Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 113201 |
| ensemblid | ENSG00000166734.20 |
| hgncid | 24892 |
| symbol | GOLM2 |
| name | golgi membrane protein 2 |
| refseq_nuc | NM_138423.4 |
| refseq_prot | NP_612432.2 |
| ensembl_nuc | ENST00000299957.11 |
| ensembl_prot | ENSP00000299957.6 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 44288719 |
| end | 44415758 |
| strand | + |
| ver | v1.2 |
| region | chr15:44288719-44415758 |
| region5000 | chr15:44283719-44420758 |
| regionname0 | GOLM2_chr15_44288719_44415758 |
| regionname5000 | GOLM2_chr15_44283719_44420758 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 436 | 146 | 58 | 18 | 54 | 6 | 8 | 34 | GOLM2_chr15_44283719_44420758 | GOLM2 | MVGFG others(431): Show |
chr15 | 44283719 | 44420758 |
| a0002 | 0/0 | 436 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | MVGFG others(431): Show |
chr15 | 44283719 | 44420758 |
| a0003 | 0/0 | 435 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | GOLM2_chr15_44283719_44420758 | GOLM2 | MVGFG others(430): Show |
chr15 | 44283719 | 44420758 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1308 | 131 | 44 | 17 | 54 | 6 | 8 | GOLM2_chr15_44283719_44420758 | GOLM2 | ATGGT others(1303): Show |
chr15 | 44283719 | 44420758 | ||
| a0001c0002 | 0/0 | 1308 | 11 | 10 | 1 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | ATGGT others(1303): Show |
chr15 | 44283719 | 44420758 | ||
| a0001c0003 | 0/0 | 1308 | 3 | 3 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | ATGGT others(1303): Show |
chr15 | 44283719 | 44420758 | ||
| a0001c0006 | 0/0 | 1308 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | ATGGT others(1303): Show |
chr15 | 44283719 | 44420758 | ||
| a0002c0005 | 0/0 | 1308 | 2 | 2 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | ATGGT others(1303): Show |
chr15 | 44283719 | 44420758 | ||
| a0003c0004 | 0/0 | 1305 | 2 | 0 | 0 | 2 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | ATGGT others(1300): Show |
chr15 | 44283719 | 44420758 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3974 | 98 | 29 | 14 | 40 | 5 | 8 | GOLM2_chr15_44283719_44420758 | GOLM2 | CCCGC others(3969): Show |
chr15 | 44283719 | 44420758 |
| a0001c0001t0002 | 0/0 | 3974 | 15 | 6 | 1 | 8 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | CCCGC others(3969): Show |
chr15 | 44283719 | 44420758 |
| a0001c0001t0003 | 0/0 | 3975 | 10 | 3 | 2 | 5 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | CCCGC others(3970): Show |
chr15 | 44283719 | 44420758 |
| a0001c0001t0005 | 0/0 | 3975 | 2 | 2 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | CCCGC others(3970): Show |
chr15 | 44283719 | 44420758 |
| a0001c0001t0007 | 0/0 | 3975 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | CCCGC others(3970): Show |
chr15 | 44283719 | 44420758 |
| a0001c0001t0008 | 0/0 | 3974 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | CCCGC others(3969): Show |
chr15 | 44283719 | 44420758 |
| a0001c0001t0010 | 0/0 | 3974 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | CCCGC others(3969): Show |
chr15 | 44283719 | 44420758 |
| a0001c0001t0011 | 0/0 | 3976 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | CCCGC others(3971): Show |
chr15 | 44283719 | 44420758 |
| a0001c0001t0012 | 0/0 | 3975 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | CCCGC others(3970): Show |
chr15 | 44283719 | 44420758 |
| a0001c0001t0013 | 0/0 | 3974 | 1 | 0 | 0 | 0 | 1 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | CCCGC others(3969): Show |
chr15 | 44283719 | 44420758 |
| a0001c0002t0001 | 0/0 | 3974 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | CCCGC others(3969): Show |
chr15 | 44283719 | 44420758 |
| a0001c0002t0003 | 0/0 | 3975 | 1 | 0 | 1 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | CCCGC others(3970): Show |
chr15 | 44283719 | 44420758 |
| a0001c0002t0004 | 0/0 | 3975 | 8 | 8 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | CCCGC others(3970): Show |
chr15 | 44283719 | 44420758 |
| a0001c0002t0006 | 0/0 | 3975 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | CCCGC others(3970): Show |
chr15 | 44283719 | 44420758 |
| a0001c0003t0001 | 0/0 | 3974 | 2 | 2 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | CCCGC others(3969): Show |
chr15 | 44283719 | 44420758 |
| a0001c0003t0009 | 0/0 | 3974 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | CCCGC others(3969): Show |
chr15 | 44283719 | 44420758 |
| a0001c0006t0001 | 0/0 | 3974 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | CCCGC others(3969): Show |
chr15 | 44283719 | 44420758 |
| a0002c0005t0001 | 0/0 | 3974 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | CCCGC others(3969): Show |
chr15 | 44283719 | 44420758 |
| a0002c0005t0003 | 0/0 | 3975 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | CCCGC others(3970): Show |
chr15 | 44283719 | 44420758 |
| a0003c0004t0002 | 0/0 | 3971 | 2 | 0 | 0 | 2 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | CCCGC others(3966): Show |
chr15 | 44283719 | 44420758 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0011 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0070 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0005g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0007g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0008g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0010g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0011g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0012g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0001t0013g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0002t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0002t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0002t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0002t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0002t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0002t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0002t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0002t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0002t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0002t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0003t0009g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0001c0006t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0002c0005t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0002c0005t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0003c0004t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| a0003c0004t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0073 | EUR | GBR | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | GBR | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG00280 | hp1 | a0001 | c0001 | t0013 | g0061 | EUR | FIN | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | FIN | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0077 | EUR | FIN | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG00408 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | CHS | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | CHS | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | CHS | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0019 | AMR | PUR | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0064 | AMR | CLM | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | CLM | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0147 | AFR | ACB | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG01891 | hp2 | a0002 | c0005 | t0001 | g0112 | AFR | ACB | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG01981 | hp2 | a0001 | c0002 | t0003 | g0114 | AMR | PEL | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | KHV | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | CDX | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0141 | AFR | ACB | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02258 | hp1 | a0001 | c0002 | t0004 | g0105 | AFR | ACB | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | ACB | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | KHV | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | KHV | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02630 | hp1 | a0001 | c0002 | t0004 | g0108 | AFR | GWD | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02886 | hp1 | a0001 | c0002 | t0004 | g0104 | AFR | GWD | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | ESN | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02965 | hp1 | a0001 | c0002 | t0004 | g0086 | AFR | ESN | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02965 | hp2 | a0001 | c0001 | t0007 | g0121 | AFR | ESN | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | ESN | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG03130 | hp1 | a0001 | c0003 | t0001 | g0148 | AFR | ESN | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG03139 | hp1 | a0001 | c0001 | t0012 | g0004 | AFR | ESN | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ESN | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | ESN | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0090 | AFR | ESN | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG03209 | hp1 | a0001 | c0001 | t0011 | g0122 | AFR | MSL | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG03225 | hp2 | a0001 | c0001 | t0005 | g0120 | AFR | MSL | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0136 | AFR | MSL | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | MSL | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | ESN | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG03516 | hp2 | a0001 | c0002 | t0004 | g0118 | AFR | ESN | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | BEB | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | STU | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | STU | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | STU | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA18906 | hp1 | a0001 | c0002 | t0006 | g0109 | AFR | YRI | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA18960 | hp1 | a0003 | c0004 | t0002 | g0129 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA18990 | hp2 | a0001 | c0001 | t0010 | g0126 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | LWK | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | LWK | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA19043 | hp1 | a0001 | c0006 | t0001 | g0150 | AFR | LWK | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0045 | AFR | LWK | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA19063 | hp2 | a0003 | c0004 | t0002 | g0128 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA19089 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ASW | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA20129 | hp2 | a0001 | c0001 | t0005 | g0119 | AFR | ASW | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02109 | hp1 | a0001 | c0003 | t0009 | g0149 | AFR | ACB | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02109 | hp2 | a0002 | c0005 | t0003 | g0117 | AFR | ACB | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | ACB | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG03471 | hp1 | a0001 | c0002 | t0004 | g0107 | AFR | MSL | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | MSL | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | USA | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| HG06807 | hp2 | a0001 | c0002 | t0004 | g0103 | AFR | USA | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | USA | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA20300 | hp2 | a0001 | c0002 | t0004 | g0106 | AFR | USA | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | LWK | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | LWK | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0011 | REF | REF | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0070 | REF | REF | GOLM2_chr15_44283719_44420758 | GOLM2 | chr15 | 44283719 | 44420758 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:44332050 | TAGC | T | 1 | a0003 | 2 | NA18960.hp1 NA19063.hp2 |
disruptive_inframe_deletion | MODERATE | c.551_553delCAG | p.Ala184del | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/10 | 862/3974 | 551/1311 | 184/436 | INFO_REALIGN_3_PRIME | chr15 | 44332050 | ||
| chr15:44337899 | A | C | 1 | a0002 | 2 | HG01891.hp2 HG02109.hp2 |
missense_variant | MODERATE | c.713A>C | p.His238Pro | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 5/10 | 1024/3974 | 713/1311 | 238/436 | chr15 | 44337899 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:44289113 | C | T | 1 | a0001c0002 | 11 | HG01981.hp2 HG02258.hp1 HG02630.hp1 others(8): Show |
synonymous_variant | LOW | c.84C>T | p.Leu28Leu | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/10 | 395/3974 | 84/1311 | 28/436 | chr15 | 44289113 | |||
| chr15:44289140 | C | G | 1 | a0001c0006 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.111C>G | p.Ser37Ser | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/10 | 422/3974 | 111/1311 | 37/436 | chr15 | 44289140 | |||
| chr15:44380834 | C | T | 2 | a0001c0003 a0001c0006 |
4 | HG01891.hp1 HG02109.hp1 HG03130.hp1 others(1): Show |
synonymous_variant | LOW | c.930C>T | p.Pro310Pro | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/10 | 1241/3974 | 930/1311 | 310/436 | chr15 | 44380834 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:44288842 | A | AG | 3 | a0001c0001t0003 a0001c0002t0003 a0002c0005t0003 |
12 | HG00408.hp2 HG00558.hp2 HG00597.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-182dupG | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/10 | 181 | INFO_REALIGN_3_PRIME | chr15 | 44288842 | |||||
| chr15:44413474 | G | A | 1 | a0001c0002t0006 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*68G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 10/10 | 68 | chr15 | 44413474 | ||||||
| chr15:44413684 | A | G | 1 | a0001c0001t0013 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*278A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 10/10 | 278 | chr15 | 44413684 | ||||||
| chr15:44413810 | C | CT | 4 | a0001c0001t0011 a0001c0001t0012 a0001c0002t0004 others(1): Show |
11 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*421dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 10/10 | 422 | INFO_REALIGN_3_PRIME | chr15 | 44413810 | |||||
| chr15:44413832 | C | CA | 3 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0011 |
4 | HG02965.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*427dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 10/10 | 428 | INFO_REALIGN_3_PRIME | chr15 | 44413832 | |||||
| chr15:44413892 | C | A | 1 | a0001c0001t0008 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*486C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 10/10 | 486 | chr15 | 44413892 | ||||||
| chr15:44413899 | C | G | 1 | a0001c0001t0010 | 1 | NA18990.hp2 | 3_prime_UTR_variant | MODIFIER | c.*493C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 10/10 | 493 | chr15 | 44413899 | ||||||
| chr15:44414225 | A | C | 1 | a0001c0001t0007 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*819A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 10/10 | 819 | chr15 | 44414225 | ||||||
| chr15:44414352 | T | C | 4 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0012 others(1): Show |
19 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*946T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 10/10 | 946 | chr15 | 44414352 | ||||||
| chr15:44414814 | T | G | 1 | a0001c0003t0009 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1408T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 10/10 | 1408 | chr15 | 44414814 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:44289402 | C | T | 65 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(62): Show |
65 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.327+46C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44289402 | |||||||
| chr15:44289485 | C | G | 4 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0009g0149 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+129C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44289485 | |||||||
| chr15:44289494 | C | G | 4 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(1): Show |
4 | HG02970.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+138C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44289494 | |||||||
| chr15:44289508 | CT | C | 2 | a0001c0003t0001g0147 a0001c0003t0001g0148 |
2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.327+156delT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44289508 | ||||||
| chr15:44289581 | G | C | 1 | a0001c0001t0001g0001 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.327+225G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44289581 | |||||||
| chr15:44290608 | T | G | 1 | a0001c0002t0004g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.327+1252T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44290608 | |||||||
| chr15:44290648 | T | C | 1 | a0001c0001t0001g0002 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.327+1292T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44290648 | |||||||
| chr15:44290688 | G | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(117): Show |
120 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.327+1332G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44290688 | |||||||
| chr15:44290843 | C | T | 4 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 others(1): Show |
4 | NA18965.hp1 NA18985.hp2 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+1487C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44290843 | |||||||
| chr15:44290890 | C | G | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG00642.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.327+1534C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44290890 | |||||||
| chr15:44290891 | C | G | 1 | a0001c0001t0001g0055 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.327+1535C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44290891 | |||||||
| chr15:44290895 | C | T | 20 | a0001c0001t0001g0123 a0001c0001t0001g0142 a0001c0001t0002g0124 others(17): Show |
20 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(17): Show |
intron_variant | MODIFIER | c.327+1539C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44290895 | |||||||
| chr15:44290960 | C | T | 24 | a0001c0001t0001g0123 a0001c0001t0001g0142 a0001c0001t0002g0124 others(21): Show |
24 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(21): Show |
intron_variant | MODIFIER | c.327+1604C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44290960 | |||||||
| chr15:44291003 | A | G | 4 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0007g0121 others(1): Show |
4 | HG02965.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+1647A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44291003 | |||||||
| chr15:44291104 | C | CT | 30 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0054 others(27): Show |
30 | HG00423.hp1 HG00673.hp2 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.327+1767dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44291104 | ||||||
| chr15:44291104 | CT | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0082 a0001c0001t0001g0087 others(2): Show |
5 | HG01891.hp1 HG02155.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+1767delT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44291104 | ||||||
| chr15:44291133 | G | A | 2 | a0001c0001t0001g0005 a0001c0001t0012g0004 |
2 | HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.327+1777G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44291133 | |||||||
| chr15:44291339 | C | T | 2 | a0001c0001t0001g0050 a0001c0001t0003g0049 |
2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.327+1983C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44291339 | |||||||
| chr15:44291397 | G | GT | 3 | a0001c0001t0001g0003 a0001c0002t0004g0118 a0002c0005t0001g0112 |
3 | HG01891.hp2 HG02155.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.327+2047dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44291397 | ||||||
| chr15:44291540 | C | T | 1 | a0002c0005t0001g0112 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.327+2184C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44291540 | |||||||
| chr15:44291600 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.327+2244C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44291600 | |||||||
| chr15:44291843 | G | GA | 12 | a0001c0001t0001g0003 a0001c0001t0001g0088 a0001c0001t0001g0089 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.327+2494dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44291843 | ||||||
| chr15:44292070 | T | G | 1 | a0001c0002t0004g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.327+2714T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44292070 | |||||||
| chr15:44292184 | C | CAT | 16 | a0001c0001t0001g0006 a0001c0001t0001g0087 a0001c0001t0001g0091 others(13): Show |
16 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.327+2845_327+2846d others(4): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44292184 | ||||||
| chr15:44292198 | TA | T | 3 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0002c0005t0003g0117 |
3 | HG01891.hp1 HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.327+2843delA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44292198 | |||||||
| chr15:44292199 | A | T | 1 | a0002c0005t0001g0112 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.327+2843A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44292199 | |||||||
| chr15:44292200 | TA | T | 14 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(11): Show |
14 | HG00738.hp2 HG01069.hp1 HG01074.hp1 others(11): Show |
intron_variant | MODIFIER | c.327+2845delA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44292200 | |||||||
| chr15:44292201 | A | AT | 5 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0110 others(2): Show |
5 | HG02109.hp1 HG02155.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.327+2860dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44292201 | ||||||
| chr15:44292201 | A | T | 6 | a0001c0001t0001g0021 a0001c0001t0003g0072 a0001c0003t0001g0147 others(3): Show |
6 | HG00642.hp1 HG01891.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.327+2845A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44292201 | |||||||
| chr15:44292201 | AT | A | 11 | a0001c0001t0001g0014 a0001c0001t0001g0123 a0001c0001t0005g0119 others(8): Show |
11 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.327+2860delT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44292201 | ||||||
| chr15:44292201 | ATT | A | 18 | a0001c0001t0001g0142 a0001c0001t0002g0124 a0001c0001t0002g0125 others(15): Show |
18 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.327+2859_327+2860d others(4): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44292201 | ||||||
| chr15:44292202 | T | TA | 3 | a0001c0001t0001g0083 a0001c0002t0003g0114 a0001c0002t0004g0086 |
3 | HG01981.hp2 HG02965.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.327+2846_327+2847i others(3): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44292202 | |||||||
| chr15:44292203 | T | A | 6 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0056 others(3): Show |
6 | HG00642.hp2 HG03139.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.327+2847T>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44292203 | |||||||
| chr15:44292220 | C | CA | 11 | a0001c0002t0001g0090 a0001c0002t0003g0114 a0001c0002t0004g0086 others(8): Show |
11 | HG01981.hp2 HG02258.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.327+2865dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44292220 | ||||||
| chr15:44292228 | C | T | 11 | a0001c0002t0001g0090 a0001c0002t0003g0114 a0001c0002t0004g0086 others(8): Show |
11 | HG01981.hp2 HG02258.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.327+2872C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44292228 | |||||||
| chr15:44292232 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.327+2876C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44292232 | |||||||
| chr15:44292233 | G | A | 1 | a0001c0001t0003g0051 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.327+2877G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44292233 | |||||||
| chr15:44292380 | T | G | 1 | a0002c0005t0003g0117 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.327+3024T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44292380 | |||||||
| chr15:44292388 | G | C | 2 | a0001c0003t0001g0147 a0001c0003t0001g0148 |
2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.327+3032G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44292388 | |||||||
| chr15:44292774 | A | C | 43 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(40): Show |
43 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.327+3418A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44292774 | |||||||
| chr15:44292968 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.327+3612C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44292968 | |||||||
| chr15:44293049 | G | C | 42 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(39): Show |
42 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.327+3693G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44293049 | |||||||
| chr15:44293150 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.327+3794C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44293150 | |||||||
| chr15:44293812 | G | A | 15 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(12): Show |
15 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.327+4456G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44293812 | |||||||
| chr15:44294149 | T | C | 1 | a0001c0001t0012g0004 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.327+4793T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44294149 | |||||||
| chr15:44294207 | C | T | 1 | a0002c0005t0003g0117 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.327+4851C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44294207 | |||||||
| chr15:44294255 | G | T | 42 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(39): Show |
42 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.327+4899G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44294255 | |||||||
| chr15:44294597 | C | T | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.327+5241C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44294597 | |||||||
| chr15:44294678 | C | T | 1 | a0001c0002t0004g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.327+5322C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44294678 | |||||||
| chr15:44294698 | C | T | 1 | a0002c0005t0001g0112 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.327+5342C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44294698 | |||||||
| chr15:44294711 | C | CA | 26 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(23): Show |
26 | HG00621.hp1 HG00735.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.327+5372dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44294711 | ||||||
| chr15:44294740 | C | CA | 7 | a0001c0001t0001g0007 a0001c0001t0001g0052 a0001c0001t0001g0082 others(4): Show |
7 | HG00408.hp1 HG00673.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.327+5393dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44294740 | ||||||
| chr15:44294939 | G | C | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.327+5583G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44294939 | |||||||
| chr15:44295392 | T | C | 17 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.327+6036T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44295392 | |||||||
| chr15:44295549 | A | G | 23 | a0001c0001t0001g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(20): Show |
23 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(20): Show |
intron_variant | MODIFIER | c.327+6193A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44295549 | |||||||
| chr15:44295732 | C | T | 1 | a0002c0005t0003g0117 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.327+6376C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44295732 | |||||||
| chr15:44295875 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.327+6519G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44295875 | |||||||
| chr15:44295917 | T | TAC | 29 | a0001c0001t0001g0010 a0001c0001t0001g0036 a0001c0001t0001g0048 others(26): Show |
29 | HG00323.hp1 HG00408.hp1 HG00423.hp1 others(26): Show |
intron_variant | MODIFIER | c.327+6591_327+6592d others(4): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44295917 | ||||||
| chr15:44295917 | T | TACAC | 11 | a0001c0001t0001g0055 a0001c0001t0001g0087 a0001c0001t0001g0095 others(8): Show |
11 | HG00280.hp1 HG00280.hp2 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.327+6589_327+6592d others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44295917 | ||||||
| chr15:44295917 | T | TACACAC | 5 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0110 others(2): Show |
5 | HG00673.hp1 HG02965.hp2 NA19043.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+6587_327+6592d others(8): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44295917 | ||||||
| chr15:44295917 | T | TACACACA others(1): Show |
8 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(5): Show |
8 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.327+6585_327+6592d others(10): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44295917 | ||||||
| chr15:44295917 | T | TACACACA others(3): Show |
6 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(3): Show |
6 | HG02970.hp1 HG03098.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.327+6583_327+6592d others(12): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44295917 | ||||||
| chr15:44295917 | T | TACACACA others(5): Show |
1 | a0001c0003t0001g0148 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.327+6581_327+6592d others(14): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44295917 | ||||||
| chr15:44295917 | T | TACACACA others(7): Show |
7 | a0001c0001t0005g0119 a0001c0002t0003g0114 a0001c0002t0004g0103 others(4): Show |
7 | HG01981.hp2 HG02258.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.327+6579_327+6592d others(16): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44295917 | ||||||
| chr15:44295917 | T | TACACACA others(9): Show |
2 | a0001c0002t0004g0104 a0001c0003t0001g0147 |
2 | HG01891.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.327+6577_327+6592d others(18): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44295917 | ||||||
| chr15:44295917 | T | TACACACA others(11): Show |
1 | a0001c0002t0001g0090 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.327+6575_327+6592d others(20): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44295917 | ||||||
| chr15:44295917 | T | TACACACA others(13): Show |
1 | a0001c0002t0004g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.327+6573_327+6592d others(22): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44295917 | ||||||
| chr15:44295949 | G | C | 42 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(39): Show |
42 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.327+6593G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44295949 | |||||||
| chr15:44296238 | A | C | 15 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(12): Show |
15 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.327+6882A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44296238 | |||||||
| chr15:44296375 | A | T | 1 | a0002c0005t0001g0112 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.327+7019A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44296375 | |||||||
| chr15:44296463 | T | A | 15 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(12): Show |
15 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.327+7107T>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44296463 | |||||||
| chr15:44296474 | A | G | 1 | a0001c0001t0001g0097 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.327+7118A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44296474 | |||||||
| chr15:44296719 | A | G | 4 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0007g0121 others(1): Show |
4 | HG02965.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+7363A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44296719 | |||||||
| chr15:44296968 | C | A | 17 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.327+7612C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44296968 | |||||||
| chr15:44297124 | T | C | 3 | a0001c0002t0004g0103 a0001c0002t0004g0118 a0001c0002t0006g0109 |
3 | HG03516.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.327+7768T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44297124 | |||||||
| chr15:44297330 | T | C | 17 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.327+7974T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44297330 | |||||||
| chr15:44297537 | A | G | 1 | a0001c0001t0001g0033 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.327+8181A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44297537 | |||||||
| chr15:44297552 | A | AT | 11 | a0001c0002t0001g0090 a0001c0002t0003g0114 a0001c0002t0004g0086 others(8): Show |
11 | HG01981.hp2 HG02258.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.327+8205dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44297552 | ||||||
| chr15:44297706 | C | T | 2 | a0001c0003t0001g0147 a0001c0003t0001g0148 |
2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.327+8350C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44297706 | |||||||
| chr15:44297719 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.327+8363G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44297719 | |||||||
| chr15:44297765 | T | C | 1 | a0001c0001t0010g0126 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.327+8409T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44297765 | |||||||
| chr15:44297858 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.327+8502G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44297858 | |||||||
| chr15:44297867 | C | CT | 5 | a0001c0001t0001g0034 a0001c0001t0001g0037 a0001c0001t0001g0053 others(2): Show |
5 | HG00642.hp2 HG01069.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.327+8529dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44297867 | ||||||
| chr15:44297867 | CT | C | 44 | a0001c0001t0001g0007 a0001c0001t0001g0083 a0001c0001t0001g0087 others(41): Show |
44 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.327+8529delT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44297867 | ||||||
| chr15:44297961 | G | A | 18 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0127 others(15): Show |
18 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.327+8605G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44297961 | |||||||
| chr15:44298014 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.327+8658C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44298014 | |||||||
| chr15:44298265 | C | CT | 5 | a0001c0001t0001g0034 a0001c0001t0001g0053 a0001c0002t0004g0118 others(2): Show |
5 | HG01891.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.327+8924dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44298265 | ||||||
| chr15:44298325 | G | A | 4 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0007g0121 others(1): Show |
4 | HG02965.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+8969G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44298325 | |||||||
| chr15:44298430 | A | AT | 24 | a0001c0001t0001g0032 a0001c0001t0001g0046 a0001c0001t0001g0047 others(21): Show |
24 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.327+9091dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44298430 | ||||||
| chr15:44298539 | G | A | 41 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(38): Show |
41 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.327+9183G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44298539 | |||||||
| chr15:44298542 | C | G | 2 | a0001c0002t0004g0107 a0001c0002t0004g0108 |
2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.327+9186C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44298542 | |||||||
| chr15:44298714 | T | C | 14 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(11): Show |
14 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.327+9358T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44298714 | |||||||
| chr15:44298733 | C | T | 63 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(60): Show |
63 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.327+9377C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44298733 | |||||||
| chr15:44298979 | A | G | 39 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(36): Show |
39 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.327+9623A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44298979 | |||||||
| chr15:44299025 | T | C | 14 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(11): Show |
14 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.327+9669T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44299025 | |||||||
| chr15:44299298 | G | GT | 11 | a0001c0001t0001g0085 a0001c0001t0002g0125 a0001c0002t0001g0090 others(8): Show |
11 | HG01891.hp2 HG01981.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.327+9954dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44299298 | ||||||
| chr15:44299299 | T | G | 4 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 others(1): Show |
4 | HG02559.hp2 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+9943T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44299299 | |||||||
| chr15:44299353 | C | T | 39 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(36): Show |
39 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.327+9997C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44299353 | |||||||
| chr15:44299360 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.327+10004T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44299360 | |||||||
| chr15:44299424 | C | G | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.327+10068C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44299424 | |||||||
| chr15:44299733 | G | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0096 |
2 | NA19007.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.327+10377G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44299733 | |||||||
| chr15:44299759 | A | G | 19 | a0001c0001t0001g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(16): Show |
19 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.327+10403A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44299759 | |||||||
| chr15:44299772 | G | A | 63 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(60): Show |
63 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.327+10416G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44299772 | |||||||
| chr15:44299824 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.327+10468G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44299824 | |||||||
| chr15:44299926 | C | CA | 31 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(28): Show |
31 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.327+10597dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44299926 | ||||||
| chr15:44299926 | C | CAA | 5 | a0001c0001t0001g0012 a0001c0001t0001g0080 a0001c0001t0001g0083 others(2): Show |
5 | HG03225.hp1 HG03927.hp2 NA18965.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+10596_327+1059 others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44299926 | ||||||
| chr15:44299926 | CA | C | 7 | a0001c0001t0001g0089 a0001c0001t0001g0143 a0001c0002t0003g0114 others(4): Show |
7 | HG01981.hp2 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.327+10597delA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44299926 | ||||||
| chr15:44299926 | CAA | C | 15 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0095 others(12): Show |
15 | HG00408.hp1 HG00735.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.327+10596_327+1059 others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44299926 | ||||||
| chr15:44299926 | CAAA | C | 20 | a0001c0001t0001g0087 a0001c0001t0001g0092 a0001c0001t0001g0094 others(17): Show |
20 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.327+10595_327+1059 others(7): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44299926 | ||||||
| chr15:44299926 | CAAAA | C | 15 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0127 others(12): Show |
15 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(12): Show |
intron_variant | MODIFIER | c.327+10594_327+1059 others(8): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44299926 | ||||||
| chr15:44299967 | A | G | 63 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(60): Show |
63 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.327+10611A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44299967 | |||||||
| chr15:44300162 | AGAAG | A | 39 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(36): Show |
39 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.327+10820_327+1082 others(8): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44300162 | ||||||
| chr15:44300242 | A | AAAAG | 41 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(38): Show |
41 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.327+10891_327+1089 others(8): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44300242 | ||||||
| chr15:44300263 | G | C | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0041 others(1): Show |
4 | HG00738.hp2 HG01069.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+10907G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44300263 | |||||||
| chr15:44300309 | C | G | 1 | a0001c0001t0012g0004 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.327+10953C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44300309 | |||||||
| chr15:44300332 | A | AAAATTTA others(317): Show |
1 | a0001c0001t0001g0091 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.327+10985_327+1098 others(328): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44300332 | ||||||
| chr15:44300378 | T | G | 1 | a0001c0001t0001g0013 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.327+11022T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44300378 | |||||||
| chr15:44300521 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.327+11165T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44300521 | |||||||
| chr15:44300649 | C | T | 41 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(38): Show |
41 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.327+11293C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44300649 | |||||||
| chr15:44301394 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.327+12038C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44301394 | |||||||
| chr15:44301532 | A | G | 1 | a0001c0001t0001g0097 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.327+12176A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44301532 | |||||||
| chr15:44301543 | C | G | 1 | a0001c0001t0001g0081 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.327+12187C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44301543 | |||||||
| chr15:44301766 | G | A | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.327+12410G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44301766 | |||||||
| chr15:44301786 | C | T | 39 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(36): Show |
39 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.327+12430C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44301786 | |||||||
| chr15:44301848 | G | A | 3 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0009g0149 |
3 | HG01891.hp1 HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.327+12492G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44301848 | |||||||
| chr15:44301912 | C | CA | 14 | a0001c0001t0001g0083 a0001c0001t0001g0088 a0001c0001t0001g0089 others(11): Show |
14 | HG01891.hp2 HG01981.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.327+12571dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44301912 | ||||||
| chr15:44301944 | A | G | 45 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(42): Show |
45 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.327+12588A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44301944 | |||||||
| chr15:44302146 | AT | A | 15 | a0001c0001t0001g0079 a0001c0001t0001g0088 a0001c0001t0001g0089 others(12): Show |
15 | HG01081.hp2 HG01891.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.327+12806delT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44302146 | ||||||
| chr15:44302147 | T | C | 2 | a0001c0001t0002g0132 a0001c0001t0002g0135 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.327+12791T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44302147 | |||||||
| chr15:44302352 | C | T | 1 | a0002c0005t0003g0117 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.327+12996C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44302352 | |||||||
| chr15:44302410 | G | T | 2 | a0001c0002t0004g0107 a0001c0002t0004g0108 |
2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.327+13054G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44302410 | |||||||
| chr15:44302450 | A | C | 1 | a0001c0003t0001g0147 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.327+13094A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44302450 | |||||||
| chr15:44302645 | C | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0079 |
2 | HG00735.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.327+13289C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44302645 | |||||||
| chr15:44302713 | A | G | 8 | a0001c0002t0001g0090 a0001c0002t0003g0114 a0001c0002t0004g0086 others(5): Show |
8 | HG01981.hp2 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.327+13357A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44302713 | |||||||
| chr15:44302777 | C | T | 4 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0009g0149 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+13421C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44302777 | |||||||
| chr15:44302918 | C | T | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.327+13562C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44302918 | |||||||
| chr15:44302932 | G | C | 10 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(7): Show |
10 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.327+13576G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44302932 | |||||||
| chr15:44303102 | C | CAATA | 4 | a0001c0001t0001g0039 a0001c0001t0001g0062 a0001c0001t0001g0083 others(1): Show |
4 | HG02559.hp2 HG04115.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+13783_327+1378 others(8): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44303102 | ||||||
| chr15:44303102 | CAATA | C | 50 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(47): Show |
50 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.327+13783_327+1378 others(8): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44303102 | ||||||
| chr15:44303102 | CAATAAAT others(1): Show |
C | 18 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(15): Show |
18 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.327+13779_327+1378 others(12): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44303102 | ||||||
| chr15:44303102 | CAATAAAT others(5): Show |
C | 4 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0009g0149 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+13775_327+1378 others(16): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44303102 | ||||||
| chr15:44303106 | A | C | 1 | a0001c0002t0004g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.327+13750A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44303106 | |||||||
| chr15:44303574 | G | GT | 19 | a0001c0001t0001g0084 a0001c0001t0002g0124 a0001c0001t0002g0125 others(16): Show |
19 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.327+14226dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44303574 | ||||||
| chr15:44303627 | A | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0003g0020 |
3 | HG00558.hp2 HG02056.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.327+14271A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44303627 | |||||||
| chr15:44303732 | A | AT | 12 | a0001c0001t0001g0005 a0001c0001t0001g0037 a0001c0001t0001g0054 others(9): Show |
12 | HG00738.hp1 HG02055.hp1 HG02056.hp2 others(9): Show |
intron_variant | MODIFIER | c.327+14398dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44303732 | ||||||
| chr15:44303732 | A | ATT | 15 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(12): Show |
15 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.327+14397_327+1439 others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44303732 | ||||||
| chr15:44303732 | AT | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0048 a0001c0001t0001g0058 others(8): Show |
11 | HG00408.hp2 HG02451.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.327+14398delT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44303732 | ||||||
| chr15:44303832 | T | G | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.327+14476T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44303832 | |||||||
| chr15:44303845 | C | T | 4 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0009g0149 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+14489C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44303845 | |||||||
| chr15:44303983 | G | T | 10 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(7): Show |
10 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.327+14627G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44303983 | |||||||
| chr15:44304073 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.327+14717A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44304073 | |||||||
| chr15:44304230 | C | CT | 18 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0018 others(15): Show |
18 | HG00423.hp2 HG00621.hp2 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.327+14903dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44304230 | ||||||
| chr15:44304230 | C | CTTCTT | 15 | a0001c0001t0001g0123 a0001c0001t0002g0125 a0001c0001t0002g0130 others(12): Show |
15 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(12): Show |
intron_variant | MODIFIER | c.327+14876_327+1487 others(9): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44304230 | ||||||
| chr15:44304230 | C | CTTTTTTT others(3): Show |
7 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0095 others(4): Show |
7 | HG00673.hp1 HG00735.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.327+14894_327+1490 others(14): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44304230 | ||||||
| chr15:44304230 | C | CTTTTTTT others(4): Show |
4 | a0001c0001t0001g0091 a0001c0001t0001g0096 a0001c0001t0001g0100 others(1): Show |
4 | HG00423.hp1 HG03927.hp1 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+14893_327+1490 others(15): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44304230 | ||||||
| chr15:44304230 | C | CTTTTTTT others(6): Show |
2 | a0001c0001t0001g0087 a0001c0001t0001g0101 |
2 | HG00597.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.327+14891_327+1490 others(17): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44304230 | ||||||
| chr15:44304230 | CT | C | 9 | a0001c0001t0001g0027 a0001c0001t0001g0058 a0001c0001t0001g0082 others(6): Show |
9 | HG01081.hp1 HG01496.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.327+14903delT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44304230 | ||||||
| chr15:44304230 | CTTTTTTT others(12): Show |
C | 1 | a0001c0001t0001g0098 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.327+14885_327+1490 others(23): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44304230 | ||||||
| chr15:44304430 | C | T | 39 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(36): Show |
39 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.327+15074C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44304430 | |||||||
| chr15:44304844 | C | T | 1 | a0001c0001t0002g0125 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.327+15488C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44304844 | |||||||
| chr15:44305541 | A | G | 64 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(61): Show |
64 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.327+16185A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44305541 | |||||||
| chr15:44305697 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.327+16341G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44305697 | |||||||
| chr15:44305737 | G | T | 1 | a0001c0001t0003g0063 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.327+16381G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44305737 | |||||||
| chr15:44305852 | C | G | 56 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(53): Show |
56 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.327+16496C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44305852 | |||||||
| chr15:44305976 | G | A | 17 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.327+16620G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44305976 | |||||||
| chr15:44306315 | T | C | 18 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0127 others(15): Show |
18 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.328-16650T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44306315 | |||||||
| chr15:44306346 | C | T | 42 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(39): Show |
42 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.328-16619C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44306346 | |||||||
| chr15:44306444 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.328-16521T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44306444 | |||||||
| chr15:44306536 | A | C | 1 | a0001c0001t0001g0001 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.328-16429A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44306536 | |||||||
| chr15:44306560 | G | T | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 |
3 | HG02055.hp1 HG02572.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.328-16405G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44306560 | |||||||
| chr15:44306694 | A | G | 14 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(11): Show |
14 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.328-16271A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44306694 | |||||||
| chr15:44306711 | C | A | 4 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0007g0121 others(1): Show |
4 | HG02965.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-16254C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44306711 | |||||||
| chr15:44306806 | G | A | 42 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(39): Show |
42 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.328-16159G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44306806 | |||||||
| chr15:44306904 | A | G | 1 | a0002c0005t0003g0117 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.328-16061A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44306904 | |||||||
| chr15:44307086 | C | T | 8 | a0001c0002t0001g0090 a0001c0002t0003g0114 a0001c0002t0004g0086 others(5): Show |
8 | HG01981.hp2 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.328-15879C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44307086 | |||||||
| chr15:44307088 | C | T | 8 | a0001c0002t0001g0090 a0001c0002t0003g0114 a0001c0002t0004g0086 others(5): Show |
8 | HG01981.hp2 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.328-15877C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44307088 | |||||||
| chr15:44307212 | CT | C | 45 | a0001c0001t0001g0002 a0001c0001t0001g0087 a0001c0001t0001g0091 others(42): Show |
45 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(42): Show |
intron_variant | MODIFIER | c.328-15735delT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44307212 | ||||||
| chr15:44307452 | T | C | 1 | a0001c0001t0001g0110 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.328-15513T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44307452 | |||||||
| chr15:44307600 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.328-15365T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44307600 | |||||||
| chr15:44307621 | T | C | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.328-15344T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44307621 | |||||||
| chr15:44307673 | C | A | 1 | a0001c0001t0003g0051 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.328-15292C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44307673 | |||||||
| chr15:44307685 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.328-15280G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44307685 | |||||||
| chr15:44308009 | G | T | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.328-14956G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44308009 | |||||||
| chr15:44308215 | T | C | 4 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0009g0149 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-14750T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44308215 | |||||||
| chr15:44308369 | A | G | 42 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(39): Show |
42 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.328-14596A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44308369 | |||||||
| chr15:44308482 | C | G | 64 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(61): Show |
64 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.328-14483C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44308482 | |||||||
| chr15:44308522 | C | T | 11 | a0001c0002t0001g0090 a0001c0002t0003g0114 a0001c0002t0004g0086 others(8): Show |
11 | HG01981.hp2 HG02258.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.328-14443C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44308522 | |||||||
| chr15:44308730 | C | T | 4 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(1): Show |
4 | HG02970.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-14235C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44308730 | |||||||
| chr15:44308731 | G | A | 43 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(40): Show |
43 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.328-14234G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44308731 | |||||||
| chr15:44309119 | G | T | 1 | a0001c0001t0001g0080 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.328-13846G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44309119 | |||||||
| chr15:44309221 | G | A | 23 | a0001c0001t0001g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(20): Show |
23 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(20): Show |
intron_variant | MODIFIER | c.328-13744G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44309221 | |||||||
| chr15:44309497 | A | T | 15 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0015 others(12): Show |
15 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.328-13468A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44309497 | |||||||
| chr15:44309669 | A | T | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.328-13296A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44309669 | |||||||
| chr15:44309710 | T | G | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.328-13255T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44309710 | |||||||
| chr15:44309738 | G | C | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.328-13227G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44309738 | |||||||
| chr15:44309906 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.328-13059C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44309906 | |||||||
| chr15:44310211 | A | G | 1 | a0001c0001t0001g0006 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.328-12754A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310211 | |||||||
| chr15:44310224 | A | T | 10 | a0001c0002t0001g0090 a0001c0002t0003g0114 a0001c0002t0004g0103 others(7): Show |
10 | HG01981.hp2 HG02258.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.328-12741A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310224 | |||||||
| chr15:44310327 | C | G | 1 | a0001c0001t0003g0065 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.328-12638C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310327 | |||||||
| chr15:44310353 | T | C | 42 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(39): Show |
42 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.328-12612T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310353 | |||||||
| chr15:44310438 | T | C | 1 | a0001c0001t0002g0132 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.328-12527T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310438 | |||||||
| chr15:44310438 | T | TTC | 8 | a0001c0001t0001g0056 a0001c0001t0001g0123 a0001c0001t0002g0133 others(5): Show |
8 | HG00642.hp2 HG01891.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.328-12511_328-1251 others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44310438 | ||||||
| chr15:44310438 | T | TTCTC | 11 | a0001c0001t0001g0059 a0001c0001t0002g0124 a0001c0001t0002g0127 others(8): Show |
11 | HG01496.hp2 HG02109.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.328-12513_328-1251 others(8): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44310438 | ||||||
| chr15:44310438 | T | TTCTCTC | 2 | a0001c0001t0001g0006 a0001c0001t0001g0111 |
2 | NA19030.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.328-12515_328-1251 others(10): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44310438 | ||||||
| chr15:44310438 | T | TTCTCTCT others(1): Show |
5 | a0001c0001t0002g0125 a0001c0001t0002g0131 a0001c0001t0002g0140 others(2): Show |
5 | HG03209.hp1 NA18951.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-12517_328-1251 others(12): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44310438 | ||||||
| chr15:44310438 | T | TTCTCTCT others(3): Show |
2 | a0001c0001t0001g0110 a0001c0001t0010g0126 |
2 | NA18990.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.328-12519_328-1251 others(14): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44310438 | ||||||
| chr15:44310438 | T | TTCTCTCT others(5): Show |
11 | a0001c0001t0001g0087 a0001c0001t0001g0093 a0001c0001t0001g0094 others(8): Show |
11 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(8): Show |
intron_variant | MODIFIER | c.328-12521_328-1251 others(16): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44310438 | ||||||
| chr15:44310438 | T | TTCTCTCT others(7): Show |
3 | a0001c0001t0001g0092 a0001c0001t0001g0097 a0001c0001t0001g0099 |
3 | HG00673.hp1 NA18985.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.328-12523_328-1251 others(18): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44310438 | ||||||
| chr15:44310438 | T | TTCTCTCT others(9): Show |
1 | a0001c0001t0001g0091 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.328-12525_328-1251 others(20): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44310438 | ||||||
| chr15:44310456 | A | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(132): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.328-12509A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310456 | |||||||
| chr15:44310458 | A | C | 70 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(67): Show |
70 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.328-12507A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310458 | |||||||
| chr15:44310460 | A | C | 39 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(36): Show |
39 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.328-12505A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310460 | |||||||
| chr15:44310462 | A | C | 36 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0093 others(33): Show |
36 | HG00408.hp1 HG00597.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.328-12503A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310462 | |||||||
| chr15:44310464 | A | C | 31 | a0001c0001t0001g0091 a0001c0001t0001g0094 a0001c0001t0001g0095 others(28): Show |
31 | HG00735.hp2 HG01496.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.328-12501A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310464 | |||||||
| chr15:44310466 | A | C | 29 | a0001c0001t0001g0091 a0001c0001t0001g0095 a0001c0001t0001g0096 others(26): Show |
29 | HG00735.hp2 HG01496.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.328-12499A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310466 | |||||||
| chr15:44310468 | A | C | 23 | a0001c0001t0001g0096 a0001c0001t0001g0110 a0001c0001t0001g0123 others(20): Show |
23 | HG01496.hp2 HG01891.hp2 HG02040.hp1 others(20): Show |
intron_variant | MODIFIER | c.328-12497A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310468 | |||||||
| chr15:44310470 | G | A | 24 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(21): Show |
24 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.328-12495G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310470 | |||||||
| chr15:44310470 | G | C | 18 | a0001c0001t0001g0110 a0001c0001t0002g0124 a0001c0001t0002g0125 others(15): Show |
18 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.328-12495G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310470 | |||||||
| chr15:44310470 | G | GTA | 3 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0012g0004 |
3 | HG00558.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.328-12476_328-1247 others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44310470 | ||||||
| chr15:44310472 | A | C | 13 | a0001c0001t0002g0124 a0001c0001t0002g0127 a0001c0001t0002g0130 others(10): Show |
13 | HG02257.hp1 HG02451.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.328-12493A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310472 | |||||||
| chr15:44310474 | A | C | 8 | a0001c0001t0002g0124 a0001c0001t0002g0130 a0001c0001t0002g0131 others(5): Show |
8 | HG02257.hp1 HG02451.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.328-12491A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310474 | |||||||
| chr15:44310476 | A | C | 3 | a0001c0001t0002g0124 a0001c0001t0002g0132 a0001c0001t0002g0141 |
3 | HG02257.hp1 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.328-12489A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310476 | |||||||
| chr15:44310487 | T | C | 2 | a0001c0003t0001g0147 a0001c0003t0001g0148 |
2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.328-12478T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310487 | |||||||
| chr15:44310489 | T | C | 17 | a0001c0001t0001g0017 a0001c0001t0001g0110 a0001c0002t0001g0090 others(14): Show |
17 | HG01891.hp1 HG01981.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.328-12476T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310489 | |||||||
| chr15:44310490 | A | ACACACAC others(3): Show |
1 | a0001c0003t0009g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.328-12466_328-1246 others(14): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44310490 | ||||||
| chr15:44310491 | C | T | 22 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0127 others(19): Show |
22 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(19): Show |
intron_variant | MODIFIER | c.328-12474C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310491 | |||||||
| chr15:44310493 | C | T | 21 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0127 others(18): Show |
21 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(18): Show |
intron_variant | MODIFIER | c.328-12472C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310493 | |||||||
| chr15:44310495 | C | T | 20 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0127 others(17): Show |
20 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(17): Show |
intron_variant | MODIFIER | c.328-12470C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310495 | |||||||
| chr15:44310496 | A | ACACC | 3 | a0001c0002t0004g0086 a0001c0003t0001g0147 a0001c0003t0001g0148 |
3 | HG01891.hp1 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.328-12466_328-1246 others(8): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44310496 | ||||||
| chr15:44310497 | C | T | 20 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0127 others(17): Show |
20 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(17): Show |
intron_variant | MODIFIER | c.328-12468C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310497 | |||||||
| chr15:44310498 | A | ACC | 10 | a0001c0002t0001g0090 a0001c0002t0003g0114 a0001c0002t0004g0103 others(7): Show |
10 | HG01981.hp2 HG02258.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.328-12466_328-1246 others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44310498 | ||||||
| chr15:44310499 | C | T | 14 | a0001c0001t0002g0124 a0001c0001t0002g0127 a0001c0001t0002g0130 others(11): Show |
14 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.328-12466C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310499 | |||||||
| chr15:44310501 | C | T | 3 | a0001c0001t0002g0124 a0001c0001t0002g0127 a0001c0001t0002g0141 |
3 | HG02257.hp1 HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.328-12464C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310501 | |||||||
| chr15:44310502 | C | A | 38 | a0001c0001t0001g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(35): Show |
38 | HG01496.hp2 HG01891.hp1 HG01981.hp2 others(35): Show |
intron_variant | MODIFIER | c.328-12463C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310502 | |||||||
| chr15:44310502 | C | CCA | 20 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0055 others(17): Show |
20 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(17): Show |
intron_variant | MODIFIER | c.328-12440_328-1243 others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44310502 | ||||||
| chr15:44310502 | C | CCACA | 8 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.328-12442_328-1243 others(8): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44310502 | ||||||
| chr15:44310508 | A | C | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0003g0051 |
3 | HG02559.hp2 HG03453.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.328-12457A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310508 | |||||||
| chr15:44310576 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.328-12389A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310576 | |||||||
| chr15:44310736 | A | AC | 42 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(39): Show |
42 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.328-12229_328-1222 others(5): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310736 | |||||||
| chr15:44310793 | C | T | 40 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(37): Show |
40 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.328-12172C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310793 | |||||||
| chr15:44310952 | G | A | 1 | a0001c0002t0004g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.328-12013G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44310952 | |||||||
| chr15:44311012 | A | G | 64 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(61): Show |
64 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.328-11953A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44311012 | |||||||
| chr15:44311339 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.328-11626A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44311339 | |||||||
| chr15:44311584 | A | G | 4 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0009g0149 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-11381A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44311584 | |||||||
| chr15:44311652 | T | TTGTG | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.328-11298_328-1129 others(8): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44311652 | ||||||
| chr15:44311658 | G | A | 4 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0009g0149 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-11307G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44311658 | |||||||
| chr15:44311960 | G | A | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.328-11005G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44311960 | |||||||
| chr15:44312118 | A | G | 1 | a0001c0001t0001g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.328-10847A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44312118 | |||||||
| chr15:44312417 | G | T | 1 | a0001c0001t0001g0032 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.328-10548G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44312417 | |||||||
| chr15:44312605 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.328-10360C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44312605 | |||||||
| chr15:44312674 | G | A | 17 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-10291G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44312674 | |||||||
| chr15:44312808 | C | T | 42 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(39): Show |
42 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.328-10157C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44312808 | |||||||
| chr15:44312846 | C | T | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.328-10119C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44312846 | |||||||
| chr15:44312963 | C | T | 1 | a0001c0001t0012g0004 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.328-10002C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44312963 | |||||||
| chr15:44312979 | C | T | 1 | a0001c0003t0009g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.328-9986C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44312979 | |||||||
| chr15:44313314 | A | G | 23 | a0001c0001t0001g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(20): Show |
23 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(20): Show |
intron_variant | MODIFIER | c.328-9651A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44313314 | |||||||
| chr15:44313372 | A | G | 17 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-9593A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44313372 | |||||||
| chr15:44313387 | T | G | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.328-9578T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44313387 | |||||||
| chr15:44313408 | T | C | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.328-9557T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44313408 | |||||||
| chr15:44313795 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.328-9170G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44313795 | |||||||
| chr15:44313868 | A | T | 1 | a0001c0001t0001g0027 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.328-9097A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44313868 | |||||||
| chr15:44313912 | C | T | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.328-9053C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44313912 | |||||||
| chr15:44314093 | C | T | 11 | a0001c0002t0001g0090 a0001c0002t0003g0114 a0001c0002t0004g0086 others(8): Show |
11 | HG01981.hp2 HG02258.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.328-8872C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44314093 | |||||||
| chr15:44314194 | G | A | 1 | a0001c0002t0004g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.328-8771G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44314194 | |||||||
| chr15:44314236 | C | CA | 10 | a0001c0001t0001g0018 a0001c0001t0001g0084 a0001c0001t0012g0004 others(7): Show |
10 | HG01255.hp1 HG01981.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.328-8716dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44314236 | ||||||
| chr15:44314559 | CA | C | 8 | a0001c0001t0001g0094 a0001c0001t0001g0143 a0001c0001t0001g0144 others(5): Show |
8 | HG01891.hp2 HG02109.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.328-8390delA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44314559 | ||||||
| chr15:44314804 | C | G | 1 | a0001c0003t0009g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.328-8161C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44314804 | |||||||
| chr15:44314962 | G | A | 5 | a0001c0002t0004g0104 a0001c0002t0004g0105 a0001c0002t0004g0106 others(2): Show |
5 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-8003G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44314962 | |||||||
| chr15:44314995 | C | G | 2 | a0001c0001t0001g0026 a0001c0001t0003g0009 |
2 | HG02895.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.328-7970C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44314995 | |||||||
| chr15:44315161 | A | G | 2 | a0001c0001t0001g0050 a0001c0001t0003g0049 |
2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.328-7804A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44315161 | |||||||
| chr15:44315263 | A | G | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.328-7702A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44315263 | |||||||
| chr15:44315431 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0003g0049 |
2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.328-7534G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44315431 | |||||||
| chr15:44315674 | A | C | 16 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(13): Show |
16 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.328-7291A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44315674 | |||||||
| chr15:44315873 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.328-7092G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44315873 | |||||||
| chr15:44315917 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.328-7048A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44315917 | |||||||
| chr15:44316532 | A | G | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 |
3 | HG02055.hp1 HG02572.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.328-6433A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44316532 | |||||||
| chr15:44316565 | C | G | 1 | a0001c0001t0001g0017 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.328-6400C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44316565 | |||||||
| chr15:44316582 | C | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.328-6383C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44316582 | |||||||
| chr15:44316640 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.328-6325A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44316640 | |||||||
| chr15:44316680 | G | A | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.328-6285G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44316680 | |||||||
| chr15:44316754 | C | CA | 26 | a0001c0001t0001g0021 a0001c0001t0001g0062 a0001c0001t0001g0066 others(23): Show |
26 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.328-6197dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44316754 | ||||||
| chr15:44316769 | C | A | 41 | a0001c0001t0001g0035 a0001c0001t0001g0087 a0001c0001t0001g0091 others(38): Show |
41 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.328-6196C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44316769 | |||||||
| chr15:44316981 | C | T | 64 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(61): Show |
64 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.328-5984C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44316981 | |||||||
| chr15:44317050 | A | G | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.328-5915A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44317050 | |||||||
| chr15:44317063 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.328-5902C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44317063 | |||||||
| chr15:44317249 | T | C | 4 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0007g0121 others(1): Show |
4 | HG02965.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-5716T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44317249 | |||||||
| chr15:44317266 | A | G | 2 | a0001c0001t0001g0050 a0001c0001t0003g0049 |
2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.328-5699A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44317266 | |||||||
| chr15:44317521 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.328-5444T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44317521 | |||||||
| chr15:44317598 | T | C | 17 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-5367T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44317598 | |||||||
| chr15:44317681 | G | A | 1 | a0001c0003t0009g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.328-5284G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44317681 | |||||||
| chr15:44317790 | T | A | 1 | a0001c0001t0003g0064 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.328-5175T>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44317790 | |||||||
| chr15:44317913 | A | G | 3 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0007g0121 |
3 | HG02965.hp2 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.328-5052A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44317913 | |||||||
| chr15:44318164 | TTTCATTT others(8): Show |
T | 1 | a0001c0001t0001g0060 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.328-4795_328-4781d others(17): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44318164 | ||||||
| chr15:44318261 | C | T | 1 | a0001c0002t0004g0103 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.328-4704C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44318261 | |||||||
| chr15:44318373 | C | G | 1 | a0001c0001t0001g0071 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.328-4592C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44318373 | |||||||
| chr15:44318430 | G | A | 2 | a0001c0003t0001g0147 a0001c0003t0001g0148 |
2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.328-4535G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44318430 | |||||||
| chr15:44318438 | G | A | 16 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(13): Show |
16 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.328-4527G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44318438 | |||||||
| chr15:44318444 | T | C | 42 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(39): Show |
42 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.328-4521T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44318444 | |||||||
| chr15:44318489 | G | A | 5 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(2): Show |
5 | HG02970.hp1 HG03098.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-4476G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44318489 | |||||||
| chr15:44318538 | G | C | 1 | a0001c0003t0009g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.328-4427G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44318538 | |||||||
| chr15:44318589 | G | T | 2 | a0001c0003t0001g0147 a0001c0003t0001g0148 |
2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.328-4376G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44318589 | |||||||
| chr15:44318613 | G | A | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.328-4352G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44318613 | |||||||
| chr15:44318642 | G | C | 3 | a0001c0002t0004g0103 a0001c0002t0004g0118 a0001c0002t0006g0109 |
3 | HG03516.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.328-4323G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44318642 | |||||||
| chr15:44318652 | C | T | 42 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(39): Show |
42 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.328-4313C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44318652 | |||||||
| chr15:44318708 | C | CA | 37 | a0001c0001t0001g0023 a0001c0001t0001g0025 a0001c0001t0001g0035 others(34): Show |
37 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(34): Show |
intron_variant | MODIFIER | c.328-4239dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44318708 | ||||||
| chr15:44318708 | CA | C | 5 | a0001c0001t0001g0036 a0001c0001t0001g0083 a0001c0002t0004g0103 others(2): Show |
5 | HG01074.hp1 HG03516.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-4239delA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44318708 | ||||||
| chr15:44318749 | T | G | 3 | a0001c0002t0004g0103 a0001c0002t0004g0118 a0001c0002t0006g0109 |
3 | HG03516.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.328-4216T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44318749 | |||||||
| chr15:44318877 | T | C | 1 | a0001c0001t0003g0072 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.328-4088T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44318877 | |||||||
| chr15:44319023 | A | T | 17 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-3942A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44319023 | |||||||
| chr15:44319211 | A | G | 2 | a0001c0001t0001g0077 a0001c0001t0013g0061 |
2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.328-3754A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44319211 | |||||||
| chr15:44320352 | A | G | 1 | a0001c0003t0009g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.328-2613A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44320352 | |||||||
| chr15:44320503 | C | T | 1 | a0001c0003t0009g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.328-2462C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44320503 | |||||||
| chr15:44320531 | C | T | 1 | a0001c0002t0004g0104 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.328-2434C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44320531 | |||||||
| chr15:44320538 | C | G | 1 | a0001c0001t0001g0071 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.328-2427C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44320538 | |||||||
| chr15:44320657 | G | C | 1 | a0001c0001t0001g0123 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.328-2308G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44320657 | |||||||
| chr15:44320851 | G | C | 1 | a0001c0001t0001g0110 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.328-2114G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44320851 | |||||||
| chr15:44321223 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.328-1742G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44321223 | |||||||
| chr15:44321321 | A | C | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | NA18965.hp1 NA18985.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.328-1644A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44321321 | |||||||
| chr15:44321467 | C | G | 1 | a0001c0001t0001g0071 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.328-1498C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44321467 | |||||||
| chr15:44321467 | CA | C | 58 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(55): Show |
58 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(55): Show |
intron_variant | MODIFIER | c.328-1481delA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr15 | 44321467 | ||||||
| chr15:44321483 | A | G | 4 | a0001c0001t0005g0120 a0001c0002t0004g0103 a0001c0002t0004g0105 others(1): Show |
4 | HG02258.hp1 HG03225.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-1482A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44321483 | |||||||
| chr15:44321484 | A | G | 18 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0007g0121 others(15): Show |
18 | HG01891.hp2 HG01981.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.328-1481A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44321484 | |||||||
| chr15:44321485 | G | C | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.328-1480G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44321485 | |||||||
| chr15:44321491 | G | A | 18 | a0001c0001t0001g0032 a0001c0001t0001g0087 a0001c0001t0001g0091 others(15): Show |
18 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.328-1474G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44321491 | |||||||
| chr15:44321655 | A | G | 1 | a0001c0001t0001g0094 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.328-1310A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44321655 | |||||||
| chr15:44321923 | A | T | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.328-1042A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44321923 | |||||||
| chr15:44322299 | G | A | 15 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0015 others(12): Show |
15 | HG01074.hp2 HG02055.hp2 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.328-666G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44322299 | |||||||
| chr15:44322420 | GT | G | 4 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0009g0149 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-544delT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44322420 | |||||||
| chr15:44322486 | A | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0032 others(2): Show |
5 | HG01074.hp2 HG04199.hp2 NA18948.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-479A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44322486 | |||||||
| chr15:44322889 | T | G | 1 | a0001c0001t0001g0123 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.328-76T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 1/9 | chr15 | 44322889 | |||||||
| chr15:44323107 | G | A | 42 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(39): Show |
42 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.382+88G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44323107 | |||||||
| chr15:44323129 | AACTC | A | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 |
3 | HG02055.hp1 HG02572.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.382+111_382+114del others(4): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44323129 | |||||||
| chr15:44323131 | C | A | 17 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.382+112C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44323131 | |||||||
| chr15:44323512 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.382+493C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44323512 | |||||||
| chr15:44323548 | G | A | 1 | a0001c0002t0006g0109 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.382+529G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44323548 | |||||||
| chr15:44323821 | T | C | 1 | a0002c0005t0003g0117 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.382+802T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44323821 | |||||||
| chr15:44324481 | A | G | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.382+1462A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44324481 | |||||||
| chr15:44324598 | G | A | 6 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(3): Show |
6 | HG00408.hp2 HG00673.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.382+1579G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44324598 | |||||||
| chr15:44324639 | A | G | 1 | a0001c0001t0003g0051 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.382+1620A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44324639 | |||||||
| chr15:44325257 | C | G | 1 | a0001c0001t0001g0002 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.382+2238C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44325257 | |||||||
| chr15:44326124 | C | T | 61 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(58): Show |
61 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.383-2561C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44326124 | |||||||
| chr15:44326187 | G | T | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.383-2498G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44326187 | |||||||
| chr15:44326597 | A | G | 2 | a0001c0003t0001g0147 a0001c0003t0001g0148 |
2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.383-2088A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44326597 | |||||||
| chr15:44326654 | G | GT | 18 | a0001c0001t0001g0034 a0001c0001t0001g0053 a0001c0001t0001g0113 others(15): Show |
18 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.383-2016dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr15 | 44326654 | ||||||
| chr15:44326721 | G | T | 2 | a0001c0003t0001g0147 a0001c0003t0001g0148 |
2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.383-1964G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44326721 | |||||||
| chr15:44326786 | G | A | 4 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0007g0121 others(1): Show |
4 | HG02965.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.383-1899G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44326786 | |||||||
| chr15:44327011 | C | T | 11 | a0001c0002t0004g0086 a0001c0002t0004g0103 a0001c0002t0004g0104 others(8): Show |
11 | HG01891.hp1 HG02258.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.383-1674C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44327011 | |||||||
| chr15:44327032 | G | A | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.383-1653G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44327032 | |||||||
| chr15:44327042 | CT | C | 2 | a0001c0003t0001g0147 a0001c0003t0001g0148 |
2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.383-1642delT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44327042 | |||||||
| chr15:44327170 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.383-1515C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44327170 | |||||||
| chr15:44327238 | A | C | 1 | a0001c0001t0001g0071 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.383-1447A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44327238 | |||||||
| chr15:44327243 | G | A | 1 | a0001c0003t0009g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.383-1442G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44327243 | |||||||
| chr15:44327292 | C | A | 2 | a0001c0002t0001g0090 a0001c0002t0003g0114 |
2 | HG01981.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.383-1393C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44327292 | |||||||
| chr15:44327331 | G | T | 5 | a0001c0002t0004g0104 a0001c0002t0004g0105 a0001c0002t0004g0106 others(2): Show |
5 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.383-1354G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44327331 | |||||||
| chr15:44327334 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.383-1351C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44327334 | |||||||
| chr15:44327592 | CT | C | 17 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0015 others(14): Show |
17 | HG01074.hp2 HG01981.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.383-1092delT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44327592 | |||||||
| chr15:44327771 | T | C | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.383-914T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44327771 | |||||||
| chr15:44327775 | T | G | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.383-910T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44327775 | |||||||
| chr15:44327776 | T | G | 1 | a0001c0001t0001g0002 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.383-909T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44327776 | |||||||
| chr15:44327792 | A | G | 1 | a0001c0003t0009g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.383-893A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44327792 | |||||||
| chr15:44327882 | T | C | 3 | a0001c0002t0004g0103 a0001c0002t0004g0118 a0001c0002t0006g0109 |
3 | HG03516.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.383-803T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44327882 | |||||||
| chr15:44327931 | C | T | 17 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.383-754C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44327931 | |||||||
| chr15:44327976 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02572.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.383-709C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 2/9 | chr15 | 44327976 | |||||||
| chr15:44329332 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.485+545A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 3/9 | chr15 | 44329332 | |||||||
| chr15:44329347 | A | C | 3 | a0001c0002t0004g0103 a0001c0002t0004g0118 a0001c0002t0006g0109 |
3 | HG03516.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.485+560A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 3/9 | chr15 | 44329347 | |||||||
| chr15:44329812 | G | A | 3 | a0001c0001t0002g0131 a0001c0001t0002g0140 a0001c0001t0010g0126 |
3 | NA18951.hp1 NA18971.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.485+1025G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 3/9 | chr15 | 44329812 | |||||||
| chr15:44329909 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.485+1122T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 3/9 | chr15 | 44329909 | |||||||
| chr15:44330036 | G | A | 17 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.485+1249G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 3/9 | chr15 | 44330036 | |||||||
| chr15:44330072 | G | A | 1 | a0001c0002t0004g0103 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.485+1285G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 3/9 | chr15 | 44330072 | |||||||
| chr15:44330208 | T | TA | 38 | a0001c0001t0001g0026 a0001c0001t0001g0041 a0001c0001t0001g0042 others(35): Show |
38 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.485+1444dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 44330208 | ||||||
| chr15:44330208 | T | TAAAA | 7 | a0001c0002t0001g0090 a0001c0002t0004g0104 a0001c0002t0004g0105 others(4): Show |
7 | HG02258.hp1 HG02886.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.485+1441_485+1444d others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 44330208 | ||||||
| chr15:44330340 | C | A | 4 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(1): Show |
4 | HG02970.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.485+1553C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 3/9 | chr15 | 44330340 | |||||||
| chr15:44330469 | C | T | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.486-1519C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 3/9 | chr15 | 44330469 | |||||||
| chr15:44330514 | G | GA | 14 | a0001c0001t0001g0037 a0001c0001t0001g0062 a0001c0001t0001g0066 others(11): Show |
14 | HG02055.hp1 HG02109.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.486-1454dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr15 | 44330514 | ||||||
| chr15:44330548 | A | G | 1 | a0001c0001t0001g0016 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.486-1440A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 3/9 | chr15 | 44330548 | |||||||
| chr15:44330615 | C | G | 11 | a0001c0002t0001g0090 a0001c0002t0003g0114 a0001c0002t0004g0086 others(8): Show |
11 | HG01981.hp2 HG02258.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.486-1373C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 3/9 | chr15 | 44330615 | |||||||
| chr15:44330766 | G | C | 1 | a0001c0001t0001g0102 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.486-1222G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 3/9 | chr15 | 44330766 | |||||||
| chr15:44330824 | G | A | 41 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(38): Show |
41 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.486-1164G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 3/9 | chr15 | 44330824 | |||||||
| chr15:44330876 | C | G | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | NA18965.hp1 NA18985.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.486-1112C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 3/9 | chr15 | 44330876 | |||||||
| chr15:44331101 | A | G | 63 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(60): Show |
63 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.486-887A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 3/9 | chr15 | 44331101 | |||||||
| chr15:44331152 | C | A | 1 | a0001c0001t0001g0071 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.486-836C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 3/9 | chr15 | 44331152 | |||||||
| chr15:44331155 | C | T | 22 | a0001c0001t0001g0123 a0001c0001t0002g0124 a0001c0001t0002g0127 others(19): Show |
22 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(19): Show |
intron_variant | MODIFIER | c.486-833C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 3/9 | chr15 | 44331155 | |||||||
| chr15:44331439 | A | G | 2 | a0001c0003t0001g0147 a0001c0003t0001g0148 |
2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.486-549A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 3/9 | chr15 | 44331439 | |||||||
| chr15:44331468 | G | C | 11 | a0001c0002t0001g0090 a0001c0002t0003g0114 a0001c0002t0004g0086 others(8): Show |
11 | HG01981.hp2 HG02258.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.486-520G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 3/9 | chr15 | 44331468 | |||||||
| chr15:44331497 | T | C | 1 | a0001c0001t0001g0102 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.486-491T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 3/9 | chr15 | 44331497 | |||||||
| chr15:44331504 | T | C | 2 | a0001c0001t0001g0077 a0001c0001t0013g0061 |
2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.486-484T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 3/9 | chr15 | 44331504 | |||||||
| chr15:44331516 | T | C | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.486-472T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 3/9 | chr15 | 44331516 | |||||||
| chr15:44331650 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.486-338T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 3/9 | chr15 | 44331650 | |||||||
| chr15:44331664 | G | A | 1 | a0001c0002t0003g0114 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.486-324G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 3/9 | chr15 | 44331664 | |||||||
| chr15:44331935 | T | G | 1 | a0001c0003t0001g0147 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.486-53T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 3/9 | chr15 | 44331935 | |||||||
| chr15:44332257 | A | G | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.576+179A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44332257 | |||||||
| chr15:44332322 | T | C | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0041 others(1): Show |
4 | HG00738.hp2 HG01069.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.576+244T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44332322 | |||||||
| chr15:44332341 | G | A | 17 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.576+263G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44332341 | |||||||
| chr15:44332488 | C | T | 6 | a0001c0001t0001g0037 a0001c0001t0001g0123 a0001c0001t0005g0119 others(3): Show |
6 | HG02965.hp2 HG03209.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.576+410C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44332488 | |||||||
| chr15:44332522 | T | C | 1 | a0001c0001t0001g0058 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.576+444T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44332522 | |||||||
| chr15:44332525 | A | C | 1 | a0001c0001t0001g0071 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.576+447A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44332525 | |||||||
| chr15:44332559 | C | CA | 62 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(59): Show |
62 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.576+495dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr15 | 44332559 | ||||||
| chr15:44332677 | C | G | 4 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0009g0149 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.576+599C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44332677 | |||||||
| chr15:44332695 | T | C | 4 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0009g0149 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.576+617T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44332695 | |||||||
| chr15:44332818 | T | G | 1 | a0001c0001t0001g0007 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.576+740T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44332818 | |||||||
| chr15:44332827 | G | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0029 |
3 | HG02040.hp2 NA18966.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.576+749G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44332827 | |||||||
| chr15:44332944 | T | G | 15 | a0001c0001t0001g0005 a0001c0001t0001g0087 a0001c0001t0001g0088 others(12): Show |
15 | HG00408.hp1 HG00597.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.576+866T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44332944 | |||||||
| chr15:44332965 | G | A | 1 | a0001c0001t0002g0132 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.576+887G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44332965 | |||||||
| chr15:44332999 | C | T | 2 | a0001c0003t0001g0147 a0001c0003t0001g0148 |
2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.576+921C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44332999 | |||||||
| chr15:44333018 | C | T | 1 | a0001c0001t0002g0136 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.576+940C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44333018 | |||||||
| chr15:44333019 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.576+941G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44333019 | |||||||
| chr15:44333093 | C | T | 1 | a0001c0001t0001g0005 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.576+1015C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44333093 | |||||||
| chr15:44333154 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.576+1076G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44333154 | |||||||
| chr15:44333226 | A | G | 52 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(49): Show |
52 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.576+1148A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44333226 | |||||||
| chr15:44333232 | A | G | 10 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0133 others(7): Show |
10 | HG02040.hp1 HG02155.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.576+1154A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44333232 | |||||||
| chr15:44333436 | A | G | 1 | a0001c0001t0001g0005 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.576+1358A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44333436 | |||||||
| chr15:44333500 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.576+1422A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44333500 | |||||||
| chr15:44333517 | A | C | 1 | a0001c0001t0001g0005 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.576+1439A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44333517 | |||||||
| chr15:44333584 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.576+1506A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44333584 | |||||||
| chr15:44333661 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0054 a0001c0001t0003g0020 |
3 | HG00558.hp2 HG02056.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.576+1583G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44333661 | |||||||
| chr15:44333695 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.576+1617A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44333695 | |||||||
| chr15:44334011 | G | A | 1 | a0001c0003t0009g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.576+1933G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44334011 | |||||||
| chr15:44334193 | GA | G | 17 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.576+2116delA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44334193 | |||||||
| chr15:44334287 | T | A | 1 | a0001c0001t0001g0005 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.576+2209T>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44334287 | |||||||
| chr15:44334888 | G | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG01255.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+2810G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44334888 | |||||||
| chr15:44335151 | G | C | 52 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(49): Show |
52 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.577-2612G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44335151 | |||||||
| chr15:44335196 | G | A | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.577-2567G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44335196 | |||||||
| chr15:44335260 | C | G | 1 | a0001c0002t0004g0104 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.577-2503C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44335260 | |||||||
| chr15:44335276 | G | A | 63 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(60): Show |
63 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.577-2487G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44335276 | |||||||
| chr15:44335757 | T | C | 39 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(36): Show |
39 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.577-2006T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44335757 | |||||||
| chr15:44335810 | C | CT | 35 | a0001c0001t0001g0080 a0001c0001t0001g0082 a0001c0001t0001g0092 others(32): Show |
35 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.577-1933dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr15 | 44335810 | ||||||
| chr15:44335810 | C | CTT | 10 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0097 others(7): Show |
10 | HG01891.hp1 HG01891.hp2 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.577-1934_577-1933d others(4): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr15 | 44335810 | ||||||
| chr15:44335841 | G | A | 1 | a0002c0005t0003g0117 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.577-1922G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44335841 | |||||||
| chr15:44336308 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.577-1455G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44336308 | |||||||
| chr15:44336366 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0043 others(1): Show |
4 | HG00642.hp1 HG02572.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-1397C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44336366 | |||||||
| chr15:44336368 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.577-1395C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44336368 | |||||||
| chr15:44336698 | C | G | 1 | a0001c0001t0001g0027 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.577-1065C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44336698 | |||||||
| chr15:44336809 | G | A | 15 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(12): Show |
15 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.577-954G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44336809 | |||||||
| chr15:44336894 | C | A | 1 | a0001c0001t0001g0021 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.577-869C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44336894 | |||||||
| chr15:44337120 | C | G | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.577-643C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 4/9 | chr15 | 44337120 | |||||||
| chr15:44338415 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.802+98A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44338415 | |||||||
| chr15:44338426 | C | T | 55 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(52): Show |
55 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(52): Show |
intron_variant | MODIFIER | c.802+109C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44338426 | |||||||
| chr15:44338487 | A | G | 1 | a0001c0001t0001g0002 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.802+170A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44338487 | |||||||
| chr15:44338653 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.802+336A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44338653 | |||||||
| chr15:44339267 | T | C | 1 | a0001c0001t0005g0119 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.802+950T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44339267 | |||||||
| chr15:44339408 | G | A | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.802+1091G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44339408 | |||||||
| chr15:44339473 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.802+1156G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44339473 | |||||||
| chr15:44339557 | C | T | 1 | a0002c0005t0003g0117 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.802+1240C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44339557 | |||||||
| chr15:44339717 | T | C | 41 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(38): Show |
41 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.802+1400T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44339717 | |||||||
| chr15:44339748 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.802+1431C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44339748 | |||||||
| chr15:44340200 | C | CCTCCCAC others(6): Show |
41 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(38): Show |
41 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.802+1889_802+1890i others(15): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44340200 | ||||||
| chr15:44340204 | C | A | 1 | a0001c0001t0001g0048 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.802+1887C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44340204 | |||||||
| chr15:44340243 | G | A | 39 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(36): Show |
39 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.802+1926G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44340243 | |||||||
| chr15:44340254 | T | G | 1 | a0001c0002t0004g0103 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.802+1937T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44340254 | |||||||
| chr15:44340256 | G | T | 4 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(1): Show |
4 | HG02970.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+1939G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44340256 | |||||||
| chr15:44340449 | G | A | 5 | a0001c0001t0001g0123 a0001c0001t0005g0119 a0001c0001t0005g0120 others(2): Show |
5 | HG02965.hp2 HG03209.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.802+2132G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44340449 | |||||||
| chr15:44340628 | A | T | 1 | a0001c0001t0002g0130 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.802+2311A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44340628 | |||||||
| chr15:44340715 | T | C | 1 | a0001c0003t0001g0147 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.802+2398T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44340715 | |||||||
| chr15:44340873 | G | A | 18 | a0001c0001t0001g0007 a0001c0001t0001g0087 a0001c0001t0001g0091 others(15): Show |
18 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.802+2556G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44340873 | |||||||
| chr15:44340970 | G | A | 39 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(36): Show |
39 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.802+2653G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44340970 | |||||||
| chr15:44341079 | CT | C | 16 | a0001c0001t0001g0087 a0001c0001t0001g0089 a0001c0001t0001g0091 others(13): Show |
16 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.802+2781delT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44341079 | ||||||
| chr15:44341084 | T | C | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.802+2767T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44341084 | |||||||
| chr15:44341086 | T | C | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.802+2769T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44341086 | |||||||
| chr15:44341318 | G | A | 17 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.802+3001G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44341318 | |||||||
| chr15:44341322 | C | T | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.802+3005C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44341322 | |||||||
| chr15:44341372 | G | A | 1 | a0001c0002t0004g0118 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.802+3055G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44341372 | |||||||
| chr15:44341565 | G | T | 8 | a0001c0002t0001g0090 a0001c0002t0003g0114 a0001c0002t0004g0086 others(5): Show |
8 | HG01981.hp2 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.802+3248G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44341565 | |||||||
| chr15:44341691 | A | AT | 15 | a0001c0001t0001g0002 a0001c0001t0001g0088 a0001c0001t0003g0051 others(12): Show |
15 | HG00597.hp1 HG00621.hp1 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.802+3397dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44341691 | ||||||
| chr15:44341691 | AT | A | 7 | a0001c0001t0001g0036 a0001c0001t0001g0066 a0001c0001t0001g0089 others(4): Show |
7 | HG01074.hp1 HG02895.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.802+3397delT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44341691 | ||||||
| chr15:44341789 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.802+3472C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44341789 | |||||||
| chr15:44342059 | T | A | 4 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0007g0121 others(1): Show |
4 | HG02965.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+3742T>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44342059 | |||||||
| chr15:44342128 | A | C | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.802+3811A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44342128 | |||||||
| chr15:44342242 | G | GT | 14 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0133 others(11): Show |
14 | HG02040.hp1 HG02155.hp2 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.802+3936dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44342242 | ||||||
| chr15:44342242 | G | GTT | 7 | a0001c0001t0002g0124 a0001c0001t0002g0127 a0001c0001t0002g0132 others(4): Show |
7 | HG01496.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.802+3935_802+3936d others(4): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44342242 | ||||||
| chr15:44342282 | T | G | 4 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0009g0149 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.802+3965T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44342282 | |||||||
| chr15:44342342 | G | A | 17 | a0001c0001t0002g0124 a0001c0001t0002g0127 a0001c0001t0002g0130 others(14): Show |
17 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(14): Show |
intron_variant | MODIFIER | c.802+4025G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44342342 | |||||||
| chr15:44342406 | G | A | 1 | a0002c0005t0001g0112 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.802+4089G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44342406 | |||||||
| chr15:44342735 | C | T | 1 | a0002c0005t0003g0117 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.802+4418C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44342735 | |||||||
| chr15:44342752 | A | G | 8 | a0001c0002t0001g0090 a0001c0002t0003g0114 a0001c0002t0004g0086 others(5): Show |
8 | HG01981.hp2 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.802+4435A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44342752 | |||||||
| chr15:44342919 | A | C | 41 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(38): Show |
41 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.802+4602A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44342919 | |||||||
| chr15:44343316 | G | GA | 11 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0058 others(8): Show |
11 | HG01891.hp2 HG02109.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.802+5014dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44343316 | ||||||
| chr15:44343483 | G | T | 1 | a0001c0001t0001g0060 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.802+5166G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44343483 | |||||||
| chr15:44343531 | A | C | 11 | a0001c0002t0001g0090 a0001c0002t0003g0114 a0001c0002t0004g0086 others(8): Show |
11 | HG01981.hp2 HG02258.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.802+5214A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44343531 | |||||||
| chr15:44343778 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.802+5461C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44343778 | |||||||
| chr15:44343779 | G | A | 39 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(36): Show |
39 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.802+5462G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44343779 | |||||||
| chr15:44343822 | T | C | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.802+5505T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44343822 | |||||||
| chr15:44343986 | C | T | 15 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(12): Show |
15 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.802+5669C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44343986 | |||||||
| chr15:44344258 | C | CA | 9 | a0001c0001t0001g0082 a0001c0001t0001g0088 a0001c0001t0001g0089 others(6): Show |
9 | HG01981.hp2 HG02055.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.802+5956dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44344258 | ||||||
| chr15:44344258 | CA | C | 40 | a0001c0001t0001g0042 a0001c0001t0001g0087 a0001c0001t0001g0091 others(37): Show |
40 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.802+5956delA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44344258 | ||||||
| chr15:44344287 | G | GTA | 8 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0050 others(5): Show |
8 | HG00140.hp1 HG00323.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.802+5993_802+5994d others(4): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44344287 | ||||||
| chr15:44344287 | G | GTATA | 19 | a0001c0001t0001g0024 a0001c0001t0001g0028 a0001c0001t0002g0124 others(16): Show |
19 | HG00140.hp2 HG01496.hp2 HG02040.hp1 others(16): Show |
intron_variant | MODIFIER | c.802+5991_802+5994d others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44344287 | ||||||
| chr15:44344287 | G | GTATATA | 10 | a0001c0001t0001g0087 a0001c0001t0001g0092 a0001c0001t0001g0093 others(7): Show |
10 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(7): Show |
intron_variant | MODIFIER | c.802+5989_802+5994d others(8): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44344287 | ||||||
| chr15:44344287 | G | GTATATAT others(1): Show |
3 | a0001c0001t0001g0091 a0001c0001t0001g0097 a0001c0001t0001g0111 |
3 | HG03927.hp1 NA19030.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.802+5987_802+5994d others(10): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44344287 | ||||||
| chr15:44344287 | G | GTATATAT others(3): Show |
2 | a0001c0001t0001g0100 a0001c0001t0001g0116 |
2 | HG02602.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.802+5985_802+5994d others(12): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44344287 | ||||||
| chr15:44344287 | G | GTATATAT others(5): Show |
1 | a0001c0001t0001g0115 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.802+5983_802+5994d others(14): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44344287 | ||||||
| chr15:44344287 | GTATA | G | 25 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0095 others(22): Show |
25 | HG00735.hp2 HG01891.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.802+5991_802+5994d others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44344287 | ||||||
| chr15:44344309 | A | T | 14 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(11): Show |
14 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(11): Show |
intron_variant | MODIFIER | c.802+5992A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44344309 | |||||||
| chr15:44344321 | T | C | 41 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(38): Show |
41 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.802+6004T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44344321 | |||||||
| chr15:44344368 | G | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0096 |
2 | NA19007.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.802+6051G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44344368 | |||||||
| chr15:44344604 | T | C | 39 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(36): Show |
39 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.802+6287T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44344604 | |||||||
| chr15:44344666 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.802+6349C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44344666 | |||||||
| chr15:44344726 | G | A | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.802+6409G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44344726 | |||||||
| chr15:44344776 | A | T | 6 | a0001c0001t0001g0018 a0001c0001t0001g0053 a0001c0001t0001g0055 others(3): Show |
6 | HG00280.hp2 HG00642.hp2 HG00738.hp1 others(3): Show |
intron_variant | MODIFIER | c.802+6459A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44344776 | |||||||
| chr15:44344780 | A | AT | 18 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0123 others(15): Show |
18 | HG01891.hp1 HG02109.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.802+6478dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44344780 | ||||||
| chr15:44344780 | A | ATT | 11 | a0001c0001t0002g0132 a0001c0001t0002g0136 a0001c0001t0002g0137 others(8): Show |
11 | HG01496.hp2 HG01981.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.802+6477_802+6478d others(4): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44344780 | ||||||
| chr15:44344780 | A | ATTT | 10 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0133 others(7): Show |
10 | HG02040.hp1 HG02155.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.802+6476_802+6478d others(5): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44344780 | ||||||
| chr15:44344781 | T | A | 1 | a0001c0001t0001g0028 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.802+6464T>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44344781 | |||||||
| chr15:44344801 | G | A | 17 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.802+6484G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44344801 | |||||||
| chr15:44345276 | AT | A | 53 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(50): Show |
53 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.802+6973delT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44345276 | ||||||
| chr15:44345409 | C | T | 17 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.802+7092C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44345409 | |||||||
| chr15:44345645 | G | A | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.802+7328G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44345645 | |||||||
| chr15:44345854 | A | C | 1 | a0001c0002t0004g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.802+7537A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44345854 | |||||||
| chr15:44345898 | T | TTG | 17 | a0001c0001t0002g0124 a0001c0001t0002g0127 a0001c0001t0002g0130 others(14): Show |
17 | HG02040.hp1 HG02155.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.802+7604_802+7605d others(4): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44345898 | ||||||
| chr15:44345898 | T | TTGTG | 18 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(15): Show |
18 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(15): Show |
intron_variant | MODIFIER | c.802+7602_802+7605d others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44345898 | ||||||
| chr15:44346025 | C | A | 1 | a0001c0001t0001g0062 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.802+7708C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44346025 | |||||||
| chr15:44346049 | C | G | 4 | a0001c0001t0001g0037 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG01255.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+7732C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44346049 | |||||||
| chr15:44346168 | T | G | 1 | a0001c0001t0001g0015 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.802+7851T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44346168 | |||||||
| chr15:44346313 | GA | G | 6 | a0001c0001t0001g0066 a0001c0001t0001g0069 a0001c0001t0001g0071 others(3): Show |
6 | HG00423.hp2 HG01496.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.802+8007delA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44346313 | ||||||
| chr15:44346793 | T | C | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.802+8476T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44346793 | |||||||
| chr15:44346927 | C | T | 1 | a0001c0003t0009g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.802+8610C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44346927 | |||||||
| chr15:44347131 | AAG | A | 41 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(38): Show |
41 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.802+8835_802+8836d others(4): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44347131 | ||||||
| chr15:44347231 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.802+8914A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44347231 | |||||||
| chr15:44347322 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.802+9005G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44347322 | |||||||
| chr15:44347337 | T | A | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.802+9020T>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44347337 | |||||||
| chr15:44347514 | C | T | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.802+9197C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44347514 | |||||||
| chr15:44347576 | C | T | 1 | a0001c0001t0001g0007 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.802+9259C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44347576 | |||||||
| chr15:44347691 | C | T | 4 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0007g0121 others(1): Show |
4 | HG02965.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.802+9374C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44347691 | |||||||
| chr15:44347692 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.802+9375G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44347692 | |||||||
| chr15:44347815 | G | A | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.802+9498G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44347815 | |||||||
| chr15:44347910 | C | G | 1 | a0001c0003t0009g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.802+9593C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44347910 | |||||||
| chr15:44347911 | C | T | 3 | a0001c0002t0004g0106 a0001c0002t0004g0107 a0001c0002t0004g0108 |
3 | HG02630.hp1 HG03471.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.802+9594C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44347911 | |||||||
| chr15:44347963 | G | A | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.802+9646G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44347963 | |||||||
| chr15:44348196 | T | C | 64 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(61): Show |
64 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.802+9879T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44348196 | |||||||
| chr15:44348404 | CCTCCCCA others(15): Show |
C | 17 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.802+10099_802+1012 others(26): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44348404 | ||||||
| chr15:44348566 | C | T | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.802+10249C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44348566 | |||||||
| chr15:44348668 | T | C | 64 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(61): Show |
64 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.802+10351T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44348668 | |||||||
| chr15:44348795 | A | G | 64 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(61): Show |
64 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.802+10478A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44348795 | |||||||
| chr15:44349052 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0013g0061 |
2 | HG00280.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.802+10735G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44349052 | |||||||
| chr15:44349215 | C | T | 1 | a0001c0002t0004g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.802+10898C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44349215 | |||||||
| chr15:44349228 | C | T | 9 | a0001c0002t0004g0086 a0001c0002t0004g0103 a0001c0002t0004g0104 others(6): Show |
9 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.802+10911C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44349228 | |||||||
| chr15:44349259 | C | CA | 20 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0030 others(17): Show |
20 | HG00621.hp1 HG00621.hp2 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.802+10959dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44349259 | ||||||
| chr15:44349259 | CA | C | 12 | a0001c0001t0001g0047 a0001c0001t0001g0123 a0001c0001t0002g0124 others(9): Show |
12 | HG01496.hp2 HG02257.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.802+10959delA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44349259 | ||||||
| chr15:44349259 | CAA | C | 10 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0133 others(7): Show |
10 | HG02040.hp1 HG02155.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.802+10958_802+1095 others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44349259 | ||||||
| chr15:44349314 | G | A | 18 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0127 others(15): Show |
18 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.802+10997G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44349314 | |||||||
| chr15:44349326 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.802+11009T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44349326 | |||||||
| chr15:44349579 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.802+11262T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44349579 | |||||||
| chr15:44349627 | A | G | 2 | a0001c0003t0001g0147 a0001c0003t0001g0148 |
2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.802+11310A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44349627 | |||||||
| chr15:44349661 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.802+11344C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44349661 | |||||||
| chr15:44349766 | C | A | 4 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0009g0149 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.802+11449C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44349766 | |||||||
| chr15:44350037 | A | G | 1 | a0001c0001t0003g0051 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.802+11720A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44350037 | |||||||
| chr15:44350183 | G | C | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.802+11866G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44350183 | |||||||
| chr15:44350337 | A | G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0069 |
2 | HG00423.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.802+12020A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44350337 | |||||||
| chr15:44350628 | G | C | 36 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(33): Show |
36 | HG01496.hp2 HG01891.hp1 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.802+12311G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44350628 | |||||||
| chr15:44351404 | G | A | 11 | a0001c0002t0001g0090 a0001c0002t0003g0114 a0001c0002t0004g0086 others(8): Show |
11 | HG01981.hp2 HG02258.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.802+13087G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44351404 | |||||||
| chr15:44351427 | A | G | 1 | a0001c0001t0001g0097 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.802+13110A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44351427 | |||||||
| chr15:44351508 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.802+13191C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44351508 | |||||||
| chr15:44351536 | C | T | 2 | a0001c0003t0001g0147 a0001c0003t0001g0148 |
2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.802+13219C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44351536 | |||||||
| chr15:44351576 | C | CA | 35 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0018 others(32): Show |
35 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(32): Show |
intron_variant | MODIFIER | c.802+13281dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44351576 | ||||||
| chr15:44351576 | C | CAA | 16 | a0001c0001t0001g0026 a0001c0001t0001g0144 a0001c0001t0001g0145 others(13): Show |
16 | HG00738.hp1 HG02040.hp1 HG02155.hp2 others(13): Show |
intron_variant | MODIFIER | c.802+13280_802+1328 others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44351576 | ||||||
| chr15:44351576 | CA | C | 15 | a0001c0001t0001g0085 a0001c0001t0001g0110 a0001c0001t0001g0111 others(12): Show |
15 | HG01981.hp2 HG02258.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.802+13281delA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44351576 | ||||||
| chr15:44351609 | C | CAAAT | 36 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(33): Show |
36 | HG01496.hp2 HG01891.hp1 HG01891.hp2 others(33): Show |
intron_variant | MODIFIER | c.802+13295_802+1329 others(8): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44351609 | ||||||
| chr15:44351693 | A | G | 11 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(8): Show |
11 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.802+13376A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44351693 | |||||||
| chr15:44351997 | T | G | 18 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0127 others(15): Show |
18 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.802+13680T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44351997 | |||||||
| chr15:44352178 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.802+13861G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44352178 | |||||||
| chr15:44352182 | C | T | 1 | a0002c0005t0001g0112 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.802+13865C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44352182 | |||||||
| chr15:44352405 | A | G | 2 | a0001c0003t0001g0147 a0001c0003t0001g0148 |
2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.802+14088A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44352405 | |||||||
| chr15:44352677 | C | T | 17 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.802+14360C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44352677 | |||||||
| chr15:44352704 | G | A | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.802+14387G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44352704 | |||||||
| chr15:44352722 | A | G | 3 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0007g0121 |
3 | HG02965.hp2 HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.802+14405A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44352722 | |||||||
| chr15:44352906 | C | CA | 6 | a0001c0001t0001g0099 a0001c0002t0004g0086 a0001c0002t0004g0103 others(3): Show |
6 | HG02109.hp1 HG02965.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.802+14602dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44352906 | ||||||
| chr15:44352915 | A | AG | 7 | a0001c0002t0001g0090 a0001c0002t0003g0114 a0001c0002t0004g0104 others(4): Show |
7 | HG01981.hp2 HG02258.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.802+14598_802+1459 others(5): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44352915 | |||||||
| chr15:44353028 | C | G | 2 | a0001c0001t0001g0050 a0001c0001t0003g0049 |
2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.802+14711C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44353028 | |||||||
| chr15:44353178 | A | G | 2 | a0001c0001t0001g0050 a0001c0001t0003g0049 |
2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.802+14861A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44353178 | |||||||
| chr15:44353186 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.802+14869A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44353186 | |||||||
| chr15:44354089 | A | T | 1 | a0001c0001t0001g0037 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.802+15772A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44354089 | |||||||
| chr15:44354245 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.802+15928A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44354245 | |||||||
| chr15:44354295 | G | A | 1 | a0001c0001t0003g0049 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.802+15978G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44354295 | |||||||
| chr15:44354396 | A | C | 19 | a0001c0001t0001g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(16): Show |
19 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.802+16079A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44354396 | |||||||
| chr15:44354519 | TATA | T | 42 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(39): Show |
42 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.802+16204_802+1620 others(7): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44354519 | ||||||
| chr15:44354555 | G | A | 5 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0041 others(2): Show |
5 | HG00738.hp2 HG01069.hp1 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.802+16238G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44354555 | |||||||
| chr15:44354693 | T | C | 11 | a0001c0002t0001g0090 a0001c0002t0003g0114 a0001c0002t0004g0086 others(8): Show |
11 | HG01981.hp2 HG02258.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.802+16376T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44354693 | |||||||
| chr15:44354823 | T | G | 7 | a0001c0002t0001g0090 a0001c0002t0003g0114 a0001c0002t0004g0104 others(4): Show |
7 | HG01981.hp2 HG02258.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.802+16506T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44354823 | |||||||
| chr15:44355169 | AGATCATC others(13): Show |
A | 1 | a0001c0001t0001g0123 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.802+16854_802+1687 others(24): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44355169 | ||||||
| chr15:44355207 | C | A | 53 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(50): Show |
53 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.802+16890C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44355207 | |||||||
| chr15:44355317 | C | T | 9 | a0001c0002t0004g0086 a0001c0002t0004g0103 a0001c0002t0004g0104 others(6): Show |
9 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.802+17000C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44355317 | |||||||
| chr15:44355357 | G | A | 1 | a0001c0001t0001g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.802+17040G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44355357 | |||||||
| chr15:44355650 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.802+17333C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44355650 | |||||||
| chr15:44355658 | T | G | 1 | a0001c0001t0001g0098 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.802+17341T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44355658 | |||||||
| chr15:44355846 | G | T | 1 | a0001c0001t0001g0007 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.802+17529G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44355846 | |||||||
| chr15:44356540 | C | T | 41 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(38): Show |
41 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.802+18223C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44356540 | |||||||
| chr15:44356617 | C | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0042 |
2 | HG00738.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.802+18300C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44356617 | |||||||
| chr15:44356859 | T | C | 8 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0111 others(5): Show |
8 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.802+18542T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44356859 | |||||||
| chr15:44356865 | T | C | 41 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(38): Show |
41 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.802+18548T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44356865 | |||||||
| chr15:44357173 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.802+18856G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44357173 | |||||||
| chr15:44357273 | A | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0033 |
2 | NA18948.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.802+18956A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44357273 | |||||||
| chr15:44357280 | G | A | 41 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(38): Show |
41 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.802+18963G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44357280 | |||||||
| chr15:44357797 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.802+19480A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44357797 | |||||||
| chr15:44358042 | A | T | 1 | a0001c0001t0002g0133 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.802+19725A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44358042 | |||||||
| chr15:44358226 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG00642.hp2 HG01069.hp2 |
intron_variant | MODIFIER | c.802+19909C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44358226 | |||||||
| chr15:44358380 | A | G | 1 | a0001c0002t0004g0106 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.802+20063A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44358380 | |||||||
| chr15:44358417 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.802+20100T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44358417 | |||||||
| chr15:44358575 | T | G | 4 | a0001c0001t0001g0087 a0001c0001t0001g0093 a0001c0001t0001g0100 others(1): Show |
4 | HG00408.hp1 HG00597.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.802+20258T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44358575 | |||||||
| chr15:44358759 | A | G | 53 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(50): Show |
53 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.802+20442A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44358759 | |||||||
| chr15:44358952 | C | T | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.802+20635C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44358952 | |||||||
| chr15:44359018 | G | A | 3 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0009g0149 |
3 | HG01891.hp1 HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.803-20672G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44359018 | |||||||
| chr15:44359054 | G | A | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.803-20636G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44359054 | |||||||
| chr15:44359082 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.803-20608G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44359082 | |||||||
| chr15:44359107 | G | A | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.803-20583G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44359107 | |||||||
| chr15:44359111 | A | G | 24 | a0001c0001t0001g0099 a0001c0001t0001g0123 a0001c0001t0002g0124 others(21): Show |
24 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(21): Show |
intron_variant | MODIFIER | c.803-20579A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44359111 | |||||||
| chr15:44359127 | G | A | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.803-20563G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44359127 | |||||||
| chr15:44359145 | G | T | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.803-20545G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44359145 | |||||||
| chr15:44359369 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0123 |
2 | NA18906.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.803-20321C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44359369 | |||||||
| chr15:44359574 | C | T | 5 | a0001c0001t0001g0123 a0001c0001t0005g0119 a0001c0001t0005g0120 others(2): Show |
5 | HG02965.hp2 HG03209.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.803-20116C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44359574 | |||||||
| chr15:44359583 | G | A | 1 | a0001c0001t0003g0009 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.803-20107G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44359583 | |||||||
| chr15:44359589 | AAAAC | A | 25 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(22): Show |
25 | HG01496.hp2 HG02040.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.803-20078_803-2007 others(8): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44359589 | ||||||
| chr15:44359625 | T | C | 1 | a0001c0001t0001g0028 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.803-20065T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44359625 | |||||||
| chr15:44359661 | G | A | 1 | a0001c0001t0001g0002 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.803-20029G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44359661 | |||||||
| chr15:44359677 | A | G | 1 | a0001c0001t0001g0002 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.803-20013A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44359677 | |||||||
| chr15:44359702 | T | C | 3 | a0001c0001t0001g0002 a0002c0005t0001g0112 a0002c0005t0003g0117 |
3 | HG00621.hp1 HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.803-19988T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44359702 | |||||||
| chr15:44359715 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.803-19975C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44359715 | |||||||
| chr15:44359766 | T | C | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.803-19924T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44359766 | |||||||
| chr15:44359782 | A | C | 1 | a0001c0001t0001g0101 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.803-19908A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44359782 | |||||||
| chr15:44359829 | G | A | 18 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0127 others(15): Show |
18 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.803-19861G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44359829 | |||||||
| chr15:44360086 | C | T | 15 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(12): Show |
15 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.803-19604C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360086 | |||||||
| chr15:44360120 | A | G | 2 | a0001c0003t0001g0147 a0001c0003t0001g0148 |
2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.803-19570A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360120 | |||||||
| chr15:44360354 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.803-19336A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360354 | |||||||
| chr15:44360627 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19063A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360627 | |||||||
| chr15:44360632 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19058T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360632 | |||||||
| chr15:44360636 | C | G | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19054C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360636 | |||||||
| chr15:44360637 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19053A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360637 | |||||||
| chr15:44360639 | A | C | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19051A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360639 | |||||||
| chr15:44360643 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19047A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360643 | |||||||
| chr15:44360645 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.803-19045G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360645 | |||||||
| chr15:44360645 | G | C | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19045G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360645 | |||||||
| chr15:44360646 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19044A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360646 | |||||||
| chr15:44360649 | C | G | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19041C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360649 | |||||||
| chr15:44360650 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19040A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360650 | |||||||
| chr15:44360652 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19038A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360652 | |||||||
| chr15:44360658 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19032A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360658 | |||||||
| chr15:44360659 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19031A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360659 | |||||||
| chr15:44360660 | C | A | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19030C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360660 | |||||||
| chr15:44360668 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19022C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360668 | |||||||
| chr15:44360669 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19021C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360669 | |||||||
| chr15:44360670 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19020C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360670 | |||||||
| chr15:44360671 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19019A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360671 | |||||||
| chr15:44360673 | G | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19017G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360673 | |||||||
| chr15:44360674 | A | C | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19016A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360674 | |||||||
| chr15:44360677 | T | A | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19013T>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360677 | |||||||
| chr15:44360678 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19012G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360678 | |||||||
| chr15:44360681 | C | A | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19009C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360681 | |||||||
| chr15:44360685 | G | C | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19005G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360685 | |||||||
| chr15:44360686 | C | A | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19004C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360686 | |||||||
| chr15:44360687 | T | G | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19003T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360687 | |||||||
| chr15:44360688 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19002C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360688 | |||||||
| chr15:44360690 | G | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-19000G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360690 | |||||||
| chr15:44360691 | C | G | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18999C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360691 | |||||||
| chr15:44360692 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18998A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360692 | |||||||
| chr15:44360693 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18997C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360693 | |||||||
| chr15:44360694 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18996C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360694 | |||||||
| chr15:44360697 | G | A | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18993G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360697 | |||||||
| chr15:44360700 | G | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18990G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360700 | |||||||
| chr15:44360702 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18988C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360702 | |||||||
| chr15:44360703 | C | G | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18987C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360703 | |||||||
| chr15:44360704 | T | G | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18986T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360704 | |||||||
| chr15:44360705 | A | C | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18985A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360705 | |||||||
| chr15:44360706 | A | C | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18984A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360706 | |||||||
| chr15:44360707 | T | A | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18983T>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360707 | |||||||
| chr15:44360711 | C | A | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18979C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360711 | |||||||
| chr15:44360712 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18978A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360712 | |||||||
| chr15:44360714 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18976C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360714 | |||||||
| chr15:44360718 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18972A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360718 | |||||||
| chr15:44360724 | C | A | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18966C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360724 | |||||||
| chr15:44360725 | T | C | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18965T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360725 | |||||||
| chr15:44360726 | C | A | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18964C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360726 | |||||||
| chr15:44360729 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18961C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360729 | |||||||
| chr15:44360731 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18959C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360731 | |||||||
| chr15:44360733 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18957A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360733 | |||||||
| chr15:44360734 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18956A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360734 | |||||||
| chr15:44360735 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18955A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360735 | |||||||
| chr15:44360737 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18953C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360737 | |||||||
| chr15:44360738 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18952A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360738 | |||||||
| chr15:44360739 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18951A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360739 | |||||||
| chr15:44360740 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18950C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360740 | |||||||
| chr15:44360741 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18949A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360741 | |||||||
| chr15:44360742 | G | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18948G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360742 | |||||||
| chr15:44360743 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18947A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360743 | |||||||
| chr15:44360744 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18946A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360744 | |||||||
| chr15:44360746 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18944A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360746 | |||||||
| chr15:44360748 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18942A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360748 | |||||||
| chr15:44360749 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18941C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360749 | |||||||
| chr15:44360750 | A | AT | 18 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0127 others(15): Show |
18 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.803-18933dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44360750 | ||||||
| chr15:44360750 | A | T | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.803-18940A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360750 | |||||||
| chr15:44360922 | T | A | 1 | a0001c0001t0001g0036 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.803-18768T>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44360922 | |||||||
| chr15:44361273 | G | T | 1 | a0001c0001t0001g0080 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.803-18417G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44361273 | |||||||
| chr15:44361294 | C | T | 2 | a0001c0001t0002g0132 a0001c0001t0002g0135 |
2 | HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.803-18396C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44361294 | |||||||
| chr15:44361372 | C | G | 1 | a0001c0002t0004g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.803-18318C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44361372 | |||||||
| chr15:44361623 | A | G | 11 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(8): Show |
11 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.803-18067A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44361623 | |||||||
| chr15:44361842 | G | A | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.803-17848G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44361842 | |||||||
| chr15:44361892 | C | T | 17 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.803-17798C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44361892 | |||||||
| chr15:44361946 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.803-17744G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44361946 | |||||||
| chr15:44361949 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.803-17741A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44361949 | |||||||
| chr15:44361957 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.803-17733G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44361957 | |||||||
| chr15:44362027 | A | G | 11 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(8): Show |
11 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.803-17663A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44362027 | |||||||
| chr15:44362158 | A | G | 2 | a0001c0002t0001g0090 a0001c0002t0003g0114 |
2 | HG01981.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.803-17532A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44362158 | |||||||
| chr15:44362191 | C | T | 1 | a0001c0003t0009g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.803-17499C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44362191 | |||||||
| chr15:44362378 | A | G | 1 | a0001c0003t0009g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.803-17312A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44362378 | |||||||
| chr15:44362482 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.803-17208C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44362482 | |||||||
| chr15:44362531 | T | G | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02572.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.803-17159T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44362531 | |||||||
| chr15:44362552 | G | C | 1 | a0001c0001t0001g0123 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.803-17138G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44362552 | |||||||
| chr15:44362577 | T | C | 2 | a0001c0003t0001g0147 a0001c0003t0001g0148 |
2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.803-17113T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44362577 | |||||||
| chr15:44362783 | C | T | 11 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(8): Show |
11 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.803-16907C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44362783 | |||||||
| chr15:44362831 | A | G | 53 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(50): Show |
53 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.803-16859A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44362831 | |||||||
| chr15:44362832 | T | C | 1 | a0001c0001t0005g0119 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.803-16858T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44362832 | |||||||
| chr15:44362888 | G | A | 4 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0007g0121 others(1): Show |
4 | HG02965.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-16802G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44362888 | |||||||
| chr15:44362975 | A | G | 11 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(8): Show |
11 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.803-16715A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44362975 | |||||||
| chr15:44363060 | T | G | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.803-16630T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44363060 | |||||||
| chr15:44363126 | G | A | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.803-16564G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44363126 | |||||||
| chr15:44363201 | G | A | 1 | a0002c0005t0001g0112 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.803-16489G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44363201 | |||||||
| chr15:44363379 | C | T | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.803-16311C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44363379 | |||||||
| chr15:44363380 | G | A | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.803-16310G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44363380 | |||||||
| chr15:44363412 | C | A | 2 | a0001c0001t0001g0043 a0001c0001t0001g0044 |
2 | HG02572.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.803-16278C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44363412 | |||||||
| chr15:44363455 | A | C | 1 | a0001c0001t0003g0064 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.803-16235A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44363455 | |||||||
| chr15:44363620 | G | A | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.803-16070G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44363620 | |||||||
| chr15:44363709 | C | G | 5 | a0001c0002t0004g0104 a0001c0002t0004g0105 a0001c0002t0004g0106 others(2): Show |
5 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.803-15981C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44363709 | |||||||
| chr15:44363743 | C | T | 17 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.803-15947C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44363743 | |||||||
| chr15:44363756 | C | A | 17 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.803-15934C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44363756 | |||||||
| chr15:44363757 | A | G | 17 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.803-15933A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44363757 | |||||||
| chr15:44363761 | C | T | 17 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.803-15929C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44363761 | |||||||
| chr15:44363805 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.803-15885A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44363805 | |||||||
| chr15:44363822 | A | C | 1 | a0001c0001t0007g0121 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.803-15868A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44363822 | |||||||
| chr15:44363870 | A | G | 9 | a0001c0002t0004g0086 a0001c0002t0004g0103 a0001c0002t0004g0104 others(6): Show |
9 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.803-15820A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44363870 | |||||||
| chr15:44364057 | C | G | 11 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(8): Show |
11 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.803-15633C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44364057 | |||||||
| chr15:44364073 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.803-15617T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44364073 | |||||||
| chr15:44364074 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.803-15616G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44364074 | |||||||
| chr15:44364114 | C | A | 1 | a0001c0003t0009g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.803-15576C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44364114 | |||||||
| chr15:44364392 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.803-15298C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44364392 | |||||||
| chr15:44364428 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.803-15262T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44364428 | |||||||
| chr15:44364495 | C | T | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.803-15195C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44364495 | |||||||
| chr15:44365142 | T | C | 40 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(37): Show |
40 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.803-14548T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44365142 | |||||||
| chr15:44365393 | G | T | 1 | a0001c0001t0001g0091 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.803-14297G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44365393 | |||||||
| chr15:44365449 | C | T | 39 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(36): Show |
39 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.803-14241C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44365449 | |||||||
| chr15:44365460 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0003g0049 |
2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.803-14230G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44365460 | |||||||
| chr15:44365505 | T | G | 3 | a0001c0002t0004g0103 a0001c0002t0004g0118 a0001c0002t0006g0109 |
3 | HG03516.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.803-14185T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44365505 | |||||||
| chr15:44365557 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.803-14133A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44365557 | |||||||
| chr15:44366166 | G | A | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.803-13524G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44366166 | |||||||
| chr15:44366260 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.803-13430G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44366260 | |||||||
| chr15:44366296 | C | CA | 10 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0053 others(7): Show |
10 | HG00423.hp2 HG01981.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.803-13376dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44366296 | ||||||
| chr15:44366296 | C | CAAAAAAA others(4): Show |
1 | a0002c0005t0003g0117 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.803-13386_803-1337 others(15): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44366296 | ||||||
| chr15:44366296 | C | CAAAAAAA others(5): Show |
1 | a0002c0005t0001g0112 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.803-13387_803-1337 others(16): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44366296 | ||||||
| chr15:44366300 | A | AAAACAAA others(2): Show |
23 | a0001c0001t0001g0111 a0001c0001t0001g0123 a0001c0001t0002g0124 others(20): Show |
23 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(20): Show |
intron_variant | MODIFIER | c.803-13387_803-1338 others(13): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44366300 | ||||||
| chr15:44366305 | A | C | 24 | a0001c0001t0001g0111 a0001c0001t0001g0123 a0001c0001t0002g0124 others(21): Show |
24 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(21): Show |
intron_variant | MODIFIER | c.803-13385A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44366305 | |||||||
| chr15:44366310 | A | AAAAACAA others(3): Show |
1 | a0001c0001t0001g0097 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.803-13376_803-1336 others(14): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44366310 | ||||||
| chr15:44366310 | A | AAAACAAA others(2): Show |
14 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0093 others(11): Show |
14 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.803-13377_803-1337 others(13): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44366310 | ||||||
| chr15:44366310 | A | C | 31 | a0001c0001t0001g0058 a0001c0001t0001g0092 a0001c0001t0001g0111 others(28): Show |
31 | HG00673.hp1 HG01496.hp2 HG02040.hp1 others(28): Show |
intron_variant | MODIFIER | c.803-13380A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44366310 | |||||||
| chr15:44366415 | G | A | 17 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.803-13275G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44366415 | |||||||
| chr15:44366421 | C | T | 1 | a0001c0001t0008g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.803-13269C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44366421 | |||||||
| chr15:44366699 | G | A | 3 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0008g0045 |
3 | HG01255.hp2 HG02970.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.803-12991G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44366699 | |||||||
| chr15:44366735 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.803-12955G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44366735 | |||||||
| chr15:44366746 | G | A | 23 | a0001c0001t0001g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(20): Show |
23 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(20): Show |
intron_variant | MODIFIER | c.803-12944G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44366746 | |||||||
| chr15:44366929 | A | G | 19 | a0001c0001t0001g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(16): Show |
19 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.803-12761A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44366929 | |||||||
| chr15:44367009 | A | G | 4 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0009g0149 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.803-12681A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44367009 | |||||||
| chr15:44367374 | C | T | 1 | a0001c0002t0004g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.803-12316C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44367374 | |||||||
| chr15:44367789 | CA | C | 22 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(19): Show |
22 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.803-11885delA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44367789 | ||||||
| chr15:44367807 | A | G | 4 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0007g0121 others(1): Show |
4 | HG02965.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-11883A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44367807 | |||||||
| chr15:44367896 | G | T | 1 | a0001c0001t0001g0036 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.803-11794G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44367896 | |||||||
| chr15:44368231 | G | A | 1 | a0002c0005t0001g0112 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.803-11459G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44368231 | |||||||
| chr15:44368303 | A | AT | 23 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0025 others(20): Show |
23 | HG00423.hp1 HG00423.hp2 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.803-11367dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44368303 | ||||||
| chr15:44368303 | A | ATT | 11 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0097 others(8): Show |
11 | HG00408.hp1 HG02965.hp2 HG03209.hp1 others(8): Show |
intron_variant | MODIFIER | c.803-11368_803-1136 others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44368303 | ||||||
| chr15:44368303 | A | ATTT | 18 | a0001c0001t0001g0110 a0001c0001t0002g0124 a0001c0001t0002g0127 others(15): Show |
18 | HG01496.hp2 HG01891.hp2 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.803-11369_803-1136 others(7): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44368303 | ||||||
| chr15:44368327 | C | T | 62 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(59): Show |
62 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.803-11363C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44368327 | |||||||
| chr15:44368403 | C | T | 1 | a0001c0001t0001g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.803-11287C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44368403 | |||||||
| chr15:44368448 | A | G | 42 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(39): Show |
42 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.803-11242A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44368448 | |||||||
| chr15:44368486 | C | G | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.803-11204C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44368486 | |||||||
| chr15:44368610 | T | A | 1 | a0001c0001t0001g0002 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.803-11080T>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44368610 | |||||||
| chr15:44368716 | C | T | 4 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0007g0121 others(1): Show |
4 | HG02965.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-10974C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44368716 | |||||||
| chr15:44368732 | TATATAC | T | 2 | a0001c0001t0001g0017 a0001c0006t0001g0150 |
2 | HG03471.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.803-10940_803-1093 others(10): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44368732 | ||||||
| chr15:44368925 | A | G | 9 | a0001c0002t0004g0086 a0001c0002t0004g0103 a0001c0002t0004g0104 others(6): Show |
9 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.803-10765A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44368925 | |||||||
| chr15:44369065 | TATTATAT others(1): Show |
T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02572.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.803-10624_803-1061 others(12): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44369065 | |||||||
| chr15:44369065 | TATTATAT others(3): Show |
T | 1 | a0001c0001t0001g0113 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.803-10624_803-1061 others(14): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44369065 | |||||||
| chr15:44369066 | A | T | 5 | a0001c0001t0001g0111 a0001c0001t0001g0143 a0001c0001t0001g0144 others(2): Show |
5 | HG02970.hp1 HG03098.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.803-10624A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44369066 | |||||||
| chr15:44369066 | ATTATATA others(11): Show |
A | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.803-10623_803-1060 others(22): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44369066 | |||||||
| chr15:44369066 | ATTATATA others(25): Show |
A | 1 | a0001c0003t0009g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.803-10623_803-1059 others(36): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44369066 | |||||||
| chr15:44369067 | T | A | 2 | a0001c0001t0003g0063 a0001c0003t0001g0148 |
2 | HG00597.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.803-10623T>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44369067 | |||||||
| chr15:44369067 | T | TTA | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0023 others(12): Show |
15 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(12): Show |
intron_variant | MODIFIER | c.803-10574_803-1057 others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369067 | ||||||
| chr15:44369067 | T | TTATA | 9 | a0001c0001t0001g0033 a0001c0001t0001g0066 a0001c0001t0001g0074 others(6): Show |
9 | HG00673.hp2 HG02040.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.803-10576_803-1057 others(8): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369067 | ||||||
| chr15:44369067 | T | TTATATA | 8 | a0001c0001t0001g0054 a0001c0001t0001g0076 a0001c0001t0001g0144 others(5): Show |
8 | HG02056.hp1 HG02056.hp2 HG02155.hp2 others(5): Show |
intron_variant | MODIFIER | c.803-10578_803-1057 others(10): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369067 | ||||||
| chr15:44369067 | T | TTATATAT others(3): Show |
2 | a0001c0001t0001g0143 a0001c0001t0001g0145 |
2 | HG03098.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.803-10582_803-1057 others(14): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369067 | ||||||
| chr15:44369067 | T | TTTTATAT others(3): Show |
1 | a0001c0002t0004g0103 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.803-10622_803-1062 others(14): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369067 | ||||||
| chr15:44369067 | T | TTTTATAT others(5): Show |
1 | a0001c0001t0001g0078 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.803-10622_803-1062 others(16): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369067 | ||||||
| chr15:44369067 | TTA | T | 14 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0035 others(11): Show |
14 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(11): Show |
intron_variant | MODIFIER | c.803-10574_803-1057 others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369067 | ||||||
| chr15:44369067 | TTATA | T | 17 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0015 others(14): Show |
17 | HG01074.hp1 HG01255.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.803-10576_803-1057 others(8): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369067 | ||||||
| chr15:44369067 | TTATATA | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0012 others(6): Show |
9 | HG01981.hp2 HG02055.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.803-10578_803-1057 others(10): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369067 | ||||||
| chr15:44369067 | TTATATAT others(1): Show |
T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0029 others(4): Show |
7 | HG00642.hp1 HG00642.hp2 HG02040.hp2 others(4): Show |
intron_variant | MODIFIER | c.803-10580_803-1057 others(12): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369067 | ||||||
| chr15:44369067 | TTATATAT others(3): Show |
T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0123 |
2 | HG03098.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.803-10582_803-1057 others(14): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369067 | ||||||
| chr15:44369067 | TTATATAT others(5): Show |
T | 1 | a0001c0001t0001g0060 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.803-10584_803-1057 others(16): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369067 | ||||||
| chr15:44369067 | TTATATAT others(9): Show |
T | 1 | a0001c0001t0001g0075 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.803-10588_803-1057 others(20): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369067 | ||||||
| chr15:44369067 | TTATATAT others(11): Show |
T | 1 | a0002c0005t0003g0117 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.803-10590_803-1057 others(22): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369067 | ||||||
| chr15:44369067 | TTATATAT others(15): Show |
T | 1 | a0002c0005t0001g0112 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.803-10594_803-1057 others(26): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369067 | ||||||
| chr15:44369067 | TTATATAT others(19): Show |
T | 2 | a0001c0001t0001g0050 a0001c0001t0003g0049 |
2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.803-10598_803-1057 others(30): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369067 | ||||||
| chr15:44369067 | TTATATAT others(23): Show |
T | 2 | a0001c0001t0002g0132 a0001c0001t0012g0004 |
2 | HG02922.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.803-10602_803-1057 others(34): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369067 | ||||||
| chr15:44369067 | TTATATAT others(27): Show |
T | 1 | a0001c0001t0001g0007 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.803-10606_803-1057 others(38): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369067 | ||||||
| chr15:44369069 | A | T | 1 | a0001c0002t0006g0109 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.803-10621A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44369069 | |||||||
| chr15:44369071 | A | T | 1 | a0001c0002t0004g0108 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.803-10619A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44369071 | |||||||
| chr15:44369073 | A | ATATATAT others(45): Show |
1 | a0001c0001t0001g0096 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.803-10610_803-1060 others(56): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369073 | ||||||
| chr15:44369073 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.803-10617A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44369073 | |||||||
| chr15:44369073 | A | T | 4 | a0001c0002t0004g0104 a0001c0002t0004g0105 a0001c0002t0004g0106 others(1): Show |
4 | HG02258.hp1 HG02886.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.803-10617A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44369073 | |||||||
| chr15:44369075 | A | ATATATTA others(43): Show |
1 | a0001c0001t0001g0094 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.803-10610_803-1060 others(54): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369075 | ||||||
| chr15:44369075 | A | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02572.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.803-10615A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44369075 | |||||||
| chr15:44369077 | A | ATATTATA others(43): Show |
1 | a0001c0001t0001g0091 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.803-10610_803-1060 others(54): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369077 | ||||||
| chr15:44369077 | A | T | 1 | a0001c0001t0001g0113 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.803-10613A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44369077 | |||||||
| chr15:44369079 | A | ATTATATA others(41): Show |
2 | a0001c0001t0001g0102 a0001c0001t0001g0116 |
2 | HG02602.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.803-10610_803-1060 others(52): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369079 | ||||||
| chr15:44369079 | A | ATTATATA others(39): Show |
9 | a0001c0001t0001g0087 a0001c0001t0001g0092 a0001c0001t0001g0093 others(6): Show |
9 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.803-10610_803-1060 others(50): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369079 | ||||||
| chr15:44369079 | A | ATTATATA others(37): Show |
1 | a0001c0001t0001g0115 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.803-10610_803-1060 others(48): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369079 | ||||||
| chr15:44369103 | A | AATATG | 15 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(12): Show |
15 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.803-10587_803-1058 others(9): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44369103 | |||||||
| chr15:44369103 | A | G | 1 | a0001c0001t0001g0110 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.803-10587A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44369103 | |||||||
| chr15:44369120 | C | T | 15 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(12): Show |
15 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.803-10570C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44369120 | |||||||
| chr15:44369192 | GTA | G | 12 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(9): Show |
12 | HG02055.hp1 HG02258.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.803-10484_803-1048 others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369192 | ||||||
| chr15:44369204 | ATATGTG | A | 8 | a0001c0001t0001g0111 a0001c0001t0001g0143 a0001c0001t0001g0144 others(5): Show |
8 | HG01891.hp1 HG02109.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.803-10484_803-1047 others(10): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369204 | ||||||
| chr15:44369204 | ATATGTGT others(1): Show |
A | 39 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(36): Show |
39 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.803-10484_803-1047 others(12): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369204 | ||||||
| chr15:44369204 | ATATGTGT others(3): Show |
A | 1 | a0002c0005t0001g0112 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.803-10484_803-1047 others(14): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369204 | ||||||
| chr15:44369206 | A | ATG | 16 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0015 others(13): Show |
16 | HG00621.hp2 HG01074.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.803-10456_803-1045 others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369206 | ||||||
| chr15:44369206 | A | ATGTG | 2 | a0001c0002t0001g0090 a0001c0002t0003g0114 |
2 | HG01981.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.803-10458_803-1045 others(8): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369206 | ||||||
| chr15:44369206 | ATG | A | 4 | a0001c0001t0001g0018 a0001c0001t0001g0067 a0001c0001t0001g0080 others(1): Show |
4 | HG01255.hp1 HG01981.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.803-10456_803-1045 others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369206 | ||||||
| chr15:44369206 | ATGTG | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0037 |
2 | HG03209.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.803-10458_803-1045 others(8): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369206 | ||||||
| chr15:44369208 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.803-10482G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44369208 | |||||||
| chr15:44369405 | C | A | 1 | a0001c0001t0005g0119 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.803-10285C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44369405 | |||||||
| chr15:44369479 | G | A | 53 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(50): Show |
53 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.803-10211G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44369479 | |||||||
| chr15:44369515 | A | T | 1 | a0001c0001t0001g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.803-10175A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44369515 | |||||||
| chr15:44369561 | C | T | 1 | a0001c0002t0006g0109 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.803-10129C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44369561 | |||||||
| chr15:44369693 | T | TAC | 32 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0038 others(29): Show |
32 | HG00423.hp2 HG00597.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.803-9967_803-9966d others(4): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369693 | ||||||
| chr15:44369693 | T | TACAC | 21 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0012 others(18): Show |
21 | HG00738.hp2 HG01069.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.803-9969_803-9966d others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369693 | ||||||
| chr15:44369693 | T | TACACAC | 12 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0032 others(9): Show |
12 | HG01074.hp2 HG01255.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.803-9971_803-9966d others(8): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369693 | ||||||
| chr15:44369693 | T | TACACACA others(1): Show |
9 | a0001c0001t0001g0092 a0001c0001t0001g0095 a0001c0001t0001g0096 others(6): Show |
9 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(6): Show |
intron_variant | MODIFIER | c.803-9973_803-9966d others(10): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369693 | ||||||
| chr15:44369693 | T | TACACACA others(3): Show |
4 | a0001c0001t0001g0087 a0001c0001t0001g0093 a0001c0001t0001g0100 others(1): Show |
4 | HG00408.hp1 HG02602.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.803-9975_803-9966d others(12): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369693 | ||||||
| chr15:44369693 | T | TACACACA others(5): Show |
3 | a0001c0001t0001g0047 a0001c0001t0001g0091 a0001c0001t0001g0094 |
3 | HG02970.hp2 HG03927.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.803-9977_803-9966d others(14): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369693 | ||||||
| chr15:44369693 | TAC | T | 9 | a0001c0002t0004g0103 a0001c0002t0004g0104 a0001c0002t0004g0105 others(6): Show |
9 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.803-9967_803-9966d others(4): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369693 | ||||||
| chr15:44369693 | TACAC | T | 7 | a0001c0001t0001g0002 a0001c0001t0001g0053 a0001c0001t0001g0055 others(4): Show |
7 | HG00280.hp2 HG00621.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.803-9969_803-9966d others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369693 | ||||||
| chr15:44369693 | TACACAC | T | 18 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(15): Show |
18 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(15): Show |
intron_variant | MODIFIER | c.803-9971_803-9966d others(8): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369693 | ||||||
| chr15:44369723 | C | CACACACA others(1): Show |
10 | a0001c0001t0002g0130 a0001c0001t0002g0131 a0001c0001t0002g0133 others(7): Show |
10 | HG02040.hp1 HG02155.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.803-9966_803-9965i others(10): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369723 | ||||||
| chr15:44369723 | C | CACACAT | 8 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0127 others(5): Show |
8 | HG01496.hp2 HG02257.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.803-9966_803-9965i others(8): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44369723 | ||||||
| chr15:44369725 | T | C | 4 | a0001c0001t0001g0040 a0001c0001t0001g0095 a0001c0003t0001g0147 others(1): Show |
4 | HG00735.hp2 HG01891.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-9965T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44369725 | |||||||
| chr15:44369897 | T | A | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 |
3 | HG02055.hp1 HG02572.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.803-9793T>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44369897 | |||||||
| chr15:44370285 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.803-9405T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44370285 | |||||||
| chr15:44370618 | G | A | 1 | a0001c0001t0005g0119 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.803-9072G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44370618 | |||||||
| chr15:44371038 | T | C | 2 | a0001c0003t0001g0147 a0001c0003t0001g0148 |
2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.803-8652T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44371038 | |||||||
| chr15:44371714 | A | C | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.803-7976A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44371714 | |||||||
| chr15:44371890 | T | C | 3 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0009g0149 |
3 | HG01891.hp1 HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.803-7800T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44371890 | |||||||
| chr15:44372185 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.803-7505T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44372185 | |||||||
| chr15:44372470 | C | A | 2 | a0001c0002t0001g0090 a0001c0002t0003g0114 |
2 | HG01981.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.803-7220C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44372470 | |||||||
| chr15:44373099 | A | T | 1 | a0001c0001t0001g0094 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.803-6591A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44373099 | |||||||
| chr15:44373456 | C | CA | 10 | a0001c0001t0001g0098 a0001c0001t0002g0131 a0001c0002t0004g0103 others(7): Show |
10 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.803-6224dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44373456 | ||||||
| chr15:44373481 | C | T | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.803-6209C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44373481 | |||||||
| chr15:44373532 | A | G | 63 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0088 others(60): Show |
63 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.803-6158A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44373532 | |||||||
| chr15:44373864 | G | A | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.803-5826G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44373864 | |||||||
| chr15:44373927 | C | T | 1 | a0001c0001t0001g0013 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.803-5763C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44373927 | |||||||
| chr15:44373967 | G | T | 1 | a0001c0001t0002g0130 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.803-5723G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44373967 | |||||||
| chr15:44374009 | A | G | 63 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0088 others(60): Show |
63 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.803-5681A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44374009 | |||||||
| chr15:44374243 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.803-5447C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44374243 | |||||||
| chr15:44374507 | GA | G | 9 | a0001c0002t0004g0086 a0001c0002t0004g0103 a0001c0002t0004g0104 others(6): Show |
9 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.803-5173delA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44374507 | ||||||
| chr15:44374974 | G | C | 42 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0091 others(39): Show |
42 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.803-4716G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44374974 | |||||||
| chr15:44375183 | G | C | 1 | a0002c0005t0003g0117 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.803-4507G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44375183 | |||||||
| chr15:44375270 | C | T | 2 | a0001c0003t0001g0147 a0001c0003t0001g0148 |
2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.803-4420C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44375270 | |||||||
| chr15:44375280 | A | C | 1 | a0002c0005t0001g0112 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.803-4410A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44375280 | |||||||
| chr15:44375323 | G | A | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.803-4367G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44375323 | |||||||
| chr15:44375443 | A | G | 1 | a0001c0001t0011g0122 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.803-4247A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44375443 | |||||||
| chr15:44375623 | A | T | 1 | a0001c0001t0002g0125 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.803-4067A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44375623 | |||||||
| chr15:44375624 | T | A | 1 | a0001c0001t0011g0122 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.803-4066T>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44375624 | |||||||
| chr15:44375683 | A | G | 1 | a0001c0001t0001g0002 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.803-4007A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44375683 | |||||||
| chr15:44375787 | A | T | 5 | a0001c0002t0004g0103 a0001c0002t0004g0118 a0001c0002t0006g0109 others(2): Show |
5 | HG01891.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.803-3903A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44375787 | |||||||
| chr15:44376109 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.803-3581T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44376109 | |||||||
| chr15:44376158 | G | A | 5 | a0001c0002t0004g0104 a0001c0002t0004g0105 a0001c0002t0004g0106 others(2): Show |
5 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.803-3532G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44376158 | |||||||
| chr15:44376230 | G | T | 1 | a0001c0001t0001g0088 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.803-3460G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44376230 | |||||||
| chr15:44376508 | A | G | 43 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0091 others(40): Show |
43 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.803-3182A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44376508 | |||||||
| chr15:44376751 | G | T | 4 | a0001c0001t0001g0087 a0001c0001t0001g0093 a0001c0001t0001g0100 others(1): Show |
4 | HG00408.hp1 HG00597.hp2 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.803-2939G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44376751 | |||||||
| chr15:44376810 | G | GTTTATAT others(3): Show |
54 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0088 others(51): Show |
54 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.803-2879_803-2878i others(12): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44376810 | ||||||
| chr15:44376867 | A | G | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.803-2823A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44376867 | |||||||
| chr15:44376868 | G | T | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.803-2822G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44376868 | |||||||
| chr15:44376869 | G | A | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 |
3 | HG03098.hp2 HG03130.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.803-2821G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44376869 | |||||||
| chr15:44377007 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.803-2683C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44377007 | |||||||
| chr15:44377663 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.803-2027C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44377663 | |||||||
| chr15:44377752 | T | C | 1 | a0001c0001t0011g0122 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.803-1938T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44377752 | |||||||
| chr15:44378023 | A | T | 3 | a0001c0002t0004g0104 a0001c0002t0004g0105 a0002c0005t0003g0117 |
3 | HG02109.hp2 HG02258.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.803-1667A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44378023 | |||||||
| chr15:44378032 | A | ATTAT | 2 | a0001c0001t0001g0123 a0001c0001t0002g0138 |
2 | HG02155.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.803-1631_803-1628d others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44378032 | ||||||
| chr15:44378032 | A | ATTATTTA others(1): Show |
16 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0127 others(13): Show |
16 | HG01496.hp2 HG02040.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.803-1635_803-1628d others(10): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44378032 | ||||||
| chr15:44378032 | A | ATTATTTA others(5): Show |
1 | a0001c0001t0002g0136 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.803-1639_803-1628d others(14): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44378032 | ||||||
| chr15:44378055 | A | T | 2 | a0001c0006t0001g0150 a0002c0005t0003g0117 |
2 | HG02109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.803-1635A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44378055 | |||||||
| chr15:44378059 | A | T | 8 | a0001c0001t0003g0020 a0001c0002t0004g0104 a0001c0002t0004g0105 others(5): Show |
8 | HG00558.hp2 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.803-1631A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44378059 | |||||||
| chr15:44378111 | T | C | 42 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0091 others(39): Show |
42 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.803-1579T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44378111 | |||||||
| chr15:44378114 | C | T | 42 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0091 others(39): Show |
42 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.803-1576C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44378114 | |||||||
| chr15:44378136 | C | T | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.803-1554C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44378136 | |||||||
| chr15:44378295 | G | T | 63 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0088 others(60): Show |
63 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.803-1395G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44378295 | |||||||
| chr15:44378345 | G | A | 12 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0111 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.803-1345G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44378345 | |||||||
| chr15:44378354 | C | CT | 22 | a0001c0001t0001g0026 a0001c0001t0001g0146 a0001c0001t0002g0124 others(19): Show |
22 | HG01496.hp2 HG01891.hp1 HG02040.hp1 others(19): Show |
intron_variant | MODIFIER | c.803-1317dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44378354 | ||||||
| chr15:44378505 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.803-1185G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44378505 | |||||||
| chr15:44378612 | A | G | 1 | a0001c0003t0001g0147 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.803-1078A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44378612 | |||||||
| chr15:44378825 | A | C | 40 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0091 others(37): Show |
40 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.803-865A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44378825 | |||||||
| chr15:44378848 | T | C | 65 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0088 others(62): Show |
65 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.803-842T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44378848 | |||||||
| chr15:44378984 | A | C | 40 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0091 others(37): Show |
40 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.803-706A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44378984 | |||||||
| chr15:44379341 | G | A | 1 | a0001c0001t0003g0051 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.803-349G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44379341 | |||||||
| chr15:44379618 | G | GT | 13 | a0001c0001t0001g0073 a0001c0001t0001g0097 a0001c0001t0003g0065 others(10): Show |
13 | HG00140.hp1 HG00408.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.803-52dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44379618 | ||||||
| chr15:44379618 | GT | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0042 a0001c0001t0001g0057 others(2): Show |
5 | HG00323.hp2 HG01069.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.803-52delT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr15 | 44379618 | ||||||
| chr15:44379640 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.803-50G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44379640 | |||||||
| chr15:44379658 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.803-32G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44379658 | |||||||
| chr15:44379659 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.803-31G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 6/9 | chr15 | 44379659 | |||||||
| chr15:44379914 | T | TA | 63 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0088 others(60): Show |
63 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.901+126_901+127ins others(1): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 7/9 | chr15 | 44379914 | |||||||
| chr15:44380095 | C | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 |
3 | HG02559.hp2 HG02630.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.901+307C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 7/9 | chr15 | 44380095 | |||||||
| chr15:44380393 | T | G | 1 | a0001c0001t0001g0066 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.902-413T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 7/9 | chr15 | 44380393 | |||||||
| chr15:44380665 | T | TA | 11 | a0001c0001t0002g0125 a0001c0001t0002g0130 a0001c0001t0002g0131 others(8): Show |
11 | HG02040.hp1 HG02155.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.902-125dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 44380665 | ||||||
| chr15:44380665 | T | TAA | 7 | a0001c0001t0002g0124 a0001c0001t0002g0127 a0001c0001t0002g0132 others(4): Show |
7 | HG01496.hp2 HG02257.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.902-126_902-125dup others(2): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr15 | 44380665 | ||||||
| chr15:44380698 | A | G | 3 | a0001c0001t0001g0058 a0001c0001t0001g0094 a0001c0001t0001g0096 |
3 | NA18948.hp1 NA19007.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.902-108A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 7/9 | chr15 | 44380698 | |||||||
| chr15:44381327 | G | T | 16 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(13): Show |
16 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.1072+351G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44381327 | |||||||
| chr15:44381969 | G | A | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1072+993G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44381969 | |||||||
| chr15:44382239 | A | C | 12 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0111 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1072+1263A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44382239 | |||||||
| chr15:44382249 | T | C | 1 | a0001c0001t0002g0132 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1072+1273T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44382249 | |||||||
| chr15:44382288 | C | T | 1 | a0001c0002t0006g0109 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1072+1312C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44382288 | |||||||
| chr15:44382615 | C | T | 18 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0127 others(15): Show |
18 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.1072+1639C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44382615 | |||||||
| chr15:44382642 | A | C | 20 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(17): Show |
20 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(17): Show |
intron_variant | MODIFIER | c.1072+1666A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44382642 | |||||||
| chr15:44382693 | T | A | 5 | a0001c0002t0004g0104 a0001c0002t0004g0105 a0001c0002t0004g0106 others(2): Show |
5 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1072+1717T>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44382693 | |||||||
| chr15:44382794 | A | G | 18 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0127 others(15): Show |
18 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.1072+1818A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44382794 | |||||||
| chr15:44382806 | C | G | 2 | a0001c0001t0005g0120 a0001c0001t0007g0121 |
2 | HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1072+1830C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44382806 | |||||||
| chr15:44382847 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG02572.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1072+1871C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44382847 | |||||||
| chr15:44382900 | G | C | 39 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(36): Show |
39 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1072+1924G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44382900 | |||||||
| chr15:44382920 | C | CA | 10 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0030 others(7): Show |
10 | HG01074.hp2 HG02630.hp1 HG03471.hp1 others(7): Show |
intron_variant | MODIFIER | c.1072+1962dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44382920 | ||||||
| chr15:44382996 | A | G | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1072+2020A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44382996 | |||||||
| chr15:44383038 | ATTTAC | A | 2 | a0001c0001t0001g0050 a0001c0001t0003g0049 |
2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1072+2066_1072+207 others(9): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44383038 | ||||||
| chr15:44383102 | C | T | 11 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(8): Show |
11 | HG01891.hp1 HG02055.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1072+2126C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44383102 | |||||||
| chr15:44383234 | T | C | 18 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0127 others(15): Show |
18 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.1072+2258T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44383234 | |||||||
| chr15:44383270 | T | C | 62 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(59): Show |
62 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1072+2294T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44383270 | |||||||
| chr15:44383417 | C | G | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1072+2441C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44383417 | |||||||
| chr15:44383496 | T | C | 1 | a0001c0001t0002g0125 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1072+2520T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44383496 | |||||||
| chr15:44383675 | C | CT | 14 | a0001c0001t0001g0035 a0001c0001t0001g0142 a0001c0001t0002g0135 others(11): Show |
14 | HG01891.hp2 HG02258.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1072+2717dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44383675 | ||||||
| chr15:44383938 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1072+2962C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44383938 | |||||||
| chr15:44383982 | G | A | 1 | a0002c0005t0003g0117 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1072+3006G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44383982 | |||||||
| chr15:44384027 | T | C | 2 | a0001c0001t0001g0050 a0001c0001t0003g0049 |
2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1072+3051T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44384027 | |||||||
| chr15:44384036 | C | T | 39 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(36): Show |
39 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1072+3060C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44384036 | |||||||
| chr15:44384197 | C | T | 1 | a0001c0001t0001g0015 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1072+3221C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44384197 | |||||||
| chr15:44384241 | AC | A | 39 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(36): Show |
39 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1072+3268delC | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44384241 | ||||||
| chr15:44384701 | C | T | 1 | a0001c0003t0009g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1072+3725C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44384701 | |||||||
| chr15:44384746 | CA | C | 5 | a0001c0001t0001g0033 a0001c0001t0001g0143 a0001c0001t0001g0144 others(2): Show |
5 | HG02970.hp1 HG03098.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.1072+3783delA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44384746 | ||||||
| chr15:44384776 | G | A | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1072+3800G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44384776 | |||||||
| chr15:44385042 | TA | T | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1072+4068delA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44385042 | ||||||
| chr15:44385064 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1072+4088A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44385064 | |||||||
| chr15:44385120 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1072+4144G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44385120 | |||||||
| chr15:44385137 | A | T | 3 | a0001c0002t0004g0103 a0001c0002t0004g0118 a0001c0002t0006g0109 |
3 | HG03516.hp2 HG06807.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1072+4161A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44385137 | |||||||
| chr15:44385358 | CCCTT | C | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1072+4386_1072+438 others(8): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44385358 | ||||||
| chr15:44385710 | C | G | 1 | a0001c0002t0004g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1072+4734C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44385710 | |||||||
| chr15:44386216 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1072+5240G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44386216 | |||||||
| chr15:44386511 | A | G | 5 | a0001c0002t0004g0104 a0001c0002t0004g0105 a0001c0002t0004g0106 others(2): Show |
5 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1072+5535A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44386511 | |||||||
| chr15:44386706 | A | T | 1 | a0001c0001t0001g0123 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1072+5730A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44386706 | |||||||
| chr15:44386730 | G | C | 17 | a0001c0001t0001g0014 a0001c0001t0001g0021 a0001c0001t0001g0036 others(14): Show |
17 | HG00642.hp1 HG00738.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1072+5754G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44386730 | |||||||
| chr15:44387007 | T | G | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 |
3 | HG02055.hp1 HG02572.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1072+6031T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44387007 | |||||||
| chr15:44387183 | G | GA | 19 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0050 others(16): Show |
19 | HG00621.hp1 HG01891.hp1 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.1072+6228dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44387183 | ||||||
| chr15:44387183 | G | GAA | 22 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0091 others(19): Show |
22 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.1072+6227_1072+622 others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44387183 | ||||||
| chr15:44387400 | T | C | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1072+6424T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44387400 | |||||||
| chr15:44387532 | G | GT | 9 | a0001c0002t0004g0086 a0001c0002t0004g0103 a0001c0002t0004g0104 others(6): Show |
9 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1072+6557dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44387532 | ||||||
| chr15:44387563 | C | G | 63 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0088 others(60): Show |
63 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.1072+6587C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44387563 | |||||||
| chr15:44387716 | G | A | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1072+6740G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44387716 | |||||||
| chr15:44387817 | T | C | 1 | a0001c0003t0009g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1072+6841T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44387817 | |||||||
| chr15:44387840 | A | G | 1 | a0001c0001t0002g0125 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1072+6864A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44387840 | |||||||
| chr15:44388273 | C | CA | 12 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0001c0001t0001g0036 others(9): Show |
12 | HG00140.hp1 HG00621.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1072+7316dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44388273 | ||||||
| chr15:44388273 | C | CAA | 14 | a0001c0001t0001g0079 a0001c0001t0001g0113 a0001c0001t0001g0143 others(11): Show |
14 | HG01081.hp2 HG02055.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1072+7315_1072+731 others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44388273 | ||||||
| chr15:44388273 | C | CAAA | 20 | a0001c0001t0001g0087 a0001c0001t0001g0092 a0001c0001t0001g0093 others(17): Show |
20 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.1072+7314_1072+731 others(7): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44388273 | ||||||
| chr15:44388273 | C | CAAAA | 27 | a0001c0001t0001g0058 a0001c0001t0001g0091 a0001c0001t0001g0099 others(24): Show |
27 | HG01496.hp2 HG01891.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.1072+7313_1072+731 others(8): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44388273 | ||||||
| chr15:44388295 | G | A | 1 | a0001c0002t0001g0090 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1072+7319G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44388295 | |||||||
| chr15:44388362 | T | A | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1072+7386T>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44388362 | |||||||
| chr15:44388761 | C | T | 9 | a0001c0002t0004g0086 a0001c0002t0004g0103 a0001c0002t0004g0104 others(6): Show |
9 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1072+7785C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44388761 | |||||||
| chr15:44388838 | C | T | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1072+7862C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44388838 | |||||||
| chr15:44388839 | G | A | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1072+7863G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44388839 | |||||||
| chr15:44388909 | G | A | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1072+7933G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44388909 | |||||||
| chr15:44389033 | A | C | 20 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(17): Show |
20 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(17): Show |
intron_variant | MODIFIER | c.1072+8057A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44389033 | |||||||
| chr15:44389522 | T | C | 8 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0111 others(5): Show |
8 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1072+8546T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44389522 | |||||||
| chr15:44389794 | T | C | 63 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0088 others(60): Show |
63 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.1072+8818T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44389794 | |||||||
| chr15:44390536 | A | G | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1072+9560A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44390536 | |||||||
| chr15:44390565 | AT | A | 7 | a0001c0001t0001g0123 a0001c0002t0004g0086 a0001c0002t0004g0104 others(4): Show |
7 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1072+9606delT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44390565 | ||||||
| chr15:44390634 | C | T | 1 | a0001c0001t0003g0020 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1072+9658C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44390634 | |||||||
| chr15:44390700 | A | G | 63 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0088 others(60): Show |
63 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.1072+9724A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44390700 | |||||||
| chr15:44390952 | T | C | 63 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0088 others(60): Show |
63 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.1072+9976T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44390952 | |||||||
| chr15:44390995 | A | G | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1072+10019A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44390995 | |||||||
| chr15:44391105 | C | T | 2 | a0001c0003t0001g0147 a0001c0003t0001g0148 |
2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1072+10129C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44391105 | |||||||
| chr15:44391156 | C | G | 1 | a0001c0002t0006g0109 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1072+10180C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44391156 | |||||||
| chr15:44391198 | G | A | 17 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0091 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.1072+10222G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44391198 | |||||||
| chr15:44391286 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1072+10310G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44391286 | |||||||
| chr15:44391373 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1072+10397C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44391373 | |||||||
| chr15:44391448 | T | C | 63 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0088 others(60): Show |
63 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.1072+10472T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44391448 | |||||||
| chr15:44391560 | G | A | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1072+10584G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44391560 | |||||||
| chr15:44391605 | AAAG | A | 40 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0091 others(37): Show |
40 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.1072+10632_1072+10 others(9): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44391605 | ||||||
| chr15:44391702 | T | C | 1 | a0001c0001t0003g0051 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1072+10726T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44391702 | |||||||
| chr15:44391914 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1072+10938A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44391914 | |||||||
| chr15:44391924 | C | T | 17 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0091 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.1072+10948C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44391924 | |||||||
| chr15:44392215 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1073-10672G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44392215 | |||||||
| chr15:44392516 | A | T | 1 | a0001c0001t0001g0071 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1073-10371A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44392516 | |||||||
| chr15:44392549 | G | A | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1073-10338G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44392549 | |||||||
| chr15:44392607 | G | A | 1 | a0001c0002t0004g0106 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1073-10280G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44392607 | |||||||
| chr15:44392891 | C | T | 1 | a0001c0001t0007g0121 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1073-9996C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44392891 | |||||||
| chr15:44392898 | G | C | 18 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0127 others(15): Show |
18 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.1073-9989G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44392898 | |||||||
| chr15:44392976 | G | T | 1 | a0001c0001t0001g0046 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1073-9911G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44392976 | |||||||
| chr15:44393325 | A | G | 4 | a0001c0001t0001g0037 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG01255.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1073-9562A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44393325 | |||||||
| chr15:44393417 | C | T | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1073-9470C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44393417 | |||||||
| chr15:44393836 | T | C | 42 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(39): Show |
42 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.1073-9051T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44393836 | |||||||
| chr15:44394691 | G | A | 42 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(39): Show |
42 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(39): Show |
intron_variant | MODIFIER | c.1073-8196G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44394691 | |||||||
| chr15:44394722 | T | C | 9 | a0001c0002t0004g0086 a0001c0002t0004g0103 a0001c0002t0004g0104 others(6): Show |
9 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1073-8165T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44394722 | |||||||
| chr15:44394971 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1073-7916C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44394971 | |||||||
| chr15:44394972 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1073-7915A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44394972 | |||||||
| chr15:44395064 | C | T | 4 | a0001c0001t0002g0130 a0001c0001t0002g0133 a0001c0001t0002g0134 others(1): Show |
4 | HG02040.hp1 HG02523.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1073-7823C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44395064 | |||||||
| chr15:44395155 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1073-7732C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44395155 | |||||||
| chr15:44395177 | A | AT | 39 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(36): Show |
39 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(36): Show |
intron_variant | MODIFIER | c.1073-7694dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44395177 | ||||||
| chr15:44395235 | C | T | 2 | a0001c0001t0001g0030 a0001c0001t0001g0033 |
2 | NA18948.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1073-7652C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44395235 | |||||||
| chr15:44395236 | C | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0033 |
2 | NA18948.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1073-7651C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44395236 | |||||||
| chr15:44395250 | C | T | 1 | a0001c0002t0004g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1073-7637C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44395250 | |||||||
| chr15:44395303 | C | G | 1 | a0001c0001t0002g0136 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1073-7584C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44395303 | |||||||
| chr15:44395412 | A | G | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1073-7475A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44395412 | |||||||
| chr15:44395491 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1073-7396T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44395491 | |||||||
| chr15:44395616 | C | T | 10 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0007g0121 others(7): Show |
10 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1073-7271C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44395616 | |||||||
| chr15:44395675 | C | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0054 others(63): Show |
66 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.1073-7212C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44395675 | |||||||
| chr15:44395797 | G | A | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1073-7090G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44395797 | |||||||
| chr15:44395834 | G | A | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1073-7053G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44395834 | |||||||
| chr15:44396521 | A | G | 1 | a0001c0001t0001g0008 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1073-6366A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44396521 | |||||||
| chr15:44396670 | C | T | 1 | a0001c0001t0001g0029 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1073-6217C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44396670 | |||||||
| chr15:44397108 | C | T | 1 | a0002c0005t0003g0117 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1073-5779C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44397108 | |||||||
| chr15:44397262 | G | A | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 |
3 | HG02055.hp1 HG02572.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1073-5625G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44397262 | |||||||
| chr15:44397295 | C | T | 17 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.1073-5592C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44397295 | |||||||
| chr15:44397296 | G | A | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1073-5591G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44397296 | |||||||
| chr15:44397303 | C | T | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1073-5584C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44397303 | |||||||
| chr15:44397331 | T | C | 40 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(37): Show |
40 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.1073-5556T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44397331 | |||||||
| chr15:44397335 | C | G | 23 | a0001c0001t0001g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(20): Show |
23 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(20): Show |
intron_variant | MODIFIER | c.1073-5552C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44397335 | |||||||
| chr15:44397455 | G | A | 1 | a0002c0005t0003g0117 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1073-5432G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44397455 | |||||||
| chr15:44397466 | G | A | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1073-5421G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44397466 | |||||||
| chr15:44397478 | C | CA | 41 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0014 others(38): Show |
41 | HG00423.hp2 HG00597.hp1 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.1073-5385dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44397478 | ||||||
| chr15:44397478 | C | CAA | 16 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0001g0052 others(13): Show |
16 | HG01891.hp1 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1073-5386_1073-538 others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44397478 | ||||||
| chr15:44397497 | A | C | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1073-5390A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44397497 | |||||||
| chr15:44397503 | C | A | 2 | a0001c0001t0005g0119 a0001c0006t0001g0150 |
2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1073-5384C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44397503 | |||||||
| chr15:44397504 | A | C | 1 | a0001c0001t0001g0085 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1073-5383A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44397504 | |||||||
| chr15:44397508 | C | CCA | 31 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(28): Show |
31 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.1073-5356_1073-535 others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44397508 | ||||||
| chr15:44397508 | CCACACAC others(7): Show |
C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0055 |
2 | HG00280.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1073-5368_1073-535 others(18): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44397508 | ||||||
| chr15:44397606 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1073-5281C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44397606 | |||||||
| chr15:44397865 | G | A | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1073-5022G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44397865 | |||||||
| chr15:44398485 | G | A | 1 | a0001c0003t0001g0147 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1073-4402G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44398485 | |||||||
| chr15:44398657 | C | CT | 13 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0014 others(10): Show |
13 | HG00621.hp2 HG00642.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.1073-4206dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44398657 | ||||||
| chr15:44398657 | CT | C | 27 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0091 others(24): Show |
27 | HG00408.hp1 HG00597.hp2 HG00673.hp1 others(24): Show |
intron_variant | MODIFIER | c.1073-4206delT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44398657 | ||||||
| chr15:44398657 | CTT | C | 26 | a0001c0001t0001g0085 a0001c0001t0001g0089 a0001c0001t0002g0124 others(23): Show |
26 | HG01496.hp2 HG01891.hp1 HG02040.hp1 others(23): Show |
intron_variant | MODIFIER | c.1073-4207_1073-420 others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44398657 | ||||||
| chr15:44398711 | G | A | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1073-4176G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44398711 | |||||||
| chr15:44398817 | C | G | 1 | a0001c0001t0001g0110 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1073-4070C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44398817 | |||||||
| chr15:44399053 | A | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0022 |
2 | HG00621.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1073-3834A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44399053 | |||||||
| chr15:44399716 | C | T | 9 | a0001c0002t0004g0086 a0001c0002t0004g0103 a0001c0002t0004g0104 others(6): Show |
9 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1073-3171C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44399716 | |||||||
| chr15:44399760 | C | T | 16 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(13): Show |
16 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.1073-3127C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44399760 | |||||||
| chr15:44399864 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1073-3023A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44399864 | |||||||
| chr15:44399923 | A | G | 17 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0091 others(14): Show |
17 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(14): Show |
intron_variant | MODIFIER | c.1073-2964A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44399923 | |||||||
| chr15:44399984 | GA | G | 5 | a0001c0001t0001g0073 a0001c0001t0001g0145 a0001c0001t0002g0131 others(2): Show |
5 | HG00140.hp1 HG01891.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.1073-2890delA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44399984 | ||||||
| chr15:44400405 | G | A | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1073-2482G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44400405 | |||||||
| chr15:44400574 | C | CT | 42 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0017 others(39): Show |
42 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.1073-2286dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44400574 | ||||||
| chr15:44400574 | C | CTT | 6 | a0001c0001t0001g0091 a0001c0001t0001g0096 a0001c0001t0001g0100 others(3): Show |
6 | HG00597.hp2 HG02602.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1073-2287_1073-228 others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44400574 | ||||||
| chr15:44400574 | CT | C | 11 | a0001c0001t0001g0085 a0001c0001t0001g0089 a0001c0001t0001g0145 others(8): Show |
11 | HG01891.hp1 HG01891.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1073-2286delT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44400574 | ||||||
| chr15:44400574 | CTT | C | 7 | a0001c0002t0004g0103 a0001c0002t0004g0104 a0001c0002t0004g0105 others(4): Show |
7 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1073-2287_1073-228 others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44400574 | ||||||
| chr15:44400769 | G | C | 1 | a0002c0005t0003g0117 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1073-2118G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44400769 | |||||||
| chr15:44400822 | G | A | 40 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0091 others(37): Show |
40 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.1073-2065G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44400822 | |||||||
| chr15:44401119 | G | T | 41 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(38): Show |
41 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.1073-1768G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44401119 | |||||||
| chr15:44401266 | AT | A | 5 | a0001c0001t0001g0085 a0001c0001t0001g0089 a0001c0001t0001g0097 others(2): Show |
5 | HG02523.hp1 HG02895.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.1073-1607delT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44401266 | ||||||
| chr15:44401395 | T | G | 63 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0088 others(60): Show |
63 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.1073-1492T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44401395 | |||||||
| chr15:44401542 | G | T | 2 | a0001c0002t0001g0090 a0001c0002t0003g0114 |
2 | HG01981.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1073-1345G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44401542 | |||||||
| chr15:44401829 | CT | C | 6 | a0001c0001t0001g0075 a0001c0001t0001g0085 a0001c0001t0002g0134 others(3): Show |
6 | HG01891.hp2 HG02109.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.1073-1041delT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr15 | 44401829 | ||||||
| chr15:44401872 | C | T | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1073-1015C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44401872 | |||||||
| chr15:44402139 | C | G | 63 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0088 others(60): Show |
63 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.1073-748C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44402139 | |||||||
| chr15:44402302 | A | G | 9 | a0001c0002t0004g0086 a0001c0002t0004g0103 a0001c0002t0004g0104 others(6): Show |
9 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1073-585A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44402302 | |||||||
| chr15:44402384 | G | A | 1 | a0001c0002t0004g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1073-503G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44402384 | |||||||
| chr15:44402397 | T | G | 52 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0091 others(49): Show |
52 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.1073-490T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44402397 | |||||||
| chr15:44402430 | A | G | 52 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0091 others(49): Show |
52 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.1073-457A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44402430 | |||||||
| chr15:44402432 | T | G | 1 | a0001c0001t0001g0068 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1073-455T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44402432 | |||||||
| chr15:44402583 | G | A | 1 | a0001c0002t0004g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1073-304G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44402583 | |||||||
| chr15:44402618 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1073-269T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44402618 | |||||||
| chr15:44402637 | T | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0055 |
2 | HG00280.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.1073-250T>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 8/9 | chr15 | 44402637 | |||||||
| chr15:44403102 | A | G | 3 | a0001c0001t0002g0124 a0001c0001t0002g0127 a0001c0001t0002g0141 |
3 | HG02257.hp1 HG02451.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1240+48A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44403102 | |||||||
| chr15:44403262 | A | C | 41 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0091 others(38): Show |
41 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.1240+208A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44403262 | |||||||
| chr15:44403453 | C | T | 18 | a0001c0001t0002g0124 a0001c0001t0002g0125 a0001c0001t0002g0127 others(15): Show |
18 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.1240+399C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44403453 | |||||||
| chr15:44403671 | C | G | 1 | a0001c0002t0004g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1240+617C>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44403671 | |||||||
| chr15:44404091 | T | A | 9 | a0001c0002t0004g0086 a0001c0002t0004g0103 a0001c0002t0004g0104 others(6): Show |
9 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1240+1037T>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44404091 | |||||||
| chr15:44404245 | T | G | 1 | a0001c0001t0001g0102 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1240+1191T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44404245 | |||||||
| chr15:44404618 | T | G | 1 | a0001c0001t0001g0002 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1240+1564T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44404618 | |||||||
| chr15:44404624 | C | T | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1240+1570C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44404624 | |||||||
| chr15:44404649 | A | T | 40 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(37): Show |
40 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.1240+1595A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44404649 | |||||||
| chr15:44404779 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1240+1725G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44404779 | |||||||
| chr15:44404949 | T | C | 9 | a0001c0002t0004g0086 a0001c0002t0004g0103 a0001c0002t0004g0104 others(6): Show |
9 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1240+1895T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44404949 | |||||||
| chr15:44404974 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1240+1920T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44404974 | |||||||
| chr15:44405236 | A | T | 2 | a0001c0003t0001g0147 a0001c0003t0001g0148 |
2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1240+2182A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44405236 | |||||||
| chr15:44405368 | G | C | 1 | a0001c0001t0001g0073 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1240+2314G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44405368 | |||||||
| chr15:44405967 | G | A | 4 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0007g0121 others(1): Show |
4 | HG02965.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+2913G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44405967 | |||||||
| chr15:44406047 | G | C | 2 | a0003c0004t0002g0128 a0003c0004t0002g0129 |
2 | NA18960.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1240+2993G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44406047 | |||||||
| chr15:44406055 | T | C | 3 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 |
3 | HG02055.hp1 HG02572.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1240+3001T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44406055 | |||||||
| chr15:44406175 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1240+3121C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44406175 | |||||||
| chr15:44406176 | G | A | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1240+3122G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44406176 | |||||||
| chr15:44406375 | G | A | 1 | a0001c0001t0002g0137 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1240+3321G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44406375 | |||||||
| chr15:44406739 | G | T | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+3685G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44406739 | |||||||
| chr15:44407111 | TTATAA | T | 9 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(6): Show |
9 | HG01891.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.1240+4062_1240+406 others(9): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44407111 | ||||||
| chr15:44407142 | T | C | 2 | a0001c0003t0001g0147 a0001c0003t0001g0148 |
2 | HG01891.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1240+4088T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44407142 | |||||||
| chr15:44407181 | A | G | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240+4127A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44407181 | |||||||
| chr15:44407365 | A | G | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1240+4311A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44407365 | |||||||
| chr15:44407423 | G | A | 4 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(1): Show |
4 | HG02970.hp1 HG03098.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240+4369G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44407423 | |||||||
| chr15:44407468 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1240+4414T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44407468 | |||||||
| chr15:44407614 | T | A | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1240+4560T>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44407614 | |||||||
| chr15:44407771 | C | CT | 8 | a0001c0001t0001g0014 a0001c0001t0001g0088 a0001c0001t0001g0089 others(5): Show |
8 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1240+4733dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44407771 | ||||||
| chr15:44407940 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1240+4886C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44407940 | |||||||
| chr15:44407969 | C | T | 16 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(13): Show |
16 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(13): Show |
intron_variant | MODIFIER | c.1240+4915C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44407969 | |||||||
| chr15:44407997 | G | A | 15 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0092 others(12): Show |
15 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.1240+4943G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44407997 | |||||||
| chr15:44408265 | G | C | 9 | a0001c0002t0004g0086 a0001c0002t0004g0103 a0001c0002t0004g0104 others(6): Show |
9 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1241-5071G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44408265 | |||||||
| chr15:44408347 | G | A | 2 | a0001c0001t0005g0120 a0001c0001t0007g0121 |
2 | HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1241-4989G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44408347 | |||||||
| chr15:44408830 | G | A | 3 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0009g0149 |
3 | HG01891.hp1 HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1241-4506G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44408830 | |||||||
| chr15:44408867 | G | A | 1 | a0001c0003t0009g0149 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1241-4469G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44408867 | |||||||
| chr15:44408943 | A | C | 8 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0111 others(5): Show |
8 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1241-4393A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44408943 | |||||||
| chr15:44408949 | C | T | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1241-4387C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44408949 | |||||||
| chr15:44409080 | A | G | 3 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0009g0149 |
3 | HG01891.hp1 HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1241-4256A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44409080 | |||||||
| chr15:44409140 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1241-4196C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44409140 | |||||||
| chr15:44409283 | C | CA | 9 | a0001c0002t0004g0086 a0001c0002t0004g0103 a0001c0002t0004g0104 others(6): Show |
9 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1241-4042dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44409283 | ||||||
| chr15:44409336 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1241-4000T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44409336 | |||||||
| chr15:44409479 | C | A | 1 | a0001c0001t0001g0083 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1241-3857C>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44409479 | |||||||
| chr15:44409524 | G | C | 2 | a0001c0001t0005g0120 a0001c0001t0007g0121 |
2 | HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1241-3812G>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44409524 | |||||||
| chr15:44409592 | C | CA | 14 | a0001c0001t0001g0012 a0001c0001t0001g0026 a0001c0001t0001g0036 others(11): Show |
14 | HG00140.hp1 HG01074.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1241-3710dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44409592 | ||||||
| chr15:44409592 | C | CAA | 6 | a0001c0001t0001g0088 a0001c0001t0001g0143 a0001c0001t0001g0144 others(3): Show |
6 | HG02258.hp1 HG02572.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1241-3711_1241-371 others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44409592 | ||||||
| chr15:44409592 | C | CAAAAAAA others(1): Show |
7 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0001g0096 others(4): Show |
7 | HG00423.hp1 HG00597.hp2 HG00673.hp1 others(4): Show |
intron_variant | MODIFIER | c.1241-3717_1241-371 others(12): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44409592 | ||||||
| chr15:44409592 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0001g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1241-3719_1241-371 others(14): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44409592 | ||||||
| chr15:44409592 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0087 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1241-3722_1241-371 others(17): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44409592 | ||||||
| chr15:44409592 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0102 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1241-3723_1241-371 others(18): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44409592 | ||||||
| chr15:44409592 | C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0100 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1241-3727_1241-371 others(22): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44409592 | ||||||
| chr15:44409592 | CA | C | 38 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(35): Show |
38 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1241-3710delA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44409592 | ||||||
| chr15:44409592 | CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0001g0116 a0001c0002t0004g0086 a0001c0003t0009g0149 |
3 | HG02109.hp1 HG02602.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1241-3721_1241-371 others(16): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44409592 | ||||||
| chr15:44409592 | CAAAAAAA others(6): Show |
C | 1 | a0001c0006t0001g0150 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1241-3722_1241-371 others(17): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44409592 | ||||||
| chr15:44409592 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0002g0125 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1241-3724_1241-371 others(19): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44409592 | ||||||
| chr15:44409592 | CAAAAAAA others(9): Show |
C | 18 | a0001c0001t0001g0123 a0001c0001t0002g0124 a0001c0001t0002g0127 others(15): Show |
18 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(15): Show |
intron_variant | MODIFIER | c.1241-3725_1241-371 others(20): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44409592 | ||||||
| chr15:44409592 | CAAAAAAA others(10): Show |
C | 4 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0007g0121 others(1): Show |
4 | HG02965.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241-3726_1241-371 others(21): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44409592 | ||||||
| chr15:44409675 | G | A | 1 | a0001c0002t0004g0105 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1241-3661G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44409675 | |||||||
| chr15:44409736 | G | A | 9 | a0001c0002t0004g0086 a0001c0002t0004g0103 a0001c0002t0004g0104 others(6): Show |
9 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1241-3600G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44409736 | |||||||
| chr15:44409745 | A | G | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1241-3591A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44409745 | |||||||
| chr15:44409789 | G | A | 5 | a0001c0002t0004g0104 a0001c0002t0004g0105 a0001c0002t0004g0106 others(2): Show |
5 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1241-3547G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44409789 | |||||||
| chr15:44409914 | T | TA | 16 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0040 others(13): Show |
16 | HG00597.hp1 HG01891.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1241-3404dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44409914 | ||||||
| chr15:44409914 | TA | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0111 a0001c0001t0002g0124 others(2): Show |
5 | HG01074.hp2 HG02451.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-3404delA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44409914 | ||||||
| chr15:44410040 | T | C | 4 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0007g0121 others(1): Show |
4 | HG02965.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241-3296T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44410040 | |||||||
| chr15:44410070 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1241-3266C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44410070 | |||||||
| chr15:44410126 | G | A | 4 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0057 others(1): Show |
4 | HG00738.hp2 HG01069.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.1241-3210G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44410126 | |||||||
| chr15:44410386 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1241-2950G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44410386 | |||||||
| chr15:44410521 | T | G | 1 | a0001c0001t0001g0035 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1241-2815T>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44410521 | |||||||
| chr15:44410852 | G | A | 2 | a0002c0005t0001g0112 a0002c0005t0003g0117 |
2 | HG01891.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1241-2484G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44410852 | |||||||
| chr15:44410874 | A | G | 1 | a0001c0002t0004g0106 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1241-2462A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44410874 | |||||||
| chr15:44410903 | C | CA | 24 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0034 others(21): Show |
24 | HG00280.hp1 HG00280.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1241-2413dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44410903 | ||||||
| chr15:44410903 | CA | C | 6 | a0001c0002t0004g0103 a0001c0002t0004g0118 a0001c0002t0006g0109 others(3): Show |
6 | HG01891.hp1 HG01891.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1241-2413delA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44410903 | ||||||
| chr15:44410996 | A | T | 1 | a0001c0001t0001g0066 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1241-2340A>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44410996 | |||||||
| chr15:44411013 | C | CT | 29 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(26): Show |
29 | HG00323.hp1 HG00323.hp2 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.1241-2297dupT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44411013 | ||||||
| chr15:44411013 | C | CTTT | 15 | a0001c0001t0001g0058 a0001c0001t0001g0087 a0001c0001t0001g0092 others(12): Show |
15 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(12): Show |
intron_variant | MODIFIER | c.1241-2299_1241-229 others(7): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44411013 | ||||||
| chr15:44411013 | CT | C | 10 | a0001c0001t0001g0029 a0001c0001t0001g0042 a0001c0001t0001g0089 others(7): Show |
10 | HG01069.hp1 HG02040.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1241-2297delT | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44411013 | ||||||
| chr15:44411013 | CTTTTTTT others(6): Show |
C | 23 | a0001c0001t0001g0123 a0001c0001t0002g0124 a0001c0001t0002g0125 others(20): Show |
23 | HG01496.hp2 HG02040.hp1 HG02155.hp2 others(20): Show |
intron_variant | MODIFIER | c.1241-2309_1241-229 others(17): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44411013 | ||||||
| chr15:44411169 | A | G | 1 | a0001c0001t0001g0116 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1241-2167A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44411169 | |||||||
| chr15:44411401 | A | C | 9 | a0001c0002t0004g0086 a0001c0002t0004g0103 a0001c0002t0004g0104 others(6): Show |
9 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1241-1935A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44411401 | |||||||
| chr15:44411538 | T | C | 4 | a0001c0001t0005g0119 a0001c0001t0005g0120 a0001c0001t0007g0121 others(1): Show |
4 | HG02965.hp2 HG03209.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241-1798T>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44411538 | |||||||
| chr15:44411563 | C | T | 1 | a0001c0001t0007g0121 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1241-1773C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44411563 | |||||||
| chr15:44411569 | C | T | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | NA18965.hp1 NA18985.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.1241-1767C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44411569 | |||||||
| chr15:44411768 | G | T | 1 | a0001c0001t0001g0042 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1241-1568G>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44411768 | |||||||
| chr15:44411808 | G | A | 1 | a0001c0001t0011g0122 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1241-1528G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44411808 | |||||||
| chr15:44411828 | C | CA | 46 | a0001c0001t0001g0026 a0001c0001t0001g0035 a0001c0001t0001g0058 others(43): Show |
46 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.1241-1488dupA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44411828 | ||||||
| chr15:44411828 | C | CAA | 7 | a0001c0001t0001g0110 a0001c0002t0004g0104 a0001c0002t0004g0105 others(4): Show |
7 | HG02258.hp1 HG02630.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1241-1489_1241-148 others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44411828 | ||||||
| chr15:44411828 | CA | C | 11 | a0001c0001t0001g0032 a0001c0001t0001g0085 a0001c0001t0001g0123 others(8): Show |
11 | HG01074.hp2 HG01496.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1241-1488delA | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44411828 | ||||||
| chr15:44411996 | T | A | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1241-1340T>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44411996 | |||||||
| chr15:44412170 | A | AAAAC | 6 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0111 others(3): Show |
6 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1241-1146_1241-114 others(8): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44412170 | ||||||
| chr15:44412280 | A | G | 5 | a0001c0001t0001g0087 a0001c0001t0001g0093 a0001c0001t0001g0100 others(2): Show |
5 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(2): Show |
intron_variant | MODIFIER | c.1241-1056A>G | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44412280 | |||||||
| chr15:44412330 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1241-1006G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44412330 | |||||||
| chr15:44412455 | C | T | 62 | a0001c0001t0001g0087 a0001c0001t0001g0088 a0001c0001t0001g0089 others(59): Show |
62 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1241-881C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44412455 | |||||||
| chr15:44412774 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1241-562G>A | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44412774 | |||||||
| chr15:44412984 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1241-352C>T | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44412984 | |||||||
| chr15:44413032 | A | C | 4 | a0001c0001t0002g0130 a0001c0001t0002g0133 a0001c0001t0002g0134 others(1): Show |
4 | HG02040.hp1 HG02523.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1241-304A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44413032 | |||||||
| chr15:44413100 | CTGTT | C | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0113 others(4): Show |
7 | HG02055.hp1 HG02572.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1241-232_1241-229d others(6): Show |
GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr15 | 44413100 | ||||||
| chr15:44413231 | A | C | 1 | a0001c0001t0001g0058 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1241-105A>C | GOLM2 | ENSG00000166734.20 | transcript | ENST00000299957.11 | protein_coding | 9/9 | chr15 | 44413231 |