0003g0061 a0001c0001t0009g0329 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.155+1898G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172898972 | |||||||
| chr5:172899261 | C | T | 31 | a0001c0001t0001g0121 a0001c0001t0001g0144 a0001c0001t0001g0289 others(28): Show |
31 | HG00639.hp1 HG00741.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.155+2187C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172899261 | |||||||
| chr5:172899311 | C | CT | 92 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(89): Show |
92 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.155+2260dupT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172899311 | ||||||
| chr5:172899311 | CT | C | 151 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(148): Show |
151 | HG00140.hp2 HG00280.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.155+2260delT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172899311 | ||||||
| chr5:172899403 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.155+2329C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172899403 | |||||||
| chr5:172899412 | A | C | 1 | a0001c0001t0005g0162 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.155+2338A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172899412 | |||||||
| chr5:172899418 | A | G | 4 | a0001c0001t0001g0121 a0001c0001t0001g0144 a0001c0001t0002g0217 others(1): Show |
4 | HG00639.hp1 HG00741.hp2 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.155+2344A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172899418 | |||||||
| chr5:172899434 | T | TA | 90 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(87): Show |
90 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.155+2360_155+2361i others(3): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172899434 | |||||||
| chr5:172899611 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.155+2537G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172899611 | |||||||
| chr5:172899752 | T | G | 1 | a0001c0001t0001g0065 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.155+2678T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172899752 | |||||||
| chr5:172899758 | G | A | 6 | a0001c0001t0001g0265 a0001c0001t0003g0055 a0001c0001t0003g0298 others(3): Show |
6 | HG01243.hp2 HG03195.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.155+2684G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172899758 | |||||||
| chr5:172899787 | A | C | 7 | a0001c0001t0001g0092 a0001c0001t0002g0024 a0001c0001t0002g0212 others(4): Show |
7 | HG03654.hp1 HG03654.hp2 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.155+2713A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172899787 | |||||||
| chr5:172900056 | T | C | 90 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(87): Show |
90 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.155+2982T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172900056 | |||||||
| chr5:172900159 | C | T | 1 | a0001c0001t0001g0305 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.155+3085C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172900159 | |||||||
| chr5:172900322 | C | T | 1 | a0001c0001t0002g0135 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.155+3248C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172900322 | |||||||
| chr5:172900358 | T | C | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(250): Show |
253 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(250): Show |
intron_variant | MODIFIER | c.155+3284T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172900358 | |||||||
| chr5:172900570 | C | T | 2 | a0001c0001t0007g0281 a0001c0001t0007g0282 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.155+3496C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172900570 | |||||||
| chr5:172900671 | C | T | 2 | a0001c0001t0003g0328 a0001c0001t0010g0058 |
2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.155+3597C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172900671 | |||||||
| chr5:172900696 | C | T | 3 | a0001c0001t0001g0313 a0001c0001t0001g0325 a0001c0001t0004g0326 |
3 | HG01884.hp1 HG02109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.155+3622C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172900696 | |||||||
| chr5:172900709 | C | CA | 10 | a0001c0001t0001g0021 a0001c0001t0001g0116 a0001c0001t0001g0295 others(7): Show |
10 | HG01109.hp2 HG02056.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.155+3647dupA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172900709 | ||||||
| chr5:172900721 | A | C | 13 | a0001c0001t0001g0265 a0001c0001t0001g0313 a0001c0001t0001g0325 others(10): Show |
13 | HG01243.hp2 HG01884.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.155+3647A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172900721 | |||||||
| chr5:172900722 | C | A | 90 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(87): Show |
90 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.155+3648C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172900722 | |||||||
| chr5:172900726 | A | AAC | 8 | a0001c0001t0001g0070 a0001c0001t0001g0159 a0001c0001t0001g0211 others(5): Show |
8 | HG02071.hp2 HG02896.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.155+3653_155+3654i others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172900726 | ||||||
| chr5:172900726 | A | AC | 52 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(49): Show |
52 | HG00323.hp2 HG00544.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.155+3652_155+3653i others(3): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172900726 | |||||||
| chr5:172900726 | A | C | 11 | a0001c0001t0001g0290 a0001c0001t0003g0334 a0001c0001t0005g0156 others(8): Show |
11 | HG01243.hp1 HG01884.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.155+3652A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172900726 | |||||||
| chr5:172900732 | C | A | 13 | a0001c0001t0001g0265 a0001c0001t0001g0313 a0001c0001t0001g0325 others(10): Show |
13 | HG01243.hp2 HG01884.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.155+3658C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172900732 | |||||||
| chr5:172900825 | T | C | 11 | a0001c0001t0001g0038 a0001c0001t0001g0059 a0001c0001t0001g0165 others(8): Show |
11 | HG01168.hp1 HG01255.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.155+3751T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172900825 | |||||||
| chr5:172901130 | C | T | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(147): Show |
150 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.155+4056C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172901130 | |||||||
| chr5:172901163 | G | A | 5 | a0001c0001t0002g0142 a0001c0001t0002g0285 a0001c0001t0003g0284 others(2): Show |
5 | HG01257.hp1 HG01952.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.155+4089G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172901163 | |||||||
| chr5:172901247 | G | C | 1 | a0001c0001t0010g0058 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.155+4173G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172901247 | |||||||
| chr5:172901305 | G | A | 19 | a0001c0001t0001g0290 a0001c0001t0001g0295 a0001c0001t0003g0155 others(16): Show |
19 | HG01243.hp1 HG01884.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.155+4231G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172901305 | |||||||
| chr5:172901375 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.155+4301C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172901375 | |||||||
| chr5:172901393 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.155+4319C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172901393 | |||||||
| chr5:172901413 | C | CT | 3 | a0001c0001t0002g0122 a0001c0001t0031g0083 a0001c0001t0032g0084 |
3 | HG02055.hp2 HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.155+4340dupT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172901413 | ||||||
| chr5:172901599 | T | C | 1 | a0001c0001t0001g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.155+4525T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172901599 | |||||||
| chr5:172901672 | T | C | 1 | a0001c0001t0002g0060 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.155+4598T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172901672 | |||||||
| chr5:172901677 | T | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(236): Show |
239 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(236): Show |
intron_variant | MODIFIER | c.155+4603T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172901677 | |||||||
| chr5:172901727 | G | A | 234 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(231): Show |
234 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.155+4653G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172901727 | |||||||
| chr5:172901791 | G | A | 40 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(37): Show |
40 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.155+4717G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172901791 | |||||||
| chr5:172901884 | C | T | 1 | a0002c0003t0002g0012 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.155+4810C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172901884 | |||||||
| chr5:172902024 | C | G | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(233): Show |
236 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.155+4950C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172902024 | |||||||
| chr5:172902470 | C | T | 1 | a0001c0001t0002g0135 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.155+5396C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172902470 | |||||||
| chr5:172902675 | A | C | 68 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(65): Show |
68 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.155+5601A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172902675 | |||||||
| chr5:172902694 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.155+5620T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172902694 | |||||||
| chr5:172902706 | G | T | 1 | a0001c0001t0001g0163 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.155+5632G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172902706 | |||||||
| chr5:172902731 | A | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(229): Show |
232 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(229): Show |
intron_variant | MODIFIER | c.155+5657A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172902731 | |||||||
| chr5:172902733 | G | A | 4 | a0001c0001t0001g0040 a0001c0001t0001g0193 a0001c0001t0001g0194 others(1): Show |
4 | HG00673.hp1 HG02155.hp2 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.155+5659G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172902733 | |||||||
| chr5:172902768 | C | T | 5 | a0001c0001t0005g0156 a0001c0001t0005g0162 a0001c0001t0005g0206 others(2): Show |
5 | HG02280.hp1 HG02622.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.155+5694C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172902768 | |||||||
| chr5:172902872 | T | G | 98 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0015 others(95): Show |
98 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.155+5798T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172902872 | |||||||
| chr5:172902951 | C | T | 3 | a0001c0001t0008g0150 a0001c0001t0008g0187 a0001c0001t0008g0205 |
3 | HG02896.hp1 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.155+5877C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172902951 | |||||||
| chr5:172903083 | C | T | 2 | a0001c0001t0003g0283 a0001c0001t0006g0004 |
2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.155+6009C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172903083 | |||||||
| chr5:172903351 | T | G | 2 | a0001c0001t0003g0055 a0001c0001t0003g0198 |
2 | HG01243.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.155+6277T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172903351 | |||||||
| chr5:172903442 | A | G | 145 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0015 others(142): Show |
145 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.156-6225A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172903442 | |||||||
| chr5:172903617 | C | T | 1 | a0001c0001t0024g0323 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.156-6050C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172903617 | |||||||
| chr5:172903716 | CAGCAACC others(4): Show |
C | 1 | a0001c0001t0003g0293 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.156-5941_156-5931d others(13): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172903716 | ||||||
| chr5:172903751 | T | C | 1 | a0001c0001t0003g0293 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.156-5916T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172903751 | |||||||
| chr5:172903828 | C | CGAACCCT others(15): Show |
9 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0163 others(6): Show |
9 | HG00609.hp2 NA18942.hp1 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.156-5817_156-5796d others(24): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172903828 | ||||||
| chr5:172903840 | G | A | 1 | a0001c0001t0003g0311 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.156-5827G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172903840 | |||||||
| chr5:172903850 | T | C | 2 | a0001c0001t0001g0231 a0001c0001t0002g0094 |
2 | HG00741.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.156-5817T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172903850 | |||||||
| chr5:172903894 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.156-5773C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172903894 | |||||||
| chr5:172903953 | G | A | 2 | a0001c0001t0001g0231 a0001c0001t0002g0094 |
2 | HG00741.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.156-5714G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172903953 | |||||||
| chr5:172903968 | T | TAC | 5 | a0001c0001t0001g0062 a0001c0001t0001g0080 a0001c0001t0001g0152 others(2): Show |
5 | HG00733.hp1 HG03831.hp2 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.156-5679_156-5678d others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172903968 | ||||||
| chr5:172903968 | T | TACAC | 103 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0029 others(100): Show |
103 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.156-5681_156-5678d others(6): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172903968 | ||||||
| chr5:172903968 | T | TACACAC | 6 | a0001c0001t0001g0009 a0001c0001t0001g0115 a0001c0001t0002g0008 others(3): Show |
6 | HG00280.hp2 HG01192.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.156-5683_156-5678d others(8): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172903968 | ||||||
| chr5:172903968 | T | TACACACA others(1): Show |
27 | a0001c0001t0001g0081 a0001c0001t0001g0092 a0001c0001t0001g0182 others(24): Show |
27 | HG00140.hp1 HG01257.hp2 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.156-5685_156-5678d others(10): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172903968 | ||||||
| chr5:172903968 | T | TACACACA others(3): Show |
6 | a0001c0001t0001g0121 a0001c0001t0001g0144 a0001c0001t0001g0295 others(3): Show |
6 | HG00639.hp1 HG01261.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.156-5687_156-5678d others(12): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172903968 | ||||||
| chr5:172903968 | T | TACACACA others(7): Show |
9 | a0001c0001t0001g0037 a0001c0001t0001g0124 a0001c0001t0001g0127 others(6): Show |
9 | HG01109.hp2 HG01358.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.156-5691_156-5678d others(16): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172903968 | ||||||
| chr5:172903968 | T | TACACACA others(9): Show |
32 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(29): Show |
32 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.156-5693_156-5678d others(18): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172903968 | ||||||
| chr5:172903968 | T | TACACACA others(11): Show |
2 | a0001c0001t0001g0158 a0001c0001t0001g0211 |
2 | NA18971.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.156-5695_156-5678d others(20): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172903968 | ||||||
| chr5:172903968 | T | TACACACA others(15): Show |
1 | a0001c0001t0001g0255 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.156-5678_156-5677i others(24): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172903968 | ||||||
| chr5:172903968 | TAC | T | 9 | a0001c0001t0001g0305 a0001c0001t0003g0293 a0001c0001t0003g0294 others(6): Show |
9 | HG02145.hp1 HG02145.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.156-5679_156-5678d others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172903968 | ||||||
| chr5:172903990 | T | A | 1 | a0001c0001t0005g0297 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.156-5677T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172903990 | |||||||
| chr5:172903991 | T | C | 1 | a0001c0001t0005g0297 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.156-5676T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172903991 | |||||||
| chr5:172904054 | C | T | 107 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(104): Show |
107 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.156-5613C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172904054 | |||||||
| chr5:172904225 | T | TGAATTTT others(36): Show |
1 | a0001c0001t0002g0160 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.156-5441_156-5399d others(45): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172904225 | ||||||
| chr5:172904330 | C | T | 1 | a0001c0001t0006g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.156-5337C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172904330 | |||||||
| chr5:172904479 | G | A | 1 | a0001c0001t0005g0297 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.156-5188G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172904479 | |||||||
| chr5:172904616 | G | A | 1 | a0001c0001t0003g0101 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.156-5051G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172904616 | |||||||
| chr5:172904679 | AG | A | 8 | a0001c0001t0001g0092 a0001c0001t0001g0182 a0001c0001t0002g0024 others(5): Show |
8 | HG00639.hp2 HG01243.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.156-4987delG | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172904679 | |||||||
| chr5:172904696 | C | A | 1 | a0001c0001t0001g0100 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.156-4971C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172904696 | |||||||
| chr5:172904783 | G | A | 1 | a0001c0001t0010g0058 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.156-4884G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172904783 | |||||||
| chr5:172904784 | A | T | 1 | a0001c0001t0001g0100 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.156-4883A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172904784 | |||||||
| chr5:172904791 | A | G | 8 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0002g0333 others(5): Show |
8 | HG01243.hp1 HG01884.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.156-4876A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172904791 | |||||||
| chr5:172904907 | C | T | 45 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(42): Show |
45 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.156-4760C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172904907 | |||||||
| chr5:172905195 | AG | A | 6 | a0001c0001t0003g0271 a0001c0001t0003g0272 a0001c0001t0003g0292 others(3): Show |
6 | HG02280.hp2 HG02647.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.156-4471delG | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172905195 | |||||||
| chr5:172905199 | G | C | 3 | a0001c0001t0003g0273 a0001c0001t0003g0274 a0001c0001t0034g0086 |
3 | HG02630.hp1 HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.156-4468G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172905199 | |||||||
| chr5:172905218 | G | T | 1 | a0001c0001t0001g0241 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.156-4449G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172905218 | |||||||
| chr5:172905262 | G | A | 2 | a0001c0001t0005g0297 a0001c0005t0018g0161 |
2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.156-4405G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172905262 | |||||||
| chr5:172905290 | A | G | 3 | a0001c0001t0001g0109 a0001c0001t0001g0149 a0001c0001t0001g0248 |
3 | HG01978.hp1 NA18959.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.156-4377A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172905290 | |||||||
| chr5:172905443 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0240 |
2 | NA18962.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.156-4224G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172905443 | |||||||
| chr5:172905555 | G | A | 45 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(42): Show |
45 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.156-4112G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172905555 | |||||||
| chr5:172905714 | C | T | 3 | a0001c0001t0003g0154 a0001c0001t0003g0284 a0001c0001t0033g0085 |
3 | HG02055.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.156-3953C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172905714 | |||||||
| chr5:172905715 | G | A | 3 | a0001c0001t0003g0154 a0001c0001t0003g0284 a0001c0001t0033g0085 |
3 | HG02055.hp1 HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.156-3952G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172905715 | |||||||
| chr5:172905738 | G | GAACA | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(174): Show |
177 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.156-3928_156-3925d others(6): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172905738 | ||||||
| chr5:172905847 | G | A | 8 | a0001c0001t0001g0092 a0001c0001t0001g0182 a0001c0001t0002g0024 others(5): Show |
8 | HG00639.hp2 HG01243.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.156-3820G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172905847 | |||||||
| chr5:172905907 | T | A | 1 | a0001c0001t0001g0100 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.156-3760T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172905907 | |||||||
| chr5:172905952 | C | A | 1 | a0001c0001t0010g0058 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.156-3715C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172905952 | |||||||
| chr5:172905953 | C | G | 1 | a0001c0001t0010g0058 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.156-3714C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172905953 | |||||||
| chr5:172906176 | C | T | 2 | a0001c0001t0010g0189 a0001c0001t0014g0173 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.156-3491C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172906176 | |||||||
| chr5:172906301 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.156-3366G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172906301 | |||||||
| chr5:172906313 | G | C | 7 | a0001c0001t0003g0155 a0001c0001t0003g0273 a0001c0001t0003g0274 others(4): Show |
7 | HG01109.hp2 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.156-3354G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172906313 | |||||||
| chr5:172906365 | G | T | 74 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0038 others(71): Show |
74 | HG00408.hp2 HG00423.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.156-3302G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172906365 | |||||||
| chr5:172906471 | T | C | 8 | a0001c0001t0001g0092 a0001c0001t0001g0182 a0001c0001t0002g0024 others(5): Show |
8 | HG00639.hp2 HG01243.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.156-3196T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172906471 | |||||||
| chr5:172906544 | A | G | 1 | a0001c0001t0002g0095 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.156-3123A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172906544 | |||||||
| chr5:172906571 | G | A | 2 | a0001c0001t0005g0297 a0001c0005t0018g0161 |
2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.156-3096G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172906571 | |||||||
| chr5:172906850 | C | T | 1 | a0001c0001t0034g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.156-2817C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172906850 | |||||||
| chr5:172907112 | C | T | 5 | a0001c0001t0002g0122 a0001c0001t0010g0189 a0001c0001t0014g0173 others(2): Show |
5 | HG02055.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.156-2555C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172907112 | |||||||
| chr5:172907231 | C | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(166): Show |
169 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.156-2436C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172907231 | |||||||
| chr5:172907372 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.156-2295A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172907372 | |||||||
| chr5:172907378 | T | A | 45 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(42): Show |
45 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.156-2289T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172907378 | |||||||
| chr5:172907437 | A | G | 1 | a0001c0001t0002g0082 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.156-2230A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172907437 | |||||||
| chr5:172907520 | T | G | 1 | a0001c0001t0001g0211 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.156-2147T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172907520 | |||||||
| chr5:172907527 | C | T | 8 | a0001c0001t0001g0092 a0001c0001t0001g0182 a0001c0001t0002g0024 others(5): Show |
8 | HG00639.hp2 HG01243.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.156-2140C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172907527 | |||||||
| chr5:172907545 | A | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(167): Show |
170 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.156-2122A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172907545 | |||||||
| chr5:172907555 | C | CA | 6 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0289 others(3): Show |
6 | HG01981.hp1 HG02056.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.156-2099dupA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172907555 | ||||||
| chr5:172907555 | CA | C | 24 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0097 others(21): Show |
24 | HG01074.hp2 HG01106.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.156-2099delA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172907555 | ||||||
| chr5:172907589 | C | T | 1 | a0001c0001t0002g0082 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.156-2078C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172907589 | |||||||
| chr5:172907813 | T | G | 1 | a0001c0001t0001g0211 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.156-1854T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172907813 | |||||||
| chr5:172907813 | T | TG | 5 | a0001c0001t0001g0021 a0001c0001t0001g0065 a0001c0001t0001g0149 others(2): Show |
5 | HG01074.hp2 HG01978.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.156-1849dupG | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172907813 | ||||||
| chr5:172907872 | A | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(167): Show |
170 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.156-1795A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172907872 | |||||||
| chr5:172908057 | G | T | 1 | a0001c0005t0018g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.156-1610G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908057 | |||||||
| chr5:172908070 | C | A | 1 | a0001c0001t0010g0058 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.156-1597C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908070 | |||||||
| chr5:172908079 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.156-1588C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908079 | |||||||
| chr5:172908120 | T | G | 1 | a0001c0001t0001g0119 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.156-1547T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908120 | |||||||
| chr5:172908121 | G | T | 1 | a0001c0001t0001g0119 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.156-1546G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908121 | |||||||
| chr5:172908122 | T | G | 1 | a0001c0001t0001g0119 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.156-1545T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908122 | |||||||
| chr5:172908172 | C | T | 45 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(42): Show |
45 | HG00323.hp2 HG00544.hp2 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.156-1495C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908172 | |||||||
| chr5:172908201 | A | G | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(167): Show |
170 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.156-1466A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908201 | |||||||
| chr5:172908287 | T | G | 3 | a0001c0001t0001g0204 a0001c0001t0002g0102 a0001c0001t0002g0195 |
3 | HG02015.hp1 NA18983.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.156-1380T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908287 | |||||||
| chr5:172908300 | C | CG | 56 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0041 others(53): Show |
56 | HG00280.hp2 HG00438.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.156-1362dupG | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908300 | ||||||
| chr5:172908304 | G | GGGCA | 36 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0051 others(33): Show |
36 | HG00280.hp1 HG00323.hp1 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.156-1362_156-1361i others(6): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908304 | ||||||
| chr5:172908304 | G | GGGCAGGT others(27): Show |
1 | a0001c0001t0028g0088 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.156-1362_156-1361i others(36): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908304 | ||||||
| chr5:172908305 | G | GGC | 23 | a0001c0001t0001g0049 a0001c0001t0001g0072 a0001c0001t0001g0100 others(20): Show |
23 | HG00741.hp2 HG01106.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.156-1362_156-1361i others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908305 | |||||||
| chr5:172908305 | G | T | 6 | a0001c0001t0001g0252 a0001c0001t0001g0313 a0001c0001t0001g0325 others(3): Show |
6 | HG01884.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.156-1362G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908305 | |||||||
| chr5:172908306 | C | A | 23 | a0001c0001t0001g0049 a0001c0001t0001g0072 a0001c0001t0001g0100 others(20): Show |
23 | HG00741.hp2 HG01106.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.156-1361C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908306 | |||||||
| chr5:172908306 | C | CG | 54 | a0001c0001t0001g0007 a0001c0001t0001g0017 a0001c0001t0001g0030 others(51): Show |
54 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(51): Show |
intron_variant | MODIFIER | c.156-1349dupG | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908306 | ||||||
| chr5:172908306 | C | CGG | 22 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0019 others(19): Show |
22 | HG00423.hp2 HG01496.hp2 HG01515.hp2 others(19): Show |
intron_variant | MODIFIER | c.156-1350_156-1349d others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908306 | ||||||
| chr5:172908306 | C | G | 91 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0016 others(88): Show |
91 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.156-1361C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908306 | |||||||
| chr5:172908307 | G | A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0041 others(38): Show |
41 | HG00438.hp1 HG01192.hp1 HG01433.hp1 others(38): Show |
intron_variant | MODIFIER | c.156-1360G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908307 | |||||||
| chr5:172908307 | G | C | 5 | a0001c0001t0001g0081 a0001c0001t0001g0092 a0001c0001t0002g0138 others(2): Show |
5 | HG00140.hp1 HG03209.hp2 HG04199.hp2 others(2): Show |
intron_variant | MODIFIER | c.156-1360G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908307 | |||||||
| chr5:172908307 | G | T | 1 | a0001c0001t0027g0091 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.156-1360G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908307 | |||||||
| chr5:172908308 | G | GGGGGGGG others(29): Show |
1 | a0001c0001t0001g0237 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.156-1350_156-1349i others(38): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908308 | ||||||
| chr5:172908308 | G | GGGGGGGG others(30): Show |
1 | a0001c0001t0001g0209 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.156-1350_156-1349i others(39): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908308 | ||||||
| chr5:172908310 | G | A | 8 | a0001c0001t0002g0125 a0001c0001t0002g0130 a0001c0001t0002g0275 others(5): Show |
8 | HG01123.hp1 HG01175.hp1 HG01261.hp2 others(5): Show |
intron_variant | MODIFIER | c.156-1357G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908310 | |||||||
| chr5:172908310 | G | T | 1 | a0001c0001t0002g0285 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.156-1357G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908310 | |||||||
| chr5:172908311 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.156-1356G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908311 | |||||||
| chr5:172908312 | G | T | 1 | a0001c0005t0018g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.156-1355G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908312 | |||||||
| chr5:172908313 | G | A | 1 | a0001c0001t0028g0088 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.156-1354G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908313 | |||||||
| chr5:172908315 | G | C | 37 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0051 others(34): Show |
37 | HG00280.hp1 HG00323.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.156-1352G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908315 | |||||||
| chr5:172908315 | G | GGGGGCGG others(26): Show |
4 | a0001c0001t0001g0109 a0001c0001t0001g0164 a0001c0001t0002g0160 others(1): Show |
4 | HG02895.hp2 HG03831.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.156-1349_156-1348i others(35): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908315 | ||||||
| chr5:172908315 | GGGGAGAG others(6): Show |
G | 1 | a0001c0001t0003g0220 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.156-1348_156-1336d others(15): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908315 | ||||||
| chr5:172908318 | G | A | 37 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0051 others(34): Show |
37 | HG00280.hp1 HG00323.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.156-1349G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908318 | |||||||
| chr5:172908318 | G | GCGGA | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0041 others(81): Show |
84 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.156-1349_156-1348i others(6): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908318 | |||||||
| chr5:172908318 | G | GGGGGGGC others(3): Show |
7 | a0001c0001t0001g0013 a0001c0001t0001g0037 a0001c0001t0001g0110 others(4): Show |
7 | HG01257.hp1 HG02129.hp2 HG02683.hp2 others(4): Show |
intron_variant | MODIFIER | c.156-1349_156-1348i others(12): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908318 | |||||||
| chr5:172908318 | G | GGGGGGGG others(4): Show |
4 | a0001c0001t0001g0144 a0001c0001t0001g0240 a0001c0001t0002g0285 others(1): Show |
4 | HG01952.hp2 HG02055.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.156-1349_156-1348i others(13): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908318 | |||||||
| chr5:172908318 | G | GGGGGGGG others(5): Show |
1 | a0001c0001t0001g0225 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.156-1349_156-1348i others(14): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908318 | |||||||
| chr5:172908318 | G | GGGGGGGG others(5): Show |
3 | a0001c0001t0001g0148 a0001c0001t0001g0252 a0001c0001t0024g0323 |
3 | HG04115.hp1 NA18995.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.156-1349_156-1348i others(14): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908318 | |||||||
| chr5:172908318 | G | GGGGGGGG others(6): Show |
7 | a0001c0001t0001g0031 a0001c0001t0001g0042 a0001c0001t0001g0070 others(4): Show |
7 | HG00323.hp2 HG00544.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.156-1349_156-1348i others(15): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908318 | |||||||
| chr5:172908318 | G | GGGGGGGG others(7): Show |
1 | a0001c0001t0001g0256 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.156-1349_156-1348i others(16): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908318 | |||||||
| chr5:172908318 | G | GGGGGGGG others(7): Show |
2 | a0001c0001t0001g0118 a0001c0001t0017g0234 |
2 | HG03669.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.156-1349_156-1348i others(16): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908318 | |||||||
| chr5:172908318 | G | GGGGGGGG others(8): Show |
3 | a0001c0001t0001g0016 a0001c0001t0001g0211 a0001c0001t0002g0122 |
3 | HG02970.hp1 NA18962.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.156-1349_156-1348i others(17): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908318 | |||||||
| chr5:172908318 | G | GGGGGGGG others(9): Show |
4 | a0001c0001t0001g0033 a0001c0001t0001g0063 a0001c0001t0001g0124 others(1): Show |
4 | HG00597.hp2 HG01081.hp2 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.156-1349_156-1348i others(18): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908318 | |||||||
| chr5:172908318 | G | GGGGGGGG others(11): Show |
1 | a0001c0001t0001g0127 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.156-1349_156-1348i others(20): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908318 | |||||||
| chr5:172908319 | A | G | 18 | a0001c0001t0001g0059 a0001c0001t0001g0109 a0001c0001t0001g0164 others(15): Show |
18 | HG00438.hp2 HG01884.hp1 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.156-1348A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908319 | |||||||
| chr5:172908321 | A | G | 2 | a0001c0001t0005g0297 a0001c0005t0018g0161 |
2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.156-1346A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908321 | |||||||
| chr5:172908323 | A | AGAGGGGA others(39): Show |
1 | a0001c0001t0001g0258 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.156-1343_156-1342i others(48): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908323 | ||||||
| chr5:172908323 | A | AGAGGGGA others(38): Show |
1 | a0001c0001t0001g0172 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.156-1343_156-1342i others(47): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908323 | ||||||
| chr5:172908323 | A | AGAGGGGA others(38): Show |
1 | a0001c0001t0029g0131 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.156-1343_156-1342i others(47): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908323 | ||||||
| chr5:172908323 | A | AGAGGGGA others(38): Show |
1 | a0001c0001t0002g0066 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.156-1343_156-1342i others(47): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908323 | ||||||
| chr5:172908323 | A | AGAGGGGA others(41): Show |
1 | a0001c0001t0001g0059 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.156-1343_156-1342i others(50): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908323 | ||||||
| chr5:172908323 | A | AGAGGGGA others(43): Show |
1 | a0001c0001t0002g0317 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.156-1343_156-1342i others(52): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908323 | ||||||
| chr5:172908323 | A | AGGGAGGG others(49): Show |
1 | a0001c0001t0001g0186 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.156-1341_156-1340i others(58): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908323 | ||||||
| chr5:172908323 | A | AGGGGAGG others(22): Show |
3 | a0001c0001t0001g0049 a0001c0001t0001g0149 a0001c0001t0033g0085 |
3 | HG01978.hp1 HG03098.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.156-1337_156-1336i others(31): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908323 | ||||||
| chr5:172908323 | A | AGGGGAGG others(37): Show |
1 | a0001c0001t0001g0062 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.156-1325_156-1324i others(46): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908323 | ||||||
| chr5:172908323 | A | AGGGGAGG others(36): Show |
1 | a0001c0001t0001g0181 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.156-1325_156-1324i others(45): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908323 | ||||||
| chr5:172908323 | A | AGGGGAGG others(62): Show |
1 | a0001c0001t0001g0242 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.156-1325_156-1324i others(71): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908323 | ||||||
| chr5:172908323 | A | AGGGGAGG others(36): Show |
2 | a0001c0001t0001g0030 a0001c0001t0002g0333 |
2 | HG02976.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.156-1325_156-1324i others(45): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908323 | ||||||
| chr5:172908323 | A | AGGGGAGG others(37): Show |
1 | a0001c0001t0001g0080 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.156-1325_156-1324i others(46): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908323 | ||||||
| chr5:172908323 | A | AGGGGAGG others(38): Show |
2 | a0001c0001t0001g0290 a0001c0001t0004g0246 |
2 | HG01243.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.156-1325_156-1324i others(47): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908323 | ||||||
| chr5:172908323 | A | G | 5 | a0001c0001t0001g0109 a0001c0001t0001g0164 a0001c0001t0002g0160 others(2): Show |
5 | HG01261.hp2 HG02895.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.156-1344A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908323 | |||||||
| chr5:172908325 | G | GGGAGGAG others(8): Show |
1 | a0001c0001t0024g0323 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.156-1337_156-1336i others(17): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908325 | ||||||
| chr5:172908328 | A | AGGGGGGG others(3): Show |
2 | a0001c0001t0001g0097 a0001c0001t0003g0292 |
2 | HG01255.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.156-1334_156-1325d others(12): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(38): Show |
1 | a0001c0001t0004g0108 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.156-1325_156-1324i others(47): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(38): Show |
1 | a0001c0001t0001g0238 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.156-1325_156-1324i others(47): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(39): Show |
1 | a0001c0001t0001g0304 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.156-1325_156-1324i others(48): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(37): Show |
1 | a0001c0001t0001g0321 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.156-1325_156-1324i others(46): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(38): Show |
1 | a0001c0001t0001g0322 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.156-1325_156-1324i others(47): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(37): Show |
8 | a0001c0001t0001g0133 a0001c0001t0001g0141 a0001c0001t0001g0168 others(5): Show |
8 | HG01169.hp1 HG01169.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.156-1325_156-1324i others(46): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(38): Show |
1 | a0001c0001t0001g0075 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.156-1325_156-1324i others(47): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(63): Show |
2 | a0001c0001t0001g0151 a0001c0001t0001g0245 |
2 | HG02129.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.156-1325_156-1324i others(72): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(67): Show |
1 | a0001c0001t0001g0261 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.156-1325_156-1324i others(76): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(38): Show |
1 | a0001c0001t0001g0079 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.156-1325_156-1324i others(47): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(38): Show |
1 | a0001c0001t0001g0152 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.156-1325_156-1324i others(47): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(39): Show |
1 | a0001c0001t0001g0040 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.156-1325_156-1324i others(48): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(40): Show |
2 | a0001c0001t0001g0116 a0001c0001t0020g0078 |
2 | HG01175.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.156-1325_156-1324i others(49): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(42): Show |
1 | a0001c0001t0001g0228 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.156-1325_156-1324i others(51): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(38): Show |
1 | a0001c0001t0004g0247 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.156-1325_156-1324i others(47): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(39): Show |
2 | a0001c0001t0004g0023 a0001c0001t0004g0178 |
2 | NA18612.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.156-1325_156-1324i others(48): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(39): Show |
1 | a0001c0001t0002g0174 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.156-1325_156-1324i others(48): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(40): Show |
1 | a0001c0001t0001g0230 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.156-1325_156-1324i others(49): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(40): Show |
2 | a0001c0001t0001g0201 a0001c0001t0002g0010 |
2 | HG00673.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.156-1325_156-1324i others(49): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(40): Show |
1 | a0001c0001t0003g0334 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.156-1325_156-1324i others(49): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(40): Show |
1 | a0001c0001t0001g0119 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.156-1332_156-1331i others(49): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(3): Show |
2 | a0001c0001t0001g0165 a0001c0001t0001g0232 |
2 | HG01106.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.156-1332_156-1331i others(12): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(21): Show |
2 | a0001c0001t0001g0222 a0001c0001t0001g0236 |
2 | NA18951.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.156-1332_156-1331i others(30): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(4): Show |
1 | a0001c0001t0001g0064 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.156-1332_156-1331i others(13): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(38): Show |
1 | a0001c0001t0004g0166 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.156-1332_156-1331i others(47): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(37): Show |
1 | a0001c0001t0002g0094 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.156-1332_156-1331i others(46): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(38): Show |
1 | a0001c0001t0001g0185 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.156-1332_156-1331i others(47): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(40): Show |
1 | a0001c0001t0002g0032 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.156-1332_156-1331i others(49): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(38): Show |
1 | a0001c0001t0001g0077 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.156-1332_156-1331i others(47): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(39): Show |
1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.156-1332_156-1331i others(48): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(39): Show |
1 | a0001c0001t0001g0111 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.156-1332_156-1331i others(48): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(40): Show |
1 | a0001c0001t0001g0233 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.156-1332_156-1331i others(49): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(41): Show |
2 | a0001c0001t0001g0090 a0001c0001t0001g0112 |
2 | HG01192.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.156-1332_156-1331i others(50): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(39): Show |
1 | a0001c0001t0013g0291 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.156-1332_156-1331i others(48): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(44): Show |
1 | a0001c0001t0001g0204 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.156-1332_156-1331i others(53): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(39): Show |
1 | a0001c0001t0001g0241 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.156-1332_156-1331i others(48): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(40): Show |
1 | a0001c0001t0001g0057 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.156-1332_156-1331i others(49): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(41): Show |
1 | a0001c0001t0001g0286 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.156-1332_156-1331i others(50): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(41): Show |
1 | a0001c0001t0001g0175 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.156-1332_156-1331i others(50): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(40): Show |
1 | a0001c0001t0002g0243 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.156-1332_156-1331i others(49): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(41): Show |
1 | a0001c0001t0001g0320 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.156-1332_156-1331i others(50): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(41): Show |
1 | a0001c0001t0001g0235 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.156-1332_156-1331i others(50): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908328 | A | AGGGGGGG others(36): Show |
2 | a0001c0001t0002g0073 a0001c0001t0002g0188 |
2 | NA18964.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.156-1332_156-1331i others(45): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908328 | ||||||
| chr5:172908329 | G | GGAGGTGG others(7): Show |
1 | a0001c0001t0001g0303 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.156-1337_156-1336i others(16): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908329 | ||||||
| chr5:172908329 | G | GGAGGTGG others(13): Show |
26 | a0001c0001t0001g0081 a0001c0001t0001g0092 a0001c0001t0001g0115 others(23): Show |
26 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.156-1337_156-1336i others(22): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908329 | ||||||
| chr5:172908329 | G | GGAGGTGG others(20): Show |
81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(78): Show |
81 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(78): Show |
intron_variant | MODIFIER | c.156-1337_156-1336i others(29): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908329 | ||||||
| chr5:172908329 | G | GGAGGTGG others(21): Show |
6 | a0001c0001t0001g0214 a0001c0001t0001g0249 a0001c0001t0001g0257 others(3): Show |
6 | HG00609.hp2 HG01109.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.156-1337_156-1336i others(30): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908329 | ||||||
| chr5:172908329 | G | GGAGGTGG others(21): Show |
2 | a0001c0001t0001g0100 a0001c0001t0001g0213 |
2 | NA18956.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.156-1337_156-1336i others(30): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908329 | ||||||
| chr5:172908329 | G | GGGGGGAG others(16): Show |
1 | a0001c0001t0010g0058 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.156-1333_156-1332i others(25): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908329 | ||||||
| chr5:172908329 | G | GGGGGGGA others(38): Show |
1 | a0001c0001t0001g0202 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.156-1325_156-1324i others(47): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908329 | ||||||
| chr5:172908329 | G | GGGGGGGA others(60): Show |
1 | a0001c0001t0001g0019 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.156-1325_156-1324i others(69): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908329 | ||||||
| chr5:172908330 | G | GAGGT | 34 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0031 others(31): Show |
34 | HG00323.hp2 HG00544.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.156-1337_156-1336i others(6): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908330 | |||||||
| chr5:172908330 | G | GAGGTGGG others(6): Show |
6 | a0001c0001t0001g0033 a0001c0001t0001g0104 a0001c0001t0001g0121 others(3): Show |
6 | HG00597.hp2 HG00639.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.156-1337_156-1336i others(15): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908330 | |||||||
| chr5:172908331 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.156-1336G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908331 | |||||||
| chr5:172908331 | G | GGGGGAGG others(19): Show |
1 | a0001c0001t0025g0045 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.156-1325_156-1324i others(28): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908331 | ||||||
| chr5:172908334 | G | A | 1 | a0001c0001t0003g0220 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.156-1333G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908334 | |||||||
| chr5:172908334 | G | GA | 3 | a0001c0001t0001g0313 a0001c0001t0003g0328 a0001c0005t0018g0161 |
3 | HG01884.hp1 HG02970.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.156-1333_156-1332i others(3): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908334 | |||||||
| chr5:172908334 | G | T | 1 | a0001c0001t0001g0256 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.156-1333G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908334 | |||||||
| chr5:172908335 | G | A | 1 | a0001c0001t0005g0297 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.156-1332G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908335 | |||||||
| chr5:172908335 | G | GGGGAGGG others(43): Show |
1 | a0001c0001t0004g0180 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.156-1332_156-1331i others(52): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908335 | |||||||
| chr5:172908336 | A | AG | 15 | a0001c0001t0001g0018 a0001c0001t0001g0038 a0001c0001t0001g0050 others(12): Show |
15 | HG01928.hp2 HG02027.hp2 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.156-1325dupG | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908336 | ||||||
| chr5:172908336 | A | AGGGGGGG others(41): Show |
1 | a0001c0001t0003g0198 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.156-1325_156-1324i others(50): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908336 | ||||||
| chr5:172908336 | A | AGGGGGGG others(42): Show |
1 | a0001c0001t0001g0140 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.156-1325_156-1324i others(51): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908336 | ||||||
| chr5:172908336 | A | AGGGGGGG others(42): Show |
2 | a0001c0001t0001g0074 a0001c0001t0004g0176 |
2 | NA18953.hp1 NA18953.hp2 |
intron_variant | MODIFIER | c.156-1325_156-1324i others(51): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908336 | ||||||
| chr5:172908336 | A | AGGGGGGG others(41): Show |
1 | a0001c0001t0016g0197 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.156-1325_156-1324i others(50): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908336 | ||||||
| chr5:172908336 | A | G | 10 | a0001c0001t0001g0209 a0001c0001t0001g0256 a0001c0001t0001g0313 others(7): Show |
10 | HG01884.hp1 HG02074.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.156-1331A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908336 | |||||||
| chr5:172908337 | G | GGA | 34 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(31): Show |
34 | HG00323.hp2 HG00544.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.156-1329_156-1328i others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908337 | ||||||
| chr5:172908338 | G | A | 1 | a0001c0001t0003g0220 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.156-1329G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908338 | |||||||
| chr5:172908339 | G | GGGGGGAG others(57): Show |
1 | a0001c0001t0002g0014 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.156-1325_156-1324i others(66): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908339 | ||||||
| chr5:172908341 | G | GGGGAGGG others(39): Show |
1 | a0001c0001t0001g0039 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.156-1325_156-1324i others(48): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908341 | ||||||
| chr5:172908341 | G | GGGGAGGG others(39): Show |
1 | a0001c0001t0001g0289 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.156-1325_156-1324i others(48): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908341 | ||||||
| chr5:172908341 | G | GGGGAGGG others(41): Show |
1 | a0001c0001t0001g0183 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.156-1325_156-1324i others(50): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908341 | ||||||
| chr5:172908342 | G | GGAGGGGG others(38): Show |
1 | a0001c0001t0004g0036 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.156-1325_156-1324i others(47): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908342 | |||||||
| chr5:172908342 | G | GGGAGGGG others(38): Show |
3 | a0001c0001t0001g0015 a0001c0001t0001g0052 a0001c0002t0001g0251 |
3 | HG02071.hp1 NA18959.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.156-1325_156-1324i others(47): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908342 | |||||||
| chr5:172908342 | G | GGGAGGGG others(65): Show |
1 | a0001c0001t0001g0129 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.156-1325_156-1324i others(74): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908342 | |||||||
| chr5:172908342 | G | GGGAGGGG others(39): Show |
1 | a0001c0001t0001g0263 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.156-1325_156-1324i others(48): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908342 | |||||||
| chr5:172908342 | G | GGGAGGGG others(40): Show |
1 | a0001c0001t0002g0221 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.156-1325_156-1324i others(49): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908342 | |||||||
| chr5:172908342 | G | GGGAGGGG others(39): Show |
1 | a0001c0001t0001g0007 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.156-1325_156-1324i others(48): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908342 | |||||||
| chr5:172908342 | G | GGGAGGGG others(39): Show |
1 | a0001c0001t0001g0043 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.156-1325_156-1324i others(48): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908342 | |||||||
| chr5:172908342 | G | GGGAGGGG others(40): Show |
1 | a0001c0001t0001g0113 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.156-1325_156-1324i others(49): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908342 | |||||||
| chr5:172908342 | G | GGGAGGGG others(13): Show |
1 | a0001c0001t0001g0022 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.156-1325_156-1324i others(22): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908342 | |||||||
| chr5:172908342 | G | GGGGAGGG others(4): Show |
1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.156-1325_156-1324i others(13): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908342 | |||||||
| chr5:172908342 | G | GGGGAGGG others(67): Show |
1 | a0001c0001t0001g0017 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.156-1325_156-1324i others(76): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908342 | |||||||
| chr5:172908342 | G | GGGGAGGG others(42): Show |
1 | a0001c0001t0001g0179 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.156-1325_156-1324i others(51): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908342 | |||||||
| chr5:172908342 | G | GGGGAGGG others(45): Show |
1 | a0001c0001t0001g0219 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.156-1325_156-1324i others(54): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908342 | |||||||
| chr5:172908342 | G | GGGGGAGG others(49): Show |
1 | a0001c0001t0001g0103 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.156-1325_156-1324i others(58): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908342 | |||||||
| chr5:172908343 | A | AT | 11 | a0001c0001t0001g0049 a0001c0001t0001g0072 a0001c0001t0001g0214 others(8): Show |
11 | HG01192.hp1 HG01261.hp2 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.156-1324_156-1323i others(3): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908343 | |||||||
| chr5:172908343 | A | G | 42 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0017 others(39): Show |
42 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(39): Show |
intron_variant | MODIFIER | c.156-1324A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908343 | |||||||
| chr5:172908343 | AG | A | 20 | a0001c0001t0001g0064 a0001c0001t0001g0121 a0001c0001t0001g0123 others(17): Show |
20 | HG00639.hp1 HG01515.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.156-1315delG | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908343 | ||||||
| chr5:172908344 | G | A | 3 | a0001c0001t0001g0033 a0001c0001t0001g0233 a0001c0001t0001g0303 |
3 | HG00597.hp2 HG01978.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.156-1323G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908344 | |||||||
| chr5:172908344 | G | GAGGGGGG others(1): Show |
3 | a0001c0001t0001g0237 a0001c0001t0003g0271 a0001c0001t0009g0330 |
3 | HG02280.hp2 HG02717.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.156-1323_156-1322i others(10): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908344 | |||||||
| chr5:172908344 | G | GAGGGGGG others(35): Show |
1 | a0001c0001t0001g0157 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.156-1323_156-1322i others(44): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908344 | |||||||
| chr5:172908344 | G | GAGGGGGG others(62): Show |
1 | a0001c0001t0002g0026 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.156-1323_156-1322i others(71): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908344 | |||||||
| chr5:172908344 | G | GAGGGGGG others(36): Show |
3 | a0001c0001t0001g0196 a0001c0001t0001g0253 a0001c0001t0002g0177 |
3 | HG02293.hp2 NA18747.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.156-1323_156-1322i others(45): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908344 | |||||||
| chr5:172908344 | G | GAGGGGGG others(38): Show |
1 | a0001c0001t0001g0069 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.156-1323_156-1322i others(47): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908344 | |||||||
| chr5:172908344 | G | GAGGGGGG others(37): Show |
1 | a0001c0001t0001g0193 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.156-1323_156-1322i others(46): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908344 | |||||||
| chr5:172908344 | G | GAGGGGGG others(43): Show |
1 | a0001c0001t0001g0021 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.156-1323_156-1322i others(52): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908344 | |||||||
| chr5:172908344 | G | GGAGGGGG others(40): Show |
1 | a0001c0001t0006g0184 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.156-1322_156-1321i others(49): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908344 | ||||||
| chr5:172908344 | G | GGGGGGGG others(36): Show |
1 | a0001c0001t0001g0018 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.156-1316_156-1315i others(45): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908344 | ||||||
| chr5:172908344 | G | GGGGGGGG others(8): Show |
1 | a0001c0001t0025g0045 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.156-1316_156-1315i others(17): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908344 | ||||||
| chr5:172908344 | G | GGGGGGGG others(35): Show |
2 | a0001c0001t0002g0044 a0001c0001t0002g0102 |
2 | HG02165.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.156-1315_156-1314i others(44): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908344 | ||||||
| chr5:172908344 | G | GGGGGGGG others(36): Show |
2 | a0001c0001t0001g0050 a0001c0001t0002g0195 |
2 | NA18960.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.156-1315_156-1314i others(45): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908344 | ||||||
| chr5:172908344 | G | GGGGGGGG others(37): Show |
1 | a0001c0001t0002g0212 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.156-1315_156-1314i others(46): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908344 | ||||||
| chr5:172908344 | G | GGGGGGGG others(38): Show |
1 | a0001c0001t0001g0038 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.156-1315_156-1314i others(47): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908344 | ||||||
| chr5:172908344 | G | GGGGGGGG others(36): Show |
1 | a0001c0001t0001g0167 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.156-1315_156-1314i others(45): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908344 | ||||||
| chr5:172908344 | G | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0019 others(88): Show |
91 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(88): Show |
intron_variant | MODIFIER | c.156-1323G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908344 | |||||||
| chr5:172908345 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.156-1322G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908345 | |||||||
| chr5:172908345 | G | GGGGAGGG others(4): Show |
1 | a0001c0001t0001g0256 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.156-1319_156-1318i others(13): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908345 | ||||||
| chr5:172908345 | G | GGGGGA | 43 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp2 HG00544.hp2 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.156-1318_156-1317i others(7): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908345 | ||||||
| chr5:172908345 | G | GGGGGGAG others(7): Show |
1 | a0001c0001t0001g0104 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.156-1317_156-1316i others(16): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908345 | ||||||
| chr5:172908345 | G | GGGGGGGA others(33): Show |
1 | a0001c0001t0015g0199 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.156-1316_156-1315i others(42): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908345 | ||||||
| chr5:172908345 | G | GGGGGGGG others(35): Show |
1 | a0001c0001t0001g0306 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.156-1315_156-1314i others(44): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908345 | ||||||
| chr5:172908345 | G | GGGGGGGG others(34): Show |
2 | a0001c0001t0002g0153 a0001c0001t0026g0215 |
2 | NA18971.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.156-1315_156-1314i others(43): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908345 | ||||||
| chr5:172908345 | G | GGGGGGGG others(35): Show |
1 | a0001c0001t0001g0006 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.156-1315_156-1314i others(44): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908345 | ||||||
| chr5:172908346 | G | GGGGGAGG others(6): Show |
1 | a0001c0001t0002g0024 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.156-1317_156-1316i others(15): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172908346 | ||||||
| chr5:172908346 | G | T | 1 | a0001c0001t0001g0057 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.156-1321G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908346 | |||||||
| chr5:172908355 | G | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(107): Show |
110 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.156-1312G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908355 | |||||||
| chr5:172908358 | C | A | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.156-1309C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908358 | |||||||
| chr5:172908498 | C | T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(167): Show |
170 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(167): Show |
intron_variant | MODIFIER | c.156-1169C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908498 | |||||||
| chr5:172908530 | C | T | 25 | a0001c0001t0001g0064 a0001c0001t0001g0097 a0001c0001t0001g0134 others(22): Show |
25 | HG01255.hp2 HG01515.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.156-1137C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908530 | |||||||
| chr5:172908621 | T | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(145): Show |
148 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.156-1046T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908621 | |||||||
| chr5:172908645 | G | A | 1 | a0001c0001t0034g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.156-1022G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908645 | |||||||
| chr5:172908653 | A | T | 1 | a0001c0001t0001g0303 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.156-1014A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908653 | |||||||
| chr5:172908702 | C | T | 5 | a0001c0001t0001g0313 a0001c0001t0001g0325 a0001c0001t0001g0327 others(2): Show |
5 | HG01884.hp1 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.156-965C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908702 | |||||||
| chr5:172908742 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(174): Show |
177 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.156-925A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908742 | |||||||
| chr5:172908744 | A | G | 3 | a0001c0001t0003g0311 a0001c0001t0007g0281 a0001c0001t0007g0282 |
3 | HG02630.hp2 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.156-923A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908744 | |||||||
| chr5:172908857 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.156-810C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908857 | |||||||
| chr5:172908909 | A | G | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(162): Show |
165 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.156-758A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172908909 | |||||||
| chr5:172909118 | C | T | 8 | a0001c0001t0001g0092 a0001c0001t0001g0182 a0001c0001t0002g0024 others(5): Show |
8 | HG00639.hp2 HG01243.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.156-549C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172909118 | |||||||
| chr5:172909127 | T | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(174): Show |
177 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.156-540T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172909127 | |||||||
| chr5:172909128 | G | C | 177 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(174): Show |
177 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.156-539G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172909128 | |||||||
| chr5:172909154 | C | T | 1 | a0001c0001t0002g0054 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.156-513C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172909154 | |||||||
| chr5:172909166 | C | CCTCTTTT others(7): Show |
1 | a0001c0001t0001g0303 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.156-501_156-500ins others(14): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172909166 | |||||||
| chr5:172909168 | C | CCTTTTTT others(4): Show |
1 | a0001c0001t0002g0324 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.156-499_156-498ins others(11): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172909168 | |||||||
| chr5:172909168 | C | CT | 22 | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0021 others(19): Show |
22 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.156-481dupT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172909168 | ||||||
| chr5:172909168 | C | CTTTTTTT others(2): Show |
6 | a0001c0001t0001g0071 a0001c0001t0001g0159 a0001c0001t0001g0248 others(3): Show |
6 | HG01167.hp2 HG02922.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.156-489_156-481dup others(9): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172909168 | ||||||
| chr5:172909168 | C | CTTTTTTT others(3): Show |
71 | a0001c0001t0001g0009 a0001c0001t0001g0041 a0001c0001t0001g0049 others(68): Show |
71 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.156-490_156-481dup others(10): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172909168 | ||||||
| chr5:172909168 | C | CTTTTTTT others(4): Show |
64 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0029 others(61): Show |
64 | HG00323.hp2 HG00438.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.156-491_156-481dup others(11): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172909168 | ||||||
| chr5:172909168 | C | CTTTTTTT others(5): Show |
20 | a0001c0001t0001g0001 a0001c0001t0001g0020 a0001c0001t0001g0047 others(17): Show |
20 | HG00741.hp2 HG01070.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.156-492_156-481dup others(12): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172909168 | ||||||
| chr5:172909168 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0002 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.156-481_156-480ins others(19): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172909168 | ||||||
| chr5:172909168 | C | CTTTTTTT others(14): Show |
1 | a0001c0001t0001g0072 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.156-481_156-480ins others(21): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172909168 | ||||||
| chr5:172909168 | C | T | 1 | a0001c0001t0001g0303 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.156-499C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172909168 | |||||||
| chr5:172909168 | CT | C | 6 | a0001c0001t0001g0040 a0001c0001t0003g0273 a0001c0001t0003g0274 others(3): Show |
6 | HG00673.hp1 HG02630.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.156-481delT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr5 | 172909168 | ||||||
| chr5:172909190 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.156-477A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172909190 | |||||||
| chr5:172909205 | T | G | 1 | a0001c0001t0001g0295 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.156-462T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172909205 | |||||||
| chr5:172909239 | G | A | 1 | a0001c0001t0003g0311 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.156-428G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172909239 | |||||||
| chr5:172909451 | C | T | 2 | a0001c0001t0002g0010 a0001c0001t0002g0011 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.156-216C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172909451 | |||||||
| chr5:172909514 | G | A | 7 | a0001c0001t0003g0061 a0001c0001t0003g0210 a0001c0001t0003g0267 others(4): Show |
7 | HG02451.hp2 HG02486.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.156-153G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172909514 | |||||||
| chr5:172909535 | G | T | 1 | a0001c0001t0001g0103 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.156-132G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172909535 | |||||||
| chr5:172909613 | C | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(163): Show |
166 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.156-54C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172909613 | |||||||
| chr5:172909656 | C | A | 5 | a0001c0001t0001g0313 a0001c0001t0001g0325 a0001c0001t0001g0327 others(2): Show |
5 | HG01884.hp1 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.156-11C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 3/9 | chr5 | 172909656 | |||||||
| chr5:172909841 | C | T | 1 | a0001c0001t0005g0266 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.250+80C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172909841 | |||||||
| chr5:172909902 | C | T | 5 | a0001c0001t0001g0313 a0001c0001t0001g0325 a0001c0001t0001g0327 others(2): Show |
5 | HG01884.hp1 HG02109.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.250+141C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172909902 | |||||||
| chr5:172909903 | G | A | 1 | a0001c0001t0003g0298 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.250+142G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172909903 | |||||||
| chr5:172909937 | A | C | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.250+176A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172909937 | |||||||
| chr5:172909999 | G | C | 4 | a0001c0001t0003g0055 a0001c0001t0003g0101 a0001c0001t0003g0145 others(1): Show |
4 | HG00639.hp2 HG01243.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.250+238G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172909999 | |||||||
| chr5:172910311 | G | A | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(158): Show |
161 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.250+550G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172910311 | |||||||
| chr5:172910324 | G | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(163): Show |
166 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.250+563G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172910324 | |||||||
| chr5:172910336 | C | T | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(163): Show |
166 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.250+575C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172910336 | |||||||
| chr5:172910398 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.250+637C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172910398 | |||||||
| chr5:172910453 | G | T | 4 | a0001c0001t0001g0313 a0001c0001t0001g0325 a0001c0001t0001g0327 others(1): Show |
4 | HG01884.hp1 HG02109.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.250+692G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172910453 | |||||||
| chr5:172910484 | C | T | 7 | a0001c0001t0003g0155 a0001c0001t0003g0273 a0001c0001t0003g0274 others(4): Show |
7 | HG01109.hp2 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.250+723C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172910484 | |||||||
| chr5:172910520 | C | CT | 51 | a0001c0001t0001g0022 a0001c0001t0001g0038 a0001c0001t0001g0040 others(48): Show |
51 | HG00673.hp1 HG01106.hp2 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.250+780dupT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 172910520 | ||||||
| chr5:172910520 | C | CTTTT | 16 | a0001c0001t0001g0092 a0001c0001t0001g0115 a0001c0001t0001g0182 others(13): Show |
16 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.250+777_250+780dup others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 172910520 | ||||||
| chr5:172910520 | CTTTTTTT others(2): Show |
C | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(141): Show |
144 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.250+772_250+780del others(9): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 172910520 | ||||||
| chr5:172910520 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0002g0269 a0003c0004t0003g0312 |
2 | HG02723.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.250+771_250+780del others(10): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 172910520 | ||||||
| chr5:172910561 | G | C | 1 | a0001c0001t0003g0328 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.250+800G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172910561 | |||||||
| chr5:172910581 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.250+820A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172910581 | |||||||
| chr5:172910671 | C | T | 4 | a0001c0001t0003g0155 a0001c0001t0003g0283 a0001c0001t0005g0105 others(1): Show |
4 | HG01109.hp2 HG02818.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.250+910C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172910671 | |||||||
| chr5:172910749 | T | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(161): Show |
164 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.250+988T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172910749 | |||||||
| chr5:172910824 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.250+1063C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172910824 | |||||||
| chr5:172910863 | G | C | 1 | a0001c0001t0001g0021 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.250+1102G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172910863 | |||||||
| chr5:172910864 | T | A | 1 | a0001c0001t0001g0021 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.250+1103T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172910864 | |||||||
| chr5:172910870 | T | C | 1 | a0001c0001t0001g0021 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.250+1109T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172910870 | |||||||
| chr5:172910871 | T | G | 1 | a0001c0001t0001g0021 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.250+1110T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172910871 | |||||||
| chr5:172910872 | G | C | 1 | a0001c0001t0001g0021 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.250+1111G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172910872 | |||||||
| chr5:172910874 | A | T | 1 | a0001c0001t0001g0021 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.250+1113A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172910874 | |||||||
| chr5:172911219 | T | G | 1 | a0001c0001t0001g0183 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.250+1458T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172911219 | |||||||
| chr5:172911369 | A | C | 1 | a0001c0001t0003g0294 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.250+1608A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172911369 | |||||||
| chr5:172911373 | A | T | 1 | a0001c0001t0001g0128 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.250+1612A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172911373 | |||||||
| chr5:172911402 | T | A | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(169): Show |
172 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.250+1641T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172911402 | |||||||
| chr5:172911586 | A | T | 9 | a0001c0001t0001g0081 a0001c0001t0001g0115 a0001c0001t0002g0027 others(6): Show |
9 | HG00140.hp1 HG00280.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.250+1825A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172911586 | |||||||
| chr5:172911591 | T | C | 1 | a0001c0001t0001g0041 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.250+1830T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172911591 | |||||||
| chr5:172911613 | A | G | 172 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(169): Show |
172 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.250+1852A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172911613 | |||||||
| chr5:172911808 | C | T | 5 | a0001c0001t0002g0122 a0001c0001t0010g0189 a0001c0001t0014g0173 others(2): Show |
5 | HG02055.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.250+2047C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172911808 | |||||||
| chr5:172911842 | AAT | A | 5 | a0001c0001t0002g0122 a0001c0001t0010g0189 a0001c0001t0014g0173 others(2): Show |
5 | HG02055.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.250+2084_250+2085d others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 172911842 | ||||||
| chr5:172911848 | T | G | 2 | a0001c0001t0005g0297 a0001c0005t0018g0161 |
2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.250+2087T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172911848 | |||||||
| chr5:172911859 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.250+2098G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172911859 | |||||||
| chr5:172911948 | C | T | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.250+2187C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172911948 | |||||||
| chr5:172911998 | T | G | 1 | a0001c0001t0001g0074 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.250+2237T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172911998 | |||||||
| chr5:172912013 | T | C | 7 | a0001c0001t0003g0061 a0001c0001t0003g0210 a0001c0001t0003g0267 others(4): Show |
7 | HG02451.hp2 HG02486.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.250+2252T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172912013 | |||||||
| chr5:172912076 | C | CT | 9 | a0001c0001t0001g0070 a0001c0001t0001g0074 a0001c0001t0001g0112 others(6): Show |
9 | HG01109.hp2 HG01261.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.250+2330dupT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 172912076 | ||||||
| chr5:172912076 | CT | C | 10 | a0001c0001t0001g0071 a0001c0001t0001g0202 a0001c0001t0001g0235 others(7): Show |
10 | HG02055.hp2 HG02647.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.250+2330delT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 172912076 | ||||||
| chr5:172912231 | C | G | 1 | a0001c0001t0001g0039 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.250+2470C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172912231 | |||||||
| chr5:172912254 | G | T | 5 | a0001c0001t0002g0122 a0001c0001t0010g0189 a0001c0001t0014g0173 others(2): Show |
5 | HG02055.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.251-2460G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172912254 | |||||||
| chr5:172912255 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.251-2459G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172912255 | |||||||
| chr5:172912465 | G | A | 2 | a0001c0001t0005g0297 a0001c0005t0018g0161 |
2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.251-2249G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172912465 | |||||||
| chr5:172912480 | C | T | 1 | a0001c0001t0003g0328 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.251-2234C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172912480 | |||||||
| chr5:172912594 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.251-2120G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172912594 | |||||||
| chr5:172912660 | T | C | 15 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0031 others(12): Show |
15 | HG00597.hp2 HG02071.hp2 HG02074.hp1 others(12): Show |
intron_variant | MODIFIER | c.251-2054T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172912660 | |||||||
| chr5:172912678 | C | T | 5 | a0001c0001t0001g0157 a0001c0001t0001g0181 a0001c0001t0001g0202 others(2): Show |
5 | HG00408.hp2 HG00423.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.251-2036C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172912678 | |||||||
| chr5:172912679 | G | A | 17 | a0001c0001t0001g0081 a0001c0001t0001g0092 a0001c0001t0001g0115 others(14): Show |
17 | HG00140.hp1 HG00280.hp2 HG00639.hp2 others(14): Show |
intron_variant | MODIFIER | c.251-2035G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172912679 | |||||||
| chr5:172912735 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.251-1979G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172912735 | |||||||
| chr5:172912775 | C | CT | 28 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0067 others(25): Show |
28 | HG00280.hp1 HG00438.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.251-1928dupT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 172912775 | ||||||
| chr5:172913008 | A | T | 50 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0049 others(47): Show |
50 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.251-1706A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172913008 | |||||||
| chr5:172913032 | G | C | 5 | a0001c0001t0002g0122 a0001c0001t0010g0189 a0001c0001t0014g0173 others(2): Show |
5 | HG02055.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.251-1682G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172913032 | |||||||
| chr5:172913077 | T | G | 9 | a0001c0001t0002g0269 a0001c0001t0003g0061 a0001c0001t0003g0210 others(6): Show |
9 | HG02451.hp2 HG02486.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.251-1637T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172913077 | |||||||
| chr5:172913273 | T | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(199): Show |
202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.251-1441T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172913273 | |||||||
| chr5:172913355 | G | C | 1 | a0001c0001t0003g0101 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.251-1359G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172913355 | |||||||
| chr5:172913425 | A | T | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0230 |
3 | HG01168.hp2 HG01169.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.251-1289A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172913425 | |||||||
| chr5:172913455 | A | G | 65 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(62): Show |
65 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.251-1259A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172913455 | |||||||
| chr5:172913556 | G | A | 14 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0003g0293 others(11): Show |
14 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.251-1158G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172913556 | |||||||
| chr5:172913671 | A | G | 5 | a0001c0001t0002g0122 a0001c0001t0010g0189 a0001c0001t0014g0173 others(2): Show |
5 | HG02055.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.251-1043A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172913671 | |||||||
| chr5:172913819 | T | C | 75 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(72): Show |
75 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.251-895T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172913819 | |||||||
| chr5:172914089 | T | A | 1 | a0001c0001t0001g0074 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.251-625T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172914089 | |||||||
| chr5:172914234 | C | CA | 48 | a0001c0001t0001g0006 a0001c0001t0001g0018 a0001c0001t0001g0021 others(45): Show |
48 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(45): Show |
intron_variant | MODIFIER | c.251-457dupA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 172914234 | ||||||
| chr5:172914234 | C | CAA | 6 | a0001c0001t0001g0059 a0001c0001t0002g0032 a0001c0001t0002g0243 others(3): Show |
6 | HG02027.hp1 HG02630.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.251-458_251-457dup others(2): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 172914234 | ||||||
| chr5:172914234 | CA | C | 6 | a0001c0001t0001g0168 a0001c0001t0001g0222 a0001c0001t0001g0236 others(3): Show |
6 | NA18951.hp1 NA18951.hp2 NA18986.hp1 others(3): Show |
intron_variant | MODIFIER | c.251-457delA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 172914234 | ||||||
| chr5:172914234 | CAAAAAAA others(1): Show |
C | 65 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(62): Show |
65 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.251-464_251-457del others(8): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 172914234 | ||||||
| chr5:172914241 | A | T | 1 | a0001c0001t0001g0213 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.251-473A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172914241 | |||||||
| chr5:172914246 | A | AAAATAAA others(1): Show |
14 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0003g0293 others(11): Show |
14 | HG01243.hp1 HG01884.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.251-465_251-464ins others(8): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 172914246 | ||||||
| chr5:172914246 | A | AAATAAAT | 7 | a0001c0001t0001g0288 a0001c0001t0002g0082 a0001c0001t0002g0107 others(4): Show |
7 | HG01167.hp2 HG01261.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.251-466_251-465ins others(7): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 172914246 | ||||||
| chr5:172914246 | A | T | 2 | a0001c0001t0001g0305 a0001c0001t0006g0270 |
2 | HG02145.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.251-468A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172914246 | |||||||
| chr5:172914250 | A | T | 23 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(20): Show |
23 | HG01167.hp2 HG01243.hp1 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.251-464A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172914250 | |||||||
| chr5:172914254 | A | AAAAAAAA others(1): Show |
11 | a0001c0001t0001g0002 a0001c0001t0001g0200 a0001c0001t0001g0223 others(8): Show |
11 | HG01109.hp2 HG01123.hp1 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.251-457_251-456ins others(8): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 172914254 | ||||||
| chr5:172914254 | A | AAAAAAAT | 63 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0041 others(60): Show |
63 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.251-457_251-456ins others(7): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 172914254 | ||||||
| chr5:172914254 | A | AAATAAAT | 11 | a0001c0001t0001g0159 a0001c0001t0001g0164 a0001c0001t0001g0190 others(8): Show |
11 | HG02572.hp1 HG02647.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.251-458_251-457ins others(7): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr5 | 172914254 | ||||||
| chr5:172914254 | A | T | 38 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0109 others(35): Show |
38 | HG00609.hp2 HG01167.hp2 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.251-460A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172914254 | |||||||
| chr5:172914268 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.251-446A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172914268 | |||||||
| chr5:172914428 | T | C | 43 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.251-286T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172914428 | |||||||
| chr5:172914444 | C | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0115 |
2 | HG00280.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.251-270C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172914444 | |||||||
| chr5:172914518 | C | G | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.251-196C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172914518 | |||||||
| chr5:172914548 | T | C | 5 | a0001c0001t0002g0122 a0001c0001t0010g0189 a0001c0001t0014g0173 others(2): Show |
5 | HG02055.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.251-166T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 4/9 | chr5 | 172914548 | |||||||
| chr5:172914890 | TC | T | 8 | a0001c0001t0001g0092 a0001c0001t0001g0182 a0001c0001t0002g0024 others(5): Show |
8 | HG00639.hp2 HG01243.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.375+56delC | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 172914890 | ||||||
| chr5:172914914 | T | C | 50 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(47): Show |
50 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.375+76T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172914914 | |||||||
| chr5:172915026 | G | GT | 49 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(46): Show |
49 | HG00323.hp2 HG00597.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.375+192dupT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 172915026 | ||||||
| chr5:172915076 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.375+238T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172915076 | |||||||
| chr5:172915248 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0070 |
2 | NA18969.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.375+410T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172915248 | |||||||
| chr5:172915501 | T | G | 1 | a0001c0001t0002g0269 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.375+663T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172915501 | |||||||
| chr5:172915619 | G | A | 1 | a0001c0001t0006g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.375+781G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172915619 | |||||||
| chr5:172915665 | C | T | 18 | a0001c0001t0001g0021 a0001c0001t0001g0038 a0001c0001t0001g0040 others(15): Show |
18 | HG00597.hp1 HG00673.hp1 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.375+827C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172915665 | |||||||
| chr5:172915745 | A | C | 1 | a0001c0001t0002g0275 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.375+907A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172915745 | |||||||
| chr5:172915850 | C | T | 1 | a0001c0001t0001g0286 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.375+1012C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172915850 | |||||||
| chr5:172915899 | C | G | 1 | a0001c0001t0002g0275 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.375+1061C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172915899 | |||||||
| chr5:172915907 | A | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0079 |
2 | HG01346.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.375+1069A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172915907 | |||||||
| chr5:172916017 | G | T | 1 | a0001c0001t0001g0143 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.375+1179G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172916017 | |||||||
| chr5:172916082 | T | G | 1 | a0001c0001t0002g0221 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.375+1244T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172916082 | |||||||
| chr5:172916372 | A | C | 1 | a0001c0001t0001g0202 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.375+1534A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172916372 | |||||||
| chr5:172916582 | C | T | 2 | a0001c0001t0001g0304 a0001c0001t0003g0198 |
2 | HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.375+1744C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172916582 | |||||||
| chr5:172916593 | G | A | 1 | a0001c0001t0003g0220 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.375+1755G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172916593 | |||||||
| chr5:172916746 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.375+1908G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172916746 | |||||||
| chr5:172916774 | G | A | 8 | a0001c0001t0003g0061 a0001c0001t0003g0210 a0001c0001t0003g0267 others(5): Show |
8 | HG02451.hp2 HG02486.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.375+1936G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172916774 | |||||||
| chr5:172916821 | C | CA | 11 | a0001c0001t0001g0092 a0001c0001t0001g0100 a0001c0001t0001g0182 others(8): Show |
11 | HG00639.hp2 HG01243.hp2 HG02523.hp2 others(8): Show |
intron_variant | MODIFIER | c.375+1992dupA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 172916821 | ||||||
| chr5:172916845 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.375+2007C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172916845 | |||||||
| chr5:172916919 | A | G | 1 | a0001c0001t0004g0108 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.375+2081A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172916919 | |||||||
| chr5:172917053 | G | A | 7 | a0001c0001t0001g0018 a0001c0001t0001g0185 a0001c0001t0001g0231 others(4): Show |
7 | HG00741.hp1 HG01081.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.375+2215G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172917053 | |||||||
| chr5:172917197 | C | T | 1 | a0001c0005t0018g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.375+2359C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172917197 | |||||||
| chr5:172917440 | A | G | 5 | a0001c0001t0002g0122 a0001c0001t0010g0189 a0001c0001t0014g0173 others(2): Show |
5 | HG02055.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.375+2602A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172917440 | |||||||
| chr5:172917486 | C | G | 1 | a0001c0001t0001g0144 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.375+2648C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172917486 | |||||||
| chr5:172917805 | G | A | 6 | a0001c0001t0001g0037 a0001c0001t0001g0080 a0001c0001t0001g0124 others(3): Show |
6 | HG01358.hp1 HG02683.hp2 HG03239.hp2 others(3): Show |
intron_variant | MODIFIER | c.375+2967G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172917805 | |||||||
| chr5:172917880 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.375+3042G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172917880 | |||||||
| chr5:172917988 | A | T | 1 | a0001c0001t0001g0148 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.375+3150A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172917988 | |||||||
| chr5:172917996 | C | T | 140 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(137): Show |
140 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.375+3158C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172917996 | |||||||
| chr5:172918029 | T | A | 1 | a0001c0001t0010g0058 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.375+3191T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172918029 | |||||||
| chr5:172918131 | C | T | 1 | a0001c0001t0003g0328 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.375+3293C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172918131 | |||||||
| chr5:172918379 | A | G | 1 | a0001c0001t0005g0308 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.375+3541A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172918379 | |||||||
| chr5:172918464 | A | T | 1 | a0001c0001t0001g0305 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.375+3626A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172918464 | |||||||
| chr5:172918499 | C | G | 1 | a0001c0001t0002g0160 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.375+3661C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172918499 | |||||||
| chr5:172918532 | A | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(215): Show |
218 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.375+3694A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172918532 | |||||||
| chr5:172918569 | A | G | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.375+3731A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172918569 | |||||||
| chr5:172918738 | G | A | 2 | a0001c0001t0002g0142 a0001c0001t0002g0285 |
2 | HG01257.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.375+3900G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172918738 | |||||||
| chr5:172918779 | G | T | 1 | a0001c0001t0001g0228 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.375+3941G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172918779 | |||||||
| chr5:172918821 | C | CTCTGTCC others(20): Show |
1 | a0001c0001t0002g0160 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.375+3984_375+4010d others(29): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 172918821 | ||||||
| chr5:172918983 | G | A | 3 | a0001c0001t0001g0121 a0001c0001t0001g0144 a0001c0001t0022g0315 |
3 | HG00639.hp1 HG02559.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.375+4145G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172918983 | |||||||
| chr5:172918986 | T | C | 55 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(52): Show |
55 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(52): Show |
intron_variant | MODIFIER | c.375+4148T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172918986 | |||||||
| chr5:172919045 | G | A | 7 | a0001c0001t0003g0271 a0001c0001t0003g0272 a0001c0001t0003g0292 others(4): Show |
7 | HG02280.hp2 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.375+4207G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172919045 | |||||||
| chr5:172919183 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.375+4345G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172919183 | |||||||
| chr5:172919336 | A | T | 7 | a0001c0001t0002g0082 a0001c0001t0003g0334 a0001c0001t0008g0150 others(4): Show |
7 | HG02809.hp1 HG02896.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.375+4498A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172919336 | |||||||
| chr5:172919469 | C | T | 1 | a0001c0001t0034g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.376-4536C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172919469 | |||||||
| chr5:172919567 | T | G | 1 | a0002c0003t0002g0012 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.376-4438T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172919567 | |||||||
| chr5:172919585 | A | G | 80 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0029 others(77): Show |
80 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.376-4420A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172919585 | |||||||
| chr5:172919625 | T | C | 3 | a0001c0001t0001g0265 a0001c0001t0001g0289 a0001c0001t0001g0290 |
3 | HG01243.hp1 HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.376-4380T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172919625 | |||||||
| chr5:172919635 | G | T | 3 | a0001c0001t0001g0265 a0001c0001t0001g0289 a0001c0001t0001g0290 |
3 | HG01243.hp1 HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.376-4370G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172919635 | |||||||
| chr5:172919645 | T | C | 56 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(53): Show |
56 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(53): Show |
intron_variant | MODIFIER | c.376-4360T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172919645 | |||||||
| chr5:172919738 | C | T | 1 | a0001c0001t0004g0178 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.376-4267C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172919738 | |||||||
| chr5:172919790 | C | T | 1 | a0001c0005t0018g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.376-4215C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172919790 | |||||||
| chr5:172919940 | A | G | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0041 others(34): Show |
37 | HG00544.hp2 HG01261.hp2 HG01433.hp2 others(34): Show |
intron_variant | MODIFIER | c.376-4065A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172919940 | |||||||
| chr5:172920150 | T | C | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.376-3855T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172920150 | |||||||
| chr5:172920437 | G | A | 64 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0029 others(61): Show |
64 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.376-3568G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172920437 | |||||||
| chr5:172920676 | A | G | 105 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0029 others(102): Show |
105 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.376-3329A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172920676 | |||||||
| chr5:172920744 | G | T | 1 | a0001c0001t0001g0263 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.376-3261G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172920744 | |||||||
| chr5:172920820 | C | A | 85 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0029 others(82): Show |
85 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.376-3185C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172920820 | |||||||
| chr5:172920872 | G | A | 1 | a0001c0001t0003g0055 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.376-3133G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172920872 | |||||||
| chr5:172920900 | T | G | 85 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0029 others(82): Show |
85 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.376-3105T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172920900 | |||||||
| chr5:172920910 | C | G | 18 | a0001c0001t0001g0304 a0001c0001t0003g0155 a0001c0001t0003g0271 others(15): Show |
18 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.376-3095C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172920910 | |||||||
| chr5:172920971 | T | C | 1 | a0001c0001t0001g0041 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.376-3034T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172920971 | |||||||
| chr5:172920988 | C | T | 12 | a0001c0001t0001g0081 a0001c0001t0001g0115 a0001c0001t0001g0209 others(9): Show |
12 | HG00140.hp1 HG00280.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.376-3017C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172920988 | |||||||
| chr5:172921025 | C | T | 1 | a0001c0001t0013g0291 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.376-2980C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172921025 | |||||||
| chr5:172921072 | A | G | 18 | a0001c0001t0001g0304 a0001c0001t0003g0155 a0001c0001t0003g0271 others(15): Show |
18 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.376-2933A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172921072 | |||||||
| chr5:172921122 | A | G | 3 | a0001c0001t0001g0265 a0001c0001t0001g0289 a0001c0001t0001g0290 |
3 | HG01243.hp1 HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.376-2883A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172921122 | |||||||
| chr5:172921202 | G | A | 1 | a0001c0001t0002g0243 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.376-2803G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172921202 | |||||||
| chr5:172921255 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.376-2750C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172921255 | |||||||
| chr5:172921267 | G | A | 2 | a0001c0001t0007g0281 a0001c0001t0007g0282 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.376-2738G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172921267 | |||||||
| chr5:172921463 | A | G | 148 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0016 others(145): Show |
148 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.376-2542A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172921463 | |||||||
| chr5:172921473 | C | G | 3 | a0001c0001t0001g0265 a0001c0001t0001g0289 a0001c0001t0001g0290 |
3 | HG01243.hp1 HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.376-2532C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172921473 | |||||||
| chr5:172921503 | TC | T | 14 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(11): Show |
14 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.376-2498delC | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 172921503 | ||||||
| chr5:172921586 | G | A | 2 | a0001c0001t0006g0004 a0001c0001t0006g0053 |
2 | HG02723.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.376-2419G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172921586 | |||||||
| chr5:172921591 | C | G | 65 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0029 others(62): Show |
65 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.376-2414C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172921591 | |||||||
| chr5:172921670 | A | G | 2 | a0001c0001t0005g0105 a0001c0001t0005g0106 |
2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.376-2335A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172921670 | |||||||
| chr5:172921671 | A | G | 1 | a0001c0005t0018g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.376-2334A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172921671 | |||||||
| chr5:172921675 | G | A | 14 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(11): Show |
14 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.376-2330G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172921675 | |||||||
| chr5:172921769 | TC | T | 66 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0029 others(63): Show |
66 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.376-2234delC | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 172921769 | ||||||
| chr5:172921793 | A | C | 96 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(93): Show |
96 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.376-2212A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172921793 | |||||||
| chr5:172921950 | C | T | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.376-2055C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172921950 | |||||||
| chr5:172922018 | C | G | 1 | a0001c0001t0001g0258 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.376-1987C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172922018 | |||||||
| chr5:172922139 | G | A | 4 | a0001c0001t0001g0157 a0001c0001t0001g0181 a0001c0001t0001g0202 others(1): Show |
4 | HG00423.hp2 NA18747.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.376-1866G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172922139 | |||||||
| chr5:172922183 | C | G | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.376-1822C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172922183 | |||||||
| chr5:172922300 | G | C | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.376-1705G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172922300 | |||||||
| chr5:172922343 | G | A | 5 | a0001c0001t0001g0157 a0001c0001t0001g0181 a0001c0001t0001g0202 others(2): Show |
5 | HG00423.hp2 HG02071.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.376-1662G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172922343 | |||||||
| chr5:172922449 | G | A | 14 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(11): Show |
14 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.376-1556G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172922449 | |||||||
| chr5:172922454 | C | T | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.376-1551C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172922454 | |||||||
| chr5:172922461 | T | C | 1 | a0001c0001t0015g0199 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.376-1544T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172922461 | |||||||
| chr5:172922518 | G | A | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.376-1487G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172922518 | |||||||
| chr5:172922619 | C | T | 1 | a0001c0001t0001g0307 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.376-1386C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172922619 | |||||||
| chr5:172922628 | G | A | 1 | a0001c0001t0015g0199 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.376-1377G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172922628 | |||||||
| chr5:172922633 | C | T | 1 | a0001c0005t0018g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.376-1372C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172922633 | |||||||
| chr5:172922645 | A | C | 19 | a0001c0001t0001g0304 a0001c0001t0003g0155 a0001c0001t0003g0271 others(16): Show |
19 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.376-1360A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172922645 | |||||||
| chr5:172922702 | G | A | 2 | a0001c0001t0001g0231 a0001c0001t0002g0094 |
2 | HG00741.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.376-1303G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172922702 | |||||||
| chr5:172922711 | C | G | 1 | a0001c0001t0001g0077 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.376-1294C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172922711 | |||||||
| chr5:172922893 | G | A | 10 | a0001c0001t0001g0081 a0001c0001t0001g0115 a0001c0001t0001g0209 others(7): Show |
10 | HG00140.hp1 HG00280.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.376-1112G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172922893 | |||||||
| chr5:172923014 | C | T | 3 | a0001c0001t0002g0138 a0001c0001t0002g0207 a0001c0001t0002g0208 |
3 | HG00140.hp1 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.376-991C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172923014 | |||||||
| chr5:172923061 | G | A | 1 | a0001c0001t0034g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.376-944G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172923061 | |||||||
| chr5:172923069 | A | C | 158 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0016 others(155): Show |
158 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.376-936A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172923069 | |||||||
| chr5:172923073 | AGGAGGAG others(52): Show |
A | 45 | a0001c0001t0001g0081 a0001c0001t0001g0115 a0001c0001t0001g0194 others(42): Show |
45 | HG00140.hp1 HG00280.hp2 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.376-805_376-747del others(59): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 172923073 | ||||||
| chr5:172923085 | AGGAGGAG others(165): Show |
A | 65 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0029 others(62): Show |
65 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.376-858_376-687del | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 172923085 | ||||||
| chr5:172923092 | G | C | 34 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0041 others(31): Show |
34 | HG00544.hp2 HG01261.hp2 HG01433.hp2 others(31): Show |
intron_variant | MODIFIER | c.376-913G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172923092 | |||||||
| chr5:172923148 | G | A | 1 | a0001c0001t0001g0228 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.376-857G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172923148 | |||||||
| chr5:172923149 | G | T | 3 | a0001c0001t0007g0281 a0001c0001t0007g0282 a0001c0001t0023g0332 |
3 | HG02630.hp2 HG02717.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.376-856G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172923149 | |||||||
| chr5:172923151 | G | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0262 |
2 | HG02155.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.376-854G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172923151 | |||||||
| chr5:172923203 | AGGAGGAG others(47): Show |
A | 1 | a0001c0001t0005g0266 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.376-746_376-693del others(54): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 172923203 | ||||||
| chr5:172923360 | AGGAGGAG others(2): Show |
A | 17 | a0001c0001t0001g0081 a0001c0001t0001g0115 a0001c0001t0001g0209 others(14): Show |
17 | HG00140.hp1 HG00280.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.376-627_376-619del others(9): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr5 | 172923360 | ||||||
| chr5:172923419 | A | C | 8 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0033 others(5): Show |
8 | HG00597.hp2 HG02074.hp1 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.376-586A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172923419 | |||||||
| chr5:172923501 | G | A | 71 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(68): Show |
71 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(68): Show |
intron_variant | MODIFIER | c.376-504G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172923501 | |||||||
| chr5:172923635 | A | G | 162 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0016 others(159): Show |
162 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.376-370A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172923635 | |||||||
| chr5:172923761 | C | A | 1 | a0001c0001t0004g0246 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.376-244C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172923761 | |||||||
| chr5:172923777 | C | T | 1 | a0001c0001t0003g0145 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.376-228C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172923777 | |||||||
| chr5:172923779 | G | A | 1 | a0001c0001t0002g0082 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.376-226G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172923779 | |||||||
| chr5:172923795 | G | A | 1 | a0001c0001t0003g0210 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.376-210G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172923795 | |||||||
| chr5:172923808 | C | T | 1 | a0001c0001t0034g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.376-197C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172923808 | |||||||
| chr5:172923910 | T | C | 1 | a0001c0001t0001g0240 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.376-95T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 5/9 | chr5 | 172923910 | |||||||
| chr5:172924127 | G | A | 5 | a0001c0001t0003g0293 a0001c0001t0006g0004 a0001c0001t0006g0053 others(2): Show |
5 | HG02145.hp2 HG02723.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.480+18G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/9 | chr5 | 172924127 | |||||||
| chr5:172924157 | G | A | 53 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(50): Show |
53 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.480+48G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/9 | chr5 | 172924157 | |||||||
| chr5:172924209 | C | T | 1 | a0001c0001t0002g0280 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.480+100C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/9 | chr5 | 172924209 | |||||||
| chr5:172924311 | C | T | 55 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0029 others(52): Show |
55 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.480+202C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/9 | chr5 | 172924311 | |||||||
| chr5:172924414 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.480+305C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/9 | chr5 | 172924414 | |||||||
| chr5:172924603 | C | G | 17 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(14): Show |
17 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.480+494C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/9 | chr5 | 172924603 | |||||||
| chr5:172924684 | C | T | 53 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(50): Show |
53 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.480+575C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/9 | chr5 | 172924684 | |||||||
| chr5:172924763 | A | T | 9 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0033 others(6): Show |
9 | HG00597.hp2 HG02074.hp1 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.480+654A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/9 | chr5 | 172924763 | |||||||
| chr5:172924826 | G | T | 108 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0029 others(105): Show |
108 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.480+717G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/9 | chr5 | 172924826 | |||||||
| chr5:172925164 | GGAGGTGG others(10): Show |
G | 1 | a0001c0001t0003g0198 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.480+1059_480+1075d others(19): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr5 | 172925164 | ||||||
| chr5:172925216 | A | T | 105 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0029 others(102): Show |
105 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.480+1107A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/9 | chr5 | 172925216 | |||||||
| chr5:172925366 | T | C | 102 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0029 others(99): Show |
102 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.481-1143T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/9 | chr5 | 172925366 | |||||||
| chr5:172925372 | C | T | 2 | a0001c0001t0003g0273 a0001c0001t0003g0274 |
2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.481-1137C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/9 | chr5 | 172925372 | |||||||
| chr5:172925379 | C | A | 1 | a0001c0001t0009g0329 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.481-1130C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/9 | chr5 | 172925379 | |||||||
| chr5:172925472 | C | T | 1 | a0001c0001t0027g0091 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.481-1037C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/9 | chr5 | 172925472 | |||||||
| chr5:172925526 | G | A | 54 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(51): Show |
54 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.481-983G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/9 | chr5 | 172925526 | |||||||
| chr5:172925587 | G | C | 162 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0016 others(159): Show |
162 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(159): Show |
intron_variant | MODIFIER | c.481-922G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/9 | chr5 | 172925587 | |||||||
| chr5:172925597 | G | A | 80 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(77): Show |
80 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.481-912G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/9 | chr5 | 172925597 | |||||||
| chr5:172925756 | C | T | 1 | a0001c0001t0003g0220 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.481-753C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/9 | chr5 | 172925756 | |||||||
| chr5:172925776 | A | G | 1 | a0001c0001t0002g0125 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.481-733A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/9 | chr5 | 172925776 | |||||||
| chr5:172925861 | C | T | 3 | a0001c0001t0007g0281 a0001c0001t0007g0282 a0001c0001t0023g0332 |
3 | HG02630.hp2 HG02717.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.481-648C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/9 | chr5 | 172925861 | |||||||
| chr5:172925910 | T | C | 159 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0016 others(156): Show |
159 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.481-599T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/9 | chr5 | 172925910 | |||||||
| chr5:172925938 | G | A | 7 | a0001c0001t0001g0039 a0001c0001t0001g0052 a0001c0001t0001g0204 others(4): Show |
7 | HG00408.hp1 HG02015.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.481-571G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/9 | chr5 | 172925938 | |||||||
| chr5:172925992 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.481-517G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/9 | chr5 | 172925992 | |||||||
| chr5:172926340 | A | G | 159 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0016 others(156): Show |
159 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.481-169A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/9 | chr5 | 172926340 | |||||||
| chr5:172926379 | C | G | 1 | a0001c0001t0001g0245 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.481-130C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/9 | chr5 | 172926379 | |||||||
| chr5:172926441 | C | T | 5 | a0001c0001t0003g0334 a0001c0001t0008g0150 a0001c0001t0008g0187 others(2): Show |
5 | HG02809.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.481-68C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 6/9 | chr5 | 172926441 | |||||||
| chr5:172926720 | T | C | 1 | a0001c0002t0001g0251 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.541+151T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172926720 | |||||||
| chr5:172926724 | A | C | 35 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0041 others(32): Show |
35 | HG00544.hp2 HG01261.hp2 HG01433.hp2 others(32): Show |
intron_variant | MODIFIER | c.541+155A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172926724 | |||||||
| chr5:172926760 | T | C | 105 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0029 others(102): Show |
105 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.541+191T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172926760 | |||||||
| chr5:172926784 | G | A | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.541+215G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172926784 | |||||||
| chr5:172926842 | C | A | 1 | a0001c0001t0001g0165 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.541+273C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172926842 | |||||||
| chr5:172926869 | T | G | 4 | a0001c0001t0002g0107 a0001c0001t0002g0132 a0001c0001t0002g0147 others(1): Show |
4 | HG01258.hp2 HG02300.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.541+300T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172926869 | |||||||
| chr5:172926999 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.541+430C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172926999 | |||||||
| chr5:172927031 | C | T | 54 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(51): Show |
54 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.541+462C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172927031 | |||||||
| chr5:172927034 | T | C | 105 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0029 others(102): Show |
105 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.541+465T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172927034 | |||||||
| chr5:172927102 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.541+533G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172927102 | |||||||
| chr5:172927170 | T | G | 2 | a0001c0001t0007g0281 a0001c0001t0007g0282 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.541+601T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172927170 | |||||||
| chr5:172927226 | T | C | 159 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0016 others(156): Show |
159 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.541+657T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172927226 | |||||||
| chr5:172927323 | C | T | 1 | a0001c0005t0018g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.541+754C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172927323 | |||||||
| chr5:172927369 | T | A | 1 | a0001c0001t0002g0082 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.541+800T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172927369 | |||||||
| chr5:172927462 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.541+893A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172927462 | |||||||
| chr5:172927518 | C | T | 15 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(12): Show |
15 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.541+949C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172927518 | |||||||
| chr5:172927579 | C | CT | 30 | a0001c0001t0001g0041 a0001c0001t0001g0074 a0001c0001t0001g0080 others(27): Show |
30 | HG00544.hp2 HG00639.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.541+1028dupT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 172927579 | ||||||
| chr5:172927579 | CT | C | 67 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0029 others(64): Show |
67 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.541+1028delT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 172927579 | ||||||
| chr5:172927599 | A | G | 105 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0029 others(102): Show |
105 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.541+1030A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172927599 | |||||||
| chr5:172927728 | T | C | 105 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0029 others(102): Show |
105 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.541+1159T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172927728 | |||||||
| chr5:172927731 | C | T | 1 | a0001c0001t0003g0284 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.541+1162C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172927731 | |||||||
| chr5:172927777 | C | T | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.541+1208C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172927777 | |||||||
| chr5:172927880 | G | A | 69 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0029 others(66): Show |
69 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.541+1311G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172927880 | |||||||
| chr5:172927901 | C | T | 1 | a0001c0001t0002g0082 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.541+1332C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172927901 | |||||||
| chr5:172928036 | T | C | 105 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0029 others(102): Show |
105 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.541+1467T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172928036 | |||||||
| chr5:172928073 | C | A | 54 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(51): Show |
54 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.541+1504C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172928073 | |||||||
| chr5:172928255 | C | T | 2 | a0001c0001t0006g0309 a0001c0001t0006g0310 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.541+1686C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172928255 | |||||||
| chr5:172928451 | C | T | 2 | a0001c0001t0006g0192 a0001c0001t0006g0270 |
2 | HG02559.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.541+1882C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172928451 | |||||||
| chr5:172928452 | G | A | 1 | a0001c0001t0011g0117 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.541+1883G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172928452 | |||||||
| chr5:172928479 | G | C | 1 | a0001c0001t0009g0329 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.541+1910G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172928479 | |||||||
| chr5:172928567 | C | G | 1 | a0001c0001t0015g0199 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.541+1998C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172928567 | |||||||
| chr5:172928602 | TATAACAT others(11): Show |
T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0185 a0001c0001t0001g0233 others(1): Show |
4 | HG01928.hp2 HG01978.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.541+2034_541+2051d others(20): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172928602 | |||||||
| chr5:172928623 | G | GT | 4 | a0001c0001t0001g0018 a0001c0001t0001g0185 a0001c0001t0001g0233 others(1): Show |
4 | HG01928.hp2 HG01978.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.541+2054_541+2055i others(3): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172928623 | |||||||
| chr5:172928667 | A | G | 91 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0029 others(88): Show |
91 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.541+2098A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172928667 | |||||||
| chr5:172928673 | TATATGAT others(5): Show |
T | 91 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0029 others(88): Show |
91 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.541+2108_541+2119d others(14): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 172928673 | ||||||
| chr5:172928775 | C | T | 1 | a0001c0001t0001g0240 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.541+2206C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172928775 | |||||||
| chr5:172928840 | G | C | 108 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0029 others(105): Show |
108 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.541+2271G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172928840 | |||||||
| chr5:172928886 | A | T | 54 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(51): Show |
54 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(51): Show |
intron_variant | MODIFIER | c.541+2317A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172928886 | |||||||
| chr5:172928898 | C | T | 6 | a0001c0001t0001g0313 a0001c0001t0001g0325 a0001c0001t0001g0327 others(3): Show |
6 | HG01109.hp2 HG01884.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.541+2329C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172928898 | |||||||
| chr5:172929112 | A | T | 1 | a0001c0001t0001g0304 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.541+2543A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172929112 | |||||||
| chr5:172929142 | C | CAT | 4 | a0001c0001t0001g0193 a0001c0001t0001g0225 a0001c0001t0001g0237 others(1): Show |
4 | HG02071.hp2 NA18956.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.541+2584_541+2585d others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 172929142 | ||||||
| chr5:172929151 | A | ATG | 39 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0020 others(36): Show |
39 | HG00323.hp2 HG00408.hp2 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.541+2583_541+2584i others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 172929151 | ||||||
| chr5:172929151 | A | ATGTG | 75 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0029 others(72): Show |
75 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.541+2583_541+2584i others(6): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 172929151 | ||||||
| chr5:172929151 | A | ATGTGTG | 8 | a0001c0001t0002g0060 a0001c0001t0002g0095 a0001c0001t0003g0055 others(5): Show |
8 | HG00639.hp2 HG01243.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.541+2583_541+2584i others(8): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 172929151 | ||||||
| chr5:172929153 | A | ATG | 32 | a0001c0001t0001g0064 a0001c0001t0001g0096 a0001c0001t0001g0097 others(29): Show |
32 | HG00639.hp1 HG00738.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.541+2602_541+2603d others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 172929153 | ||||||
| chr5:172929153 | A | ATGTG | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0041 others(45): Show |
48 | HG00544.hp2 HG01261.hp2 HG01433.hp2 others(45): Show |
intron_variant | MODIFIER | c.541+2600_541+2603d others(6): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 172929153 | ||||||
| chr5:172929153 | A | ATGTGTGT others(1): Show |
18 | a0001c0001t0001g0081 a0001c0001t0001g0115 a0001c0001t0001g0209 others(15): Show |
18 | HG00140.hp1 HG00280.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.541+2596_541+2603d others(10): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 172929153 | ||||||
| chr5:172929153 | A | G | 127 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0016 others(124): Show |
127 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.541+2584A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172929153 | |||||||
| chr5:172929167 | G | GTT | 3 | a0001c0001t0001g0158 a0001c0001t0001g0211 a0001c0001t0001g0256 |
3 | NA18971.hp1 NA18998.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.541+2599_541+2600i others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 172929167 | ||||||
| chr5:172929171 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0118 a0001c0001t0001g0303 |
3 | NA18979.hp1 NA19007.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.541+2602G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172929171 | |||||||
| chr5:172929173 | A | G | 14 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0074 others(11): Show |
14 | HG01070.hp1 HG01071.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.541+2604A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172929173 | |||||||
| chr5:172929311 | C | T | 1 | a0001c0001t0013g0291 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.541+2742C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172929311 | |||||||
| chr5:172929375 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.541+2806G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172929375 | |||||||
| chr5:172929470 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.541+2901C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172929470 | |||||||
| chr5:172929514 | C | G | 1 | a0001c0001t0034g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.542-2922C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172929514 | |||||||
| chr5:172929668 | C | A | 1 | a0001c0001t0034g0086 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.542-2768C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172929668 | |||||||
| chr5:172929824 | A | G | 14 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(11): Show |
14 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.542-2612A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172929824 | |||||||
| chr5:172929848 | A | G | 4 | a0001c0001t0003g0154 a0001c0001t0003g0284 a0001c0001t0003g0298 others(1): Show |
4 | HG02055.hp1 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.542-2588A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172929848 | |||||||
| chr5:172929925 | C | T | 5 | a0001c0001t0002g0026 a0001c0001t0002g0073 a0001c0001t0002g0177 others(2): Show |
5 | NA18747.hp2 NA18944.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.542-2511C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172929925 | |||||||
| chr5:172929954 | A | G | 159 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0016 others(156): Show |
159 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.542-2482A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172929954 | |||||||
| chr5:172930039 | T | C | 14 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(11): Show |
14 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.542-2397T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172930039 | |||||||
| chr5:172930187 | C | CA | 20 | a0001c0001t0001g0041 a0001c0001t0001g0228 a0001c0001t0001g0261 others(17): Show |
20 | HG00609.hp1 HG01175.hp2 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.542-2234dupA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 172930187 | ||||||
| chr5:172930187 | C | CAA | 61 | a0001c0001t0001g0009 a0001c0001t0001g0029 a0001c0001t0001g0049 others(58): Show |
61 | HG00280.hp1 HG00323.hp1 HG00609.hp2 others(58): Show |
intron_variant | MODIFIER | c.542-2235_542-2234d others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 172930187 | ||||||
| chr5:172930187 | C | CAAA | 12 | a0001c0001t0001g0081 a0001c0001t0001g0115 a0001c0001t0001g0209 others(9): Show |
12 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(9): Show |
intron_variant | MODIFIER | c.542-2236_542-2234d others(5): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 172930187 | ||||||
| chr5:172930355 | A | AT | 10 | a0001c0001t0001g0031 a0001c0001t0001g0069 a0001c0001t0001g0112 others(7): Show |
10 | HG00597.hp1 HG01261.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.542-2068dupT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 172930355 | ||||||
| chr5:172930355 | AT | A | 141 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0020 others(138): Show |
141 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.542-2068delT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 172930355 | ||||||
| chr5:172930355 | ATT | A | 12 | a0001c0001t0001g0081 a0001c0001t0001g0115 a0001c0001t0001g0209 others(9): Show |
12 | HG00140.hp1 HG00280.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.542-2069_542-2068d others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 172930355 | ||||||
| chr5:172930733 | G | A | 1 | a0001c0001t0007g0314 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.542-1703G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172930733 | |||||||
| chr5:172930791 | C | A | 50 | a0001c0001t0001g0009 a0001c0001t0001g0049 a0001c0001t0001g0051 others(47): Show |
50 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.542-1645C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172930791 | |||||||
| chr5:172930869 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.542-1567C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172930869 | |||||||
| chr5:172930989 | T | C | 3 | a0001c0001t0002g0138 a0001c0001t0002g0207 a0001c0001t0002g0208 |
3 | HG00140.hp1 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.542-1447T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172930989 | |||||||
| chr5:172931047 | G | A | 1 | a0001c0001t0001g0231 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.542-1389G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172931047 | |||||||
| chr5:172931173 | G | A | 7 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(4): Show |
7 | HG02280.hp2 HG02647.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.542-1263G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172931173 | |||||||
| chr5:172931179 | C | T | 1 | a0001c0005t0018g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.542-1257C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172931179 | |||||||
| chr5:172931299 | T | C | 156 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0020 others(153): Show |
156 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.542-1137T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172931299 | |||||||
| chr5:172931362 | A | G | 330 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(327): Show |
330 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.542-1074A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172931362 | |||||||
| chr5:172931559 | T | G | 3 | a0001c0001t0010g0189 a0001c0001t0014g0173 a0001c0001t0031g0083 |
3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.542-877T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172931559 | |||||||
| chr5:172931584 | T | G | 39 | a0001c0001t0001g0081 a0001c0001t0001g0115 a0001c0001t0001g0209 others(36): Show |
39 | HG00140.hp1 HG00280.hp2 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.542-852T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172931584 | |||||||
| chr5:172931719 | A | G | 1 | a0001c0001t0002g0046 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.542-717A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172931719 | |||||||
| chr5:172931857 | C | CT | 19 | a0001c0001t0001g0064 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
19 | HG01070.hp1 HG01071.hp2 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.542-560dupT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 172931857 | ||||||
| chr5:172931857 | C | CTT | 7 | a0001c0001t0002g0160 a0001c0001t0003g0154 a0001c0001t0003g0284 others(4): Show |
7 | HG02055.hp1 HG02559.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.542-561_542-560dup others(2): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 172931857 | ||||||
| chr5:172931857 | C | CTTT | 60 | a0001c0001t0001g0009 a0001c0001t0001g0047 a0001c0001t0001g0049 others(57): Show |
60 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.542-562_542-560dup others(3): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 172931857 | ||||||
| chr5:172931857 | C | CTTTT | 66 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0033 others(63): Show |
66 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.542-563_542-560dup others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 172931857 | ||||||
| chr5:172931857 | CT | C | 10 | a0001c0001t0001g0013 a0001c0001t0001g0048 a0001c0001t0001g0172 others(7): Show |
10 | HG01993.hp1 HG03453.hp2 HG03688.hp2 others(7): Show |
intron_variant | MODIFIER | c.542-560delT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 172931857 | ||||||
| chr5:172931857 | CTTTTT | C | 17 | a0001c0001t0001g0081 a0001c0001t0001g0115 a0001c0001t0001g0209 others(14): Show |
17 | HG00140.hp1 HG00280.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.542-564_542-560del others(5): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr5 | 172931857 | ||||||
| chr5:172931895 | A | G | 4 | a0001c0001t0001g0304 a0001c0001t0006g0184 a0001c0001t0013g0291 others(1): Show |
4 | HG03139.hp2 HG03195.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.542-541A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172931895 | |||||||
| chr5:172931898 | G | A | 2 | a0001c0001t0007g0281 a0001c0001t0007g0282 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.542-538G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172931898 | |||||||
| chr5:172932106 | A | G | 153 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0020 others(150): Show |
153 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.542-330A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172932106 | |||||||
| chr5:172932249 | T | C | 3 | a0001c0001t0010g0189 a0001c0001t0014g0173 a0001c0001t0031g0083 |
3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.542-187T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172932249 | |||||||
| chr5:172932330 | G | T | 1 | a0001c0001t0003g0293 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.542-106G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172932330 | |||||||
| chr5:172932358 | C | T | 3 | a0001c0001t0001g0168 a0001c0001t0001g0244 a0001c0001t0001g0320 |
3 | NA18986.hp1 NA18986.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.542-78C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 7/9 | chr5 | 172932358 | |||||||
| chr5:172932552 | C | T | 1 | a0001c0001t0003g0061 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.642+16C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 8/9 | chr5 | 172932552 | |||||||
| chr5:172932717 | T | C | 16 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(13): Show |
16 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.642+181T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 8/9 | chr5 | 172932717 | |||||||
| chr5:172932814 | G | GA | 156 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0020 others(153): Show |
156 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.642+278_642+279ins others(1): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 8/9 | chr5 | 172932814 | |||||||
| chr5:172932815 | G | T | 156 | a0001c0001t0001g0009 a0001c0001t0001g0016 a0001c0001t0001g0020 others(153): Show |
156 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.642+279G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 8/9 | chr5 | 172932815 | |||||||
| chr5:172932838 | T | C | 9 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0072 others(6): Show |
9 | HG01433.hp2 HG01928.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.642+302T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 8/9 | chr5 | 172932838 | |||||||
| chr5:172933031 | G | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(63): Show |
66 | HG00544.hp2 HG00639.hp1 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.642+495G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 8/9 | chr5 | 172933031 | |||||||
| chr5:172933291 | T | G | 4 | a0001c0001t0002g0138 a0001c0001t0002g0191 a0001c0001t0002g0207 others(1): Show |
4 | HG00140.hp1 HG01257.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.642+755T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 8/9 | chr5 | 172933291 | |||||||
| chr5:172933432 | ATTT | A | 3 | a0001c0001t0008g0150 a0001c0001t0008g0187 a0001c0001t0008g0205 |
3 | HG02896.hp1 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.642+897_642+899del others(3): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 8/9 | chr5 | 172933432 | |||||||
| chr5:172933441 | T | C | 3 | a0001c0001t0001g0227 a0001c0001t0001g0257 a0001c0001t0001g0259 |
3 | HG01433.hp2 HG01928.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.642+905T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 8/9 | chr5 | 172933441 | |||||||
| chr5:172933642 | C | T | 10 | a0001c0001t0005g0005 a0001c0001t0005g0156 a0001c0001t0005g0162 others(7): Show |
10 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.642+1106C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 8/9 | chr5 | 172933642 | |||||||
| chr5:172933647 | GC | G | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(219): Show |
222 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.642+1115delC | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 172933647 | ||||||
| chr5:172933727 | A | G | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(183): Show |
186 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(183): Show |
intron_variant | MODIFIER | c.642+1191A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 8/9 | chr5 | 172933727 | |||||||
| chr5:172933912 | C | CA | 31 | a0001c0001t0001g0081 a0001c0001t0001g0115 a0001c0001t0001g0209 others(28): Show |
31 | HG00140.hp1 HG00280.hp2 HG01257.hp2 others(28): Show |
intron_variant | MODIFIER | c.643-1265dupA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr5 | 172933912 | ||||||
| chr5:172933938 | G | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(34): Show |
37 | HG00544.hp2 HG01261.hp2 HG01433.hp2 others(34): Show |
intron_variant | MODIFIER | c.643-1250G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 8/9 | chr5 | 172933938 | |||||||
| chr5:172934106 | C | T | 4 | a0001c0001t0001g0112 a0001c0001t0001g0169 a0001c0001t0001g0170 others(1): Show |
4 | HG01106.hp1 HG01261.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.643-1082C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 8/9 | chr5 | 172934106 | |||||||
| chr5:172934254 | A | G | 32 | a0001c0001t0001g0081 a0001c0001t0001g0115 a0001c0001t0001g0209 others(29): Show |
32 | HG00140.hp1 HG00280.hp2 HG01257.hp2 others(29): Show |
intron_variant | MODIFIER | c.643-934A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 8/9 | chr5 | 172934254 | |||||||
| chr5:172934413 | G | T | 3 | a0001c0001t0007g0281 a0001c0001t0007g0282 a0001c0001t0023g0332 |
3 | HG02630.hp2 HG02717.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.643-775G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 8/9 | chr5 | 172934413 | |||||||
| chr5:172934428 | C | T | 1 | a0001c0001t0012g0331 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.643-760C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 8/9 | chr5 | 172934428 | |||||||
| chr5:172934524 | C | G | 1 | a0001c0001t0003g0035 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.643-664C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 8/9 | chr5 | 172934524 | |||||||
| chr5:172934525 | G | A | 2 | a0001c0001t0007g0281 a0001c0001t0007g0282 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.643-663G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 8/9 | chr5 | 172934525 | |||||||
| chr5:172934685 | A | G | 223 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(220): Show |
223 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(220): Show |
intron_variant | MODIFIER | c.643-503A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 8/9 | chr5 | 172934685 | |||||||
| chr5:172934713 | A | T | 7 | a0001c0001t0005g0005 a0001c0001t0005g0156 a0001c0001t0005g0162 others(4): Show |
7 | HG01884.hp2 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.643-475A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 8/9 | chr5 | 172934713 | |||||||
| chr5:172935135 | C | T | 2 | a0001c0001t0007g0281 a0001c0001t0007g0282 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.643-53C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 8/9 | chr5 | 172935135 | |||||||
| chr5:172935143 | CT | C | 5 | a0001c0001t0003g0055 a0001c0001t0003g0101 a0001c0001t0003g0145 others(2): Show |
5 | HG00639.hp2 HG01243.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.643-44delT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 8/9 | chr5 | 172935143 | |||||||
| chr5:172935173 | T | C | 2 | a0001c0001t0005g0105 a0001c0001t0005g0106 |
2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.643-15T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 8/9 | chr5 | 172935173 | |||||||
| chr5:172935503 | G | A | 2 | a0001c0001t0007g0281 a0001c0001t0007g0282 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.765+193G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172935503 | |||||||
| chr5:172935596 | T | A | 1 | a0001c0001t0001g0016 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.765+286T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172935596 | |||||||
| chr5:172935849 | T | C | 4 | a0001c0001t0006g0004 a0001c0001t0006g0053 a0001c0001t0006g0309 others(1): Show |
4 | HG02723.hp1 HG02896.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.765+539T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172935849 | |||||||
| chr5:172936164 | G | A | 1 | a0001c0001t0001g0041 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.765+854G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172936164 | |||||||
| chr5:172936258 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.765+948A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172936258 | |||||||
| chr5:172936526 | GGGC | G | 10 | a0001c0001t0001g0081 a0001c0001t0001g0115 a0001c0001t0001g0209 others(7): Show |
10 | HG00140.hp1 HG00280.hp2 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.765+1217_765+1219d others(5): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172936526 | |||||||
| chr5:172936571 | C | T | 5 | a0001c0001t0001g0157 a0001c0001t0001g0181 a0001c0001t0001g0202 others(2): Show |
5 | HG00423.hp2 HG02071.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.765+1261C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172936571 | |||||||
| chr5:172936674 | T | C | 17 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(14): Show |
17 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.765+1364T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172936674 | |||||||
| chr5:172936866 | A | G | 17 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(14): Show |
17 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.765+1556A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172936866 | |||||||
| chr5:172937026 | A | G | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.765+1716A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172937026 | |||||||
| chr5:172937150 | G | C | 53 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0029 others(50): Show |
53 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.765+1840G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172937150 | |||||||
| chr5:172937165 | G | A | 17 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(14): Show |
17 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.765+1855G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172937165 | |||||||
| chr5:172937309 | G | A | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(219): Show |
222 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.765+1999G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172937309 | |||||||
| chr5:172937313 | TATTGGC | T | 17 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(14): Show |
17 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.765+2005_765+2010d others(8): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 172937313 | ||||||
| chr5:172937329 | A | G | 2 | a0001c0001t0007g0281 a0001c0001t0007g0282 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.765+2019A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172937329 | |||||||
| chr5:172937390 | A | T | 1 | a0001c0001t0006g0004 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.765+2080A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172937390 | |||||||
| chr5:172937509 | A | G | 4 | a0001c0001t0003g0154 a0001c0001t0003g0284 a0001c0001t0003g0298 others(1): Show |
4 | HG02055.hp1 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.765+2199A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172937509 | |||||||
| chr5:172937593 | G | A | 1 | a0001c0001t0002g0243 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.765+2283G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172937593 | |||||||
| chr5:172937735 | G | A | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.765+2425G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172937735 | |||||||
| chr5:172937756 | G | C | 17 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(14): Show |
17 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.765+2446G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172937756 | |||||||
| chr5:172937823 | A | G | 17 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(14): Show |
17 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.765+2513A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172937823 | |||||||
| chr5:172937843 | C | T | 1 | a0001c0001t0002g0229 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.765+2533C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172937843 | |||||||
| chr5:172937854 | G | A | 18 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(15): Show |
18 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.765+2544G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172937854 | |||||||
| chr5:172938006 | A | AAAAAG | 17 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(14): Show |
17 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.765+2699_765+2700i others(7): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 172938006 | ||||||
| chr5:172938056 | G | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(170): Show |
173 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(170): Show |
intron_variant | MODIFIER | c.765+2746G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172938056 | |||||||
| chr5:172938084 | G | A | 4 | a0001c0001t0003g0154 a0001c0001t0003g0284 a0001c0001t0003g0298 others(1): Show |
4 | HG02055.hp1 HG02976.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.765+2774G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172938084 | |||||||
| chr5:172938117 | A | T | 2 | a0001c0001t0002g0024 a0001c0001t0002g0285 |
2 | HG01952.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.765+2807A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172938117 | |||||||
| chr5:172938136 | C | T | 53 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0029 others(50): Show |
53 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.765+2826C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172938136 | |||||||
| chr5:172938143 | A | G | 2 | a0001c0001t0007g0281 a0001c0001t0007g0282 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.765+2833A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172938143 | |||||||
| chr5:172938481 | G | A | 1 | a0001c0005t0018g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.765+3171G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172938481 | |||||||
| chr5:172938495 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.765+3185G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172938495 | |||||||
| chr5:172938685 | G | A | 12 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(9): Show |
12 | HG02055.hp2 HG02280.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.765+3375G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172938685 | |||||||
| chr5:172938749 | T | G | 1 | a0001c0001t0001g0167 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.765+3439T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172938749 | |||||||
| chr5:172938759 | A | AG | 12 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(9): Show |
12 | HG02055.hp2 HG02280.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.765+3449_765+3450i others(3): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172938759 | |||||||
| chr5:172938764 | G | A | 12 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(9): Show |
12 | HG02055.hp2 HG02280.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.765+3454G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172938764 | |||||||
| chr5:172938765 | A | G | 12 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(9): Show |
12 | HG02055.hp2 HG02280.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.765+3455A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172938765 | |||||||
| chr5:172938782 | G | A | 10 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(7): Show |
10 | HG02055.hp2 HG02280.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.765+3472G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172938782 | |||||||
| chr5:172938841 | A | G | 30 | a0001c0001t0001g0081 a0001c0001t0001g0115 a0001c0001t0001g0209 others(27): Show |
30 | HG00140.hp1 HG00280.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.765+3531A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172938841 | |||||||
| chr5:172938852 | G | A | 12 | a0001c0001t0002g0130 a0001c0001t0002g0275 a0001c0001t0003g0155 others(9): Show |
12 | HG01123.hp1 HG01993.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.765+3542G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172938852 | |||||||
| chr5:172938962 | G | C | 10 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(7): Show |
10 | HG02055.hp2 HG02280.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.765+3652G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172938962 | |||||||
| chr5:172939062 | CA | C | 36 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(33): Show |
36 | HG00544.hp2 HG01261.hp2 HG01433.hp2 others(33): Show |
intron_variant | MODIFIER | c.765+3763delA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 172939062 | ||||||
| chr5:172939063 | A | C | 60 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0029 others(57): Show |
60 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.765+3753A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172939063 | |||||||
| chr5:172939076 | A | AAAAAG | 10 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(7): Show |
10 | HG02055.hp2 HG02280.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.765+3770_765+3774d others(7): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 172939076 | ||||||
| chr5:172939152 | A | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(45): Show |
48 | HG00544.hp2 HG01261.hp2 HG01433.hp2 others(45): Show |
intron_variant | MODIFIER | c.765+3842A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172939152 | |||||||
| chr5:172939192 | C | T | 1 | a0001c0001t0004g0178 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.765+3882C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172939192 | |||||||
| chr5:172939206 | G | T | 3 | a0001c0001t0008g0150 a0001c0001t0008g0187 a0001c0001t0008g0205 |
3 | HG02896.hp1 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.765+3896G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172939206 | |||||||
| chr5:172939381 | C | T | 2 | a0001c0001t0003g0273 a0001c0001t0003g0274 |
2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.765+4071C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172939381 | |||||||
| chr5:172939408 | C | T | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(219): Show |
222 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.765+4098C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172939408 | |||||||
| chr5:172939426 | G | A | 2 | a0001c0001t0003g0273 a0001c0001t0003g0274 |
2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.765+4116G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172939426 | |||||||
| chr5:172939426 | G | C | 11 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.765+4116G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172939426 | |||||||
| chr5:172939461 | A | G | 23 | a0001c0001t0001g0081 a0001c0001t0001g0115 a0001c0001t0001g0209 others(20): Show |
23 | HG00140.hp1 HG00280.hp2 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.765+4151A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172939461 | |||||||
| chr5:172939540 | A | G | 89 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0029 others(86): Show |
89 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.765+4230A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172939540 | |||||||
| chr5:172939703 | T | C | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.765+4393T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172939703 | |||||||
| chr5:172939745 | G | A | 1 | a0001c0005t0018g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.765+4435G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172939745 | |||||||
| chr5:172939906 | G | A | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.765+4596G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172939906 | |||||||
| chr5:172939909 | G | A | 2 | a0001c0001t0002g0024 a0001c0001t0002g0285 |
2 | HG01952.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.765+4599G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172939909 | |||||||
| chr5:172939987 | G | A | 48 | a0001c0001t0001g0009 a0001c0001t0001g0049 a0001c0001t0001g0051 others(45): Show |
48 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.765+4677G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172939987 | |||||||
| chr5:172940214 | T | C | 11 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(8): Show |
11 | HG02055.hp2 HG02280.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.765+4904T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172940214 | |||||||
| chr5:172940264 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.765+4954G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172940264 | |||||||
| chr5:172940328 | C | T | 26 | a0001c0001t0002g0024 a0001c0001t0002g0285 a0001c0001t0003g0034 others(23): Show |
26 | HG00408.hp2 HG00639.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.765+5018C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172940328 | |||||||
| chr5:172940699 | C | A | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.765+5389C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172940699 | |||||||
| chr5:172940892 | C | G | 3 | a0001c0001t0006g0184 a0001c0001t0013g0291 a0001c0001t0016g0197 |
3 | HG03139.hp2 HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.765+5582C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172940892 | |||||||
| chr5:172940903 | C | G | 3 | a0001c0001t0006g0184 a0001c0001t0013g0291 a0001c0001t0016g0197 |
3 | HG03139.hp2 HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.765+5593C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172940903 | |||||||
| chr5:172940936 | C | G | 1 | a0001c0001t0001g0050 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.765+5626C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172940936 | |||||||
| chr5:172941100 | G | A | 1 | a0001c0001t0003g0283 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.765+5790G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172941100 | |||||||
| chr5:172941104 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.765+5794C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172941104 | |||||||
| chr5:172941201 | C | T | 1 | a0001c0005t0018g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.765+5891C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172941201 | |||||||
| chr5:172941221 | G | A | 3 | a0001c0001t0010g0189 a0001c0001t0014g0173 a0001c0001t0031g0083 |
3 | HG02895.hp1 HG02897.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.765+5911G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172941221 | |||||||
| chr5:172941324 | C | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0277 |
2 | HG02602.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.765+6014C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172941324 | |||||||
| chr5:172941329 | T | G | 1 | a0001c0001t0002g0212 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.765+6019T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172941329 | |||||||
| chr5:172941526 | T | A | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(34): Show |
37 | HG00544.hp2 HG01261.hp2 HG01433.hp2 others(34): Show |
intron_variant | MODIFIER | c.765+6216T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172941526 | |||||||
| chr5:172941533 | C | T | 2 | a0001c0001t0007g0281 a0001c0001t0007g0282 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.765+6223C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172941533 | |||||||
| chr5:172941552 | A | G | 1 | a0001c0001t0001g0305 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.765+6242A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172941552 | |||||||
| chr5:172941568 | A | C | 16 | a0001c0001t0005g0005 a0001c0001t0005g0105 a0001c0001t0005g0106 others(13): Show |
16 | HG01109.hp2 HG01884.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.765+6258A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172941568 | |||||||
| chr5:172941671 | A | G | 222 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(219): Show |
222 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(219): Show |
intron_variant | MODIFIER | c.765+6361A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172941671 | |||||||
| chr5:172941945 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(61): Show |
64 | HG00408.hp2 HG00544.hp2 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.765+6635G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172941945 | |||||||
| chr5:172942275 | G | T | 1 | a0001c0001t0001g0286 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.765+6965G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172942275 | |||||||
| chr5:172942470 | C | T | 1 | a0001c0001t0017g0234 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.765+7160C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172942470 | |||||||
| chr5:172942670 | A | T | 2 | a0001c0001t0007g0281 a0001c0001t0007g0282 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.765+7360A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172942670 | |||||||
| chr5:172942766 | C | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(132): Show |
135 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.765+7456C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172942766 | |||||||
| chr5:172942864 | C | T | 1 | a0001c0001t0013g0291 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.765+7554C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172942864 | |||||||
| chr5:172942997 | T | G | 1 | a0001c0001t0002g0094 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.765+7687T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172942997 | |||||||
| chr5:172943013 | G | C | 4 | a0001c0001t0001g0043 a0001c0001t0001g0119 a0001c0001t0001g0201 others(1): Show |
4 | HG00673.hp2 NA18952.hp1 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.766-7696G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172943013 | |||||||
| chr5:172943091 | A | G | 21 | a0001c0001t0001g0067 a0001c0001t0001g0081 a0001c0001t0001g0115 others(18): Show |
21 | HG00140.hp1 HG00280.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.766-7618A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172943091 | |||||||
| chr5:172943229 | C | T | 17 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(14): Show |
17 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.766-7480C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172943229 | |||||||
| chr5:172943656 | T | C | 6 | a0001c0001t0003g0154 a0001c0001t0003g0273 a0001c0001t0003g0274 others(3): Show |
6 | HG02055.hp1 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.766-7053T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172943656 | |||||||
| chr5:172943690 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.766-7019A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172943690 | |||||||
| chr5:172943861 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.766-6848C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172943861 | |||||||
| chr5:172943996 | A | C | 2 | a0001c0001t0001g0204 a0001c0001t0001g0255 |
2 | HG02015.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.766-6713A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172943996 | |||||||
| chr5:172944218 | A | T | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.766-6491A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172944218 | |||||||
| chr5:172944294 | G | C | 2 | a0001c0001t0002g0027 a0001c0001t0002g0028 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.766-6415G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172944294 | |||||||
| chr5:172944359 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.766-6350C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172944359 | |||||||
| chr5:172944360 | C | CT | 44 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(41): Show |
44 | HG00544.hp2 HG00741.hp1 HG01261.hp2 others(41): Show |
intron_variant | MODIFIER | c.766-6336dupT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 172944360 | ||||||
| chr5:172944361 | T | C | 1 | a0001c0001t0001g0238 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.766-6348T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172944361 | |||||||
| chr5:172944380 | C | T | 1 | a0001c0001t0013g0291 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.766-6329C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172944380 | |||||||
| chr5:172944423 | A | G | 2 | a0001c0001t0002g0044 a0001c0001t0002g0212 |
2 | HG02165.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.766-6286A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172944423 | |||||||
| chr5:172944555 | C | T | 1 | a0001c0001t0001g0327 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.766-6154C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172944555 | |||||||
| chr5:172944559 | T | A | 58 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0029 others(55): Show |
58 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.766-6150T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172944559 | |||||||
| chr5:172944718 | G | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(92): Show |
95 | HG00323.hp2 HG00408.hp1 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.766-5991G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172944718 | |||||||
| chr5:172944776 | A | G | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.766-5933A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172944776 | |||||||
| chr5:172944849 | A | G | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(212): Show |
215 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.766-5860A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172944849 | |||||||
| chr5:172944939 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.766-5770G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172944939 | |||||||
| chr5:172944940 | C | T | 2 | a0001c0001t0010g0058 a0001c0001t0032g0084 |
2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.766-5769C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172944940 | |||||||
| chr5:172944970 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0163 |
2 | HG02056.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.766-5739C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172944970 | |||||||
| chr5:172945034 | C | T | 1 | a0001c0001t0002g0333 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.766-5675C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172945034 | |||||||
| chr5:172945055 | C | T | 1 | a0001c0001t0003g0328 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.766-5654C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172945055 | |||||||
| chr5:172945122 | TGA | T | 4 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0220 others(1): Show |
4 | HG00408.hp2 HG02523.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.766-5583_766-5582d others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 172945122 | ||||||
| chr5:172945413 | A | G | 3 | a0001c0001t0001g0043 a0001c0001t0001g0119 a0001c0001t0001g0201 |
3 | HG00673.hp2 NA18963.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.766-5296A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172945413 | |||||||
| chr5:172945552 | G | A | 42 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0055 others(39): Show |
42 | HG00408.hp2 HG00639.hp2 HG01243.hp2 others(39): Show |
intron_variant | MODIFIER | c.766-5157G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172945552 | |||||||
| chr5:172945660 | AG | A | 15 | a0001c0001t0003g0334 a0001c0001t0005g0005 a0001c0001t0005g0156 others(12): Show |
15 | HG01884.hp2 HG02280.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.766-5045delG | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 172945660 | ||||||
| chr5:172945669 | G | C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(309): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.766-5040G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172945669 | |||||||
| chr5:172945671 | C | T | 4 | a0001c0001t0010g0189 a0001c0001t0013g0291 a0001c0001t0014g0173 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.766-5038C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172945671 | |||||||
| chr5:172945672 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.766-5037G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172945672 | |||||||
| chr5:172945680 | T | C | 2 | a0001c0001t0002g0217 a0001c0001t0002g0218 |
2 | HG00741.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.766-5029T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172945680 | |||||||
| chr5:172945809 | C | T | 2 | a0001c0001t0006g0309 a0001c0001t0006g0310 |
2 | HG02896.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.766-4900C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172945809 | |||||||
| chr5:172945892 | C | T | 4 | a0001c0001t0010g0189 a0001c0001t0013g0291 a0001c0001t0014g0173 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.766-4817C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172945892 | |||||||
| chr5:172945908 | T | C | 6 | a0001c0001t0001g0157 a0001c0001t0001g0181 a0001c0001t0001g0183 others(3): Show |
6 | HG00423.hp2 HG00438.hp2 HG02071.hp2 others(3): Show |
intron_variant | MODIFIER | c.766-4801T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172945908 | |||||||
| chr5:172945997 | T | C | 16 | a0001c0001t0003g0155 a0001c0001t0003g0271 a0001c0001t0003g0272 others(13): Show |
16 | HG02055.hp2 HG02145.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.766-4712T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172945997 | |||||||
| chr5:172946002 | A | G | 2 | a0001c0001t0003g0035 a0001c0001t0003g0220 |
2 | HG00408.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.766-4707A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172946002 | |||||||
| chr5:172946036 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.766-4673G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172946036 | |||||||
| chr5:172946154 | C | A | 2 | a0001c0001t0003g0273 a0001c0001t0003g0274 |
2 | HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.766-4555C>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172946154 | |||||||
| chr5:172946263 | G | A | 1 | a0001c0001t0002g0191 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.766-4446G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172946263 | |||||||
| chr5:172946352 | A | C | 39 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0013 others(36): Show |
39 | HG00544.hp2 HG01261.hp2 HG01433.hp2 others(36): Show |
intron_variant | MODIFIER | c.766-4357A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172946352 | |||||||
| chr5:172946539 | G | A | 7 | a0001c0001t0005g0005 a0001c0001t0005g0156 a0001c0001t0005g0162 others(4): Show |
7 | HG01884.hp2 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.766-4170G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172946539 | |||||||
| chr5:172946674 | G | C | 1 | a0001c0001t0002g0139 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.766-4035G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172946674 | |||||||
| chr5:172946765 | C | T | 1 | a0001c0001t0002g0229 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.766-3944C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172946765 | |||||||
| chr5:172946772 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0163 |
2 | HG02056.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.766-3937C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172946772 | |||||||
| chr5:172946877 | AT | A | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(238): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.766-3818delT | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 172946877 | ||||||
| chr5:172946877 | ATT | A | 67 | a0001c0001t0001g0009 a0001c0001t0001g0049 a0001c0001t0001g0051 others(64): Show |
67 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(64): Show |
intron_variant | MODIFIER | c.766-3819_766-3818d others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 172946877 | ||||||
| chr5:172946899 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.766-3810G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172946899 | |||||||
| chr5:172946978 | G | A | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.766-3731G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172946978 | |||||||
| chr5:172947183 | CA | C | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(298): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.766-3509delA | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 172947183 | ||||||
| chr5:172947249 | A | G | 54 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0029 others(51): Show |
54 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.766-3460A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172947249 | |||||||
| chr5:172947281 | C | G | 12 | a0001c0001t0001g0081 a0001c0001t0001g0115 a0001c0001t0001g0209 others(9): Show |
12 | HG00140.hp1 HG00280.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.766-3428C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172947281 | |||||||
| chr5:172947370 | A | T | 4 | a0001c0001t0010g0189 a0001c0001t0013g0291 a0001c0001t0014g0173 others(1): Show |
4 | HG02895.hp1 HG02897.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.766-3339A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172947370 | |||||||
| chr5:172947419 | C | T | 3 | a0001c0001t0001g0119 a0001c0001t0001g0201 a0001c0001t0001g0279 |
3 | HG00673.hp2 NA18952.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.766-3290C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172947419 | |||||||
| chr5:172947566 | G | A | 1 | a0001c0001t0013g0291 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.766-3143G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172947566 | |||||||
| chr5:172947797 | A | T | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.766-2912A>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172947797 | |||||||
| chr5:172947826 | GTCATAAG others(148): Show |
G | 1 | a0001c0001t0002g0285 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.766-2882_766-2728d others(2): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172947826 | |||||||
| chr5:172947848 | A | G | 1 | a0001c0001t0023g0332 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.766-2861A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172947848 | |||||||
| chr5:172947876 | T | TGTG | 4 | a0001c0001t0001g0015 a0001c0001t0001g0113 a0001c0001t0001g0168 others(1): Show |
4 | HG00544.hp1 HG02071.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.766-2833_766-2832i others(5): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172947876 | |||||||
| chr5:172947876 | T | TGTGTGTG others(4): Show |
1 | a0001c0001t0001g0182 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.766-2833_766-2832i others(13): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172947876 | |||||||
| chr5:172947876 | T | TTG | 115 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(112): Show |
115 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.766-2798_766-2797d others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 172947876 | ||||||
| chr5:172947876 | T | TTGTG | 36 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0018 others(33): Show |
36 | HG00423.hp2 HG00438.hp2 HG01070.hp2 others(33): Show |
intron_variant | MODIFIER | c.766-2800_766-2797d others(6): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 172947876 | ||||||
| chr5:172947876 | T | TTGTGTG | 23 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0030 others(20): Show |
23 | HG00597.hp2 HG01261.hp2 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.766-2802_766-2797d others(8): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 172947876 | ||||||
| chr5:172947876 | T | TTGTGTGT others(1): Show |
9 | a0001c0001t0001g0041 a0001c0001t0001g0126 a0001c0001t0001g0164 others(6): Show |
9 | HG03041.hp1 HG03491.hp2 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.766-2804_766-2797d others(10): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 172947876 | ||||||
| chr5:172947876 | T | TTGTGTGT others(3): Show |
12 | a0001c0001t0001g0120 a0001c0001t0001g0204 a0001c0001t0001g0214 others(9): Show |
12 | HG00544.hp2 HG01884.hp2 HG02015.hp1 others(9): Show |
intron_variant | MODIFIER | c.766-2806_766-2797d others(12): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 172947876 | ||||||
| chr5:172947876 | T | TTGTGTGT others(5): Show |
1 | a0001c0001t0001g0165 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.766-2808_766-2797d others(14): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 172947876 | ||||||
| chr5:172947876 | T | TTGTGTGT others(7): Show |
2 | a0001c0001t0008g0150 a0001c0001t0008g0187 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.766-2810_766-2797d others(16): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 172947876 | ||||||
| chr5:172947876 | TTG | T | 91 | a0001c0001t0001g0009 a0001c0001t0001g0049 a0001c0001t0001g0051 others(88): Show |
91 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(88): Show |
intron_variant | MODIFIER | c.766-2798_766-2797d others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 172947876 | ||||||
| chr5:172947876 | TTGTG | T | 7 | a0001c0001t0003g0154 a0001c0001t0003g0284 a0001c0001t0003g0298 others(4): Show |
7 | HG02055.hp1 HG02055.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.766-2800_766-2797d others(6): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 172947876 | ||||||
| chr5:172947942 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.766-2767G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172947942 | |||||||
| chr5:172947994 | A | C | 1 | a0001c0001t0004g0246 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.766-2715A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172947994 | |||||||
| chr5:172948075 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.766-2634G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172948075 | |||||||
| chr5:172948598 | C | G | 2 | a0001c0001t0002g0046 a0001c0001t0002g0280 |
2 | HG01952.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.766-2111C>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172948598 | |||||||
| chr5:172948796 | C | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(184): Show |
187 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.766-1913C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172948796 | |||||||
| chr5:172948808 | G | T | 32 | a0001c0001t0003g0034 a0001c0001t0003g0035 a0001c0001t0003g0055 others(29): Show |
32 | HG00408.hp2 HG00639.hp2 HG01109.hp2 others(29): Show |
intron_variant | MODIFIER | c.766-1901G>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172948808 | |||||||
| chr5:172948822 | A | G | 328 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(325): Show |
328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.766-1887A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172948822 | |||||||
| chr5:172948924 | A | G | 31 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0003g0271 others(28): Show |
31 | HG02055.hp1 HG02145.hp2 HG02280.hp2 others(28): Show |
intron_variant | MODIFIER | c.766-1785A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172948924 | |||||||
| chr5:172948947 | C | T | 8 | a0001c0001t0005g0005 a0001c0001t0005g0156 a0001c0001t0005g0162 others(5): Show |
8 | HG01884.hp2 HG02280.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.766-1762C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172948947 | |||||||
| chr5:172948980 | G | A | 7 | a0001c0001t0005g0005 a0001c0001t0005g0156 a0001c0001t0005g0162 others(4): Show |
7 | HG01884.hp2 HG02280.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.766-1729G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172948980 | |||||||
| chr5:172949175 | A | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(253): Show |
256 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.766-1534A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172949175 | |||||||
| chr5:172949282 | C | T | 2 | a0001c0001t0010g0058 a0001c0001t0032g0084 |
2 | HG02055.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.766-1427C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172949282 | |||||||
| chr5:172949333 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.766-1376G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172949333 | |||||||
| chr5:172949499 | T | C | 2 | a0001c0001t0005g0105 a0001c0001t0005g0106 |
2 | HG01109.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.766-1210T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172949499 | |||||||
| chr5:172949655 | C | CG | 173 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(170): Show |
173 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.766-1045dupG | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 172949655 | ||||||
| chr5:172949655 | C | CGG | 34 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0021 others(31): Show |
34 | HG00408.hp1 HG00423.hp2 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.766-1046_766-1045d others(4): Show |
ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr5 | 172949655 | ||||||
| chr5:172949656 | G | C | 1 | a0001c0001t0002g0082 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.766-1053G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172949656 | |||||||
| chr5:172949665 | T | G | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(253): Show |
256 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.766-1044T>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172949665 | |||||||
| chr5:172949764 | G | A | 1 | a0001c0001t0002g0317 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.766-945G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172949764 | |||||||
| chr5:172949882 | G | A | 2 | a0001c0001t0007g0281 a0001c0001t0007g0282 |
2 | HG02630.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.766-827G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172949882 | |||||||
| chr5:172949900 | T | C | 256 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(253): Show |
256 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.766-809T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172949900 | |||||||
| chr5:172949936 | G | A | 8 | a0001c0001t0005g0005 a0001c0001t0005g0156 a0001c0001t0005g0162 others(5): Show |
8 | HG01884.hp2 HG02280.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.766-773G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172949936 | |||||||
| chr5:172949960 | C | T | 2 | a0001c0001t0001g0222 a0001c0001t0001g0236 |
2 | NA18951.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.766-749C>T | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172949960 | |||||||
| chr5:172949986 | T | A | 1 | a0001c0005t0018g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.766-723T>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172949986 | |||||||
| chr5:172949990 | G | A | 5 | a0001c0001t0003g0334 a0001c0001t0008g0150 a0001c0001t0008g0187 others(2): Show |
5 | HG02809.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.766-719G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172949990 | |||||||
| chr5:172950028 | A | G | 29 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0029 others(26): Show |
29 | HG00323.hp2 HG00408.hp1 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.766-681A>G | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172950028 | |||||||
| chr5:172950036 | G | C | 2 | a0001c0001t0008g0150 a0001c0001t0008g0187 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.766-673G>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172950036 | |||||||
| chr5:172950131 | T | C | 5 | a0001c0001t0010g0058 a0001c0001t0010g0189 a0001c0001t0014g0173 others(2): Show |
5 | HG02055.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.766-578T>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172950131 | |||||||
| chr5:172950342 | G | A | 6 | a0001c0001t0001g0237 a0001c0001t0004g0108 a0001c0001t0004g0166 others(3): Show |
6 | HG02074.hp2 NA18612.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.766-367G>A | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172950342 | |||||||
| chr5:172950632 | A | C | 1 | a0001c0005t0018g0161 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.766-77A>C | ERGIC1 | ENSG00000113719.17 | transcript | ENST00000393784.8 | protein_coding | 9/9 | chr5 | 172950632 |