Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 23637 |
| ensemblid | ENSG00000011454.18 |
| hgncid | 17155 |
| symbol | RABGAP1 |
| name | RAB GTPase activating protein 1 |
| refseq_nuc | NM_012197.4 |
| refseq_prot | NP_036329.3 |
| ensembl_nuc | ENST00000373647.9 |
| ensembl_prot | ENSP00000362751.4 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 122941020 |
| end | 123104866 |
| strand | + |
| ver | v1.2 |
| region | chr9:122941020-123104866 |
| region5000 | chr9:122936020-123109866 |
| regionname0 | RABGAP1_chr9_122941020_123104866 |
| regionname5000 | RABGAP1_chr9_122936020_123109866 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1069 | 251 | 72 | 52 | 100 | 10 | 15 | 72 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | MDDKA others(1064): Show |
chr9 | 122936020 | 123109866 |
| a0002 | 0/0 | 1069 | 5 | 0 | 0 | 5 | 0 | 0 | 3 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | MDDKA others(1064): Show |
chr9 | 122936020 | 123109866 |
| a0003 | 0/0 | 1069 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | MDDKA others(1064): Show |
chr9 | 122936020 | 123109866 |
| a0004 | 0/0 | 1069 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | MDDKA others(1064): Show |
chr9 | 122936020 | 123109866 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3207 | 228 | 72 | 51 | 82 | 8 | 13 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | ATGGA others(3202): Show |
chr9 | 122936020 | 123109866 | ||
| a0001c0002 | 0/0 | 3207 | 21 | 0 | 1 | 16 | 2 | 2 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | ATGGA others(3202): Show |
chr9 | 122936020 | 123109866 | ||
| a0001c0006 | 0/0 | 3207 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | ATGGA others(3202): Show |
chr9 | 122936020 | 123109866 | ||
| a0001c0007 | 0/0 | 3207 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | ATGGA others(3202): Show |
chr9 | 122936020 | 123109866 | ||
| a0002c0003 | 0/0 | 3207 | 5 | 0 | 0 | 5 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | ATGGA others(3202): Show |
chr9 | 122936020 | 123109866 | ||
| a0003c0005 | 0/0 | 3207 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | ATGGA others(3202): Show |
chr9 | 122936020 | 123109866 | ||
| a0004c0004 | 0/0 | 3207 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | ATGGA others(3202): Show |
chr9 | 122936020 | 123109866 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4989 | 60 | 9 | 11 | 38 | 1 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4984): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0002 | 0/0 | 4993 | 40 | 3 | 15 | 15 | 2 | 5 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4988): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0003 | 0/0 | 4983 | 14 | 1 | 7 | 0 | 2 | 4 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4978): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0004 | 0/0 | 4993 | 14 | 13 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4988): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0005 | 0/0 | 4987 | 10 | 9 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4982): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0006 | 0/0 | 4987 | 10 | 5 | 4 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4982): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0007 | 0/0 | 4995 | 9 | 9 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4990): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0008 | 1/0 | 4986 | 9 | 8 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4981): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0010 | 0/0 | 4995 | 5 | 0 | 0 | 5 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4990): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0012 | 0/0 | 4989 | 5 | 0 | 0 | 5 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4984): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0013 | 0/0 | 4993 | 5 | 0 | 1 | 3 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4988): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0014 | 0/0 | 4989 | 3 | 0 | 1 | 1 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4984): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0015 | 0/0 | 4993 | 3 | 0 | 0 | 3 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4988): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0016 | 0/0 | 4991 | 3 | 2 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4986): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0017 | 0/0 | 4995 | 3 | 0 | 2 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4990): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0018 | 0/0 | 4997 | 3 | 2 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4992): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0019 | 0/0 | 4991 | 2 | 0 | 0 | 2 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4986): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0020 | 0/0 | 4975 | 2 | 0 | 0 | 2 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4970): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0021 | 0/0 | 4991 | 2 | 2 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4986): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0024 | 0/0 | 4986 | 2 | 2 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4981): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0027 | 0/0 | 4989 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTGT others(4984): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0028 | 0/0 | 4989 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4984): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0029 | 0/1 | 4981 | 1 | 0 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4976): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0030 | 0/0 | 4983 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4978): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0031 | 0/0 | 4983 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4978): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0032 | 0/0 | 4987 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4982): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0033 | 0/0 | 4989 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4984): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0034 | 0/0 | 4992 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4987): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0035 | 0/0 | 4997 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4992): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0036 | 0/0 | 4997 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4992): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0037 | 0/0 | 4999 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4994): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0038 | 0/0 | 4997 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4992): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0039 | 0/0 | 5003 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4998): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0040 | 0/0 | 4986 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4981): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0041 | 0/0 | 4989 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4984): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0042 | 0/0 | 4989 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4984): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0043 | 0/0 | 4988 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4983): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0044 | 0/0 | 4991 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4986): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0045 | 0/0 | 4991 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4986): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0046 | 0/0 | 5007 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(5002): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0047 | 0/0 | 4947 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4942): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0048 | 0/0 | 4982 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4977): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0055 | 0/0 | 4988 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4983): Show |
chr9 | 122936020 | 123109866 |
| a0001c0001t0057 | 0/0 | 4995 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4990): Show |
chr9 | 122936020 | 123109866 |
| a0001c0002t0009 | 0/0 | 4978 | 7 | 0 | 0 | 6 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4973): Show |
chr9 | 122936020 | 123109866 |
| a0001c0002t0022 | 0/0 | 4982 | 2 | 0 | 0 | 2 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4977): Show |
chr9 | 122936020 | 123109866 |
| a0001c0002t0023 | 0/0 | 4976 | 2 | 0 | 0 | 2 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4971): Show |
chr9 | 122936020 | 123109866 |
| a0001c0002t0025 | 0/0 | 4982 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4977): Show |
chr9 | 122936020 | 123109866 |
| a0001c0002t0026 | 0/0 | 4993 | 2 | 0 | 1 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4988): Show |
chr9 | 122936020 | 123109866 |
| a0001c0002t0049 | 0/0 | 4974 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4969): Show |
chr9 | 122936020 | 123109866 |
| a0001c0002t0050 | 0/0 | 4976 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4971): Show |
chr9 | 122936020 | 123109866 |
| a0001c0002t0051 | 0/0 | 4972 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4967): Show |
chr9 | 122936020 | 123109866 |
| a0001c0002t0052 | 0/0 | 4977 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4972): Show |
chr9 | 122936020 | 123109866 |
| a0001c0002t0053 | 0/0 | 4980 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4975): Show |
chr9 | 122936020 | 123109866 |
| a0001c0002t0054 | 0/0 | 4984 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4979): Show |
chr9 | 122936020 | 123109866 |
| a0001c0002t0056 | 0/0 | 4988 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4983): Show |
chr9 | 122936020 | 123109866 |
| a0001c0006t0010 | 0/0 | 4995 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4990): Show |
chr9 | 122936020 | 123109866 |
| a0001c0007t0025 | 0/0 | 4982 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4977): Show |
chr9 | 122936020 | 123109866 |
| a0002c0003t0011 | 0/0 | 4985 | 5 | 0 | 0 | 5 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4980): Show |
chr9 | 122936020 | 123109866 |
| a0003c0005t0001 | 0/0 | 4989 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4984): Show |
chr9 | 122936020 | 123109866 |
| a0004c0004t0011 | 0/0 | 4985 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | GGTTT others(4980): Show |
chr9 | 122936020 | 123109866 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0004g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0005g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0005g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0005g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0005g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0005g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0005g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0005g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0006g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0006g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0006g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0006g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0006g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0006g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0006g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0007g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0007g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0007g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0007g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0007g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0008g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0008g0091 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0008g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0008g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0008g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0008g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0008g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0008g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0010g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0010g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0010g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0010g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0010g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0012g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0012g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0012g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0012g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0012g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0013g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0013g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0013g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0013g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0013g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0014g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0014g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0014g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0015g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0015g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0015g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0016g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0016g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0016g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0017g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0017g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0017g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0018g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0018g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0018g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0019g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0019g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0020g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0020g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0021g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0024g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0024g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0027g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0028g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0029g0183 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0030g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0031g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0032g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0033g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0034g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0035g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0036g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0037g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0038g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0039g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0040g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0041g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0042g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0043g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0044g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0045g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0046g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0047g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0048g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0055g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0001t0057g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0009g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0009g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0009g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0009g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0009g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0009g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0009g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0022g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0022g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0023g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0023g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0025g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0026g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0026g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0049g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0050g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0051g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0052g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0053g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0054g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0002t0056g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0006t0010g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0001c0007t0025g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0002c0003t0011g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0002c0003t0011g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0002c0003t0011g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0002c0003t0011g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0002c0003t0011g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0003c0005t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| a0004c0004t0011g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0047 | g0199 | EUR | GBR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0220 | EUR | GBR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00280 | hp1 | a0001 | c0002 | t0026 | g0043 | EUR | FIN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00280 | hp2 | a0001 | c0001 | t0014 | g0189 | EUR | FIN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00323 | hp1 | a0001 | c0001 | t0006 | g0081 | EUR | FIN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00323 | hp2 | a0001 | c0002 | t0025 | g0038 | EUR | FIN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00544 | hp1 | a0002 | c0003 | t0011 | g0062 | EAS | CHS | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | CHS | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | CHS | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00558 | hp2 | a0001 | c0001 | t0012 | g0116 | EAS | CHS | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | CHS | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00621 | hp1 | a0001 | c0001 | t0041 | g0133 | EAS | CHS | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | CHS | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00639 | hp1 | a0001 | c0001 | t0039 | g0234 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00639 | hp2 | a0001 | c0001 | t0017 | g0203 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00642 | hp1 | a0001 | c0001 | t0014 | g0208 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0219 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | CHS | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0215 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00735 | hp2 | a0001 | c0001 | t0017 | g0204 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00738 | hp2 | a0001 | c0001 | t0006 | g0060 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG00741 | hp2 | a0001 | c0002 | t0026 | g0045 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0217 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01069 | hp2 | a0001 | c0001 | t0034 | g0013 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0211 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01070 | hp2 | a0001 | c0001 | t0013 | g0198 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0218 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01099 | hp1 | a0001 | c0001 | t0046 | g0190 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01099 | hp2 | a0001 | c0001 | t0016 | g0073 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0182 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0241 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01109 | hp2 | a0001 | c0001 | t0006 | g0088 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01167 | hp1 | a0001 | c0001 | t0004 | g0022 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01167 | hp2 | a0001 | c0001 | t0036 | g0228 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01175 | hp2 | a0001 | c0001 | t0006 | g0080 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01243 | hp1 | a0001 | c0001 | t0018 | g0251 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01243 | hp2 | a0001 | c0001 | t0006 | g0089 | AMR | PUR | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | CLM | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01256 | hp2 | a0001 | c0001 | t0043 | g0135 | AMR | CLM | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | CLM | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | CLM | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0229 | EUR | IBS | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0225 | EUR | IBS | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0090 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01884 | hp2 | a0001 | c0001 | t0007 | g0056 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0206 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01993 | hp1 | a0001 | c0001 | t0030 | g0210 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0214 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02027 | hp1 | a0001 | c0001 | t0012 | g0084 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02027 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02040 | hp1 | a0001 | c0001 | t0032 | g0160 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02055 | hp1 | a0001 | c0001 | t0035 | g0058 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02055 | hp2 | a0001 | c0001 | t0005 | g0247 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02056 | hp1 | a0001 | c0001 | t0013 | g0205 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02071 | hp1 | a0001 | c0001 | t0045 | g0130 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02071 | hp2 | a0001 | c0001 | t0014 | g0170 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02129 | hp1 | a0001 | c0001 | t0010 | g0003 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02132 | hp2 | a0001 | c0007 | t0025 | g0035 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02145 | hp1 | a0001 | c0001 | t0004 | g0010 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0082 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02155 | hp1 | a0002 | c0003 | t0011 | g0079 | EAS | CDX | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02155 | hp2 | a0001 | c0001 | t0020 | g0115 | EAS | CDX | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02165 | hp1 | a0001 | c0001 | t0020 | g0114 | EAS | CDX | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02165 | hp2 | a0001 | c0002 | t0022 | g0049 | EAS | CDX | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0027 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02257 | hp2 | a0001 | c0001 | t0006 | g0061 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02258 | hp1 | a0001 | c0001 | t0021 | g0001 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02280 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PEL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02572 | hp2 | a0001 | c0001 | t0007 | g0029 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02717 | hp1 | a0001 | c0001 | t0018 | g0249 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02717 | hp2 | a0001 | c0001 | t0007 | g0021 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02723 | hp1 | a0001 | c0001 | t0033 | g0023 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02723 | hp2 | a0001 | c0001 | t0048 | g0233 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02735 | hp1 | a0001 | c0002 | t0054 | g0042 | SAS | PJL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0163 | SAS | PJL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0179 | SAS | PJL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02738 | hp2 | a0003 | c0005 | t0001 | g0156 | SAS | PJL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02809 | hp1 | a0001 | c0001 | t0018 | g0026 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02809 | hp2 | a0001 | c0001 | t0008 | g0099 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02818 | hp1 | a0001 | c0001 | t0005 | g0244 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02818 | hp2 | a0001 | c0001 | t0016 | g0071 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0245 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02886 | hp2 | a0001 | c0001 | t0037 | g0055 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02895 | hp2 | a0001 | c0001 | t0006 | g0068 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02896 | hp1 | a0001 | c0001 | t0005 | g0239 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02896 | hp2 | a0001 | c0001 | t0007 | g0019 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02897 | hp1 | a0001 | c0001 | t0005 | g0248 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0024 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02965 | hp1 | a0001 | c0001 | t0008 | g0094 | AFR | ESN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | ESN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02970 | hp1 | a0001 | c0001 | t0055 | g0065 | AFR | ESN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | ESN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | ESN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0096 | AFR | ESN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | MSL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0015 | AFR | MSL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03130 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | ESN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | ESN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0240 | AFR | ESN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03139 | hp2 | a0001 | c0001 | t0006 | g0077 | AFR | ESN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03195 | hp1 | a0001 | c0001 | t0024 | g0067 | AFR | ESN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03195 | hp2 | a0001 | c0001 | t0008 | g0095 | AFR | ESN | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0100 | AFR | MSL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03225 | hp2 | a0001 | c0001 | t0007 | g0025 | AFR | MSL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0216 | SAS | PJL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03453 | hp1 | a0001 | c0001 | t0040 | g0093 | AFR | MSL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03486 | hp1 | a0001 | c0001 | t0005 | g0242 | AFR | MSL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0020 | AFR | GWD | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03579 | hp1 | a0001 | c0001 | t0005 | g0243 | AFR | MSL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03579 | hp2 | a0001 | c0001 | t0007 | g0256 | AFR | MSL | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03831 | hp1 | a0001 | c0001 | t0003 | g0181 | SAS | BEB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | BEB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03834 | hp1 | a0001 | c0001 | t0044 | g0150 | SAS | BEB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03834 | hp2 | a0001 | c0002 | t0009 | g0052 | SAS | BEB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0180 | SAS | BEB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0162 | SAS | BEB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0178 | SAS | STU | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | STU | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG04199 | hp1 | a0001 | c0001 | t0031 | g0222 | SAS | STU | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG04199 | hp2 | a0001 | c0001 | t0013 | g0226 | SAS | STU | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0246 | AFR | YRI | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18522 | hp2 | a0001 | c0001 | t0008 | g0098 | AFR | YRI | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | CHB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0097 | AFR | YRI | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | YRI | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18939 | hp1 | a0001 | c0001 | t0015 | g0187 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18939 | hp2 | a0001 | c0001 | t0028 | g0252 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18944 | hp1 | a0001 | c0001 | t0012 | g0108 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18944 | hp2 | a0002 | c0003 | t0011 | g0078 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18945 | hp1 | a0004 | c0004 | t0011 | g0076 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18945 | hp2 | a0001 | c0002 | t0056 | g0047 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18949 | hp1 | a0001 | c0002 | t0023 | g0044 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18951 | hp2 | a0001 | c0001 | t0015 | g0200 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18952 | hp2 | a0001 | c0002 | t0009 | g0036 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18956 | hp1 | a0001 | c0001 | t0057 | g0174 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18959 | hp1 | a0001 | c0001 | t0012 | g0120 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18959 | hp2 | a0001 | c0001 | t0019 | g0231 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18961 | hp2 | a0001 | c0001 | t0013 | g0202 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18964 | hp1 | a0001 | c0001 | t0015 | g0197 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18969 | hp2 | a0001 | c0001 | t0012 | g0118 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18970 | hp2 | a0001 | c0001 | t0010 | g0004 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18975 | hp2 | a0001 | c0001 | t0019 | g0227 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18979 | hp2 | a0001 | c0006 | t0010 | g0008 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18983 | hp1 | a0001 | c0001 | t0042 | g0147 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18984 | hp2 | a0001 | c0001 | t0010 | g0006 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18986 | hp1 | a0001 | c0001 | t0027 | g0158 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18986 | hp2 | a0001 | c0002 | t0050 | g0041 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18992 | hp1 | a0001 | c0002 | t0009 | g0051 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19001 | hp1 | a0001 | c0002 | t0049 | g0031 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19004 | hp1 | a0002 | c0003 | t0011 | g0075 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19011 | hp2 | a0001 | c0002 | t0009 | g0034 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0053 | AFR | LWK | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | LWK | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19058 | hp2 | a0001 | c0001 | t0013 | g0230 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19065 | hp2 | a0001 | c0001 | t0017 | g0191 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19067 | hp2 | a0001 | c0002 | t0022 | g0046 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19068 | hp2 | a0002 | c0003 | t0011 | g0074 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19072 | hp2 | a0001 | c0002 | t0053 | g0048 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19074 | hp1 | a0001 | c0001 | t0010 | g0005 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19074 | hp2 | a0001 | c0002 | t0009 | g0040 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19077 | hp2 | a0001 | c0002 | t0051 | g0050 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19080 | hp1 | a0001 | c0002 | t0009 | g0033 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19082 | hp2 | a0001 | c0002 | t0023 | g0032 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19088 | hp2 | a0001 | c0002 | t0009 | g0037 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19091 | hp1 | a0001 | c0001 | t0010 | g0007 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0213 | EUR | TSI | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | TSI | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02109 | hp1 | a0001 | c0001 | t0021 | g0001 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02109 | hp2 | a0001 | c0001 | t0024 | g0066 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0221 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0250 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0011 | AFR | ACB | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | USA | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| HG06807 | hp2 | a0001 | c0001 | t0008 | g0092 | AFR | USA | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18955 | hp1 | a0001 | c0002 | t0052 | g0039 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | USA | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA20300 | hp2 | a0001 | c0001 | t0038 | g0057 | AFR | USA | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA21309 | hp1 | a0001 | c0001 | t0016 | g0054 | AFR | LWK | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | LWK | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0029 | g0183 | REF | REF | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0008 | g0091 | REF | REF | RABGAP1_chr9_122936020_123109866 | RABGAP1 | chr9 | 122936020 | 123109866 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:122986335 | G | A | 1 | a0004 | 1 | NA18945.hp1 | missense_variant | MODERATE | c.506G>A | p.Arg169Lys | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/26 | 629/4986 | 506/3210 | 169/1069 | chr9 | 122986335 | |||
| chr9:123020458 | A | G | 2 | a0002 a0004 |
6 | HG00544.hp1 HG02155.hp1 NA18944.hp2 others(3): Show |
missense_variant&splice_region_variant | MODERATE | c.1793A>G | p.Lys598Arg | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/26 | 1916/4986 | 1793/3210 | 598/1069 | chr9 | 123020458 | |||
| chr9:123101585 | A | G | 1 | a0003 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.2909A>G | p.Glu970Gly | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 25/26 | 3032/4986 | 2909/3210 | 970/1069 | chr9 | 123101585 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:122986249 | C | T | 1 | a0001c0007 | 1 | HG02132.hp2 | synonymous_variant | LOW | c.420C>T | p.Ala140Ala | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/26 | 543/4986 | 420/3210 | 140/1069 | chr9 | 122986249 | |||
| chr9:123010485 | A | G | 1 | a0001c0006 | 1 | NA18979.hp2 | synonymous_variant | LOW | c.1506A>G | p.Gln502Gln | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/26 | 1629/4986 | 1506/3210 | 502/1069 | chr9 | 123010485 | |||
| chr9:123020384 | A | G | 2 | a0001c0002 a0001c0007 |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
synonymous_variant | LOW | c.1719A>G | p.Gly573Gly | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/26 | 1842/4986 | 1719/3210 | 573/1069 | chr9 | 123020384 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:122941023 | T | G | 1 | a0001c0001t0027 | 1 | NA18986.hp1 | 5_prime_UTR_variant | MODIFIER | c.-120T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/26 | 16037 | chr9 | 122941023 | ||||||
| chr9:123103357 | C | T | 2 | a0001c0001t0013 a0001c0001t0057 |
6 | HG01070.hp2 HG02056.hp1 HG04199.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*144C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 144 | chr9 | 123103357 | ||||||
| chr9:123103581 | T | A | 1 | a0001c0001t0028 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*368T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 368 | chr9 | 123103581 | ||||||
| chr9:123103582 | A | T | 16 | a0001c0001t0024 a0001c0001t0048 a0001c0001t0055 others(13): Show |
26 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*369A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 369 | chr9 | 123103582 | ||||||
| chr9:123103582 | AATATACA others(29): Show |
A | 1 | a0001c0001t0047 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*375_*410delCATATA others(30): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 375 | INFO_REALIGN_3_PRIME | chr9 | 123103582 | |||||
| chr9:123103583 | ATATACAT others(4): Show |
A | 1 | a0001c0002t0056 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*371_*381delTATACA others(5): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 371 | chr9 | 123103583 | ||||||
| chr9:123103583 | ATATACAT others(6): Show |
A | 3 | a0001c0001t0055 a0001c0002t0025 a0001c0007t0025 |
3 | HG00323.hp2 HG02132.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*371_*383delTATACA others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 371 | chr9 | 123103583 | ||||||
| chr9:123103583 | ATATACAT others(8): Show |
A | 4 | a0001c0001t0024 a0001c0002t0023 a0001c0002t0053 others(1): Show |
6 | HG02109.hp2 HG02735.hp1 HG03195.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*371_*385delTATACA others(9): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 371 | chr9 | 123103583 | ||||||
| chr9:123103583 | ATATACAT others(10): Show |
A | 4 | a0001c0002t0009 a0001c0002t0022 a0001c0002t0051 others(1): Show |
11 | HG02165.hp2 HG03834.hp2 NA18952.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*371_*387delTATACA others(11): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 371 | chr9 | 123103583 | ||||||
| chr9:123103583 | ATATACAT others(12): Show |
A | 2 | a0001c0002t0049 a0001c0002t0050 |
2 | NA18986.hp2 NA19001.hp1 |
3_prime_UTR_variant | MODIFIER | c.*371_*389delTATACA others(13): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 371 | chr9 | 123103583 | ||||||
| chr9:123103583 | ATATACAT others(18): Show |
A | 1 | a0001c0001t0048 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*371_*395delTATACA others(19): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 371 | chr9 | 123103583 | ||||||
| chr9:123103588 | C | CAT | 5 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(2): Show |
17 | HG00280.hp2 HG00597.hp1 HG00673.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*423_*424dupTA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 425 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | |||||
| chr9:123103588 | C | CATAT | 5 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0008 others(2): Show |
9 | HG00558.hp1 HG00673.hp1 HG01934.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*421_*424dupTATA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 425 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | |||||
| chr9:123103588 | C | CATATACA others(5): Show |
1 | a0001c0001t0002 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*380_*381insCATATA others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 381 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | |||||
| chr9:123103588 | C | CATATAT | 5 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(2): Show |
9 | HG00099.hp2 HG01167.hp2 HG01515.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*419_*424dupTATATA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 425 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | |||||
| chr9:123103588 | C | CATATATA others(3): Show |
4 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0014 others(1): Show |
4 | HG02071.hp2 HG02165.hp1 HG02896.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*415_*424dupTATATA others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 425 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | |||||
| chr9:123103588 | C | CATATATA others(5): Show |
9 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(6): Show |
13 | HG00544.hp2 HG00735.hp1 HG01256.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*413_*424dupTATATA others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 425 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | |||||
| chr9:123103588 | C | CATATATA others(7): Show |
6 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0015 others(3): Show |
7 | HG00639.hp1 NA18747.hp2 NA18964.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*411_*424dupTATATA others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 425 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | |||||
| chr9:123103588 | C | CATATATA others(9): Show |
2 | a0001c0001t0002 a0001c0001t0019 |
2 | HG02735.hp2 NA18959.hp2 |
3_prime_UTR_variant | MODIFIER | c.*409_*424dupTATATA others(10): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 425 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | |||||
| chr9:123103588 | C | CATATATA others(11): Show |
4 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(1): Show |
4 | HG01081.hp1 HG03486.hp1 NA18939.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*407_*424dupTATATA others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 425 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | |||||
| chr9:123103588 | C | CATATATA others(13): Show |
3 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0010 |
4 | HG01106.hp2 HG02055.hp2 NA19004.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*405_*424dupTATATA others(14): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 425 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | |||||
| chr9:123103588 | C | CATATATA others(15): Show |
2 | a0001c0001t0010 a0001c0001t0012 |
2 | NA18959.hp1 NA18970.hp2 |
3_prime_UTR_variant | MODIFIER | c.*403_*424dupTATATA others(16): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 425 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | |||||
| chr9:123103588 | C | CATATATA others(17): Show |
1 | a0001c0001t0001 | 1 | NA18992.hp2 | 3_prime_UTR_variant | MODIFIER | c.*401_*424dupTATATA others(18): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 425 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | |||||
| chr9:123103588 | C | CATATATA others(19): Show |
1 | a0001c0001t0012 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*399_*424dupTATATA others(20): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 425 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | |||||
| chr9:123103588 | C | T | 1 | a0001c0001t0001 | 2 | NA18952.hp1 NA19077.hp1 |
3_prime_UTR_variant | MODIFIER | c.*375C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 375 | chr9 | 123103588 | ||||||
| chr9:123103588 | CAT | C | 9 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(6): Show |
20 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*423_*424delTA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 423 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | |||||
| chr9:123103588 | CATAT | C | 7 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(4): Show |
9 | HG00597.hp2 HG00642.hp1 HG00642.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*421_*424delTATA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 421 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | |||||
| chr9:123103588 | CATATAT | C | 6 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0013 others(3): Show |
12 | HG01952.hp2 HG01981.hp1 HG02135.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*419_*424delTATATA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 419 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | |||||
| chr9:123103588 | CATATATA others(1): Show |
C | 6 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(3): Show |
11 | HG00544.hp1 HG00733.hp1 HG00733.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*417_*424delTATATA others(2): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 417 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | |||||
| chr9:123103588 | CATATATA others(3): Show |
C | 7 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(4): Show |
14 | HG01070.hp1 HG01081.hp2 HG01106.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*415_*424delTATATA others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 415 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | |||||
| chr9:123103588 | CATATATA others(5): Show |
C | 4 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0042 others(1): Show |
9 | HG01167.hp1 HG01993.hp2 HG02257.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*413_*424delTATATA others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 413 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | |||||
| chr9:123103588 | CATATATA others(7): Show |
C | 3 | a0001c0001t0004 a0001c0001t0007 a0001c0001t0034 |
6 | HG01069.hp2 HG02145.hp1 HG02559.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*411_*424delTATATA others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 411 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | |||||
| chr9:123103588 | CATATATA others(9): Show |
C | 6 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(3): Show |
13 | HG00621.hp2 HG02055.hp1 HG02280.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*409_*424delTATATA others(10): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 409 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | |||||
| chr9:123103588 | CATATATA others(11): Show |
C | 9 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(6): Show |
21 | HG01099.hp2 HG01109.hp1 HG01109.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*407_*424delTATATA others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 407 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | |||||
| chr9:123103588 | CATATATA others(15): Show |
C | 3 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0015 |
3 | HG03579.hp2 HG03942.hp1 NA18951.hp2 |
3_prime_UTR_variant | MODIFIER | c.*403_*424delTATATA others(16): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 403 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | |||||
| chr9:123103588 | CATATATA others(19): Show |
C | 1 | a0001c0001t0001 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*399_*424delTATATA others(20): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 399 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | |||||
| chr9:123103588 | CATATATA others(21): Show |
C | 2 | a0001c0001t0001 a0001c0001t0018 |
4 | HG01243.hp1 HG02717.hp1 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*397_*424delTATATA others(22): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 397 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | |||||
| chr9:123103588 | CATATATA others(25): Show |
C | 3 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0021 |
11 | HG00323.hp1 HG00738.hp2 HG01175.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*393_*424delTATATA others(26): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 393 | INFO_REALIGN_3_PRIME | chr9 | 123103588 | |||||
| chr9:123103596 | T | C | 1 | a0001c0002t0026 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*383T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 383 | chr9 | 123103596 | ||||||
| chr9:123103598 | T | C | 1 | a0001c0002t0026 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*385T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 385 | chr9 | 123103598 | ||||||
| chr9:123103600 | T | C | 1 | a0001c0002t0056 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*387T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 387 | chr9 | 123103600 | ||||||
| chr9:123103602 | T | C | 3 | a0001c0001t0055 a0001c0002t0025 a0001c0007t0025 |
3 | HG00323.hp2 HG02132.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*389T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 389 | chr9 | 123103602 | ||||||
| chr9:123103604 | T | C | 4 | a0001c0001t0024 a0001c0002t0023 a0001c0002t0053 others(1): Show |
6 | HG02109.hp2 HG02735.hp1 HG03195.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*391T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 391 | chr9 | 123103604 | ||||||
| chr9:123103606 | T | C | 4 | a0001c0002t0009 a0001c0002t0022 a0001c0002t0051 others(1): Show |
11 | HG02165.hp2 HG03834.hp2 NA18952.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*393T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 393 | chr9 | 123103606 | ||||||
| chr9:123103608 | T | C | 2 | a0001c0002t0049 a0001c0002t0050 |
2 | NA18986.hp2 NA19001.hp1 |
3_prime_UTR_variant | MODIFIER | c.*395T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 395 | chr9 | 123103608 | ||||||
| chr9:123103614 | T | C | 1 | a0001c0001t0048 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*401T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 401 | chr9 | 123103614 | ||||||
| chr9:123103623 | A | ATATATAT others(5): Show |
1 | a0001c0001t0046 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*421_*422insGTATAT others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 422 | INFO_REALIGN_3_PRIME | chr9 | 123103623 | |||||
| chr9:123103791 | G | C | 42 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(39): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*578G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 578 | chr9 | 123103791 | ||||||
| chr9:123103825 | C | T | 2 | a0001c0001t0012 a0001c0001t0045 |
6 | HG00558.hp2 HG02027.hp1 HG02071.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*612C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 612 | chr9 | 123103825 | ||||||
| chr9:123103861 | C | A | 1 | a0001c0001t0030 | 1 | HG01993.hp1 | 3_prime_UTR_variant | MODIFIER | c.*648C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 648 | chr9 | 123103861 | ||||||
| chr9:123103933 | C | G | 4 | a0001c0001t0024 a0001c0001t0039 a0001c0001t0048 others(1): Show |
5 | HG00639.hp1 HG02109.hp2 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*720C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 720 | chr9 | 123103933 | ||||||
| chr9:123103963 | T | TTG | 11 | a0001c0001t0001 a0001c0001t0012 a0001c0001t0019 others(8): Show |
77 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*782_*783dupGT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 784 | INFO_REALIGN_3_PRIME | chr9 | 123103963 | |||||
| chr9:123103963 | T | TTGTG | 3 | a0001c0001t0016 a0001c0001t0044 a0001c0001t0045 |
5 | HG01099.hp2 HG02071.hp1 HG02818.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*780_*783dupGTGT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 784 | INFO_REALIGN_3_PRIME | chr9 | 123103963 | |||||
| chr9:123103963 | T | TTGTGTGT others(3): Show |
1 | a0001c0001t0038 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*774_*783dupGTGTGT others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 784 | INFO_REALIGN_3_PRIME | chr9 | 123103963 | |||||
| chr9:123103963 | TTG | T | 2 | a0002c0003t0011 a0004c0004t0011 |
6 | HG00544.hp1 HG02155.hp1 NA18944.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*782_*783delGT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 782 | INFO_REALIGN_3_PRIME | chr9 | 123103963 | |||||
| chr9:123103963 | TTGTGTGT others(5): Show |
T | 1 | a0001c0001t0020 | 2 | HG02155.hp2 HG02165.hp1 |
3_prime_UTR_variant | MODIFIER | c.*772_*783delGTGTGT others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 772 | INFO_REALIGN_3_PRIME | chr9 | 123103963 | |||||
| chr9:123103991 | G | A | 4 | a0001c0001t0003 a0001c0001t0030 a0001c0001t0031 others(1): Show |
17 | HG00099.hp1 HG00642.hp2 HG00733.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*778G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 778 | chr9 | 123103991 | ||||||
| chr9:123103993 | G | GTGTGTGT others(1): Show |
1 | a0001c0001t0017 | 3 | HG00639.hp2 HG00735.hp2 NA19065.hp2 |
3_prime_UTR_variant | MODIFIER | c.*783_*784insGTGTAT others(2): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 784 | INFO_REALIGN_3_PRIME | chr9 | 123103993 | |||||
| chr9:123103993 | G | GTGTGTGT others(5): Show |
1 | a0001c0002t0054 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*783_*784insGTGTGT others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 784 | INFO_REALIGN_3_PRIME | chr9 | 123103993 | |||||
| chr9:123103993 | GTGTA | G | 4 | a0001c0001t0003 a0001c0001t0030 a0001c0001t0031 others(1): Show |
17 | HG00099.hp1 HG00642.hp2 HG00733.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*786_*789delGTAT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 786 | INFO_REALIGN_3_PRIME | chr9 | 123103993 | |||||
| chr9:123103995 | G | A | 1 | a0001c0001t0005 | 10 | HG01109.hp1 HG02055.hp2 HG02818.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*782G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 782 | chr9 | 123103995 | ||||||
| chr9:123103997 | A | G | 30 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(27): Show |
120 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*784A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 784 | chr9 | 123103997 | ||||||
| chr9:123103999 | G | A | 7 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0017 others(4): Show |
31 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*786G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 786 | chr9 | 123103999 | ||||||
| chr9:123103999 | G | GTA | 6 | a0001c0001t0014 a0001c0001t0019 a0001c0001t0021 others(3): Show |
11 | HG00280.hp2 HG00642.hp1 HG02071.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*799_*800dupTA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 801 | INFO_REALIGN_3_PRIME | chr9 | 123103999 | |||||
| chr9:123103999 | G | GTATGTA | 6 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0013 others(3): Show |
63 | HG00099.hp2 HG00280.hp1 HG00544.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*789_*790insGTATAT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 790 | INFO_REALIGN_3_PRIME | chr9 | 123103999 | |||||
| chr9:123103999 | G | GTGTATGT others(1): Show |
11 | a0001c0001t0007 a0001c0001t0010 a0001c0001t0046 others(8): Show |
29 | HG00323.hp2 HG01099.hp1 HG01884.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*787_*788insGTATGT others(2): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 788 | INFO_REALIGN_3_PRIME | chr9 | 123103999 | |||||
| chr9:123103999 | G | GTGTGTA | 1 | a0001c0001t0015 | 3 | NA18939.hp1 NA18951.hp2 NA18964.hp1 |
3_prime_UTR_variant | MODIFIER | c.*787_*788insGTGTAT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 788 | INFO_REALIGN_3_PRIME | chr9 | 123103999 | |||||
| chr9:123103999 | G | GTGTGTAT others(3): Show |
3 | a0001c0001t0018 a0001c0001t0035 a0001c0001t0036 |
5 | HG01167.hp2 HG01243.hp1 HG02055.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*787_*788insGTGTAT others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 788 | INFO_REALIGN_3_PRIME | chr9 | 123103999 | |||||
| chr9:123103999 | G | GTGTGTGT others(5): Show |
5 | a0001c0001t0024 a0001c0001t0037 a0001c0001t0055 others(2): Show |
7 | HG02109.hp2 HG02165.hp2 HG02886.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*787_*788insGTGTGT others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 788 | INFO_REALIGN_3_PRIME | chr9 | 123103999 | |||||
| chr9:123103999 | G | GTGTGTGT others(9): Show |
1 | a0001c0001t0039 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*787_*788insGTGTGT others(10): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 788 | INFO_REALIGN_3_PRIME | chr9 | 123103999 | |||||
| chr9:123103999 | G | GTGTGTGT others(13): Show |
1 | a0001c0001t0048 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*787_*788insGTGTGT others(14): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 788 | INFO_REALIGN_3_PRIME | chr9 | 123103999 | |||||
| chr9:123104081 | T | A | 1 | a0001c0001t0018 | 3 | HG01243.hp1 HG02717.hp1 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*868T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 868 | chr9 | 123104081 | ||||||
| chr9:123104132 | T | A | 2 | a0001c0001t0039 a0001c0001t0048 |
2 | HG00639.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*919T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 919 | chr9 | 123104132 | ||||||
| chr9:123104288 | T | TCC | 2 | a0001c0001t0024 a0001c0001t0055 |
3 | HG02109.hp2 HG02970.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1076_*1077dupCC | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 1078 | INFO_REALIGN_3_PRIME | chr9 | 123104288 | |||||
| chr9:123104417 | T | TA | 55 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(52): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
3_prime_UTR_variant | MODIFIER | c.*1218dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 1219 | INFO_REALIGN_3_PRIME | chr9 | 123104417 | |||||
| chr9:123104481 | T | C | 1 | a0001c0001t0041 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1268T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 1268 | chr9 | 123104481 | ||||||
| chr9:123104493 | C | G | 17 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0010 others(14): Show |
84 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*1280C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 1280 | chr9 | 123104493 | ||||||
| chr9:123104517 | G | A | 1 | a0001c0001t0040 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1304G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 1304 | chr9 | 123104517 | ||||||
| chr9:123104646 | C | T | 1 | a0001c0001t0031 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1433C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 26/26 | 1433 | chr9 | 123104646 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:122941126 | C | G | 1 | a0001c0001t0001g0257 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-50+33C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122941126 | |||||||
| chr9:122941183 | T | C | 1 | a0001c0001t0001g0002 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-50+90T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122941183 | |||||||
| chr9:122941241 | C | T | 1 | a0001c0001t0007g0256 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-50+148C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122941241 | |||||||
| chr9:122941348 | C | G | 1 | a0001c0001t0001g0255 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-50+255C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122941348 | |||||||
| chr9:122941536 | C | T | 1 | a0001c0001t0002g0254 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-50+443C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122941536 | |||||||
| chr9:122941711 | G | C | 6 | a0001c0001t0010g0003 a0001c0001t0010g0004 a0001c0001t0010g0005 others(3): Show |
6 | HG02129.hp1 NA18970.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.-50+618G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122941711 | |||||||
| chr9:122941756 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-50+663A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122941756 | |||||||
| chr9:122941785 | C | G | 1 | a0001c0001t0028g0252 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-50+692C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122941785 | |||||||
| chr9:122941907 | A | C | 3 | a0001c0001t0006g0250 a0001c0001t0018g0249 a0001c0001t0018g0251 |
3 | HG01243.hp1 HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-50+814A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122941907 | |||||||
| chr9:122941946 | G | A | 22 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(19): Show |
22 | HG01069.hp2 HG01167.hp1 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.-50+853G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122941946 | |||||||
| chr9:122942322 | A | G | 10 | a0001c0001t0005g0239 a0001c0001t0005g0240 a0001c0001t0005g0241 others(7): Show |
10 | HG01109.hp1 HG02055.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.-50+1229A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122942322 | |||||||
| chr9:122942499 | G | T | 3 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0253 |
3 | HG02056.hp2 HG02132.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.-50+1406G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122942499 | |||||||
| chr9:122942563 | G | C | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.-50+1470G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122942563 | |||||||
| chr9:122942664 | C | T | 106 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(103): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.-50+1571C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122942664 | |||||||
| chr9:122942669 | C | CA | 27 | a0001c0001t0001g0002 a0001c0001t0001g0064 a0001c0001t0001g0069 others(24): Show |
28 | HG00323.hp1 HG00673.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.-50+1595dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122942669 | ||||||
| chr9:122942669 | C | CAA | 8 | a0001c0001t0001g0059 a0001c0001t0001g0063 a0001c0001t0006g0060 others(5): Show |
8 | HG00544.hp1 HG00639.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.-50+1594_-50+1595d others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122942669 | ||||||
| chr9:122942669 | C | CAAA | 17 | a0001c0001t0004g0030 a0001c0002t0009g0036 a0001c0002t0009g0037 others(14): Show |
17 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.-50+1593_-50+1595d others(5): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122942669 | ||||||
| chr9:122942669 | C | CAAAA | 29 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0015 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.-50+1592_-50+1595d others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122942669 | ||||||
| chr9:122942669 | C | CAAAAA | 19 | a0001c0001t0002g0223 a0001c0001t0002g0224 a0001c0001t0002g0225 others(16): Show |
19 | HG00741.hp1 HG01167.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.-50+1591_-50+1595d others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122942669 | ||||||
| chr9:122942669 | C | CAAAAAA | 40 | a0001c0001t0002g0184 a0001c0001t0002g0185 a0001c0001t0002g0186 others(37): Show |
40 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.-50+1590_-50+1595d others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122942669 | ||||||
| chr9:122942669 | C | CAAAAAAA | 25 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(22): Show |
25 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.-50+1589_-50+1595d others(9): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122942669 | ||||||
| chr9:122942669 | CA | C | 20 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(17): Show |
20 | HG00733.hp1 HG01993.hp2 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.-50+1595delA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122942669 | ||||||
| chr9:122943023 | TAAAAA | T | 8 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG01081.hp1 HG01106.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.-50+1933_-50+1937d others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122943023 | ||||||
| chr9:122943034 | CA | C | 67 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0085 others(64): Show |
67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.-50+1947delA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122943034 | ||||||
| chr9:122943050 | T | TAGTC | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.-50+1959_-50+1962d others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122943050 | ||||||
| chr9:122943061 | T | A | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.-50+1968T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122943061 | |||||||
| chr9:122943072 | CTTT | C | 18 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(15): Show |
18 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50+2006_-50+2008d others(5): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122943072 | ||||||
| chr9:122943072 | CTTTTT | C | 39 | a0001c0001t0001g0063 a0001c0001t0001g0129 a0001c0001t0001g0131 others(36): Show |
39 | HG00621.hp1 HG01069.hp2 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.-50+2004_-50+2008d others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122943072 | ||||||
| chr9:122943072 | CTTTTTT | C | 73 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0069 others(70): Show |
74 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.-50+2003_-50+2008d others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122943072 | ||||||
| chr9:122943072 | CTTTTTTT | C | 16 | a0001c0001t0001g0064 a0001c0001t0005g0239 a0001c0001t0005g0240 others(13): Show |
16 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.-50+2002_-50+2008d others(9): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122943072 | ||||||
| chr9:122943072 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0004g0011 a0001c0001t0004g0012 |
2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-50+1997_-50+2008d others(14): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122943072 | ||||||
| chr9:122943072 | CTTTTTTT others(6): Show |
C | 18 | a0001c0001t0002g0178 a0001c0001t0002g0180 a0001c0001t0002g0212 others(15): Show |
18 | HG00099.hp2 HG00621.hp2 HG00642.hp2 others(15): Show |
intron_variant | MODIFIER | c.-50+1996_-50+2008d others(15): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122943072 | ||||||
| chr9:122943072 | CTTTTTTT others(7): Show |
C | 64 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(61): Show |
64 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.-50+1995_-50+2008d others(16): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122943072 | ||||||
| chr9:122943072 | CTTTTTTT others(9): Show |
C | 2 | a0001c0001t0001g0101 a0001c0001t0001g0102 |
2 | NA18747.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.-50+1993_-50+2008d others(18): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122943072 | ||||||
| chr9:122943072 | CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0018g0249 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-50+1991_-50+2008d others(20): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122943072 | ||||||
| chr9:122943196 | A | C | 1 | a0001c0001t0001g0128 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-50+2103A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122943196 | |||||||
| chr9:122943199 | T | C | 106 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(103): Show |
106 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.-50+2106T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122943199 | |||||||
| chr9:122943256 | A | C | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.-50+2163A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122943256 | |||||||
| chr9:122943477 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-50+2384A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122943477 | |||||||
| chr9:122943669 | G | A | 4 | a0001c0001t0001g0064 a0001c0001t0024g0066 a0001c0001t0024g0067 others(1): Show |
4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-50+2576G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122943669 | |||||||
| chr9:122943733 | A | G | 1 | a0001c0001t0004g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-50+2640A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122943733 | |||||||
| chr9:122943794 | A | T | 1 | a0001c0001t0002g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-50+2701A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122943794 | |||||||
| chr9:122943862 | A | G | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.-50+2769A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122943862 | |||||||
| chr9:122943877 | C | T | 67 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0085 others(64): Show |
67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.-50+2784C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122943877 | |||||||
| chr9:122943952 | C | CA | 52 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0085 others(49): Show |
52 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.-50+2869dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122943952 | ||||||
| chr9:122943972 | G | T | 1 | a0001c0001t0031g0222 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-50+2879G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122943972 | |||||||
| chr9:122944229 | CT | C | 8 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0104 others(5): Show |
8 | HG01069.hp2 HG01496.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.-50+3150delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122944229 | ||||||
| chr9:122944243 | T | A | 10 | a0001c0001t0005g0239 a0001c0001t0005g0240 a0001c0001t0005g0241 others(7): Show |
10 | HG01109.hp1 HG02055.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.-50+3150T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122944243 | |||||||
| chr9:122944566 | G | A | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-50+3473G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122944566 | |||||||
| chr9:122944664 | G | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG02258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.-50+3571G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122944664 | |||||||
| chr9:122944737 | A | AT | 12 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(9): Show |
12 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.-50+3657dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122944737 | ||||||
| chr9:122944744 | T | C | 1 | a0001c0001t0048g0233 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-50+3651T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122944744 | |||||||
| chr9:122944751 | A | T | 1 | a0001c0001t0048g0233 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-50+3658A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122944751 | |||||||
| chr9:122944872 | C | T | 2 | a0001c0001t0006g0080 a0001c0001t0006g0081 |
2 | HG00323.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-50+3779C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122944872 | |||||||
| chr9:122945068 | C | G | 135 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.-50+3975C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122945068 | |||||||
| chr9:122945147 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-50+4061_-50+4070d others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122945147 | ||||||
| chr9:122945147 | C | CTTTTTTT others(6): Show |
3 | a0001c0001t0016g0054 a0001c0002t0025g0038 a0001c0002t0052g0039 |
3 | HG00323.hp2 NA18955.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-50+4058_-50+4070d others(15): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122945147 | ||||||
| chr9:122945147 | C | CTTTTTTT others(7): Show |
32 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0012 others(29): Show |
32 | HG00280.hp1 HG01884.hp2 HG02132.hp2 others(29): Show |
intron_variant | MODIFIER | c.-50+4057_-50+4070d others(16): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122945147 | ||||||
| chr9:122945147 | C | CTTTTTTT others(8): Show |
14 | a0001c0001t0004g0010 a0001c0001t0004g0022 a0001c0001t0004g0028 others(11): Show |
14 | HG00741.hp2 HG01069.hp2 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.-50+4056_-50+4070d others(17): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122945147 | ||||||
| chr9:122945147 | C | CTTTTTTT others(9): Show |
1 | a0001c0001t0007g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-50+4055_-50+4070d others(18): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122945147 | ||||||
| chr9:122945147 | C | CTTTTTTT others(10): Show |
3 | a0001c0001t0002g0185 a0001c0001t0002g0186 a0001c0001t0032g0160 |
3 | HG02040.hp1 HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-50+4070_-50+4071i others(19): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122945147 | ||||||
| chr9:122945147 | C | CTTTTTTT others(11): Show |
23 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(20): Show |
23 | HG00280.hp2 HG01099.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.-50+4070_-50+4071i others(20): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122945147 | ||||||
| chr9:122945147 | C | CTTTTTTT others(12): Show |
28 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 others(25): Show |
28 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.-50+4070_-50+4071i others(21): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122945147 | ||||||
| chr9:122945147 | C | CTTTTTTT others(13): Show |
20 | a0001c0001t0002g0173 a0001c0001t0002g0175 a0001c0001t0002g0176 others(17): Show |
20 | HG00544.hp2 HG00642.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.-50+4070_-50+4071i others(22): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122945147 | ||||||
| chr9:122945147 | C | CTTTTTTT others(14): Show |
5 | a0001c0001t0002g0220 a0001c0001t0002g0232 a0001c0001t0003g0182 others(2): Show |
5 | HG00099.hp2 HG00642.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.-50+4070_-50+4071i others(23): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122945147 | ||||||
| chr9:122945147 | C | CTTTTTTT others(16): Show |
2 | a0001c0001t0003g0221 a0001c0001t0031g0222 |
2 | HG02486.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-50+4070_-50+4071i others(25): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122945147 | ||||||
| chr9:122945147 | CT | C | 96 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(93): Show |
97 | HG00323.hp1 HG00558.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.-50+4070delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122945147 | ||||||
| chr9:122945372 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0127 |
2 | NA18952.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.-50+4279G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122945372 | |||||||
| chr9:122945534 | T | G | 1 | a0001c0001t0010g0003 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-50+4441T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122945534 | |||||||
| chr9:122945615 | T | C | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.-50+4522T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122945615 | |||||||
| chr9:122945934 | T | C | 107 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(104): Show |
108 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.-50+4841T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122945934 | |||||||
| chr9:122946036 | A | C | 2 | a0001c0001t0002g0164 a0001c0001t0002g0195 |
2 | HG01175.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.-50+4943A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122946036 | |||||||
| chr9:122946070 | A | T | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-50+4977A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122946070 | |||||||
| chr9:122946193 | A | C | 1 | a0001c0001t0001g0132 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-50+5100A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122946193 | |||||||
| chr9:122946265 | G | C | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-50+5172G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122946265 | |||||||
| chr9:122946661 | A | G | 1 | a0001c0001t0004g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-50+5568A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122946661 | |||||||
| chr9:122946809 | A | G | 1 | a0001c0001t0003g0217 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-50+5716A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122946809 | |||||||
| chr9:122946995 | C | T | 1 | a0001c0001t0027g0158 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-50+5902C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122946995 | |||||||
| chr9:122947044 | A | G | 63 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(60): Show |
63 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.-50+5951A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122947044 | |||||||
| chr9:122947135 | C | T | 245 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.-50+6042C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122947135 | |||||||
| chr9:122947236 | T | C | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-50+6143T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122947236 | |||||||
| chr9:122947292 | A | G | 32 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0002g0194 others(29): Show |
32 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.-50+6199A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122947292 | |||||||
| chr9:122947328 | G | T | 1 | a0001c0001t0010g0003 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-50+6235G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122947328 | |||||||
| chr9:122947456 | C | G | 1 | a0001c0001t0001g0157 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-50+6363C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122947456 | |||||||
| chr9:122947480 | T | A | 2 | a0001c0001t0006g0080 a0001c0001t0006g0081 |
2 | HG00323.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.-50+6387T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122947480 | |||||||
| chr9:122947586 | T | C | 2 | a0001c0001t0005g0239 a0001c0001t0005g0248 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-50+6493T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122947586 | |||||||
| chr9:122947601 | A | C | 1 | a0001c0001t0006g0061 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-50+6508A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122947601 | |||||||
| chr9:122947652 | C | T | 1 | a0001c0001t0013g0205 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-50+6559C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122947652 | |||||||
| chr9:122947676 | G | A | 7 | a0001c0001t0002g0161 a0001c0001t0002g0165 a0001c0001t0002g0166 others(4): Show |
7 | HG01361.hp2 HG01934.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50+6583G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122947676 | |||||||
| chr9:122947693 | T | C | 1 | a0001c0002t0009g0040 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-50+6600T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122947693 | |||||||
| chr9:122948042 | A | AAC | 63 | a0001c0001t0001g0059 a0001c0001t0001g0063 a0001c0001t0001g0064 others(60): Show |
63 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.-50+6989_-50+6990d others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122948042 | ||||||
| chr9:122948042 | A | AACAC | 19 | a0001c0001t0001g0123 a0001c0001t0001g0124 a0001c0001t0001g0125 others(16): Show |
19 | HG00738.hp2 HG01884.hp1 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.-50+6987_-50+6990d others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122948042 | ||||||
| chr9:122948042 | A | AACACAC | 17 | a0001c0001t0001g0102 a0001c0001t0001g0104 a0001c0001t0001g0126 others(14): Show |
17 | HG00544.hp1 HG00639.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.-50+6985_-50+6990d others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122948042 | ||||||
| chr9:122948042 | A | AACACACA others(3): Show |
1 | a0002c0003t0011g0079 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-50+6981_-50+6990d others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122948042 | ||||||
| chr9:122948042 | AAC | A | 16 | a0001c0001t0001g0106 a0001c0001t0001g0155 a0001c0001t0001g0157 others(13): Show |
16 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.-50+6989_-50+6990d others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122948042 | ||||||
| chr9:122948042 | AACACAC | A | 21 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(18): Show |
21 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-50+6985_-50+6990d others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122948042 | ||||||
| chr9:122948042 | AACACACA others(3): Show |
A | 8 | a0001c0001t0002g0164 a0001c0001t0002g0177 a0001c0001t0002g0195 others(5): Show |
8 | HG01070.hp1 HG01175.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.-50+6981_-50+6990d others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122948042 | ||||||
| chr9:122948042 | AACACACA others(5): Show |
A | 76 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(73): Show |
76 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.-50+6979_-50+6990d others(14): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122948042 | ||||||
| chr9:122948213 | T | G | 2 | a0001c0001t0004g0011 a0001c0001t0004g0012 |
2 | HG02559.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.-50+7120T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122948213 | |||||||
| chr9:122948358 | A | G | 7 | a0001c0001t0006g0077 a0002c0003t0011g0062 a0002c0003t0011g0074 others(4): Show |
7 | HG00544.hp1 HG02155.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-50+7265A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122948358 | |||||||
| chr9:122948574 | T | C | 2 | a0001c0001t0015g0187 a0001c0001t0015g0197 |
2 | NA18939.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.-50+7481T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122948574 | |||||||
| chr9:122948611 | T | G | 1 | a0001c0001t0013g0230 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-50+7518T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122948611 | |||||||
| chr9:122948915 | T | C | 1 | a0001c0001t0002g0159 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-50+7822T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122948915 | |||||||
| chr9:122948998 | G | A | 245 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.-50+7905G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122948998 | |||||||
| chr9:122949073 | C | T | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.-49-7938C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122949073 | |||||||
| chr9:122949323 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-49-7688G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122949323 | |||||||
| chr9:122949324 | C | A | 80 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(77): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.-49-7687C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122949324 | |||||||
| chr9:122949438 | T | G | 4 | a0001c0001t0001g0064 a0001c0001t0024g0066 a0001c0001t0024g0067 others(1): Show |
4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-49-7573T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122949438 | |||||||
| chr9:122949594 | C | G | 5 | a0001c0001t0005g0239 a0001c0001t0005g0242 a0001c0001t0005g0243 others(2): Show |
5 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-7417C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122949594 | |||||||
| chr9:122949693 | C | CA | 16 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0109 others(13): Show |
16 | HG00639.hp1 HG01081.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.-49-7300dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122949693 | ||||||
| chr9:122949693 | C | CAA | 7 | a0001c0001t0006g0077 a0001c0001t0007g0053 a0002c0003t0011g0074 others(4): Show |
7 | HG02155.hp1 HG03139.hp2 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-7301_-49-7300d others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122949693 | ||||||
| chr9:122949693 | C | CAAA | 28 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0012 others(25): Show |
28 | HG00544.hp1 HG01069.hp2 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.-49-7302_-49-7300d others(5): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122949693 | ||||||
| chr9:122949693 | CAA | C | 21 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(18): Show |
21 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.-49-7301_-49-7300d others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122949693 | ||||||
| chr9:122949713 | G | A | 1 | a0001c0001t0003g0179 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-49-7298G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122949713 | |||||||
| chr9:122949817 | T | A | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.-49-7194T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122949817 | |||||||
| chr9:122950198 | T | G | 1 | a0001c0001t0013g0198 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-49-6813T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122950198 | |||||||
| chr9:122950377 | C | CT | 114 | a0001c0001t0001g0059 a0001c0001t0001g0069 a0001c0001t0001g0070 others(111): Show |
115 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.-49-6612dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122950377 | ||||||
| chr9:122950377 | C | CTT | 61 | a0001c0001t0001g0002 a0001c0001t0001g0064 a0001c0001t0001g0072 others(58): Show |
61 | HG00280.hp1 HG00544.hp1 HG00642.hp1 others(58): Show |
intron_variant | MODIFIER | c.-49-6613_-49-6612d others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122950377 | ||||||
| chr9:122950377 | C | CTTT | 58 | a0001c0001t0001g0063 a0001c0001t0001g0085 a0001c0001t0001g0086 others(55): Show |
58 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.-49-6614_-49-6612d others(5): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122950377 | ||||||
| chr9:122950465 | C | T | 1 | a0001c0001t0002g0232 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-49-6546C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122950465 | |||||||
| chr9:122950628 | A | G | 1 | a0001c0001t0005g0241 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-49-6383A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122950628 | |||||||
| chr9:122950986 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-49-6025G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122950986 | |||||||
| chr9:122951115 | T | C | 1 | a0001c0001t0002g0184 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-49-5896T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122951115 | |||||||
| chr9:122951247 | T | G | 80 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(77): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.-49-5764T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122951247 | |||||||
| chr9:122951272 | T | A | 1 | a0001c0001t0002g0180 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-49-5739T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122951272 | |||||||
| chr9:122951308 | G | A | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-49-5703G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122951308 | |||||||
| chr9:122951446 | G | A | 1 | a0001c0001t0024g0066 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-49-5565G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122951446 | |||||||
| chr9:122951623 | C | T | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-49-5388C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122951623 | |||||||
| chr9:122951951 | G | A | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-49-5060G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122951951 | |||||||
| chr9:122951995 | T | A | 2 | a0001c0001t0002g0168 a0001c0001t0002g0225 |
2 | HG00735.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.-49-5016T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122951995 | |||||||
| chr9:122952069 | T | A | 1 | a0001c0001t0001g0128 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-49-4942T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122952069 | |||||||
| chr9:122952193 | C | T | 1 | a0001c0001t0007g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-49-4818C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122952193 | |||||||
| chr9:122952492 | T | G | 7 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0148 others(4): Show |
7 | HG01993.hp2 HG02135.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-4519T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122952492 | |||||||
| chr9:122952519 | C | T | 1 | a0001c0002t0022g0046 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-49-4492C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122952519 | |||||||
| chr9:122952562 | C | G | 7 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0148 others(4): Show |
7 | HG01993.hp2 HG02135.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-4449C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122952562 | |||||||
| chr9:122952687 | G | C | 1 | a0001c0001t0002g0164 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-49-4324G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122952687 | |||||||
| chr9:122952839 | A | G | 2 | a0001c0001t0015g0187 a0001c0001t0015g0197 |
2 | NA18939.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.-49-4172A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122952839 | |||||||
| chr9:122952851 | T | C | 1 | a0001c0001t0007g0256 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-49-4160T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122952851 | |||||||
| chr9:122952906 | C | A | 2 | a0001c0001t0018g0249 a0001c0001t0018g0251 |
2 | HG01243.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-49-4105C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122952906 | |||||||
| chr9:122953064 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-49-3947A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122953064 | |||||||
| chr9:122953097 | C | T | 1 | a0001c0001t0028g0252 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-49-3914C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122953097 | |||||||
| chr9:122953252 | C | T | 1 | a0001c0001t0002g0188 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-49-3759C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122953252 | |||||||
| chr9:122953405 | C | CT | 14 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0069 others(11): Show |
15 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(12): Show |
intron_variant | MODIFIER | c.-49-3591dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122953405 | ||||||
| chr9:122953466 | A | G | 1 | a0001c0001t0006g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-49-3545A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122953466 | |||||||
| chr9:122953506 | A | T | 3 | a0001c0001t0001g0087 a0001c0001t0001g0122 a0001c0001t0001g0131 |
3 | HG00673.hp2 NA18951.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.-49-3505A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122953506 | |||||||
| chr9:122953621 | G | A | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.-49-3390G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122953621 | |||||||
| chr9:122953666 | T | A | 2 | a0001c0001t0002g0206 a0001c0001t0047g0199 |
2 | HG00099.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.-49-3345T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122953666 | |||||||
| chr9:122953679 | G | A | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-49-3332G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122953679 | |||||||
| chr9:122953722 | A | T | 245 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.-49-3289A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122953722 | |||||||
| chr9:122953987 | A | G | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.-49-3024A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122953987 | |||||||
| chr9:122954038 | T | C | 135 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.-49-2973T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122954038 | |||||||
| chr9:122954180 | G | T | 1 | a0001c0001t0004g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-49-2831G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122954180 | |||||||
| chr9:122954292 | C | T | 3 | a0001c0001t0002g0220 a0001c0001t0003g0215 a0001c0001t0003g0221 |
3 | HG00099.hp2 HG00733.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.-49-2719C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122954292 | |||||||
| chr9:122954487 | G | C | 1 | a0001c0001t0002g0184 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-49-2524G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122954487 | |||||||
| chr9:122954488 | C | T | 1 | a0002c0003t0011g0079 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-49-2523C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122954488 | |||||||
| chr9:122954595 | C | T | 1 | a0001c0001t0045g0130 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-49-2416C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122954595 | |||||||
| chr9:122954633 | A | G | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.-49-2378A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122954633 | |||||||
| chr9:122954784 | G | A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0069 others(9): Show |
13 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.-49-2227G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122954784 | |||||||
| chr9:122954856 | C | T | 4 | a0001c0001t0006g0060 a0001c0001t0006g0061 a0001c0001t0006g0080 others(1): Show |
4 | HG00323.hp1 HG00738.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.-49-2155C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122954856 | |||||||
| chr9:122955130 | G | A | 245 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.-49-1881G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122955130 | |||||||
| chr9:122955194 | G | A | 3 | a0001c0001t0002g0223 a0001c0001t0002g0224 a0001c0001t0002g0232 |
3 | HG00741.hp1 HG01258.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.-49-1817G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122955194 | |||||||
| chr9:122955270 | G | A | 15 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0148 others(12): Show |
15 | HG00733.hp1 HG01993.hp2 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.-49-1741G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122955270 | |||||||
| chr9:122955364 | A | G | 1 | a0001c0001t0005g0241 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-49-1647A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122955364 | |||||||
| chr9:122955365 | A | G | 1 | a0001c0001t0001g0149 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-49-1646A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122955365 | |||||||
| chr9:122955455 | A | C | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.-49-1556A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122955455 | |||||||
| chr9:122955949 | G | C | 5 | a0001c0001t0005g0239 a0001c0001t0005g0242 a0001c0001t0005g0243 others(2): Show |
5 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-49-1062G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122955949 | |||||||
| chr9:122955961 | A | G | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-49-1050A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122955961 | |||||||
| chr9:122956104 | A | G | 1 | a0001c0001t0017g0191 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-49-907A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122956104 | |||||||
| chr9:122956297 | CATGTTAA others(129): Show |
C | 1 | a0001c0001t0007g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-49-712_-49-577del | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122956297 | ||||||
| chr9:122956366 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-49-645G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122956366 | |||||||
| chr9:122956375 | A | G | 1 | a0001c0001t0016g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-49-636A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122956375 | |||||||
| chr9:122956409 | G | T | 7 | a0001c0001t0006g0077 a0002c0003t0011g0062 a0002c0003t0011g0074 others(4): Show |
7 | HG00544.hp1 HG02155.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-49-602G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122956409 | |||||||
| chr9:122956416 | C | T | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.-49-595C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122956416 | |||||||
| chr9:122956425 | C | T | 2 | a0001c0001t0017g0203 a0001c0001t0017g0204 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.-49-586C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122956425 | |||||||
| chr9:122956433 | G | T | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.-49-578G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122956433 | |||||||
| chr9:122956450 | A | G | 2 | a0001c0001t0017g0203 a0001c0001t0017g0204 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.-49-561A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122956450 | |||||||
| chr9:122956598 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-49-413C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122956598 | |||||||
| chr9:122956649 | C | CA | 185 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(182): Show |
186 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.-49-344dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122956649 | ||||||
| chr9:122956649 | C | CAA | 57 | a0001c0001t0001g0064 a0001c0001t0001g0154 a0001c0001t0002g0168 others(54): Show |
57 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.-49-345_-49-344dup others(2): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr9 | 122956649 | ||||||
| chr9:122956690 | C | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0121 |
2 | HG02129.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.-49-321C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122956690 | |||||||
| chr9:122956783 | T | C | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-49-228T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 1/25 | chr9 | 122956783 | |||||||
| chr9:122957314 | G | A | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.150+105G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122957314 | |||||||
| chr9:122957502 | C | G | 10 | a0001c0001t0005g0239 a0001c0001t0005g0240 a0001c0001t0005g0241 others(7): Show |
10 | HG01109.hp1 HG02055.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.150+293C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122957502 | |||||||
| chr9:122957512 | T | TGGGGGGG others(132): Show |
1 | a0001c0001t0007g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.150+303_150+304ins others(139): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122957512 | |||||||
| chr9:122957513 | T | G | 1 | a0001c0001t0007g0019 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.150+304T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122957513 | |||||||
| chr9:122957644 | C | G | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.150+435C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122957644 | |||||||
| chr9:122957720 | T | C | 1 | a0001c0001t0005g0241 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.150+511T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122957720 | |||||||
| chr9:122957735 | G | A | 1 | a0001c0001t0002g0185 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.150+526G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122957735 | |||||||
| chr9:122957884 | C | CT | 22 | a0001c0001t0017g0191 a0001c0002t0009g0033 a0001c0002t0009g0034 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.150+690dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122957884 | ||||||
| chr9:122957884 | CT | C | 108 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(105): Show |
109 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.150+690delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122957884 | ||||||
| chr9:122958102 | C | T | 12 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0069 others(9): Show |
13 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.150+893C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122958102 | |||||||
| chr9:122958151 | G | A | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.150+942G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122958151 | |||||||
| chr9:122958155 | A | G | 1 | a0001c0001t0002g0161 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.150+946A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122958155 | |||||||
| chr9:122958196 | A | G | 1 | a0001c0001t0041g0133 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.150+987A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122958196 | |||||||
| chr9:122958348 | A | G | 2 | a0001c0001t0002g0206 a0001c0001t0047g0199 |
2 | HG00099.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.150+1139A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122958348 | |||||||
| chr9:122958365 | T | C | 3 | a0001c0001t0003g0181 a0001c0001t0003g0211 a0001c0001t0030g0210 |
3 | HG01070.hp1 HG01993.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.150+1156T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122958365 | |||||||
| chr9:122958475 | A | G | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.150+1266A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122958475 | |||||||
| chr9:122958565 | A | T | 1 | a0001c0001t0037g0055 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.150+1356A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122958565 | |||||||
| chr9:122958670 | A | G | 1 | a0001c0002t0009g0052 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.150+1461A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122958670 | |||||||
| chr9:122958694 | T | A | 245 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.150+1485T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122958694 | |||||||
| chr9:122958709 | G | C | 1 | a0001c0001t0019g0231 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.150+1500G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122958709 | |||||||
| chr9:122958789 | A | G | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.150+1580A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122958789 | |||||||
| chr9:122959095 | A | T | 3 | a0001c0001t0007g0056 a0001c0001t0035g0058 a0001c0001t0037g0055 |
3 | HG01884.hp2 HG02055.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.150+1886A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122959095 | |||||||
| chr9:122959336 | G | A | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0021g0001 |
4 | HG01496.hp1 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+2127G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122959336 | |||||||
| chr9:122959364 | C | CA | 195 | a0001c0001t0001g0002 a0001c0001t0001g0064 a0001c0001t0001g0083 others(192): Show |
195 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.150+2175dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122959364 | ||||||
| chr9:122959364 | C | CAA | 40 | a0001c0001t0001g0059 a0001c0001t0001g0063 a0001c0001t0001g0069 others(37): Show |
41 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.150+2174_150+2175d others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122959364 | ||||||
| chr9:122959407 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.150+2198T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122959407 | |||||||
| chr9:122959543 | T | C | 10 | a0001c0001t0005g0239 a0001c0001t0005g0240 a0001c0001t0005g0241 others(7): Show |
10 | HG01109.hp1 HG02055.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.150+2334T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122959543 | |||||||
| chr9:122959604 | A | T | 1 | a0001c0001t0004g0100 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.150+2395A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122959604 | |||||||
| chr9:122959688 | T | C | 2 | a0001c0001t0002g0165 a0001c0001t0002g0235 |
2 | HG01361.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.150+2479T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122959688 | |||||||
| chr9:122959719 | G | T | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.150+2510G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122959719 | |||||||
| chr9:122959726 | A | G | 1 | a0001c0001t0033g0023 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.150+2517A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122959726 | |||||||
| chr9:122959781 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.150+2572C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122959781 | |||||||
| chr9:122959886 | G | A | 8 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG01081.hp1 HG01106.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.150+2677G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122959886 | |||||||
| chr9:122959946 | G | C | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.150+2737G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122959946 | |||||||
| chr9:122960161 | G | C | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.150+2952G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122960161 | |||||||
| chr9:122960657 | C | T | 4 | a0001c0001t0006g0060 a0001c0001t0006g0061 a0001c0001t0006g0080 others(1): Show |
4 | HG00323.hp1 HG00738.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+3448C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122960657 | |||||||
| chr9:122960860 | G | A | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.150+3651G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122960860 | |||||||
| chr9:122960922 | A | G | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.150+3713A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122960922 | |||||||
| chr9:122960948 | T | A | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.150+3739T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122960948 | |||||||
| chr9:122961182 | T | A | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.150+3973T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961182 | |||||||
| chr9:122961208 | C | T | 245 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.150+3999C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961208 | |||||||
| chr9:122961226 | TGATAAA | T | 6 | a0001c0001t0006g0088 a0001c0001t0006g0089 a0001c0001t0006g0090 others(3): Show |
6 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.150+4021_150+4026d others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122961226 | ||||||
| chr9:122961303 | A | G | 1 | a0002c0003t0011g0078 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.150+4094A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961303 | |||||||
| chr9:122961311 | A | G | 2 | a0001c0001t0019g0227 a0001c0001t0019g0231 |
2 | NA18959.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.150+4102A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961311 | |||||||
| chr9:122961404 | C | T | 1 | a0001c0001t0006g0077 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.150+4195C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961404 | |||||||
| chr9:122961441 | C | T | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.150+4232C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961441 | |||||||
| chr9:122961489 | T | C | 7 | a0001c0001t0006g0077 a0002c0003t0011g0062 a0002c0003t0011g0074 others(4): Show |
7 | HG00544.hp1 HG02155.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.150+4280T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961489 | |||||||
| chr9:122961522 | C | G | 1 | a0001c0001t0002g0212 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.150+4313C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961522 | |||||||
| chr9:122961535 | T | C | 1 | a0001c0001t0001g0145 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.150+4326T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961535 | |||||||
| chr9:122961550 | A | G | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.150+4341A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961550 | |||||||
| chr9:122961661 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.150+4452G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961661 | |||||||
| chr9:122961775 | A | G | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.150+4566A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961775 | |||||||
| chr9:122961818 | T | C | 248 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(245): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.150+4609T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961818 | |||||||
| chr9:122961863 | T | C | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.150+4654T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122961863 | |||||||
| chr9:122962248 | T | A | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.150+5039T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122962248 | |||||||
| chr9:122962403 | G | GA | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.150+5196dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122962403 | ||||||
| chr9:122962420 | C | G | 1 | a0001c0001t0001g0002 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.150+5211C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122962420 | |||||||
| chr9:122962452 | T | C | 6 | a0001c0001t0002g0184 a0001c0001t0002g0192 a0001c0001t0002g0193 others(3): Show |
6 | HG00597.hp2 HG00621.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.150+5243T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122962452 | |||||||
| chr9:122962529 | A | T | 63 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(60): Show |
63 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.150+5320A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122962529 | |||||||
| chr9:122962729 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.150+5520C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122962729 | |||||||
| chr9:122962863 | A | G | 11 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(8): Show |
11 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.150+5654A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122962863 | |||||||
| chr9:122963366 | C | G | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.150+6157C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122963366 | |||||||
| chr9:122963467 | A | C | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.150+6258A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122963467 | |||||||
| chr9:122963507 | A | G | 3 | a0001c0001t0001g0104 a0001c0001t0001g0119 a0001c0001t0001g0126 |
3 | HG00597.hp1 HG02040.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.150+6298A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122963507 | |||||||
| chr9:122963606 | G | A | 1 | a0001c0001t0034g0013 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.150+6397G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122963606 | |||||||
| chr9:122963624 | C | A | 1 | a0001c0001t0002g0111 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.150+6415C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122963624 | |||||||
| chr9:122963694 | G | C | 135 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.150+6485G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122963694 | |||||||
| chr9:122963736 | A | T | 1 | a0001c0001t0001g0086 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.150+6527A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122963736 | |||||||
| chr9:122963742 | C | T | 7 | a0001c0001t0006g0077 a0002c0003t0011g0062 a0002c0003t0011g0074 others(4): Show |
7 | HG00544.hp1 HG02155.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.150+6533C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122963742 | |||||||
| chr9:122963759 | A | AAAG | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.150+6553_150+6555d others(5): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122963759 | ||||||
| chr9:122963935 | C | T | 5 | a0001c0001t0007g0014 a0001c0001t0007g0019 a0001c0001t0007g0020 others(2): Show |
5 | HG02280.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.150+6726C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122963935 | |||||||
| chr9:122964015 | A | T | 1 | a0001c0001t0016g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.150+6806A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122964015 | |||||||
| chr9:122964208 | C | T | 1 | a0001c0001t0012g0118 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.150+6999C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122964208 | |||||||
| chr9:122964274 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0154 |
2 | NA18961.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.150+7065C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122964274 | |||||||
| chr9:122964616 | A | T | 1 | a0001c0001t0001g0141 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.150+7407A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122964616 | |||||||
| chr9:122964771 | A | G | 67 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0085 others(64): Show |
67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.150+7562A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122964771 | |||||||
| chr9:122964811 | G | A | 245 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.150+7602G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122964811 | |||||||
| chr9:122964852 | C | T | 2 | a0001c0001t0018g0249 a0001c0001t0018g0251 |
2 | HG01243.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.150+7643C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122964852 | |||||||
| chr9:122964993 | T | C | 15 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0148 others(12): Show |
15 | HG00733.hp1 HG01993.hp2 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.150+7784T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122964993 | |||||||
| chr9:122965286 | A | G | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.150+8077A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122965286 | |||||||
| chr9:122965396 | A | T | 4 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(1): Show |
4 | HG02258.hp2 HG02486.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+8187A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122965396 | |||||||
| chr9:122965444 | C | T | 1 | a0001c0001t0002g0177 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.150+8235C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122965444 | |||||||
| chr9:122965487 | G | A | 6 | a0001c0001t0006g0088 a0001c0001t0006g0089 a0001c0001t0006g0090 others(3): Show |
6 | HG01109.hp2 HG01243.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.150+8278G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122965487 | |||||||
| chr9:122965603 | C | T | 1 | a0002c0003t0011g0078 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.150+8394C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122965603 | |||||||
| chr9:122965739 | G | A | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.150+8530G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122965739 | |||||||
| chr9:122965769 | A | C | 13 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0069 others(10): Show |
14 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.150+8560A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122965769 | |||||||
| chr9:122965967 | A | T | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.150+8758A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122965967 | |||||||
| chr9:122966098 | T | C | 67 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0085 others(64): Show |
67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.150+8889T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122966098 | |||||||
| chr9:122966253 | A | G | 1 | a0001c0002t0022g0049 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.150+9044A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122966253 | |||||||
| chr9:122966694 | A | T | 1 | a0001c0001t0044g0150 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.150+9485A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122966694 | |||||||
| chr9:122966707 | C | T | 2 | a0001c0001t0019g0227 a0001c0001t0019g0231 |
2 | NA18959.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.150+9498C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122966707 | |||||||
| chr9:122966856 | G | A | 4 | a0001c0001t0001g0064 a0001c0001t0024g0066 a0001c0001t0024g0067 others(1): Show |
4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+9647G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122966856 | |||||||
| chr9:122966868 | C | T | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.150+9659C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122966868 | |||||||
| chr9:122967091 | G | A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0069 others(9): Show |
13 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.150+9882G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122967091 | |||||||
| chr9:122967387 | A | C | 107 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(104): Show |
108 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.150+10178A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122967387 | |||||||
| chr9:122967728 | C | CT | 254 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(251): Show |
255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.150+10526dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122967728 | ||||||
| chr9:122967782 | G | A | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.150+10573G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122967782 | |||||||
| chr9:122967843 | C | G | 1 | a0001c0001t0001g0153 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.150+10634C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122967843 | |||||||
| chr9:122967902 | A | G | 1 | a0001c0001t0044g0150 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.150+10693A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122967902 | |||||||
| chr9:122968089 | TGTA | T | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.150+10881_150+1088 others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122968089 | |||||||
| chr9:122968094 | AT | A | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.150+10886delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122968094 | |||||||
| chr9:122968220 | C | CT | 20 | a0001c0001t0001g0063 a0001c0001t0001g0087 a0001c0001t0002g0180 others(17): Show |
20 | HG00099.hp1 HG00099.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.150+11031dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122968220 | ||||||
| chr9:122968220 | CT | C | 6 | a0001c0001t0001g0064 a0001c0001t0004g0012 a0001c0001t0004g0022 others(3): Show |
6 | HG01167.hp1 HG02109.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.150+11031delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122968220 | ||||||
| chr9:122968491 | A | T | 1 | a0001c0001t0001g0151 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.150+11282A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122968491 | |||||||
| chr9:122968659 | C | G | 245 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.150+11450C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122968659 | |||||||
| chr9:122969161 | A | C | 1 | a0001c0001t0003g0219 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.150+11952A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122969161 | |||||||
| chr9:122969211 | CT | C | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.150+12003delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122969211 | |||||||
| chr9:122969264 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.150+12055A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122969264 | |||||||
| chr9:122969522 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.150+12313C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122969522 | |||||||
| chr9:122969576 | G | A | 30 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(27): Show |
30 | HG01069.hp2 HG01109.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.150+12367G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122969576 | |||||||
| chr9:122969736 | C | CATTTT | 135 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.150+12533_150+1253 others(9): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122969736 | ||||||
| chr9:122969753 | A | G | 135 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.150+12544A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122969753 | |||||||
| chr9:122969857 | C | T | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.150+12648C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122969857 | |||||||
| chr9:122970074 | A | AT | 79 | a0001c0001t0002g0159 a0001c0001t0002g0163 a0001c0001t0002g0164 others(76): Show |
79 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.150+12881dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122970074 | ||||||
| chr9:122970453 | A | C | 1 | a0001c0001t0001g0117 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.150+13244A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122970453 | |||||||
| chr9:122970522 | A | G | 1 | a0001c0001t0001g0145 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.150+13313A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122970522 | |||||||
| chr9:122970906 | T | G | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.151-13579T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122970906 | |||||||
| chr9:122971275 | T | G | 1 | a0001c0002t0054g0042 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.151-13210T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122971275 | |||||||
| chr9:122971454 | G | T | 1 | a0001c0001t0002g0192 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.151-13031G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122971454 | |||||||
| chr9:122971849 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.151-12636A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122971849 | |||||||
| chr9:122972051 | G | C | 2 | a0001c0002t0026g0043 a0001c0002t0026g0045 |
2 | HG00280.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.151-12434G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122972051 | |||||||
| chr9:122972730 | A | C | 21 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(18): Show |
21 | HG00544.hp2 HG00673.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.151-11755A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122972730 | |||||||
| chr9:122972736 | A | T | 1 | a0001c0001t0036g0228 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.151-11749A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122972736 | |||||||
| chr9:122972978 | T | TA | 110 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(107): Show |
111 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.151-11495dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122972978 | ||||||
| chr9:122972978 | T | TAA | 30 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(27): Show |
30 | HG00639.hp1 HG01069.hp2 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.151-11496_151-1149 others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122972978 | ||||||
| chr9:122972978 | T | TAAA | 103 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(100): Show |
103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.151-11497_151-1149 others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122972978 | ||||||
| chr9:122973048 | C | T | 1 | a0001c0001t0033g0023 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.151-11437C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122973048 | |||||||
| chr9:122973052 | A | G | 67 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0085 others(64): Show |
67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.151-11433A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122973052 | |||||||
| chr9:122973250 | G | T | 245 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.151-11235G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122973250 | |||||||
| chr9:122973356 | G | T | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151-11129G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122973356 | |||||||
| chr9:122973362 | C | G | 2 | a0001c0001t0017g0203 a0001c0001t0017g0204 |
2 | HG00639.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.151-11123C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122973362 | |||||||
| chr9:122973393 | T | C | 4 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0109 others(1): Show |
4 | HG00597.hp1 NA18747.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-11092T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122973393 | |||||||
| chr9:122973397 | C | T | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.151-11088C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122973397 | |||||||
| chr9:122973426 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.151-11059T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122973426 | |||||||
| chr9:122973430 | G | C | 1 | a0001c0001t0002g0168 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.151-11055G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122973430 | |||||||
| chr9:122973484 | C | T | 52 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0085 others(49): Show |
52 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.151-11001C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122973484 | |||||||
| chr9:122973690 | T | C | 81 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(78): Show |
81 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.151-10795T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122973690 | |||||||
| chr9:122973735 | C | T | 1 | a0001c0001t0003g0216 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.151-10750C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122973735 | |||||||
| chr9:122973893 | C | T | 2 | a0001c0001t0006g0088 a0001c0001t0006g0089 |
2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.151-10592C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122973893 | |||||||
| chr9:122974009 | C | CA | 14 | a0001c0001t0002g0180 a0001c0001t0002g0207 a0001c0001t0003g0179 others(11): Show |
14 | HG00642.hp2 HG00733.hp2 HG01069.hp1 others(11): Show |
intron_variant | MODIFIER | c.151-10476_151-1047 others(5): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122974009 | |||||||
| chr9:122974010 | C | A | 244 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(241): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.151-10475C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122974010 | |||||||
| chr9:122974056 | A | G | 4 | a0001c0002t0049g0031 a0001c0002t0050g0041 a0001c0002t0051g0050 others(1): Show |
4 | NA18955.hp1 NA18986.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-10429A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122974056 | |||||||
| chr9:122974067 | T | C | 1 | a0001c0001t0042g0147 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.151-10418T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122974067 | |||||||
| chr9:122974247 | T | C | 4 | a0001c0001t0001g0064 a0001c0001t0024g0066 a0001c0001t0024g0067 others(1): Show |
4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-10238T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122974247 | |||||||
| chr9:122974311 | G | C | 6 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0014g0189 others(3): Show |
6 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(3): Show |
intron_variant | MODIFIER | c.151-10174G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122974311 | |||||||
| chr9:122974415 | C | CT | 71 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(68): Show |
72 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.151-10044dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122974415 | ||||||
| chr9:122974415 | C | CTT | 33 | a0001c0001t0001g0064 a0001c0001t0001g0085 a0001c0001t0001g0128 others(30): Show |
33 | HG00621.hp1 HG00639.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.151-10045_151-1004 others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122974415 | ||||||
| chr9:122974415 | CT | C | 45 | a0001c0001t0002g0196 a0001c0001t0004g0009 a0001c0001t0004g0010 others(42): Show |
45 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(42): Show |
intron_variant | MODIFIER | c.151-10044delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122974415 | ||||||
| chr9:122974415 | CTT | C | 81 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0164 others(78): Show |
81 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.151-10045_151-1004 others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122974415 | ||||||
| chr9:122974443 | G | A | 1 | a0001c0001t0010g0003 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.151-10042G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122974443 | |||||||
| chr9:122974478 | C | T | 1 | a0001c0001t0004g0022 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.151-10007C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122974478 | |||||||
| chr9:122974696 | G | A | 3 | a0001c0001t0002g0223 a0001c0001t0002g0224 a0001c0001t0002g0232 |
3 | HG00741.hp1 HG01258.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.151-9789G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122974696 | |||||||
| chr9:122975077 | C | T | 21 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(18): Show |
21 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.151-9408C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122975077 | |||||||
| chr9:122975162 | C | A | 1 | a0001c0002t0022g0049 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.151-9323C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122975162 | |||||||
| chr9:122975244 | T | C | 83 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(80): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.151-9241T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122975244 | |||||||
| chr9:122975417 | G | T | 1 | a0001c0001t0003g0219 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.151-9068G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122975417 | |||||||
| chr9:122975691 | C | T | 21 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(18): Show |
21 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.151-8794C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122975691 | |||||||
| chr9:122976046 | T | C | 2 | a0001c0001t0016g0071 a0001c0001t0016g0073 |
2 | HG01099.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.151-8439T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122976046 | |||||||
| chr9:122976191 | TA | T | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.151-8291delA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122976191 | ||||||
| chr9:122976399 | G | T | 1 | a0001c0001t0001g0144 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.151-8086G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122976399 | |||||||
| chr9:122976610 | G | T | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.151-7875G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122976610 | |||||||
| chr9:122976926 | T | C | 1 | a0001c0001t0006g0061 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.151-7559T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122976926 | |||||||
| chr9:122976979 | G | T | 1 | a0001c0001t0024g0066 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.151-7506G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122976979 | |||||||
| chr9:122977013 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.151-7472A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122977013 | |||||||
| chr9:122977434 | G | A | 2 | a0001c0001t0008g0096 a0001c0001t0008g0097 |
2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.151-7051G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122977434 | |||||||
| chr9:122977513 | C | G | 1 | a0001c0001t0002g0161 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.151-6972C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122977513 | |||||||
| chr9:122977574 | C | T | 1 | a0001c0001t0013g0226 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.151-6911C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122977574 | |||||||
| chr9:122977575 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.151-6910G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122977575 | |||||||
| chr9:122977687 | G | A | 1 | a0001c0001t0010g0003 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.151-6798G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122977687 | |||||||
| chr9:122978055 | A | G | 13 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0069 others(10): Show |
14 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.151-6430A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122978055 | |||||||
| chr9:122978131 | A | AT | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.151-6353dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122978131 | ||||||
| chr9:122978256 | A | G | 1 | a0001c0001t0006g0077 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.151-6229A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122978256 | |||||||
| chr9:122978461 | A | G | 1 | a0001c0001t0012g0118 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.151-6024A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122978461 | |||||||
| chr9:122978709 | G | C | 67 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0085 others(64): Show |
67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.151-5776G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122978709 | |||||||
| chr9:122978792 | A | T | 1 | a0001c0001t0006g0061 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.151-5693A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122978792 | |||||||
| chr9:122978819 | C | T | 134 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.151-5666C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122978819 | |||||||
| chr9:122978834 | C | A | 4 | a0001c0001t0001g0064 a0001c0001t0024g0066 a0001c0001t0024g0067 others(1): Show |
4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.151-5651C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122978834 | |||||||
| chr9:122978877 | CATTTT | C | 133 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(130): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.151-5586_151-5582d others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122978877 | ||||||
| chr9:122978877 | CATTTTAT others(3): Show |
C | 1 | a0001c0001t0001g0153 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.151-5591_151-5582d others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122978877 | ||||||
| chr9:122978932 | C | T | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.151-5553C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122978932 | |||||||
| chr9:122978963 | G | T | 1 | a0001c0001t0041g0133 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.151-5522G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122978963 | |||||||
| chr9:122979141 | A | C | 2 | a0001c0001t0008g0095 a0001c0001t0008g0098 |
2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.151-5344A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122979141 | |||||||
| chr9:122979212 | T | C | 5 | a0001c0001t0007g0014 a0001c0001t0007g0019 a0001c0001t0007g0020 others(2): Show |
5 | HG02280.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.151-5273T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122979212 | |||||||
| chr9:122979422 | G | A | 2 | a0001c0001t0002g0201 a0001c0001t0013g0198 |
2 | HG01070.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.151-5063G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122979422 | |||||||
| chr9:122979535 | A | G | 5 | a0001c0001t0001g0064 a0001c0001t0024g0066 a0001c0001t0024g0067 others(2): Show |
5 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.151-4950A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122979535 | |||||||
| chr9:122979590 | T | G | 1 | a0001c0001t0002g0207 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.151-4895T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122979590 | |||||||
| chr9:122980293 | A | T | 21 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(18): Show |
21 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.151-4192A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122980293 | |||||||
| chr9:122980294 | C | G | 1 | a0001c0001t0006g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.151-4191C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122980294 | |||||||
| chr9:122980835 | T | C | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151-3650T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122980835 | |||||||
| chr9:122980853 | G | A | 1 | a0001c0001t0008g0092 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.151-3632G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122980853 | |||||||
| chr9:122981024 | T | TTTGTTG | 3 | a0001c0001t0006g0250 a0001c0001t0018g0249 a0001c0001t0018g0251 |
3 | HG01243.hp1 HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.151-3440_151-3435d others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122981024 | ||||||
| chr9:122981236 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.151-3249G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122981236 | |||||||
| chr9:122981388 | A | G | 135 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.151-3097A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122981388 | |||||||
| chr9:122981398 | C | T | 1 | a0001c0001t0024g0066 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.151-3087C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122981398 | |||||||
| chr9:122981585 | T | C | 6 | a0001c0002t0049g0031 a0001c0002t0050g0041 a0001c0002t0051g0050 others(3): Show |
6 | NA18945.hp2 NA18955.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.151-2900T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122981585 | |||||||
| chr9:122981604 | G | A | 2 | a0001c0001t0006g0088 a0001c0001t0006g0089 |
2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.151-2881G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122981604 | |||||||
| chr9:122981880 | C | A | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.151-2605C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122981880 | |||||||
| chr9:122982048 | C | CA | 7 | a0001c0001t0001g0064 a0001c0001t0001g0110 a0001c0001t0002g0176 others(4): Show |
7 | HG00741.hp1 HG02109.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.151-2420dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122982048 | ||||||
| chr9:122982403 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.151-2082C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122982403 | |||||||
| chr9:122982621 | A | C | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.151-1864A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122982621 | |||||||
| chr9:122982763 | G | A | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.151-1722G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122982763 | |||||||
| chr9:122982778 | G | A | 3 | a0001c0001t0006g0250 a0001c0001t0018g0249 a0001c0001t0018g0251 |
3 | HG01243.hp1 HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.151-1707G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122982778 | |||||||
| chr9:122982826 | A | G | 1 | a0001c0001t0002g0235 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.151-1659A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122982826 | |||||||
| chr9:122982862 | G | A | 1 | a0001c0001t0003g0219 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.151-1623G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122982862 | |||||||
| chr9:122982950 | G | T | 2 | a0001c0002t0053g0048 a0001c0002t0056g0047 |
2 | NA18945.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.151-1535G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122982950 | |||||||
| chr9:122983166 | C | CA | 14 | a0001c0001t0001g0083 a0001c0001t0001g0110 a0001c0001t0001g0119 others(11): Show |
14 | HG00597.hp1 HG01175.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.151-1305dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr9 | 122983166 | ||||||
| chr9:122983176 | A | C | 21 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(18): Show |
21 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.151-1309A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122983176 | |||||||
| chr9:122983181 | C | A | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.151-1304C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122983181 | |||||||
| chr9:122983273 | C | T | 3 | a0001c0001t0004g0009 a0001c0001t0004g0024 a0001c0001t0004g0030 |
3 | HG02895.hp1 HG02897.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.151-1212C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122983273 | |||||||
| chr9:122983330 | A | G | 3 | a0001c0001t0005g0240 a0001c0001t0005g0245 a0001c0001t0005g0246 |
3 | HG02886.hp1 HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.151-1155A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122983330 | |||||||
| chr9:122984001 | A | G | 1 | a0001c0001t0006g0068 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.151-484A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122984001 | |||||||
| chr9:122984272 | A | G | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.151-213A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122984272 | |||||||
| chr9:122984333 | A | T | 67 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0085 others(64): Show |
67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.151-152A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122984333 | |||||||
| chr9:122984354 | A | T | 1 | a0001c0001t0045g0130 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.151-131A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 2/25 | chr9 | 122984354 | |||||||
| chr9:122984759 | G | T | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.385+40G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | chr9 | 122984759 | |||||||
| chr9:122984877 | T | C | 67 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0085 others(64): Show |
67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.385+158T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | chr9 | 122984877 | |||||||
| chr9:122984991 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.385+272C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | chr9 | 122984991 | |||||||
| chr9:122984997 | A | C | 1 | a0001c0001t0001g0086 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.385+278A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | chr9 | 122984997 | |||||||
| chr9:122984997 | AG | A | 244 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(241): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.385+280delG | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr9 | 122984997 | ||||||
| chr9:122984998 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.385+279G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | chr9 | 122984998 | |||||||
| chr9:122985229 | A | G | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.385+510A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | chr9 | 122985229 | |||||||
| chr9:122985430 | G | A | 133 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(130): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.385+711G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | chr9 | 122985430 | |||||||
| chr9:122985611 | C | CA | 85 | a0001c0001t0001g0155 a0001c0001t0002g0159 a0001c0001t0002g0161 others(82): Show |
85 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.386-583dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr9 | 122985611 | ||||||
| chr9:122985611 | C | CAA | 27 | a0001c0001t0001g0148 a0001c0001t0002g0168 a0001c0001t0002g0169 others(24): Show |
27 | HG00544.hp2 HG00558.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.386-584_386-583dup others(2): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr9 | 122985611 | ||||||
| chr9:122985611 | C | CAAA | 5 | a0001c0001t0010g0003 a0001c0001t0010g0004 a0001c0001t0010g0005 others(2): Show |
5 | HG02129.hp1 NA18970.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.386-585_386-583dup others(3): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr9 | 122985611 | ||||||
| chr9:122985611 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0004g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.386-593_386-583del others(11): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr9 | 122985611 | ||||||
| chr9:122985680 | A | G | 3 | a0001c0001t0002g0201 a0001c0001t0003g0182 a0001c0001t0013g0198 |
3 | HG01070.hp2 HG01106.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.386-535A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | chr9 | 122985680 | |||||||
| chr9:122985965 | T | G | 1 | a0001c0001t0001g0087 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.386-250T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | chr9 | 122985965 | |||||||
| chr9:122986025 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.386-190T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 3/25 | chr9 | 122986025 | |||||||
| chr9:122986449 | A | G | 1 | a0002c0003t0011g0074 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.590+30A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122986449 | |||||||
| chr9:122986588 | G | C | 83 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(80): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.590+169G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122986588 | |||||||
| chr9:122986624 | G | A | 23 | a0001c0001t0005g0239 a0001c0001t0005g0240 a0001c0001t0005g0241 others(20): Show |
23 | HG00544.hp1 HG01109.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.590+205G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122986624 | |||||||
| chr9:122986817 | C | T | 2 | a0001c0001t0006g0088 a0001c0001t0006g0089 |
2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.590+398C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122986817 | |||||||
| chr9:122987098 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.590+679C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122987098 | |||||||
| chr9:122987221 | T | C | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.590+802T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122987221 | |||||||
| chr9:122987434 | G | C | 1 | a0001c0001t0044g0150 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.590+1015G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122987434 | |||||||
| chr9:122987460 | A | G | 245 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.590+1041A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122987460 | |||||||
| chr9:122987908 | T | C | 1 | a0001c0001t0004g0011 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.591-1389T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122987908 | |||||||
| chr9:122987929 | A | G | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.591-1368A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122987929 | |||||||
| chr9:122987986 | T | C | 1 | a0001c0001t0007g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.591-1311T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122987986 | |||||||
| chr9:122988257 | C | T | 1 | a0001c0001t0046g0190 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.591-1040C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122988257 | |||||||
| chr9:122988499 | A | AT | 55 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(52): Show |
55 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.591-785dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr9 | 122988499 | ||||||
| chr9:122988499 | A | ATT | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.591-786_591-785dup others(2): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr9 | 122988499 | ||||||
| chr9:122988851 | G | C | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.591-446G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122988851 | |||||||
| chr9:122988883 | C | T | 2 | a0001c0001t0004g0016 a0001c0001t0004g0018 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.591-414C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122988883 | |||||||
| chr9:122988899 | C | T | 2 | a0001c0001t0002g0161 a0001c0001t0002g0166 |
2 | HG01934.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.591-398C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122988899 | |||||||
| chr9:122988942 | C | CA | 10 | a0001c0001t0001g0105 a0001c0001t0001g0127 a0001c0001t0002g0175 others(7): Show |
10 | HG00544.hp2 HG00621.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.591-337dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr9 | 122988942 | ||||||
| chr9:122989083 | A | G | 4 | a0001c0001t0001g0064 a0001c0001t0024g0066 a0001c0001t0024g0067 others(1): Show |
4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.591-214A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122989083 | |||||||
| chr9:122989084 | A | ACATGATA others(91): Show |
2 | a0001c0001t0002g0168 a0001c0001t0002g0225 |
2 | HG00735.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.591-209_591-112dup others(98): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr9 | 122989084 | ||||||
| chr9:122989121 | G | A | 1 | a0001c0001t0006g0077 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.591-176G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122989121 | |||||||
| chr9:122989183 | C | T | 21 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(18): Show |
21 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.591-114C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 4/25 | chr9 | 122989183 | |||||||
| chr9:122989731 | C | T | 135 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.765+260C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 5/25 | chr9 | 122989731 | |||||||
| chr9:122990325 | A | T | 1 | a0001c0001t0004g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.923+112A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990325 | |||||||
| chr9:122990334 | C | G | 135 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.923+121C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990334 | |||||||
| chr9:122990354 | AATACATA others(8): Show |
A | 1 | a0001c0001t0004g0100 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.923+143_923+157del others(15): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990354 | ||||||
| chr9:122990431 | C | T | 1 | a0001c0001t0005g0247 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.923+218C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990431 | |||||||
| chr9:122990690 | A | T | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0021g0001 |
4 | HG01496.hp1 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.923+477A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990690 | |||||||
| chr9:122990711 | G | A | 5 | a0001c0001t0005g0239 a0001c0001t0005g0242 a0001c0001t0005g0243 others(2): Show |
5 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.923+498G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990711 | |||||||
| chr9:122990764 | C | T | 11 | a0001c0001t0004g0015 a0001c0001t0005g0239 a0001c0001t0005g0240 others(8): Show |
11 | HG01109.hp1 HG02055.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.923+551C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990764 | |||||||
| chr9:122990769 | C | CAA | 6 | a0001c0001t0001g0002 a0001c0001t0001g0069 a0001c0001t0001g0070 others(3): Show |
7 | HG01496.hp1 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.923+583_923+584dup others(2): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990769 | ||||||
| chr9:122990769 | CAAA | C | 5 | a0001c0001t0002g0166 a0001c0001t0002g0178 a0001c0001t0002g0223 others(2): Show |
5 | HG00673.hp1 HG01099.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.923+582_923+584del others(3): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990769 | ||||||
| chr9:122990769 | CAAAAA | C | 8 | a0001c0001t0002g0161 a0001c0001t0002g0165 a0001c0001t0002g0167 others(5): Show |
8 | HG00544.hp2 HG01361.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.923+580_923+584del others(5): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990769 | ||||||
| chr9:122990769 | CAAAAAA | C | 6 | a0001c0001t0002g0164 a0001c0001t0002g0201 a0001c0001t0002g0254 others(3): Show |
6 | HG00597.hp2 HG01175.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.923+579_923+584del others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990769 | ||||||
| chr9:122990769 | CAAAAAAA others(1): Show |
C | 6 | a0001c0001t0002g0169 a0001c0001t0002g0195 a0001c0001t0010g0003 others(3): Show |
6 | HG00558.hp1 HG01167.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.923+577_923+584del others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990769 | ||||||
| chr9:122990769 | CAAAAAAA others(2): Show |
C | 7 | a0001c0001t0002g0176 a0001c0001t0002g0224 a0001c0001t0002g0232 others(4): Show |
7 | HG00741.hp1 HG01258.hp1 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.923+576_923+584del others(9): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990769 | ||||||
| chr9:122990769 | CAAAAAAA others(3): Show |
C | 5 | a0001c0001t0002g0168 a0001c0001t0015g0197 a0001c0001t0015g0200 others(2): Show |
5 | HG00735.hp1 HG02040.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.923+575_923+584del others(10): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990769 | ||||||
| chr9:122990769 | CAAAAAAA others(4): Show |
C | 7 | a0001c0001t0002g0172 a0001c0001t0002g0206 a0001c0001t0002g0207 others(4): Show |
7 | HG00639.hp2 HG00735.hp2 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.923+574_923+584del others(11): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990769 | ||||||
| chr9:122990769 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0002g0225 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.923+573_923+584del others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990769 | ||||||
| chr9:122990786 | A | AATATATA others(3): Show |
1 | a0001c0001t0002g0163 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.923+574_923+575ins others(10): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990786 | ||||||
| chr9:122990786 | AAAAAAAA others(5): Show |
A | 2 | a0001c0001t0019g0227 a0001c0001t0019g0231 |
2 | NA18959.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.923+575_923+586del others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990786 | ||||||
| chr9:122990786 | AAAAAAAA others(25): Show |
A | 1 | a0001c0001t0014g0170 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.923+575_923+606del others(32): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990786 | ||||||
| chr9:122990787 | AAAAAAAA others(4): Show |
A | 3 | a0001c0001t0002g0171 a0001c0001t0003g0221 a0001c0001t0014g0189 |
3 | HG00280.hp2 HG00738.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.923+576_923+586del others(11): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990787 | ||||||
| chr9:122990787 | AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0002g0194 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.923+576_923+588del others(13): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990787 | ||||||
| chr9:122990788 | A | T | 4 | a0001c0001t0002g0163 a0001c0001t0002g0188 a0001c0001t0002g0196 others(1): Show |
4 | HG00099.hp2 HG02027.hp2 HG02135.hp1 others(1): Show |
intron_variant | MODIFIER | c.923+575A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990788 | |||||||
| chr9:122990788 | AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0002g0212 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.923+577_923+586del others(10): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990788 | ||||||
| chr9:122990788 | AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0002g0193 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.923+577_923+588del others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990788 | ||||||
| chr9:122990788 | AAAAAAAA others(27): Show |
A | 1 | a0001c0001t0002g0180 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.923+577_923+610del others(34): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990788 | ||||||
| chr9:122990789 | AAAAAAAA others(4): Show |
A | 5 | a0001c0001t0003g0181 a0001c0001t0003g0182 a0001c0001t0013g0198 others(2): Show |
5 | HG00099.hp1 HG00642.hp1 HG01070.hp2 others(2): Show |
intron_variant | MODIFIER | c.923+578_923+588del others(11): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990789 | ||||||
| chr9:122990789 | AAAAAAAA others(6): Show |
A | 1 | a0001c0001t0003g0215 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.923+578_923+590del others(13): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990789 | ||||||
| chr9:122990790 | A | T | 8 | a0001c0001t0002g0163 a0001c0001t0002g0166 a0001c0001t0002g0188 others(5): Show |
8 | HG00099.hp2 HG00673.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.923+577A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990790 | |||||||
| chr9:122990790 | AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0003g0211 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.923+579_923+590del others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990790 | ||||||
| chr9:122990791 | AAAAAAAT others(4): Show |
A | 1 | a0001c0001t0003g0216 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.923+580_923+590del others(11): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990791 | ||||||
| chr9:122990792 | A | T | 15 | a0001c0001t0002g0163 a0001c0001t0002g0165 a0001c0001t0002g0166 others(12): Show |
15 | HG00099.hp2 HG00673.hp1 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.923+579A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990792 | |||||||
| chr9:122990792 | AAAAAATA others(5): Show |
A | 1 | a0001c0001t0004g0011 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.923+581_923+592del others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990792 | ||||||
| chr9:122990794 | A | T | 24 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(21): Show |
24 | HG00099.hp2 HG00544.hp2 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.923+581A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990794 | |||||||
| chr9:122990794 | AAAATATA others(9): Show |
A | 2 | a0001c0001t0018g0249 a0001c0001t0018g0251 |
2 | HG01243.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.923+583_923+598del others(16): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990794 | ||||||
| chr9:122990796 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0006g0088 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.923+584_923+585ins others(20): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | ||||||
| chr9:122990796 | A | AAAAAAAA others(4): Show |
1 | a0001c0001t0006g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.923+584_923+585ins others(11): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | ||||||
| chr9:122990796 | A | AAAAAAAA others(12): Show |
1 | a0001c0001t0006g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.923+584_923+585ins others(19): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | ||||||
| chr9:122990796 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0005g0247 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.923+584_923+585ins others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | ||||||
| chr9:122990796 | A | AAAAAAAT others(12): Show |
1 | a0001c0001t0006g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.923+584_923+585ins others(19): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | ||||||
| chr9:122990796 | A | AAAATATA others(3): Show |
1 | a0001c0001t0006g0060 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.923+584_923+585ins others(10): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | ||||||
| chr9:122990796 | A | AAAATATA others(5): Show |
1 | a0001c0001t0005g0244 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.923+584_923+585ins others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | ||||||
| chr9:122990796 | A | AAATATAT others(4): Show |
1 | a0001c0001t0005g0245 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.923+584_923+585ins others(11): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | ||||||
| chr9:122990796 | A | AAATATAT others(6): Show |
1 | a0001c0001t0039g0234 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.923+584_923+585ins others(13): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | ||||||
| chr9:122990796 | A | AATATATA others(3): Show |
1 | a0001c0001t0048g0233 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.923+614_923+623dup others(10): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | ||||||
| chr9:122990796 | A | T | 42 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(39): Show |
42 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.923+583A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990796 | |||||||
| chr9:122990796 | AAT | A | 6 | a0001c0001t0001g0063 a0001c0001t0001g0086 a0001c0001t0001g0112 others(3): Show |
6 | HG02896.hp1 HG02897.hp1 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.923+622_923+623del others(2): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | ||||||
| chr9:122990796 | AATAT | A | 7 | a0001c0001t0001g0106 a0001c0001t0001g0128 a0001c0001t0004g0010 others(4): Show |
7 | HG02055.hp1 HG02145.hp1 HG03579.hp2 others(4): Show |
intron_variant | MODIFIER | c.923+620_923+623del others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | ||||||
| chr9:122990796 | AATATAT | A | 23 | a0001c0001t0001g0083 a0001c0001t0001g0119 a0001c0001t0001g0126 others(20): Show |
23 | HG00597.hp1 HG01081.hp1 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.923+618_923+623del others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | ||||||
| chr9:122990796 | AATATATA others(1): Show |
A | 6 | a0001c0001t0001g0101 a0001c0001t0001g0109 a0001c0001t0001g0151 others(3): Show |
6 | HG00733.hp1 HG02056.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.923+616_923+623del others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | ||||||
| chr9:122990796 | AATATATA others(11): Show |
A | 3 | a0001c0002t0009g0034 a0001c0002t0009g0051 a0001c0002t0023g0032 |
3 | NA18992.hp1 NA19011.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.923+606_923+623del others(18): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | ||||||
| chr9:122990796 | AATATATA others(13): Show |
A | 11 | a0001c0001t0001g0142 a0001c0002t0009g0036 a0001c0002t0009g0037 others(8): Show |
11 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(8): Show |
intron_variant | MODIFIER | c.923+604_923+623del others(20): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122990796 | ||||||
| chr9:122990797 | AT | A | 8 | a0001c0001t0005g0242 a0001c0001t0006g0080 a0001c0001t0008g0092 others(5): Show |
8 | HG01175.hp2 HG02809.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.923+585delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990797 | |||||||
| chr9:122990797 | ATAT | A | 5 | a0001c0001t0001g0113 a0001c0001t0004g0012 a0001c0001t0016g0071 others(2): Show |
5 | HG00544.hp1 HG01099.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.923+585_923+587del others(3): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990797 | |||||||
| chr9:122990797 | ATATAT | A | 15 | a0001c0001t0001g0146 a0001c0001t0001g0257 a0001c0001t0004g0015 others(12): Show |
15 | HG00621.hp1 HG01884.hp2 HG01952.hp1 others(12): Show |
intron_variant | MODIFIER | c.923+585_923+589del others(5): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990797 | |||||||
| chr9:122990797 | ATATATAT | A | 35 | a0001c0001t0001g0085 a0001c0001t0001g0087 a0001c0001t0001g0102 others(32): Show |
35 | HG00558.hp2 HG00673.hp2 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.923+585_923+591del others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990797 | |||||||
| chr9:122990797 | ATATATAT others(4): Show |
A | 2 | a0001c0001t0005g0240 a0001c0001t0005g0246 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.923+585_923+595del others(11): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990797 | |||||||
| chr9:122990797 | ATATATAT others(10): Show |
A | 1 | a0001c0002t0009g0052 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.923+585_923+601del others(17): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990797 | |||||||
| chr9:122990797 | ATATATAT others(12): Show |
A | 6 | a0001c0002t0009g0033 a0001c0002t0022g0046 a0001c0002t0023g0044 others(3): Show |
6 | NA18945.hp2 NA18949.hp1 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.923+585_923+603del others(19): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990797 | |||||||
| chr9:122990797 | ATATATAT others(14): Show |
A | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0002t0050g0041 |
3 | HG02258.hp2 HG02572.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.923+585_923+605del others(21): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990797 | |||||||
| chr9:122990797 | ATATATAT others(16): Show |
A | 1 | a0001c0001t0008g0095 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.923+585_923+607del others(23): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990797 | |||||||
| chr9:122990798 | T | A | 10 | a0001c0001t0001g0002 a0001c0001t0001g0064 a0001c0001t0001g0069 others(7): Show |
11 | HG00323.hp1 HG01496.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.923+585T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990798 | |||||||
| chr9:122990800 | T | A | 17 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0064 others(14): Show |
17 | HG00323.hp1 HG01175.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.923+587T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990800 | |||||||
| chr9:122990802 | T | A | 19 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0086 others(16): Show |
19 | HG01099.hp2 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.923+589T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990802 | |||||||
| chr9:122990804 | T | A | 43 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0086 others(40): Show |
43 | HG00597.hp1 HG00621.hp1 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.923+591T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990804 | |||||||
| chr9:122990806 | T | A | 69 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0085 others(66): Show |
69 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.923+593T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990806 | |||||||
| chr9:122990808 | T | A | 56 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0085 others(53): Show |
56 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.923+595T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990808 | |||||||
| chr9:122990810 | T | A | 26 | a0001c0001t0001g0063 a0001c0001t0001g0085 a0001c0001t0001g0103 others(23): Show |
26 | HG00733.hp1 HG01361.hp1 HG01981.hp2 others(23): Show |
intron_variant | MODIFIER | c.923+597T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990810 | |||||||
| chr9:122990816 | T | A | 4 | a0001c0002t0009g0034 a0001c0002t0009g0051 a0001c0002t0009g0052 others(1): Show |
4 | HG03834.hp2 NA18992.hp1 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.923+603T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990816 | |||||||
| chr9:122990818 | T | A | 21 | a0001c0001t0001g0142 a0001c0002t0009g0033 a0001c0002t0009g0034 others(18): Show |
21 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.923+605T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990818 | |||||||
| chr9:122990820 | T | A | 21 | a0001c0001t0001g0144 a0001c0002t0009g0033 a0001c0002t0009g0034 others(18): Show |
21 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.923+607T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990820 | |||||||
| chr9:122990822 | T | A | 13 | a0001c0002t0009g0033 a0001c0002t0009g0036 a0001c0002t0009g0037 others(10): Show |
13 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.923+609T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990822 | |||||||
| chr9:122990824 | T | A | 1 | a0001c0002t0051g0050 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.923+611T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990824 | |||||||
| chr9:122990886 | G | T | 1 | a0001c0001t0016g0073 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.923+673G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990886 | |||||||
| chr9:122990929 | C | T | 1 | a0001c0007t0025g0035 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.923+716C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990929 | |||||||
| chr9:122990942 | G | A | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.923+729G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122990942 | |||||||
| chr9:122991133 | A | G | 1 | a0001c0001t0002g0178 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.923+920A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122991133 | |||||||
| chr9:122991157 | A | G | 245 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.923+944A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122991157 | |||||||
| chr9:122991335 | G | C | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.923+1122G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122991335 | |||||||
| chr9:122991543 | G | A | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.923+1330G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122991543 | |||||||
| chr9:122991556 | CATT | C | 21 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(18): Show |
21 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.923+1344_923+1346d others(5): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122991556 | |||||||
| chr9:122991605 | C | CT | 34 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(31): Show |
34 | HG01109.hp2 HG01167.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.923+1408dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122991605 | ||||||
| chr9:122991605 | CT | C | 7 | a0001c0001t0001g0109 a0001c0001t0002g0159 a0001c0001t0002g0220 others(4): Show |
7 | HG00099.hp2 HG00323.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.923+1408delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122991605 | ||||||
| chr9:122991607 | T | C | 66 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0085 others(63): Show |
66 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.923+1394T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122991607 | |||||||
| chr9:122991608 | T | C | 1 | a0001c0001t0001g0109 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.923+1395T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122991608 | |||||||
| chr9:122991875 | A | G | 83 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(80): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.923+1662A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122991875 | |||||||
| chr9:122991984 | T | A | 1 | a0001c0001t0002g0180 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.923+1771T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122991984 | |||||||
| chr9:122992150 | C | T | 1 | a0001c0001t0018g0026 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.923+1937C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122992150 | |||||||
| chr9:122992256 | C | T | 4 | a0001c0001t0001g0064 a0001c0001t0024g0066 a0001c0001t0024g0067 others(1): Show |
4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.923+2043C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122992256 | |||||||
| chr9:122992280 | C | G | 3 | a0001c0001t0003g0181 a0001c0001t0003g0211 a0001c0001t0030g0210 |
3 | HG01070.hp1 HG01993.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.923+2067C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122992280 | |||||||
| chr9:122992347 | T | C | 2 | a0001c0001t0004g0024 a0001c0001t0004g0030 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.923+2134T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122992347 | |||||||
| chr9:122992442 | C | G | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.923+2229C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122992442 | |||||||
| chr9:122992620 | A | T | 1 | a0001c0001t0001g0131 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.923+2407A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122992620 | |||||||
| chr9:122992622 | A | G | 21 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(18): Show |
21 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.923+2409A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122992622 | |||||||
| chr9:122992749 | T | C | 1 | a0001c0001t0018g0251 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.923+2536T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122992749 | |||||||
| chr9:122992909 | A | G | 1 | a0001c0001t0003g0216 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.923+2696A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122992909 | |||||||
| chr9:122992917 | C | T | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.923+2704C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122992917 | |||||||
| chr9:122993265 | T | A | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.924-2776T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122993265 | |||||||
| chr9:122993292 | C | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(98): Show |
102 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.924-2749C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122993292 | |||||||
| chr9:122993365 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.924-2676G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122993365 | |||||||
| chr9:122993424 | G | A | 27 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0002g0177 others(24): Show |
27 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.924-2617G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122993424 | |||||||
| chr9:122993428 | C | T | 4 | a0001c0001t0006g0068 a0001c0001t0006g0088 a0001c0001t0006g0089 others(1): Show |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.924-2613C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122993428 | |||||||
| chr9:122993460 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.924-2581C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122993460 | |||||||
| chr9:122993559 | A | G | 17 | a0001c0001t0002g0180 a0001c0001t0003g0179 a0001c0001t0003g0181 others(14): Show |
17 | HG00099.hp1 HG00642.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.924-2482A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122993559 | |||||||
| chr9:122993645 | G | T | 1 | a0001c0001t0002g0206 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.924-2396G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122993645 | |||||||
| chr9:122993715 | G | A | 2 | a0001c0001t0005g0240 a0001c0001t0005g0246 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.924-2326G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122993715 | |||||||
| chr9:122993824 | C | T | 1 | a0001c0001t0004g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.924-2217C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122993824 | |||||||
| chr9:122994240 | A | C | 2 | a0001c0001t0004g0028 a0001c0001t0007g0025 |
2 | HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.924-1801A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122994240 | |||||||
| chr9:122994952 | C | T | 1 | a0001c0001t0010g0003 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.924-1089C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122994952 | |||||||
| chr9:122994975 | G | A | 1 | a0001c0001t0004g0022 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.924-1066G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122994975 | |||||||
| chr9:122995298 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.924-743C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122995298 | |||||||
| chr9:122995348 | A | G | 107 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(104): Show |
108 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.924-693A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122995348 | |||||||
| chr9:122995566 | A | AT | 139 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(136): Show |
140 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.924-455dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122995566 | ||||||
| chr9:122995566 | A | ATT | 101 | a0001c0001t0001g0087 a0001c0001t0001g0113 a0001c0001t0002g0159 others(98): Show |
101 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.924-456_924-455dup others(2): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr9 | 122995566 | ||||||
| chr9:122995600 | G | T | 1 | a0001c0001t0002g0177 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.924-441G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 6/25 | chr9 | 122995600 | |||||||
| chr9:122996332 | T | TA | 6 | a0001c0001t0010g0003 a0001c0001t0010g0004 a0001c0001t0010g0005 others(3): Show |
6 | HG02129.hp1 NA18970.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.1034+182dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 7/25 | INFO_REALIGN_3_PRIME | chr9 | 122996332 | ||||||
| chr9:122996334 | C | T | 1 | a0001c0001t0018g0026 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1034+183C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 7/25 | chr9 | 122996334 | |||||||
| chr9:122997162 | A | G | 1 | a0001c0001t0017g0191 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1102-97A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 8/25 | chr9 | 122997162 | |||||||
| chr9:122997213 | T | C | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1102-46T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 8/25 | chr9 | 122997213 | |||||||
| chr9:122997219 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1102-40C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 8/25 | chr9 | 122997219 | |||||||
| chr9:122997428 | C | A | 1 | a0001c0001t0001g0237 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1204+67C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 9/25 | chr9 | 122997428 | |||||||
| chr9:122997582 | TTTTC | T | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1204+231_1204+234d others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr9 | 122997582 | ||||||
| chr9:122997613 | C | G | 1 | a0001c0001t0013g0202 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1204+252C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 9/25 | chr9 | 122997613 | |||||||
| chr9:122997743 | G | A | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1204+382G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 9/25 | chr9 | 122997743 | |||||||
| chr9:122997787 | G | A | 4 | a0001c0001t0001g0064 a0001c0001t0024g0066 a0001c0001t0024g0067 others(1): Show |
4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1204+426G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 9/25 | chr9 | 122997787 | |||||||
| chr9:122997873 | A | G | 4 | a0001c0001t0006g0068 a0001c0001t0006g0088 a0001c0001t0006g0089 others(1): Show |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.1204+512A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 9/25 | chr9 | 122997873 | |||||||
| chr9:122997989 | A | G | 28 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(25): Show |
28 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1205-608A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 9/25 | chr9 | 122997989 | |||||||
| chr9:122998235 | G | A | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1205-362G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 9/25 | chr9 | 122998235 | |||||||
| chr9:122998432 | C | T | 135 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1205-165C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 9/25 | chr9 | 122998432 | |||||||
| chr9:122998584 | T | C | 80 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(77): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.1205-13T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 9/25 | chr9 | 122998584 | |||||||
| chr9:122998772 | G | A | 80 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(77): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(77): Show |
splice_region_variant&intron_variant | LOW | c.1374+6G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 122998772 | |||||||
| chr9:122998772 | G | C | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
splice_region_variant&intron_variant | LOW | c.1374+6G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 122998772 | |||||||
| chr9:122998780 | C | T | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1374+14C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 122998780 | |||||||
| chr9:122998795 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0127 |
2 | NA18952.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1374+29G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 122998795 | |||||||
| chr9:122998913 | C | T | 1 | a0001c0001t0007g0256 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1374+147C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 122998913 | |||||||
| chr9:122999124 | T | G | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1374+358T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 122999124 | |||||||
| chr9:122999209 | C | T | 1 | a0001c0001t0002g0220 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1374+443C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 122999209 | |||||||
| chr9:122999245 | G | A | 1 | a0001c0001t0020g0114 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1374+479G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 122999245 | |||||||
| chr9:122999270 | G | A | 4 | a0001c0001t0001g0064 a0001c0001t0024g0066 a0001c0001t0024g0067 others(1): Show |
4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1374+504G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 122999270 | |||||||
| chr9:122999323 | A | AC | 245 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1374+557_1374+558i others(3): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 122999323 | |||||||
| chr9:122999406 | G | A | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1374+640G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 122999406 | |||||||
| chr9:122999780 | C | T | 1 | a0001c0001t0037g0055 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1374+1014C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 122999780 | |||||||
| chr9:122999933 | A | C | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1374+1167A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 122999933 | |||||||
| chr9:123000126 | A | G | 1 | a0001c0001t0002g0225 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1374+1360A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123000126 | |||||||
| chr9:123000228 | C | G | 1 | a0001c0001t0006g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1374+1462C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123000228 | |||||||
| chr9:123000314 | G | A | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1374+1548G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123000314 | |||||||
| chr9:123000350 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1374+1584C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123000350 | |||||||
| chr9:123000428 | T | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(107): Show |
111 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.1374+1662T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123000428 | |||||||
| chr9:123000433 | A | G | 2 | a0001c0001t0004g0010 a0001c0001t0004g0027 |
2 | HG02145.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1374+1667A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123000433 | |||||||
| chr9:123000819 | A | T | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1374+2053A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123000819 | |||||||
| chr9:123001138 | G | A | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1374+2372G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123001138 | |||||||
| chr9:123001147 | C | T | 1 | a0001c0001t0002g0177 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1374+2381C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123001147 | |||||||
| chr9:123001242 | C | T | 1 | a0001c0001t0004g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1374+2476C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123001242 | |||||||
| chr9:123001625 | A | T | 3 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0109 |
3 | NA18747.hp1 NA18984.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1374+2859A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123001625 | |||||||
| chr9:123001829 | G | A | 135 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1374+3063G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123001829 | |||||||
| chr9:123001859 | A | G | 1 | a0001c0001t0042g0147 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1374+3093A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123001859 | |||||||
| chr9:123001934 | G | A | 2 | a0001c0001t0014g0189 a0001c0001t0014g0208 |
2 | HG00280.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.1374+3168G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123001934 | |||||||
| chr9:123001958 | G | A | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1374+3192G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123001958 | |||||||
| chr9:123002122 | A | T | 1 | a0001c0001t0003g0211 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1374+3356A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123002122 | |||||||
| chr9:123002346 | T | C | 2 | a0001c0001t0006g0080 a0001c0001t0006g0081 |
2 | HG00323.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1374+3580T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123002346 | |||||||
| chr9:123002356 | T | TTA | 30 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0002g0171 others(27): Show |
30 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.1374+3602_1374+360 others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123002356 | ||||||
| chr9:123002368 | A | AT | 48 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0069 others(45): Show |
49 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.1374+3612dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123002368 | ||||||
| chr9:123002369 | T | TA | 163 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0083 others(160): Show |
163 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.1374+3603_1374+360 others(5): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123002369 | |||||||
| chr9:123002370 | T | A | 10 | a0001c0001t0007g0053 a0001c0001t0008g0082 a0001c0001t0008g0092 others(7): Show |
10 | HG02145.hp2 HG02809.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1374+3604T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123002370 | |||||||
| chr9:123002371 | T | A | 70 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0085 others(67): Show |
70 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.1374+3605T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123002371 | |||||||
| chr9:123002373 | T | A | 1 | a0001c0001t0001g0124 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1374+3607T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123002373 | |||||||
| chr9:123002473 | A | G | 1 | a0001c0001t0002g0224 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1374+3707A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123002473 | |||||||
| chr9:123002522 | C | T | 32 | a0001c0001t0002g0175 a0001c0001t0002g0176 a0001c0001t0002g0236 others(29): Show |
32 | HG00544.hp2 HG00673.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.1374+3756C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123002522 | |||||||
| chr9:123002704 | AATATT | A | 80 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(77): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.1374+3941_1374+394 others(9): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123002704 | ||||||
| chr9:123002728 | C | G | 3 | a0001c0001t0001g0064 a0001c0001t0024g0067 a0001c0001t0055g0065 |
3 | HG02970.hp1 HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1374+3962C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123002728 | |||||||
| chr9:123002748 | A | G | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1374+3982A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123002748 | |||||||
| chr9:123002822 | A | G | 1 | a0001c0001t0006g0060 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1374+4056A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123002822 | |||||||
| chr9:123002883 | G | T | 1 | a0001c0001t0038g0057 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1374+4117G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123002883 | |||||||
| chr9:123002888 | C | G | 52 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0085 others(49): Show |
52 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1374+4122C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123002888 | |||||||
| chr9:123003226 | G | T | 245 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1374+4460G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123003226 | |||||||
| chr9:123003284 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1374+4518A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123003284 | |||||||
| chr9:123003835 | G | A | 67 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0085 others(64): Show |
67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1374+5069G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123003835 | |||||||
| chr9:123004167 | T | G | 13 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0069 others(10): Show |
14 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.1374+5401T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123004167 | |||||||
| chr9:123004252 | G | T | 5 | a0001c0001t0005g0239 a0001c0001t0005g0242 a0001c0001t0005g0243 others(2): Show |
5 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1374+5486G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123004252 | |||||||
| chr9:123004266 | A | G | 133 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(130): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1374+5500A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123004266 | |||||||
| chr9:123004361 | C | G | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1374+5595C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123004361 | |||||||
| chr9:123004593 | T | A | 2 | a0001c0001t0008g0092 a0001c0001t0008g0094 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1375-5761T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123004593 | |||||||
| chr9:123004970 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1375-5384C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123004970 | |||||||
| chr9:123005010 | C | G | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1375-5344C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123005010 | |||||||
| chr9:123005012 | C | T | 12 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0069 others(9): Show |
13 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1375-5342C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123005012 | |||||||
| chr9:123005056 | C | CA | 91 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0064 others(88): Show |
92 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(89): Show |
intron_variant | MODIFIER | c.1375-5277dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123005056 | ||||||
| chr9:123005056 | C | CAA | 10 | a0001c0001t0001g0063 a0001c0001t0001g0113 a0001c0001t0001g0119 others(7): Show |
10 | HG00597.hp1 HG00621.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.1375-5278_1375-527 others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123005056 | ||||||
| chr9:123005056 | CA | C | 8 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(5): Show |
8 | HG00741.hp2 HG02055.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1375-5277delA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123005056 | ||||||
| chr9:123005056 | CAA | C | 129 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(126): Show |
129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.1375-5278_1375-527 others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123005056 | ||||||
| chr9:123005261 | C | G | 107 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(104): Show |
108 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1375-5093C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123005261 | |||||||
| chr9:123005288 | AT | A | 132 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(129): Show |
132 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1375-5055delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123005288 | ||||||
| chr9:123005299 | T | C | 1 | a0001c0001t0002g0166 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1375-5055T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123005299 | |||||||
| chr9:123005301 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1375-5053C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123005301 | |||||||
| chr9:123005707 | A | G | 1 | a0001c0001t0002g0220 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1375-4647A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123005707 | |||||||
| chr9:123005800 | A | T | 2 | a0001c0001t0018g0249 a0001c0001t0018g0251 |
2 | HG01243.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1375-4554A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123005800 | |||||||
| chr9:123005808 | C | T | 1 | a0001c0002t0025g0038 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1375-4546C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123005808 | |||||||
| chr9:123006152 | T | A | 4 | a0001c0001t0001g0064 a0001c0001t0024g0066 a0001c0001t0024g0067 others(1): Show |
4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1375-4202T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123006152 | |||||||
| chr9:123006171 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1375-4183G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123006171 | |||||||
| chr9:123006401 | T | G | 107 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(104): Show |
108 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1375-3953T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123006401 | |||||||
| chr9:123006428 | T | C | 1 | a0001c0001t0006g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1375-3926T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123006428 | |||||||
| chr9:123006590 | T | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(107): Show |
111 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.1375-3764T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123006590 | |||||||
| chr9:123007089 | A | AT | 245 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1375-3259dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123007089 | ||||||
| chr9:123007369 | C | T | 1 | a0001c0001t0007g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1375-2985C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123007369 | |||||||
| chr9:123007373 | C | CT | 11 | a0001c0001t0001g0144 a0001c0001t0002g0176 a0001c0001t0002g0223 others(8): Show |
11 | HG00597.hp2 HG00741.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1375-2961dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123007373 | ||||||
| chr9:123007373 | CT | C | 97 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(94): Show |
98 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.1375-2961delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123007373 | ||||||
| chr9:123007470 | C | T | 80 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(77): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.1375-2884C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123007470 | |||||||
| chr9:123007553 | A | AT | 113 | a0001c0001t0001g0002 a0001c0001t0001g0112 a0001c0001t0002g0159 others(110): Show |
113 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.1375-2779dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123007553 | ||||||
| chr9:123007553 | A | ATT | 13 | a0001c0001t0002g0168 a0001c0001t0002g0171 a0001c0001t0002g0172 others(10): Show |
13 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.1375-2780_1375-277 others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123007553 | ||||||
| chr9:123007553 | AT | A | 13 | a0001c0001t0001g0083 a0001c0001t0001g0103 a0001c0001t0001g0140 others(10): Show |
13 | HG01109.hp1 HG01109.hp2 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1375-2779delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123007553 | ||||||
| chr9:123007629 | G | A | 1 | a0001c0001t0057g0174 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1375-2725G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123007629 | |||||||
| chr9:123007669 | A | G | 1 | a0001c0001t0048g0233 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1375-2685A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123007669 | |||||||
| chr9:123007723 | A | T | 3 | a0001c0001t0001g0064 a0001c0001t0024g0067 a0001c0001t0055g0065 |
3 | HG02970.hp1 HG03098.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1375-2631A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123007723 | |||||||
| chr9:123008413 | C | T | 1 | a0001c0001t0046g0190 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1375-1941C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123008413 | |||||||
| chr9:123008544 | C | CA | 12 | a0001c0001t0001g0127 a0001c0001t0002g0161 a0001c0001t0002g0166 others(9): Show |
12 | HG00558.hp1 HG01243.hp1 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.1375-1792dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123008544 | ||||||
| chr9:123008560 | AAAG | A | 23 | a0001c0001t0002g0176 a0001c0002t0009g0033 a0001c0002t0009g0034 others(20): Show |
23 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1375-1792_1375-179 others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123008560 | ||||||
| chr9:123008775 | C | CT | 23 | a0001c0001t0002g0176 a0001c0002t0009g0033 a0001c0002t0009g0034 others(20): Show |
23 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1375-1578dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123008775 | ||||||
| chr9:123009206 | T | C | 3 | a0001c0001t0003g0181 a0001c0001t0003g0211 a0001c0001t0030g0210 |
3 | HG01070.hp1 HG01993.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1375-1148T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123009206 | |||||||
| chr9:123009316 | C | T | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1375-1038C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123009316 | |||||||
| chr9:123009806 | T | TC | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1375-546dupC | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123009806 | ||||||
| chr9:123009835 | A | T | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1375-519A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123009835 | |||||||
| chr9:123010046 | G | A | 1 | a0001c0001t0004g0018 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1375-308G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | chr9 | 123010046 | |||||||
| chr9:123010196 | T | TA | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1375-157dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr9 | 123010196 | ||||||
| chr9:123010592 | G | A | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1549+64G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123010592 | |||||||
| chr9:123010970 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1549+442C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123010970 | |||||||
| chr9:123011475 | ACTTT | A | 3 | a0001c0001t0006g0250 a0001c0001t0018g0249 a0001c0001t0018g0251 |
3 | HG01243.hp1 HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1549+951_1549+954d others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 123011475 | ||||||
| chr9:123011738 | T | G | 17 | a0001c0001t0002g0180 a0001c0001t0003g0179 a0001c0001t0003g0181 others(14): Show |
17 | HG00099.hp1 HG00642.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.1549+1210T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123011738 | |||||||
| chr9:123011798 | CA | C | 245 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1549+1277delA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 123011798 | ||||||
| chr9:123011955 | T | TCAA | 3 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0003c0005t0001g0156 |
3 | HG00733.hp1 HG02738.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1549+1449_1549+145 others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 123011955 | ||||||
| chr9:123012824 | A | G | 13 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0069 others(10): Show |
14 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.1549+2296A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123012824 | |||||||
| chr9:123012870 | G | A | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1549+2342G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123012870 | |||||||
| chr9:123013040 | A | G | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1550-2503A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123013040 | |||||||
| chr9:123013086 | A | G | 1 | a0001c0001t0007g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1550-2457A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123013086 | |||||||
| chr9:123013148 | T | C | 1 | a0001c0001t0003g0181 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1550-2395T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123013148 | |||||||
| chr9:123013338 | C | CT | 80 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(77): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.1550-2194dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 123013338 | ||||||
| chr9:123013556 | C | T | 1 | a0001c0001t0007g0056 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1550-1987C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123013556 | |||||||
| chr9:123013581 | C | T | 21 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(18): Show |
21 | HG00544.hp2 HG00673.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.1550-1962C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123013581 | |||||||
| chr9:123013601 | G | A | 1 | a0001c0001t0005g0245 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1550-1942G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123013601 | |||||||
| chr9:123013867 | A | T | 2 | a0001c0001t0035g0058 a0001c0001t0037g0055 |
2 | HG02055.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1550-1676A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123013867 | |||||||
| chr9:123014011 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1550-1532G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123014011 | |||||||
| chr9:123014051 | A | C | 6 | a0002c0003t0011g0062 a0002c0003t0011g0074 a0002c0003t0011g0075 others(3): Show |
6 | HG00544.hp1 HG02155.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.1550-1492A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123014051 | |||||||
| chr9:123014149 | G | A | 80 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(77): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.1550-1394G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123014149 | |||||||
| chr9:123014175 | C | T | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1550-1368C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123014175 | |||||||
| chr9:123014345 | A | G | 1 | a0001c0001t0041g0133 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1550-1198A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123014345 | |||||||
| chr9:123014573 | G | A | 3 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0003c0005t0001g0156 |
3 | HG00733.hp1 HG02738.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1550-970G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123014573 | |||||||
| chr9:123014658 | AT | A | 151 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(148): Show |
152 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1550-864delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 123014658 | ||||||
| chr9:123014658 | ATT | A | 90 | a0001c0001t0001g0085 a0001c0001t0001g0145 a0001c0001t0001g0146 others(87): Show |
90 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.1550-865_1550-864d others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 123014658 | ||||||
| chr9:123014999 | A | T | 6 | a0001c0002t0049g0031 a0001c0002t0050g0041 a0001c0002t0051g0050 others(3): Show |
6 | NA18945.hp2 NA18955.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.1550-544A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123014999 | |||||||
| chr9:123015029 | C | T | 1 | a0001c0001t0037g0055 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1550-514C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123015029 | |||||||
| chr9:123015289 | C | CT | 44 | a0001c0001t0001g0103 a0001c0001t0001g0121 a0001c0001t0001g0124 others(41): Show |
44 | HG00099.hp1 HG00544.hp2 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.1550-235dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 123015289 | ||||||
| chr9:123015289 | C | CTT | 32 | a0001c0001t0002g0161 a0001c0001t0002g0165 a0001c0001t0002g0166 others(29): Show |
32 | HG00280.hp1 HG00741.hp2 HG01069.hp1 others(29): Show |
intron_variant | MODIFIER | c.1550-236_1550-235d others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 123015289 | ||||||
| chr9:123015289 | CT | C | 42 | a0001c0001t0001g0064 a0001c0001t0001g0087 a0001c0001t0001g0104 others(39): Show |
42 | HG00099.hp2 HG00323.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.1550-235delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 123015289 | ||||||
| chr9:123015289 | CTT | C | 10 | a0001c0001t0001g0059 a0001c0001t0001g0072 a0001c0001t0001g0126 others(7): Show |
11 | HG01099.hp2 HG02040.hp2 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1550-236_1550-235d others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 123015289 | ||||||
| chr9:123015289 | CTTT | C | 9 | a0001c0001t0001g0002 a0001c0001t0001g0069 a0001c0001t0001g0070 others(6): Show |
9 | HG01243.hp1 HG01243.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.1550-237_1550-235d others(5): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | INFO_REALIGN_3_PRIME | chr9 | 123015289 | ||||||
| chr9:123015368 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1550-175A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123015368 | |||||||
| chr9:123015425 | G | T | 1 | a0001c0001t0001g0125 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1550-118G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123015425 | |||||||
| chr9:123015512 | T | C | 1 | a0001c0001t0002g0224 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1550-31T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 11/25 | chr9 | 123015512 | |||||||
| chr9:123015648 | T | C | 5 | a0001c0001t0003g0179 a0001c0001t0003g0213 a0001c0001t0003g0214 others(2): Show |
5 | HG01081.hp2 HG01515.hp1 HG02004.hp1 others(2): Show |
intron_variant | MODIFIER | c.1643+12T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123015648 | |||||||
| chr9:123015663 | T | A | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1643+27T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123015663 | |||||||
| chr9:123015711 | C | G | 1 | a0001c0001t0002g0111 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1643+75C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123015711 | |||||||
| chr9:123015774 | A | T | 67 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0085 others(64): Show |
67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1643+138A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123015774 | |||||||
| chr9:123015909 | G | A | 135 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1643+273G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123015909 | |||||||
| chr9:123016001 | C | T | 5 | a0001c0001t0005g0239 a0001c0001t0005g0242 a0001c0001t0005g0243 others(2): Show |
5 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1643+365C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123016001 | |||||||
| chr9:123016215 | A | G | 5 | a0001c0001t0005g0239 a0001c0001t0005g0242 a0001c0001t0005g0243 others(2): Show |
5 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1643+579A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123016215 | |||||||
| chr9:123016366 | G | A | 1 | a0001c0001t0055g0065 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1643+730G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123016366 | |||||||
| chr9:123016368 | G | A | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1643+732G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123016368 | |||||||
| chr9:123016477 | A | G | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1643+841A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123016477 | |||||||
| chr9:123016562 | T | TTTA | 135 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1643+927_1643+929d others(5): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | INFO_REALIGN_3_PRIME | chr9 | 123016562 | ||||||
| chr9:123016646 | A | G | 2 | a0001c0001t0019g0227 a0001c0001t0019g0231 |
2 | NA18959.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1643+1010A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123016646 | |||||||
| chr9:123016685 | C | A | 1 | a0001c0001t0002g0188 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1643+1049C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123016685 | |||||||
| chr9:123017014 | G | C | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1643+1378G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123017014 | |||||||
| chr9:123017224 | A | G | 1 | a0001c0001t0007g0056 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1643+1588A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123017224 | |||||||
| chr9:123017261 | TA | T | 5 | a0001c0001t0005g0239 a0001c0001t0005g0242 a0001c0001t0005g0243 others(2): Show |
5 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1643+1626delA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123017261 | |||||||
| chr9:123017312 | C | T | 67 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0085 others(64): Show |
67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1643+1676C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123017312 | |||||||
| chr9:123017529 | T | C | 1 | a0001c0001t0002g0196 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1643+1893T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123017529 | |||||||
| chr9:123017905 | C | T | 1 | a0001c0001t0005g0246 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1643+2269C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123017905 | |||||||
| chr9:123018033 | G | T | 12 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0069 others(9): Show |
13 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1644-2276G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123018033 | |||||||
| chr9:123018196 | G | A | 2 | a0001c0001t0002g0193 a0001c0001t0002g0194 |
2 | NA18969.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1644-2113G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123018196 | |||||||
| chr9:123018360 | T | C | 1 | a0001c0001t0057g0174 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1644-1949T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123018360 | |||||||
| chr9:123018420 | A | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0134 |
2 | NA20300.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1644-1889A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123018420 | |||||||
| chr9:123018435 | A | G | 11 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(8): Show |
11 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1644-1874A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123018435 | |||||||
| chr9:123018578 | T | C | 135 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1644-1731T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123018578 | |||||||
| chr9:123018653 | A | C | 135 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1644-1656A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123018653 | |||||||
| chr9:123018978 | C | T | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1644-1331C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123018978 | |||||||
| chr9:123019012 | G | C | 12 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0069 others(9): Show |
13 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1644-1297G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123019012 | |||||||
| chr9:123019043 | C | T | 2 | a0001c0002t0023g0032 a0001c0002t0023g0044 |
2 | NA18949.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1644-1266C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123019043 | |||||||
| chr9:123019064 | G | A | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1644-1245G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123019064 | |||||||
| chr9:123019450 | G | A | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1644-859G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123019450 | |||||||
| chr9:123019473 | G | A | 1 | a0001c0001t0015g0200 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1644-836G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123019473 | |||||||
| chr9:123019542 | T | G | 1 | a0001c0001t0001g0132 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1644-767T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123019542 | |||||||
| chr9:123019623 | G | A | 244 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(241): Show |
245 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(242): Show |
intron_variant | MODIFIER | c.1644-686G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123019623 | |||||||
| chr9:123019686 | T | TTTTG | 133 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(130): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1644-603_1644-600d others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | INFO_REALIGN_3_PRIME | chr9 | 123019686 | ||||||
| chr9:123019847 | G | C | 2 | a0002c0003t0011g0075 a0004c0004t0011g0076 |
2 | NA18945.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.1644-462G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123019847 | |||||||
| chr9:123019935 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1644-374C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123019935 | |||||||
| chr9:123019954 | G | A | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1644-355G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123019954 | |||||||
| chr9:123020038 | C | T | 1 | a0001c0001t0057g0174 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1644-271C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123020038 | |||||||
| chr9:123020043 | T | G | 1 | a0001c0001t0057g0174 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1644-266T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123020043 | |||||||
| chr9:123020044 | T | G | 175 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0064 others(172): Show |
176 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1644-265T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123020044 | |||||||
| chr9:123020050 | T | G | 1 | a0001c0001t0047g0199 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1644-259T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123020050 | |||||||
| chr9:123020051 | T | C | 1 | a0001c0001t0036g0228 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1644-258T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123020051 | |||||||
| chr9:123020120 | A | G | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1644-189A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123020120 | |||||||
| chr9:123020133 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1644-176C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123020133 | |||||||
| chr9:123020161 | C | G | 1 | a0001c0001t0044g0150 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1644-148C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 12/25 | chr9 | 123020161 | |||||||
| chr9:123020706 | G | T | 1 | a0001c0001t0006g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1794+247G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123020706 | |||||||
| chr9:123021051 | C | T | 2 | a0001c0001t0002g0193 a0001c0001t0002g0194 |
2 | NA18969.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1794+592C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123021051 | |||||||
| chr9:123021091 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1794+632A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123021091 | |||||||
| chr9:123021203 | A | G | 11 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(8): Show |
11 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1794+744A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123021203 | |||||||
| chr9:123021291 | T | C | 67 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0085 others(64): Show |
67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1794+832T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123021291 | |||||||
| chr9:123021293 | TA | T | 41 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0064 others(38): Show |
42 | HG00323.hp1 HG00544.hp1 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.1794+850delA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123021293 | ||||||
| chr9:123021311 | C | T | 80 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(77): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.1794+852C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123021311 | |||||||
| chr9:123021317 | A | T | 17 | a0001c0001t0002g0180 a0001c0001t0003g0179 a0001c0001t0003g0181 others(14): Show |
17 | HG00099.hp1 HG00642.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.1794+858A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123021317 | |||||||
| chr9:123021330 | C | CT | 36 | a0001c0001t0001g0119 a0001c0001t0001g0131 a0001c0001t0001g0253 others(33): Show |
36 | HG00597.hp1 HG01069.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1794+890dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123021330 | ||||||
| chr9:123021416 | C | T | 1 | a0001c0001t0034g0013 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1794+957C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123021416 | |||||||
| chr9:123021470 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.1794+1011C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123021470 | |||||||
| chr9:123021495 | A | T | 245 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1794+1036A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123021495 | |||||||
| chr9:123021560 | A | G | 4 | a0001c0001t0006g0068 a0001c0001t0006g0088 a0001c0001t0006g0089 others(1): Show |
4 | HG01109.hp2 HG01243.hp2 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.1794+1101A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123021560 | |||||||
| chr9:123021701 | C | T | 135 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1794+1242C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123021701 | |||||||
| chr9:123021809 | C | A | 1 | a0001c0001t0045g0130 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1794+1350C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123021809 | |||||||
| chr9:123021986 | T | C | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1794+1527T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123021986 | |||||||
| chr9:123022086 | T | G | 1 | a0001c0001t0047g0199 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1794+1627T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123022086 | |||||||
| chr9:123022315 | A | G | 1 | a0001c0001t0007g0056 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1794+1856A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123022315 | |||||||
| chr9:123022634 | T | C | 12 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0069 others(9): Show |
13 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1794+2175T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123022634 | |||||||
| chr9:123022660 | C | T | 4 | a0001c0001t0001g0064 a0001c0001t0024g0066 a0001c0001t0024g0067 others(1): Show |
4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1794+2201C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123022660 | |||||||
| chr9:123022695 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1794+2236G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123022695 | |||||||
| chr9:123022696 | C | T | 80 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(77): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.1794+2237C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123022696 | |||||||
| chr9:123022724 | T | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(107): Show |
111 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.1794+2265T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123022724 | |||||||
| chr9:123022746 | G | T | 2 | a0001c0002t0051g0050 a0001c0002t0052g0039 |
2 | NA18955.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1794+2287G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123022746 | |||||||
| chr9:123022748 | A | G | 2 | a0001c0002t0051g0050 a0001c0002t0052g0039 |
2 | NA18955.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1794+2289A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123022748 | |||||||
| chr9:123022764 | G | T | 4 | a0001c0001t0001g0064 a0001c0001t0024g0066 a0001c0001t0024g0067 others(1): Show |
4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1794+2305G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123022764 | |||||||
| chr9:123023138 | A | G | 83 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(80): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.1794+2679A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123023138 | |||||||
| chr9:123023139 | T | C | 1 | a0001c0002t0054g0042 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1794+2680T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123023139 | |||||||
| chr9:123023141 | A | T | 1 | a0001c0002t0054g0042 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1794+2682A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123023141 | |||||||
| chr9:123023301 | C | T | 2 | a0001c0001t0002g0168 a0001c0001t0002g0225 |
2 | HG00735.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1794+2842C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123023301 | |||||||
| chr9:123023373 | G | A | 1 | a0001c0001t0048g0233 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1794+2914G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123023373 | |||||||
| chr9:123023656 | G | A | 1 | a0001c0001t0018g0026 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1794+3197G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123023656 | |||||||
| chr9:123023698 | G | A | 2 | a0001c0001t0002g0172 a0001c0001t0002g0207 |
2 | HG01952.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1794+3239G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123023698 | |||||||
| chr9:123023943 | G | T | 1 | a0001c0001t0002g0178 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1794+3484G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123023943 | |||||||
| chr9:123024289 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1794+3830C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123024289 | |||||||
| chr9:123024370 | A | G | 1 | a0001c0001t0016g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1794+3911A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123024370 | |||||||
| chr9:123024460 | G | A | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1794+4001G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123024460 | |||||||
| chr9:123024699 | A | G | 1 | a0001c0001t0002g0111 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1794+4240A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123024699 | |||||||
| chr9:123024708 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1794+4249G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123024708 | |||||||
| chr9:123024960 | A | T | 2 | a0001c0001t0019g0227 a0001c0001t0019g0231 |
2 | NA18959.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.1794+4501A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123024960 | |||||||
| chr9:123025112 | C | G | 2 | a0001c0001t0006g0068 a0001c0001t0006g0090 |
2 | HG01884.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1794+4653C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123025112 | |||||||
| chr9:123025117 | C | T | 2 | a0001c0001t0012g0116 a0001c0001t0012g0120 |
2 | HG00558.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.1794+4658C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123025117 | |||||||
| chr9:123025471 | A | G | 4 | a0001c0001t0001g0064 a0001c0001t0024g0066 a0001c0001t0024g0067 others(1): Show |
4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1794+5012A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123025471 | |||||||
| chr9:123025543 | C | CTTTTTTT | 72 | a0001c0001t0002g0161 a0001c0001t0002g0164 a0001c0001t0002g0165 others(69): Show |
72 | HG00099.hp1 HG00280.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.1794+5095_1794+510 others(11): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123025543 | ||||||
| chr9:123025543 | C | CTTTTTTT others(1): Show |
56 | a0001c0001t0002g0159 a0001c0001t0002g0163 a0001c0001t0002g0166 others(53): Show |
56 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.1794+5094_1794+510 others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123025543 | ||||||
| chr9:123025543 | C | CTTTTTTT others(2): Show |
6 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0024 others(3): Show |
6 | HG02145.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1794+5093_1794+510 others(13): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123025543 | ||||||
| chr9:123025543 | CT | C | 17 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0069 others(14): Show |
18 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.1794+5101delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123025543 | ||||||
| chr9:123025637 | G | A | 1 | a0001c0002t0049g0031 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1794+5178G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123025637 | |||||||
| chr9:123025663 | T | C | 1 | a0002c0003t0011g0062 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1794+5204T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123025663 | |||||||
| chr9:123025781 | G | A | 1 | a0001c0001t0032g0160 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1794+5322G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123025781 | |||||||
| chr9:123026005 | C | CT | 73 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0083 others(70): Show |
73 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.1794+5564dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123026005 | ||||||
| chr9:123026005 | C | CTT | 19 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0148 others(16): Show |
19 | HG00733.hp1 HG01109.hp1 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.1794+5563_1794+556 others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123026005 | ||||||
| chr9:123026005 | CT | C | 132 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(129): Show |
132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.1794+5564delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123026005 | ||||||
| chr9:123026536 | A | G | 3 | a0001c0001t0002g0223 a0001c0001t0002g0224 a0001c0001t0002g0232 |
3 | HG00741.hp1 HG01258.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1794+6077A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123026536 | |||||||
| chr9:123026876 | A | C | 2 | a0001c0001t0008g0095 a0001c0001t0008g0098 |
2 | HG03195.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1794+6417A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123026876 | |||||||
| chr9:123026881 | A | G | 135 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1794+6422A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123026881 | |||||||
| chr9:123027066 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1794+6607G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123027066 | |||||||
| chr9:123027108 | C | CT | 7 | a0001c0001t0001g0104 a0001c0001t0001g0106 a0001c0001t0006g0068 others(4): Show |
7 | HG01884.hp1 HG02895.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1794+6668dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123027108 | ||||||
| chr9:123027108 | CT | C | 135 | a0001c0001t0001g0153 a0001c0001t0002g0159 a0001c0001t0002g0161 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1794+6668delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123027108 | ||||||
| chr9:123027112 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1794+6653T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123027112 | |||||||
| chr9:123027203 | G | A | 2 | a0001c0001t0002g0161 a0001c0001t0002g0166 |
2 | HG01934.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1794+6744G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123027203 | |||||||
| chr9:123027472 | G | T | 107 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(104): Show |
108 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1794+7013G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123027472 | |||||||
| chr9:123027628 | G | A | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1794+7169G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123027628 | |||||||
| chr9:123027690 | C | T | 4 | a0001c0001t0001g0064 a0001c0001t0024g0066 a0001c0001t0024g0067 others(1): Show |
4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1794+7231C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123027690 | |||||||
| chr9:123027848 | G | T | 1 | a0001c0001t0006g0077 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1794+7389G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123027848 | |||||||
| chr9:123028575 | G | A | 1 | a0001c0001t0039g0234 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1794+8116G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123028575 | |||||||
| chr9:123028736 | A | G | 1 | a0001c0001t0007g0256 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1794+8277A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123028736 | |||||||
| chr9:123028962 | T | C | 2 | a0001c0002t0026g0043 a0001c0002t0026g0045 |
2 | HG00280.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1794+8503T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123028962 | |||||||
| chr9:123029060 | A | C | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1794+8601A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123029060 | |||||||
| chr9:123029259 | A | G | 2 | a0001c0001t0002g0171 a0001c0001t0030g0210 |
2 | HG00738.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1794+8800A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123029259 | |||||||
| chr9:123029544 | C | G | 111 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(108): Show |
112 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.1794+9085C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123029544 | |||||||
| chr9:123029725 | G | C | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1794+9266G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123029725 | |||||||
| chr9:123029872 | T | C | 1 | a0003c0005t0001g0156 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1794+9413T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123029872 | |||||||
| chr9:123029982 | C | G | 1 | a0001c0001t0012g0116 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1794+9523C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123029982 | |||||||
| chr9:123029995 | G | A | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1794+9536G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123029995 | |||||||
| chr9:123030018 | G | A | 1 | a0001c0001t0006g0077 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1794+9559G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123030018 | |||||||
| chr9:123030026 | G | C | 2 | a0001c0001t0035g0058 a0001c0001t0037g0055 |
2 | HG02055.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1794+9567G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123030026 | |||||||
| chr9:123030125 | A | G | 4 | a0001c0001t0001g0064 a0001c0001t0024g0066 a0001c0001t0024g0067 others(1): Show |
4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1794+9666A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123030125 | |||||||
| chr9:123030191 | A | G | 3 | a0001c0001t0001g0145 a0001c0001t0001g0152 a0001c0002t0053g0048 |
3 | NA18964.hp2 NA19072.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1794+9732A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123030191 | |||||||
| chr9:123030216 | AT | A | 27 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(24): Show |
27 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1794+9759delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123030216 | ||||||
| chr9:123030520 | G | A | 1 | a0001c0001t0031g0222 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1794+10061G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123030520 | |||||||
| chr9:123030590 | A | C | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1794+10131A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123030590 | |||||||
| chr9:123030675 | T | C | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1794+10216T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123030675 | |||||||
| chr9:123030784 | A | G | 1 | a0001c0001t0003g0216 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1794+10325A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123030784 | |||||||
| chr9:123031357 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | NA18973.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.1794+10898G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123031357 | |||||||
| chr9:123031441 | G | A | 1 | a0001c0001t0004g0018 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1794+10982G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123031441 | |||||||
| chr9:123031708 | G | T | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1794+11249G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123031708 | |||||||
| chr9:123031720 | A | G | 1 | a0001c0001t0002g0166 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1794+11261A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123031720 | |||||||
| chr9:123032069 | A | G | 4 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0001t0001g0139 others(1): Show |
4 | HG01081.hp1 HG01106.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.1794+11610A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123032069 | |||||||
| chr9:123032367 | A | G | 1 | a0001c0001t0002g0178 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1794+11908A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123032367 | |||||||
| chr9:123032431 | A | G | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1794+11972A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123032431 | |||||||
| chr9:123032442 | G | A | 1 | a0001c0001t0006g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1794+11983G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123032442 | |||||||
| chr9:123032475 | C | T | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1794+12016C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123032475 | |||||||
| chr9:123032882 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1794+12423T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123032882 | |||||||
| chr9:123033063 | T | A | 10 | a0001c0001t0005g0239 a0001c0001t0005g0240 a0001c0001t0005g0241 others(7): Show |
10 | HG01109.hp1 HG02055.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1794+12604T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123033063 | |||||||
| chr9:123033138 | C | G | 1 | a0001c0001t0002g0171 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1794+12679C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123033138 | |||||||
| chr9:123034064 | C | T | 2 | a0001c0002t0023g0032 a0001c0002t0023g0044 |
2 | NA18949.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1794+13605C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123034064 | |||||||
| chr9:123034110 | G | A | 8 | a0001c0001t0001g0059 a0001c0001t0001g0069 a0001c0001t0001g0070 others(5): Show |
9 | HG01099.hp2 HG01496.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1794+13651G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123034110 | |||||||
| chr9:123034267 | G | A | 1 | a0001c0001t0042g0147 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1794+13808G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123034267 | |||||||
| chr9:123034589 | A | G | 1 | a0001c0001t0002g0185 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1794+14130A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123034589 | |||||||
| chr9:123034962 | T | C | 1 | a0001c0001t0047g0199 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1794+14503T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123034962 | |||||||
| chr9:123035005 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1794+14546C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123035005 | |||||||
| chr9:123035200 | T | G | 3 | a0001c0001t0006g0068 a0001c0001t0016g0071 a0001c0001t0016g0073 |
3 | HG01099.hp2 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.1794+14741T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123035200 | |||||||
| chr9:123035214 | C | T | 1 | a0001c0001t0002g0171 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1794+14755C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123035214 | |||||||
| chr9:123035245 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1794+14786G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123035245 | |||||||
| chr9:123035639 | CGT | C | 4 | a0001c0001t0006g0061 a0001c0001t0008g0096 a0001c0002t0009g0036 others(1): Show |
4 | HG02257.hp2 HG02976.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.1794+15223_1794+15 others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123035639 | ||||||
| chr9:123035639 | CGTGT | C | 5 | a0001c0001t0024g0066 a0001c0001t0055g0065 a0001c0002t0009g0037 others(2): Show |
5 | HG02109.hp2 HG02165.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1794+15221_1794+15 others(10): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123035639 | ||||||
| chr9:123035639 | CGTGTGT | C | 28 | a0001c0001t0001g0064 a0001c0001t0001g0086 a0001c0001t0001g0145 others(25): Show |
28 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1794+15219_1794+15 others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123035639 | ||||||
| chr9:123035639 | CGTGTGTG others(1): Show |
C | 42 | a0001c0001t0001g0059 a0001c0001t0001g0069 a0001c0001t0001g0070 others(39): Show |
43 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(40): Show |
intron_variant | MODIFIER | c.1794+15217_1794+15 others(14): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123035639 | ||||||
| chr9:123035639 | CGTGTGTG others(3): Show |
C | 90 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0083 others(87): Show |
90 | HG00099.hp1 HG00558.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.1794+15215_1794+15 others(16): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123035639 | ||||||
| chr9:123035639 | CGTGTGTG others(5): Show |
C | 44 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0109 others(41): Show |
44 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.1794+15213_1794+15 others(18): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123035639 | ||||||
| chr9:123035639 | CGTGTGTG others(7): Show |
C | 28 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(25): Show |
28 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.1794+15211_1794+15 others(20): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123035639 | ||||||
| chr9:123035639 | CGTGTGTG others(9): Show |
C | 1 | a0001c0001t0002g0159 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1794+15209_1794+15 others(22): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123035639 | ||||||
| chr9:123035639 | CGTGTGTG others(11): Show |
C | 1 | a0001c0001t0006g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1794+15207_1794+15 others(24): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123035639 | ||||||
| chr9:123035802 | A | G | 1 | a0001c0001t0006g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1794+15343A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123035802 | |||||||
| chr9:123035896 | G | C | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1794+15437G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123035896 | |||||||
| chr9:123036856 | G | T | 11 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(8): Show |
11 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1794+16397G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123036856 | |||||||
| chr9:123037248 | T | C | 1 | a0001c0001t0045g0130 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1794+16789T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123037248 | |||||||
| chr9:123037588 | T | C | 7 | a0001c0001t0006g0077 a0002c0003t0011g0062 a0002c0003t0011g0074 others(4): Show |
7 | HG00544.hp1 HG02155.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1794+17129T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123037588 | |||||||
| chr9:123037648 | T | C | 70 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0085 others(67): Show |
70 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.1794+17189T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123037648 | |||||||
| chr9:123037725 | T | TTG | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1794+17274_1794+17 others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123037725 | ||||||
| chr9:123037735 | A | G | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1794+17276A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123037735 | |||||||
| chr9:123037735 | A | T | 2 | a0001c0002t0023g0032 a0001c0002t0023g0044 |
2 | NA18949.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1794+17276A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123037735 | |||||||
| chr9:123037852 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1794+17393A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123037852 | |||||||
| chr9:123037866 | A | G | 2 | a0001c0001t0008g0096 a0001c0001t0008g0097 |
2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1794+17407A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123037866 | |||||||
| chr9:123038226 | A | G | 10 | a0001c0001t0005g0239 a0001c0001t0005g0240 a0001c0001t0005g0241 others(7): Show |
10 | HG01109.hp1 HG02055.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1794+17767A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123038226 | |||||||
| chr9:123038440 | G | A | 1 | a0001c0001t0001g0123 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1794+17981G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123038440 | |||||||
| chr9:123038517 | C | CT | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1794+18060dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123038517 | ||||||
| chr9:123038819 | G | A | 1 | a0001c0002t0056g0047 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1794+18360G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123038819 | |||||||
| chr9:123039467 | C | T | 2 | a0001c0001t0020g0114 a0001c0001t0020g0115 |
2 | HG02155.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1794+19008C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123039467 | |||||||
| chr9:123039607 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1794+19148T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123039607 | |||||||
| chr9:123039886 | T | A | 1 | a0001c0001t0006g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1794+19427T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123039886 | |||||||
| chr9:123039899 | TC | T | 27 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(24): Show |
27 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1794+19442delC | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123039899 | ||||||
| chr9:123039978 | T | C | 1 | a0001c0001t0003g0181 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1794+19519T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123039978 | |||||||
| chr9:123040148 | A | G | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1794+19689A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123040148 | |||||||
| chr9:123040191 | A | G | 133 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(130): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.1794+19732A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123040191 | |||||||
| chr9:123040241 | C | G | 1 | a0001c0001t0013g0198 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1794+19782C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123040241 | |||||||
| chr9:123040351 | A | G | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1794+19892A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123040351 | |||||||
| chr9:123040391 | G | A | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1794+19932G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123040391 | |||||||
| chr9:123040553 | C | G | 1 | a0001c0001t0001g0072 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1794+20094C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123040553 | |||||||
| chr9:123041101 | G | A | 2 | a0001c0002t0023g0032 a0001c0002t0023g0044 |
2 | NA18949.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1794+20642G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123041101 | |||||||
| chr9:123041418 | T | C | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1794+20959T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123041418 | |||||||
| chr9:123041566 | T | C | 1 | a0001c0001t0004g0012 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1794+21107T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123041566 | |||||||
| chr9:123041787 | A | G | 2 | a0001c0001t0015g0187 a0001c0001t0015g0197 |
2 | NA18939.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1794+21328A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123041787 | |||||||
| chr9:123042068 | G | A | 1 | a0001c0001t0028g0252 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1794+21609G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123042068 | |||||||
| chr9:123042767 | A | T | 245 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1794+22308A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123042767 | |||||||
| chr9:123042822 | A | T | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1794+22363A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123042822 | |||||||
| chr9:123043083 | T | C | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1795-22265T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123043083 | |||||||
| chr9:123043092 | A | G | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1795-22256A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123043092 | |||||||
| chr9:123043304 | G | A | 10 | a0001c0001t0005g0239 a0001c0001t0005g0240 a0001c0001t0005g0241 others(7): Show |
10 | HG01109.hp1 HG02055.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1795-22044G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123043304 | |||||||
| chr9:123043384 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1795-21964G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123043384 | |||||||
| chr9:123043504 | T | C | 135 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1795-21844T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123043504 | |||||||
| chr9:123043634 | G | C | 63 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(60): Show |
63 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.1795-21714G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123043634 | |||||||
| chr9:123043900 | C | CT | 24 | a0001c0001t0001g0064 a0001c0001t0001g0069 a0001c0001t0001g0070 others(21): Show |
25 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.1795-21430dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123043900 | ||||||
| chr9:123043900 | CT | C | 9 | a0001c0001t0002g0165 a0001c0001t0005g0248 a0001c0001t0006g0077 others(6): Show |
9 | HG00323.hp2 HG00639.hp1 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.1795-21430delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123043900 | ||||||
| chr9:123043986 | C | T | 1 | a0001c0001t0006g0250 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1795-21362C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123043986 | |||||||
| chr9:123043987 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1795-21361G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123043987 | |||||||
| chr9:123044112 | C | T | 3 | a0001c0001t0007g0014 a0001c0001t0007g0019 a0001c0001t0007g0020 |
3 | HG02280.hp1 HG02896.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1795-21236C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123044112 | |||||||
| chr9:123044138 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1795-21210C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123044138 | |||||||
| chr9:123044461 | T | G | 135 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1795-20887T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123044461 | |||||||
| chr9:123044497 | A | G | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1795-20851A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123044497 | |||||||
| chr9:123044626 | C | CGT | 42 | a0001c0001t0001g0087 a0001c0001t0001g0122 a0001c0001t0001g0131 others(39): Show |
42 | HG00280.hp1 HG00323.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.1795-20695_1795-20 others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123044626 | ||||||
| chr9:123044626 | C | CGTGTGT | 23 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(20): Show |
23 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.1795-20699_1795-20 others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123044626 | ||||||
| chr9:123044626 | C | CGTGTGTG others(1): Show |
3 | a0001c0001t0004g0028 a0001c0001t0007g0025 a0001c0001t0033g0023 |
3 | HG02723.hp1 HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1795-20701_1795-20 others(14): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123044626 | ||||||
| chr9:123044626 | C | CGTGTGTG others(5): Show |
2 | a0001c0001t0004g0016 a0001c0001t0004g0018 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1795-20705_1795-20 others(18): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123044626 | ||||||
| chr9:123044626 | CGT | C | 77 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(74): Show |
77 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(74): Show |
intron_variant | MODIFIER | c.1795-20695_1795-20 others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123044626 | ||||||
| chr9:123044626 | CGTGT | C | 5 | a0001c0001t0017g0191 a0001c0001t0017g0203 a0001c0001t0017g0204 others(2): Show |
5 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(2): Show |
intron_variant | MODIFIER | c.1795-20697_1795-20 others(10): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123044626 | ||||||
| chr9:123044626 | CGTGTGTG others(3): Show |
C | 1 | a0001c0002t0022g0049 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1795-20703_1795-20 others(16): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123044626 | ||||||
| chr9:123044626 | CGTGTGTG others(11): Show |
C | 1 | a0001c0001t0007g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1795-20711_1795-20 others(24): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123044626 | ||||||
| chr9:123044741 | C | T | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1795-20607C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123044741 | |||||||
| chr9:123044743 | T | C | 1 | a0001c0001t0004g0100 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1795-20605T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123044743 | |||||||
| chr9:123045017 | C | T | 12 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0069 others(9): Show |
13 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.1795-20331C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123045017 | |||||||
| chr9:123045140 | TTCTG | T | 3 | a0001c0001t0001g0087 a0001c0001t0001g0122 a0001c0001t0001g0131 |
3 | HG00673.hp2 NA18951.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1795-20204_1795-20 others(10): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123045140 | ||||||
| chr9:123045266 | G | A | 7 | a0001c0001t0006g0077 a0002c0003t0011g0062 a0002c0003t0011g0074 others(4): Show |
7 | HG00544.hp1 HG02155.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1795-20082G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123045266 | |||||||
| chr9:123045393 | C | T | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-19955C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123045393 | |||||||
| chr9:123045417 | G | A | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1795-19931G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123045417 | |||||||
| chr9:123045452 | C | T | 3 | a0001c0001t0002g0223 a0001c0001t0002g0224 a0001c0001t0002g0232 |
3 | HG00741.hp1 HG01258.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1795-19896C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123045452 | |||||||
| chr9:123045502 | G | A | 2 | a0001c0001t0006g0088 a0001c0001t0006g0089 |
2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1795-19846G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123045502 | |||||||
| chr9:123045608 | G | A | 1 | a0001c0001t0015g0200 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1795-19740G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123045608 | |||||||
| chr9:123045655 | T | A | 2 | a0001c0001t0008g0096 a0001c0001t0008g0097 |
2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1795-19693T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123045655 | |||||||
| chr9:123045664 | A | T | 1 | a0001c0001t0002g0177 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1795-19684A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123045664 | |||||||
| chr9:123045889 | A | G | 120 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(117): Show |
121 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.1795-19459A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123045889 | |||||||
| chr9:123046197 | A | G | 2 | a0001c0001t0006g0068 a0001c0001t0006g0090 |
2 | HG01884.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1795-19151A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123046197 | |||||||
| chr9:123046221 | G | T | 1 | a0001c0001t0044g0150 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1795-19127G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123046221 | |||||||
| chr9:123046582 | C | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(117): Show |
121 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.1795-18766C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123046582 | |||||||
| chr9:123046617 | A | G | 1 | a0001c0001t0048g0233 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1795-18731A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123046617 | |||||||
| chr9:123046815 | T | C | 1 | a0001c0001t0021g0001 | 2 | HG02109.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.1795-18533T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123046815 | |||||||
| chr9:123046866 | C | A | 120 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(117): Show |
121 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.1795-18482C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123046866 | |||||||
| chr9:123047012 | A | T | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1795-18336A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123047012 | |||||||
| chr9:123047919 | G | GT | 27 | a0001c0001t0002g0163 a0001c0001t0002g0168 a0001c0001t0002g0169 others(24): Show |
27 | HG00558.hp1 HG00597.hp2 HG00642.hp1 others(24): Show |
intron_variant | MODIFIER | c.1795-17393dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123047919 | ||||||
| chr9:123047919 | G | GTT | 13 | a0001c0001t0002g0161 a0001c0001t0002g0172 a0001c0001t0002g0175 others(10): Show |
13 | HG00544.hp2 HG00621.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.1795-17394_1795-17 others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123047919 | ||||||
| chr9:123047919 | G | GTTT | 6 | a0001c0001t0002g0164 a0001c0001t0002g0186 a0001c0001t0002g0195 others(3): Show |
6 | HG01175.hp1 HG01981.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.1795-17395_1795-17 others(9): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123047919 | ||||||
| chr9:123047919 | G | GTTTTTTT others(10): Show |
1 | a0001c0001t0046g0190 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1795-17409_1795-17 others(23): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123047919 | ||||||
| chr9:123047919 | GTTTTTT | G | 17 | a0001c0001t0004g0010 a0001c0001t0004g0015 a0001c0001t0004g0016 others(14): Show |
17 | HG00323.hp2 HG02055.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1795-17398_1795-17 others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123047919 | ||||||
| chr9:123047919 | GTTTTTTT | G | 32 | a0001c0001t0004g0009 a0001c0001t0004g0011 a0001c0001t0004g0012 others(29): Show |
32 | HG00280.hp1 HG00639.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.1795-17399_1795-17 others(13): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123047919 | ||||||
| chr9:123047919 | GTTTTTTT others(1): Show |
G | 5 | a0001c0001t0002g0185 a0001c0001t0048g0233 a0001c0002t0009g0051 others(2): Show |
5 | HG02723.hp2 HG03130.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.1795-17400_1795-17 others(14): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123047919 | ||||||
| chr9:123047919 | GTTTTTTT others(8): Show |
G | 19 | a0001c0001t0001g0064 a0001c0001t0001g0085 a0001c0001t0001g0142 others(16): Show |
19 | HG00544.hp1 HG00621.hp1 HG01175.hp2 others(16): Show |
intron_variant | MODIFIER | c.1795-17407_1795-17 others(21): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123047919 | ||||||
| chr9:123047919 | GTTTTTTT others(9): Show |
G | 87 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(84): Show |
88 | HG00323.hp1 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.1795-17408_1795-17 others(22): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123047919 | ||||||
| chr9:123047919 | GTTTTTTT others(10): Show |
G | 12 | a0001c0001t0001g0109 a0001c0001t0001g0126 a0001c0001t0001g0140 others(9): Show |
12 | HG01943.hp1 HG02040.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.1795-17409_1795-17 others(23): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123047919 | ||||||
| chr9:123047919 | GTTTTTTT others(11): Show |
G | 2 | a0001c0001t0008g0092 a0001c0001t0008g0094 |
2 | HG02965.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1795-17410_1795-17 others(24): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123047919 | ||||||
| chr9:123048260 | C | G | 1 | a0001c0001t0004g0100 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1795-17088C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123048260 | |||||||
| chr9:123048365 | C | G | 1 | a0001c0001t0013g0226 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1795-16983C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123048365 | |||||||
| chr9:123048564 | C | A | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-16784C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123048564 | |||||||
| chr9:123048710 | T | C | 1 | a0001c0001t0018g0251 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1795-16638T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123048710 | |||||||
| chr9:123048843 | A | G | 107 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(104): Show |
108 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.1795-16505A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123048843 | |||||||
| chr9:123048877 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0154 |
2 | NA18961.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1795-16471G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123048877 | |||||||
| chr9:123049114 | T | C | 67 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0085 others(64): Show |
67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1795-16234T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123049114 | |||||||
| chr9:123049189 | T | TGTTAAA | 119 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(116): Show |
120 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.1795-16157_1795-16 others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123049189 | ||||||
| chr9:123049290 | T | TTTG | 5 | a0001c0001t0007g0014 a0001c0001t0007g0019 a0001c0001t0007g0020 others(2): Show |
5 | HG02280.hp1 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1795-16037_1795-16 others(9): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123049290 | ||||||
| chr9:123049290 | T | TTTGTTG | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1795-16040_1795-16 others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123049290 | ||||||
| chr9:123049364 | A | C | 1 | a0001c0001t0004g0022 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1795-15984A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123049364 | |||||||
| chr9:123050182 | CTG | C | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1795-15161_1795-15 others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123050182 | ||||||
| chr9:123051049 | A | G | 1 | a0001c0001t0005g0247 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1795-14299A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051049 | |||||||
| chr9:123051124 | T | A | 1 | a0002c0003t0011g0062 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1795-14224T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051124 | |||||||
| chr9:123051216 | G | GTTTTTTT others(9): Show |
1 | a0001c0001t0003g0219 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1795-14099_1795-14 others(22): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | ||||||
| chr9:123051216 | GTTTTTT | G | 6 | a0001c0001t0002g0169 a0001c0001t0002g0172 a0001c0001t0002g0185 others(3): Show |
6 | HG00558.hp1 HG01952.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1795-14089_1795-14 others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | ||||||
| chr9:123051216 | GTTTTTTT | G | 23 | a0001c0001t0002g0161 a0001c0001t0002g0164 a0001c0001t0002g0168 others(20): Show |
23 | HG00621.hp2 HG00639.hp2 HG00642.hp1 others(20): Show |
intron_variant | MODIFIER | c.1795-14090_1795-14 others(13): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | ||||||
| chr9:123051216 | GTTTTTTT others(1): Show |
G | 21 | a0001c0001t0002g0165 a0001c0001t0002g0167 a0001c0001t0002g0171 others(18): Show |
21 | HG00673.hp1 HG00738.hp1 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.1795-14091_1795-14 others(14): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | ||||||
| chr9:123051216 | GTTTTTTT others(2): Show |
G | 16 | a0001c0001t0002g0159 a0001c0001t0002g0163 a0001c0001t0002g0175 others(13): Show |
16 | HG00280.hp2 HG00544.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1795-14092_1795-14 others(15): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | ||||||
| chr9:123051216 | GTTTTTTT others(3): Show |
G | 6 | a0001c0001t0004g0015 a0001c0001t0004g0028 a0001c0001t0007g0014 others(3): Show |
6 | HG01884.hp2 HG02280.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1795-14093_1795-14 others(16): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | ||||||
| chr9:123051216 | GTTTTTTT others(4): Show |
G | 13 | a0001c0001t0001g0255 a0001c0001t0004g0016 a0001c0001t0004g0017 others(10): Show |
13 | HG01069.hp2 HG01167.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.1795-14094_1795-14 others(17): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | ||||||
| chr9:123051216 | GTTTTTTT others(5): Show |
G | 38 | a0001c0001t0001g0087 a0001c0001t0001g0106 a0001c0001t0001g0107 others(35): Show |
38 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.1795-14095_1795-14 others(18): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | ||||||
| chr9:123051216 | GTTTTTTT others(6): Show |
G | 72 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(69): Show |
73 | HG00323.hp1 HG00558.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.1795-14096_1795-14 others(19): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | ||||||
| chr9:123051216 | GTTTTTTT others(7): Show |
G | 8 | a0001c0001t0003g0182 a0001c0001t0006g0060 a0002c0003t0011g0062 others(5): Show |
8 | HG00544.hp1 HG00738.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.1795-14097_1795-14 others(20): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | ||||||
| chr9:123051216 | GTTTTTTT others(10): Show |
G | 1 | a0001c0001t0031g0222 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1795-14100_1795-14 others(23): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | ||||||
| chr9:123051216 | GTTTTTTT others(16): Show |
G | 1 | a0001c0001t0013g0205 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1795-14106_1795-14 others(29): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | ||||||
| chr9:123051216 | GTTTTTTT others(17): Show |
G | 2 | a0001c0001t0004g0027 a0001c0001t0019g0231 |
2 | HG02257.hp1 NA18959.hp2 |
intron_variant | MODIFIER | c.1795-14107_1795-14 others(30): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | ||||||
| chr9:123051216 | GTTTTTTT others(18): Show |
G | 1 | a0001c0001t0019g0227 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1795-14108_1795-14 others(31): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | ||||||
| chr9:123051216 | GTTTTTTT others(20): Show |
G | 3 | a0001c0002t0009g0040 a0001c0002t0051g0050 a0001c0002t0052g0039 |
3 | NA18955.hp1 NA19074.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.1795-14110_1795-14 others(33): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | ||||||
| chr9:123051216 | GTTTTTTT others(21): Show |
G | 19 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(16): Show |
19 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.1795-14111_1795-14 others(34): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | ||||||
| chr9:123051216 | GTTTTTTT others(23): Show |
G | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-14113_1795-14 others(36): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | ||||||
| chr9:123051216 | GTTTTTTT others(27): Show |
G | 2 | a0001c0001t0002g0166 a0001c0001t0002g0206 |
2 | HG01934.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.1795-14117_1795-14 others(40): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | ||||||
| chr9:123051216 | GTTTTTTT others(28): Show |
G | 1 | a0001c0001t0002g0220 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1795-14118_1795-14 others(41): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051216 | ||||||
| chr9:123051237 | T | G | 4 | a0001c0001t0001g0255 a0001c0001t0004g0022 a0001c0001t0006g0089 others(1): Show |
4 | HG01167.hp1 HG01243.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.1795-14111T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051237 | |||||||
| chr9:123051238 | T | G | 41 | a0001c0001t0001g0087 a0001c0001t0001g0106 a0001c0001t0001g0107 others(38): Show |
41 | HG00621.hp1 HG00673.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.1795-14110T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051238 | |||||||
| chr9:123051239 | T | G | 110 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(107): Show |
111 | HG00323.hp1 HG00558.hp2 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.1795-14109T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051239 | |||||||
| chr9:123051240 | T | G | 80 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(77): Show |
81 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(78): Show |
intron_variant | MODIFIER | c.1795-14108T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051240 | |||||||
| chr9:123051241 | T | G | 7 | a0001c0001t0006g0060 a0002c0003t0011g0062 a0002c0003t0011g0074 others(4): Show |
7 | HG00544.hp1 HG00738.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.1795-14107T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051241 | |||||||
| chr9:123051297 | G | C | 1 | a0002c0003t0011g0078 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1795-14051G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051297 | |||||||
| chr9:123051406 | G | C | 173 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(170): Show |
174 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.1795-13942G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051406 | |||||||
| chr9:123051409 | G | C | 4 | a0001c0001t0001g0064 a0001c0001t0024g0066 a0001c0001t0024g0067 others(1): Show |
4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1795-13939G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051409 | |||||||
| chr9:123051449 | G | A | 2 | a0001c0001t0002g0167 a0001c0001t0002g0173 |
2 | NA19060.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1795-13899G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051449 | |||||||
| chr9:123051548 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1795-13800C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051548 | |||||||
| chr9:123051720 | A | C | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-13628A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051720 | |||||||
| chr9:123051742 | CTATTT | C | 118 | a0001c0001t0001g0064 a0001c0001t0001g0125 a0001c0001t0002g0111 others(115): Show |
118 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.1795-13556_1795-13 others(11): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051742 | ||||||
| chr9:123051742 | CTATTTTA others(3): Show |
C | 112 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(109): Show |
113 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.1795-13561_1795-13 others(16): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051742 | ||||||
| chr9:123051742 | CTATTTTA others(8): Show |
C | 1 | a0001c0001t0018g0249 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1795-13566_1795-13 others(21): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051742 | ||||||
| chr9:123051742 | CTATTTTA others(13): Show |
C | 6 | a0001c0001t0001g0157 a0001c0001t0005g0239 a0001c0001t0005g0242 others(3): Show |
6 | HG02818.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1795-13571_1795-13 others(26): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051742 | ||||||
| chr9:123051779 | ATTTTATT others(5): Show |
A | 1 | a0001c0001t0016g0071 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1795-13566_1795-13 others(18): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051779 | ||||||
| chr9:123051815 | G | A | 40 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0064 others(37): Show |
41 | HG00323.hp1 HG00544.hp1 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.1795-13533G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051815 | |||||||
| chr9:123051958 | A | AT | 11 | a0001c0001t0001g0064 a0001c0001t0001g0112 a0001c0001t0001g0113 others(8): Show |
11 | HG00597.hp2 HG00621.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1795-13370dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051958 | ||||||
| chr9:123051958 | AT | A | 17 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0069 others(14): Show |
18 | HG00323.hp1 HG00558.hp1 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.1795-13370delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051958 | ||||||
| chr9:123051958 | ATT | A | 10 | a0001c0001t0004g0100 a0001c0001t0008g0082 a0001c0001t0008g0092 others(7): Show |
10 | HG02145.hp2 HG02809.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1795-13371_1795-13 others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051958 | ||||||
| chr9:123051958 | ATTTTTTT | A | 30 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(27): Show |
30 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.1795-13376_1795-13 others(13): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123051958 | ||||||
| chr9:123051987 | C | T | 1 | a0001c0001t0004g0100 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1795-13361C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123051987 | |||||||
| chr9:123052345 | A | G | 10 | a0001c0001t0004g0100 a0001c0001t0008g0082 a0001c0001t0008g0092 others(7): Show |
10 | HG02145.hp2 HG02809.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1795-13003A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123052345 | |||||||
| chr9:123052437 | C | G | 1 | a0001c0001t0003g0162 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1795-12911C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123052437 | |||||||
| chr9:123052614 | G | T | 173 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(170): Show |
174 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.1795-12734G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123052614 | |||||||
| chr9:123052667 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1795-12681C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123052667 | |||||||
| chr9:123052727 | C | T | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-12621C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123052727 | |||||||
| chr9:123053064 | T | C | 1 | a0001c0001t0037g0055 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1795-12284T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123053064 | |||||||
| chr9:123053156 | T | G | 5 | a0001c0001t0001g0059 a0001c0001t0001g0069 a0001c0001t0001g0070 others(2): Show |
6 | HG01496.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1795-12192T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123053156 | |||||||
| chr9:123053216 | A | G | 2 | a0001c0001t0018g0249 a0001c0001t0018g0251 |
2 | HG01243.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1795-12132A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123053216 | |||||||
| chr9:123053529 | T | G | 3 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0003c0005t0001g0156 |
3 | HG00733.hp1 HG02738.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1795-11819T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123053529 | |||||||
| chr9:123053539 | C | G | 10 | a0001c0001t0004g0100 a0001c0001t0008g0082 a0001c0001t0008g0092 others(7): Show |
10 | HG02145.hp2 HG02809.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1795-11809C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123053539 | |||||||
| chr9:123054100 | G | A | 6 | a0002c0003t0011g0062 a0002c0003t0011g0074 a0002c0003t0011g0075 others(3): Show |
6 | HG00544.hp1 HG02155.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.1795-11248G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123054100 | |||||||
| chr9:123054181 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1795-11167C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123054181 | |||||||
| chr9:123054421 | C | T | 2 | a0001c0001t0006g0088 a0001c0001t0006g0089 |
2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1795-10927C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123054421 | |||||||
| chr9:123054890 | T | G | 173 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(170): Show |
174 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.1795-10458T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123054890 | |||||||
| chr9:123054907 | G | C | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1795-10441G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123054907 | |||||||
| chr9:123055129 | C | T | 1 | a0001c0001t0002g0177 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1795-10219C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123055129 | |||||||
| chr9:123055254 | C | G | 1 | a0001c0001t0001g0144 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1795-10094C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123055254 | |||||||
| chr9:123055364 | G | A | 10 | a0001c0001t0004g0100 a0001c0001t0008g0082 a0001c0001t0008g0092 others(7): Show |
10 | HG02145.hp2 HG02809.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.1795-9984G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123055364 | |||||||
| chr9:123055389 | G | A | 3 | a0001c0001t0006g0088 a0001c0001t0006g0089 a0001c0001t0006g0090 |
3 | HG01109.hp2 HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1795-9959G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123055389 | |||||||
| chr9:123055432 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1795-9916G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123055432 | |||||||
| chr9:123055440 | C | T | 1 | a0001c0001t0002g0225 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1795-9908C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123055440 | |||||||
| chr9:123055514 | G | A | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1795-9834G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123055514 | |||||||
| chr9:123055546 | C | CT | 15 | a0001c0001t0001g0106 a0001c0001t0001g0117 a0001c0001t0001g0154 others(12): Show |
15 | HG00639.hp1 HG01069.hp2 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.1795-9782dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123055546 | ||||||
| chr9:123055546 | CT | C | 17 | a0001c0001t0001g0140 a0001c0001t0003g0217 a0001c0001t0003g0229 others(14): Show |
17 | HG00099.hp1 HG00544.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.1795-9782delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123055546 | ||||||
| chr9:123055549 | T | C | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1795-9799T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123055549 | |||||||
| chr9:123055588 | C | T | 3 | a0001c0001t0007g0056 a0001c0001t0035g0058 a0001c0001t0037g0055 |
3 | HG01884.hp2 HG02055.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1795-9760C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123055588 | |||||||
| chr9:123055706 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1795-9642C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123055706 | |||||||
| chr9:123055769 | C | T | 120 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(117): Show |
121 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.1795-9579C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123055769 | |||||||
| chr9:123055905 | T | G | 1 | a0001c0001t0006g0089 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1795-9443T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123055905 | |||||||
| chr9:123056177 | G | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(117): Show |
121 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.1795-9171G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056177 | |||||||
| chr9:123056245 | T | C | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-9103T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056245 | |||||||
| chr9:123056278 | T | C | 7 | a0001c0001t0006g0077 a0002c0003t0011g0062 a0002c0003t0011g0074 others(4): Show |
7 | HG00544.hp1 HG02155.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1795-9070T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056278 | |||||||
| chr9:123056323 | A | C | 67 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0085 others(64): Show |
67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.1795-9025A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056323 | |||||||
| chr9:123056481 | CT | C | 9 | a0001c0001t0001g0140 a0001c0001t0002g0169 a0001c0001t0003g0211 others(6): Show |
9 | HG00558.hp1 HG01070.hp1 HG01070.hp2 others(6): Show |
intron_variant | MODIFIER | c.1795-8850delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123056481 | ||||||
| chr9:123056484 | T | C | 1 | a0001c0001t0007g0256 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1795-8864T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056484 | |||||||
| chr9:123056485 | T | C | 12 | a0001c0002t0009g0033 a0001c0002t0009g0052 a0001c0002t0022g0046 others(9): Show |
12 | HG00323.hp2 HG02132.hp2 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.1795-8863T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056485 | |||||||
| chr9:123056486 | T | C | 1 | a0001c0001t0006g0077 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1795-8862T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056486 | |||||||
| chr9:123056487 | T | C | 3 | a0001c0001t0002g0173 a0001c0001t0017g0203 a0001c0001t0017g0204 |
3 | HG00639.hp2 HG00735.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.1795-8861T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056487 | |||||||
| chr9:123056523 | T | C | 135 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1795-8825T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056523 | |||||||
| chr9:123056530 | T | G | 135 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1795-8818T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056530 | |||||||
| chr9:123056549 | G | A | 135 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1795-8799G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056549 | |||||||
| chr9:123056638 | T | C | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1795-8710T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056638 | |||||||
| chr9:123056687 | C | T | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1795-8661C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056687 | |||||||
| chr9:123056735 | G | A | 2 | a0001c0001t0006g0068 a0001c0001t0006g0090 |
2 | HG01884.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1795-8613G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056735 | |||||||
| chr9:123056746 | A | G | 1 | a0001c0001t0015g0200 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1795-8602A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056746 | |||||||
| chr9:123056911 | A | G | 1 | a0001c0001t0006g0077 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1795-8437A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056911 | |||||||
| chr9:123056937 | C | G | 4 | a0001c0002t0009g0040 a0001c0002t0022g0046 a0001c0002t0025g0038 others(1): Show |
4 | HG00323.hp2 HG02132.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.1795-8411C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123056937 | |||||||
| chr9:123057072 | C | T | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-8276C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057072 | |||||||
| chr9:123057098 | C | T | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1795-8250C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057098 | |||||||
| chr9:123057110 | CCCCCCAC others(39): Show |
C | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-8217_1795-817 others(50): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123057110 | ||||||
| chr9:123057126 | C | T | 2 | a0001c0001t0006g0088 a0001c0001t0006g0089 |
2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1795-8222C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057126 | |||||||
| chr9:123057127 | G | A | 1 | a0001c0001t0004g0028 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1795-8221G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057127 | |||||||
| chr9:123057136 | G | A | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1795-8212G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057136 | |||||||
| chr9:123057144 | T | G | 4 | a0001c0001t0001g0064 a0001c0001t0024g0066 a0001c0001t0024g0067 others(1): Show |
4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1795-8204T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057144 | |||||||
| chr9:123057228 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1795-8120C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057228 | |||||||
| chr9:123057458 | G | A | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1795-7890G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057458 | |||||||
| chr9:123057471 | T | C | 1 | a0001c0001t0046g0190 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1795-7877T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057471 | |||||||
| chr9:123057473 | C | T | 4 | a0001c0002t0009g0040 a0001c0002t0022g0046 a0001c0002t0025g0038 others(1): Show |
4 | HG00323.hp2 HG02132.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.1795-7875C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057473 | |||||||
| chr9:123057537 | C | T | 2 | a0001c0001t0005g0240 a0001c0001t0005g0246 |
2 | HG03139.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1795-7811C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057537 | |||||||
| chr9:123057551 | C | T | 4 | a0001c0001t0001g0064 a0001c0001t0024g0066 a0001c0001t0024g0067 others(1): Show |
4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1795-7797C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057551 | |||||||
| chr9:123057618 | A | T | 3 | a0001c0001t0002g0175 a0001c0001t0002g0176 a0001c0001t0002g0236 |
3 | HG00544.hp2 HG00673.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1795-7730A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057618 | |||||||
| chr9:123057658 | G | A | 1 | a0001c0001t0003g0215 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1795-7690G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057658 | |||||||
| chr9:123057710 | G | T | 1 | a0001c0002t0023g0032 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1795-7638G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057710 | |||||||
| chr9:123057746 | A | T | 17 | a0001c0001t0003g0162 a0001c0001t0003g0179 a0001c0001t0003g0181 others(14): Show |
17 | HG00099.hp1 HG00642.hp2 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.1795-7602A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057746 | |||||||
| chr9:123057801 | A | G | 135 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1795-7547A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057801 | |||||||
| chr9:123057808 | C | T | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1795-7540C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057808 | |||||||
| chr9:123057827 | G | A | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.1795-7521G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057827 | |||||||
| chr9:123057921 | C | T | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-7427C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057921 | |||||||
| chr9:123057925 | C | G | 1 | a0001c0002t0052g0039 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1795-7423C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123057925 | |||||||
| chr9:123058050 | A | AGGGGAGA others(1): Show |
239 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(236): Show |
240 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.1795-7283_1795-727 others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123058050 | ||||||
| chr9:123058050 | A | AGGGGAGA others(9): Show |
1 | a0001c0001t0017g0191 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1795-7291_1795-727 others(20): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123058050 | ||||||
| chr9:123058050 | A | AGGGGAGA others(17): Show |
1 | a0001c0001t0046g0190 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1795-7276_1795-727 others(28): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123058050 | ||||||
| chr9:123058313 | A | G | 1 | a0001c0001t0001g0002 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1795-7035A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123058313 | |||||||
| chr9:123058394 | G | T | 1 | a0001c0001t0002g0177 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1795-6954G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123058394 | |||||||
| chr9:123058545 | A | AT | 26 | a0001c0001t0001g0110 a0001c0001t0006g0250 a0001c0001t0018g0249 others(23): Show |
26 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.1795-6791dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123058545 | ||||||
| chr9:123058545 | AT | A | 114 | a0001c0001t0001g0129 a0001c0001t0001g0134 a0001c0001t0002g0159 others(111): Show |
114 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.1795-6791delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | INFO_REALIGN_3_PRIME | chr9 | 123058545 | ||||||
| chr9:123058552 | T | G | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1795-6796T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123058552 | |||||||
| chr9:123058702 | T | C | 1 | a0001c0001t0010g0003 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1795-6646T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123058702 | |||||||
| chr9:123059336 | C | T | 1 | a0001c0002t0022g0046 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1795-6012C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123059336 | |||||||
| chr9:123059337 | G | A | 1 | a0001c0001t0057g0174 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1795-6011G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123059337 | |||||||
| chr9:123059423 | C | G | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-5925C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123059423 | |||||||
| chr9:123059480 | G | C | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-5868G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123059480 | |||||||
| chr9:123059795 | T | C | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1795-5553T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123059795 | |||||||
| chr9:123059796 | T | A | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1795-5552T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123059796 | |||||||
| chr9:123060033 | G | A | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1795-5315G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123060033 | |||||||
| chr9:123060044 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1795-5304C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123060044 | |||||||
| chr9:123060176 | C | G | 1 | a0001c0001t0001g0106 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1795-5172C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123060176 | |||||||
| chr9:123060258 | T | C | 110 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(107): Show |
111 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.1795-5090T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123060258 | |||||||
| chr9:123060628 | A | T | 1 | a0001c0001t0002g0180 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1795-4720A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123060628 | |||||||
| chr9:123060852 | T | G | 1 | a0001c0001t0015g0197 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1795-4496T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123060852 | |||||||
| chr9:123061017 | C | A | 1 | a0001c0001t0001g0083 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1795-4331C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123061017 | |||||||
| chr9:123061018 | A | C | 1 | a0001c0001t0001g0083 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1795-4330A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123061018 | |||||||
| chr9:123061108 | A | G | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-4240A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123061108 | |||||||
| chr9:123061372 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1795-3976C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123061372 | |||||||
| chr9:123061416 | G | A | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1795-3932G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123061416 | |||||||
| chr9:123061417 | C | T | 2 | a0001c0002t0009g0036 a0001c0002t0009g0037 |
2 | NA18952.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1795-3931C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123061417 | |||||||
| chr9:123061421 | T | A | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1795-3927T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123061421 | |||||||
| chr9:123061677 | T | A | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1795-3671T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123061677 | |||||||
| chr9:123061776 | G | A | 113 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(110): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1795-3572G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123061776 | |||||||
| chr9:123061849 | A | T | 245 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1795-3499A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123061849 | |||||||
| chr9:123061892 | G | C | 3 | a0001c0002t0009g0040 a0001c0002t0022g0046 a0001c0002t0025g0038 |
3 | HG00323.hp2 NA19067.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1795-3456G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123061892 | |||||||
| chr9:123062097 | G | A | 1 | a0001c0002t0056g0047 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1795-3251G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123062097 | |||||||
| chr9:123062132 | G | A | 1 | a0001c0001t0057g0174 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1795-3216G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123062132 | |||||||
| chr9:123062154 | G | A | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1795-3194G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123062154 | |||||||
| chr9:123062194 | G | A | 1 | a0001c0001t0007g0256 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1795-3154G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123062194 | |||||||
| chr9:123062199 | C | T | 113 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(110): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1795-3149C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123062199 | |||||||
| chr9:123062203 | G | T | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1795-3145G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123062203 | |||||||
| chr9:123062294 | G | C | 1 | a0001c0001t0001g0117 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1795-3054G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123062294 | |||||||
| chr9:123062845 | G | T | 3 | a0001c0001t0002g0223 a0001c0001t0002g0224 a0001c0001t0002g0232 |
3 | HG00741.hp1 HG01258.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1795-2503G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123062845 | |||||||
| chr9:123063897 | C | T | 1 | a0001c0001t0037g0055 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1795-1451C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123063897 | |||||||
| chr9:123063957 | A | G | 2 | a0001c0001t0002g0168 a0001c0001t0002g0225 |
2 | HG00735.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.1795-1391A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123063957 | |||||||
| chr9:123064095 | G | C | 1 | a0001c0001t0002g0178 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1795-1253G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123064095 | |||||||
| chr9:123064627 | T | C | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-721T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123064627 | |||||||
| chr9:123064723 | T | C | 2 | a0001c0002t0009g0040 a0001c0002t0025g0038 |
2 | HG00323.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1795-625T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123064723 | |||||||
| chr9:123064996 | C | T | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1795-352C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123064996 | |||||||
| chr9:123064999 | C | A | 3 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0003c0005t0001g0156 |
3 | HG00733.hp1 HG02738.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1795-349C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123064999 | |||||||
| chr9:123065069 | A | G | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1795-279A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123065069 | |||||||
| chr9:123065227 | A | C | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1795-121A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 13/25 | chr9 | 123065227 | |||||||
| chr9:123065657 | G | A | 1 | a0001c0001t0003g0221 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1908+196G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123065657 | |||||||
| chr9:123065800 | G | C | 6 | a0002c0003t0011g0062 a0002c0003t0011g0074 a0002c0003t0011g0075 others(3): Show |
6 | HG00544.hp1 HG02155.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.1908+339G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123065800 | |||||||
| chr9:123066148 | G | A | 1 | a0001c0001t0017g0191 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1908+687G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123066148 | |||||||
| chr9:123066165 | A | G | 1 | a0001c0006t0010g0008 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1908+704A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123066165 | |||||||
| chr9:123066313 | T | C | 135 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.1908+852T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123066313 | |||||||
| chr9:123066635 | G | A | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1908+1174G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123066635 | |||||||
| chr9:123066723 | T | C | 6 | a0002c0003t0011g0062 a0002c0003t0011g0074 a0002c0003t0011g0075 others(3): Show |
6 | HG00544.hp1 HG02155.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.1908+1262T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123066723 | |||||||
| chr9:123066912 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1908+1451C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123066912 | |||||||
| chr9:123067209 | G | A | 245 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1908+1748G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123067209 | |||||||
| chr9:123067476 | C | T | 1 | a0001c0001t0004g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1908+2015C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123067476 | |||||||
| chr9:123067637 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1908+2176C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123067637 | |||||||
| chr9:123067820 | A | T | 1 | a0004c0004t0011g0076 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1908+2359A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123067820 | |||||||
| chr9:123067821 | T | C | 1 | a0004c0004t0011g0076 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1908+2360T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123067821 | |||||||
| chr9:123068171 | G | A | 3 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0021g0001 |
4 | HG01496.hp1 HG02109.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1909-2179G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123068171 | |||||||
| chr9:123068348 | C | CA | 7 | a0001c0001t0002g0176 a0001c0001t0005g0240 a0001c0001t0006g0068 others(4): Show |
7 | HG00558.hp2 HG01109.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1909-1984dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr9 | 123068348 | ||||||
| chr9:123068348 | CA | C | 27 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(24): Show |
27 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1909-1984delA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr9 | 123068348 | ||||||
| chr9:123068656 | A | G | 2 | a0001c0001t0006g0088 a0001c0001t0006g0089 |
2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.1909-1694A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123068656 | |||||||
| chr9:123068679 | C | T | 1 | a0001c0001t0036g0228 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1909-1671C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123068679 | |||||||
| chr9:123068695 | C | CTG | 245 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.1909-1654_1909-165 others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr9 | 123068695 | ||||||
| chr9:123068738 | C | T | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1909-1612C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123068738 | |||||||
| chr9:123068814 | T | A | 23 | a0001c0001t0031g0222 a0001c0002t0009g0033 a0001c0002t0009g0034 others(20): Show |
23 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.1909-1536T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123068814 | |||||||
| chr9:123069575 | TA | T | 113 | a0001c0001t0001g0083 a0001c0001t0002g0159 a0001c0001t0002g0161 others(110): Show |
113 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.1909-761delA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr9 | 123069575 | ||||||
| chr9:123069589 | A | G | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1909-761A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123069589 | |||||||
| chr9:123069714 | T | G | 27 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(24): Show |
27 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1909-636T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123069714 | |||||||
| chr9:123069729 | T | A | 1 | a0001c0001t0001g0121 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1909-621T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123069729 | |||||||
| chr9:123070247 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1909-103G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 14/25 | chr9 | 123070247 | |||||||
| chr9:123070600 | T | C | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1983+176T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123070600 | |||||||
| chr9:123071220 | T | C | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.1983+796T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123071220 | |||||||
| chr9:123071296 | A | T | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.1983+872A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123071296 | |||||||
| chr9:123071345 | A | G | 27 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(24): Show |
27 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.1983+921A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123071345 | |||||||
| chr9:123071390 | G | T | 80 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(77): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.1983+966G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123071390 | |||||||
| chr9:123071468 | C | T | 1 | a0001c0002t0009g0036 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1983+1044C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123071468 | |||||||
| chr9:123071475 | T | A | 1 | a0001c0001t0004g0100 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1983+1051T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123071475 | |||||||
| chr9:123071583 | A | G | 2 | a0001c0001t0018g0249 a0001c0001t0018g0251 |
2 | HG01243.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1983+1159A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123071583 | |||||||
| chr9:123071975 | C | G | 1 | a0001c0001t0047g0199 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1983+1551C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123071975 | |||||||
| chr9:123072056 | C | G | 1 | a0001c0001t0001g0104 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1984-1496C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123072056 | |||||||
| chr9:123072606 | C | T | 1 | a0001c0001t0002g0178 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1984-946C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123072606 | |||||||
| chr9:123072874 | A | G | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1984-678A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123072874 | |||||||
| chr9:123072963 | T | G | 15 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0148 others(12): Show |
15 | HG00733.hp1 HG01993.hp2 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.1984-589T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123072963 | |||||||
| chr9:123072984 | G | A | 1 | a0001c0001t0002g0168 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1984-568G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 15/25 | chr9 | 123072984 | |||||||
| chr9:123073788 | T | A | 2 | a0001c0001t0018g0249 a0001c0001t0018g0251 |
2 | HG01243.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2109+111T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 16/25 | chr9 | 123073788 | |||||||
| chr9:123073797 | G | A | 2 | a0001c0002t0023g0032 a0001c0002t0023g0044 |
2 | NA18949.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.2109+120G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 16/25 | chr9 | 123073797 | |||||||
| chr9:123073799 | T | A | 7 | a0001c0001t0006g0077 a0002c0003t0011g0062 a0002c0003t0011g0074 others(4): Show |
7 | HG00544.hp1 HG02155.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.2109+122T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 16/25 | chr9 | 123073799 | |||||||
| chr9:123074661 | T | C | 1 | a0001c0001t0005g0247 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2253+233T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 17/25 | chr9 | 123074661 | |||||||
| chr9:123074909 | A | C | 1 | a0001c0001t0004g0015 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2253+481A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 17/25 | chr9 | 123074909 | |||||||
| chr9:123075058 | C | T | 4 | a0001c0001t0006g0060 a0001c0001t0006g0061 a0001c0001t0006g0080 others(1): Show |
4 | HG00323.hp1 HG00738.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.2253+630C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 17/25 | chr9 | 123075058 | |||||||
| chr9:123075630 | C | A | 1 | a0001c0001t0018g0026 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2254-615C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 17/25 | chr9 | 123075630 | |||||||
| chr9:123075680 | A | G | 4 | a0001c0001t0001g0064 a0001c0001t0024g0066 a0001c0001t0024g0067 others(1): Show |
4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2254-565A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 17/25 | chr9 | 123075680 | |||||||
| chr9:123075686 | T | G | 1 | a0001c0001t0003g0215 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2254-559T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 17/25 | chr9 | 123075686 | |||||||
| chr9:123075824 | T | G | 1 | a0001c0001t0007g0256 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2254-421T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 17/25 | chr9 | 123075824 | |||||||
| chr9:123076430 | GAAGAAAT others(81): Show |
G | 1 | a0001c0001t0002g0235 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2295+150_2296-111d others(90): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr9 | 123076430 | ||||||
| chr9:123076595 | C | G | 1 | a0001c0001t0017g0191 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2296-39C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 18/25 | chr9 | 123076595 | |||||||
| chr9:123076960 | A | C | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2424+198A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123076960 | |||||||
| chr9:123077026 | A | AG | 245 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.2424+265dupG | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077026 | ||||||
| chr9:123077051 | G | GA | 136 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(133): Show |
136 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.2424+290dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077051 | ||||||
| chr9:123077163 | TG | T | 27 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(24): Show |
27 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.2424+402delG | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077163 | |||||||
| chr9:123077164 | G | T | 2 | a0001c0001t0004g0027 a0001c0001t0004g0028 |
2 | HG02257.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2424+402G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077164 | |||||||
| chr9:123077164 | GT | G | 86 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(83): Show |
86 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(83): Show |
intron_variant | MODIFIER | c.2424+415delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077164 | ||||||
| chr9:123077166 | T | C | 2 | a0001c0002t0051g0050 a0001c0002t0052g0039 |
2 | NA18955.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.2424+404T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077166 | |||||||
| chr9:123077170 | T | G | 66 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0085 others(63): Show |
66 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(63): Show |
intron_variant | MODIFIER | c.2424+408T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077170 | |||||||
| chr9:123077462 | A | G | 2 | a0001c0001t0002g0166 a0001c0001t0002g0220 |
2 | HG00099.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.2424+700A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077462 | |||||||
| chr9:123077508 | T | C | 2 | a0001c0001t0006g0088 a0001c0001t0006g0089 |
2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.2424+746T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077508 | |||||||
| chr9:123077610 | C | CATTGT | 9 | a0001c0001t0001g0152 a0001c0001t0001g0255 a0001c0001t0002g0167 others(6): Show |
9 | HG01070.hp2 HG01175.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.2424+927_2424+931d others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077610 | ||||||
| chr9:123077610 | C | CATTGTAT others(3): Show |
6 | a0001c0001t0001g0122 a0001c0001t0002g0207 a0001c0001t0014g0189 others(3): Show |
6 | HG00280.hp2 HG00642.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2424+922_2424+931d others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077610 | ||||||
| chr9:123077610 | C | CATTGTAT others(8): Show |
5 | a0001c0001t0006g0060 a0001c0001t0006g0061 a0001c0001t0006g0081 others(2): Show |
5 | HG00323.hp1 HG00738.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2424+917_2424+931d others(17): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077610 | ||||||
| chr9:123077610 | C | CATTGTAT others(13): Show |
2 | a0001c0001t0002g0169 a0001c0001t0010g0003 |
2 | HG00558.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.2424+912_2424+931d others(22): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077610 | ||||||
| chr9:123077610 | C | CATTGTAT others(18): Show |
1 | a0001c0001t0002g0171 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2424+907_2424+931d others(27): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077610 | ||||||
| chr9:123077610 | C | CATTGTAT others(228): Show |
1 | a0001c0001t0036g0228 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2424+931_2424+932i others(237): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077610 | ||||||
| chr9:123077610 | CATTGT | C | 54 | a0001c0001t0001g0059 a0001c0001t0001g0119 a0001c0001t0001g0121 others(51): Show |
54 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.2424+927_2424+931d others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077610 | ||||||
| chr9:123077610 | CATTGTAT others(3): Show |
C | 74 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0069 others(71): Show |
75 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.2424+922_2424+931d others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077610 | ||||||
| chr9:123077610 | CATTGTAT others(8): Show |
C | 34 | a0001c0001t0001g0109 a0001c0001t0001g0134 a0001c0001t0001g0136 others(31): Show |
34 | HG00558.hp2 HG00639.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.2424+917_2424+931d others(17): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077610 | ||||||
| chr9:123077610 | CATTGTAT others(13): Show |
C | 13 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(10): Show |
13 | HG01934.hp2 HG02258.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2424+912_2424+931d others(22): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077610 | ||||||
| chr9:123077610 | CATTGTAT others(18): Show |
C | 17 | a0001c0001t0004g0015 a0001c0001t0008g0096 a0001c0001t0008g0097 others(14): Show |
17 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.2424+907_2424+931d others(27): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123077610 | ||||||
| chr9:123077640 | T | C | 1 | a0003c0005t0001g0156 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2424+878T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077640 | |||||||
| chr9:123077691 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.2424+929A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077691 | |||||||
| chr9:123077809 | G | A | 1 | a0001c0001t0024g0066 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2424+1047G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077809 | |||||||
| chr9:123077835 | A | T | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.2424+1073A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077835 | |||||||
| chr9:123077874 | T | C | 1 | a0001c0001t0036g0228 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2424+1112T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077874 | |||||||
| chr9:123077875 | A | T | 1 | a0001c0001t0036g0228 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2424+1113A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077875 | |||||||
| chr9:123077898 | C | T | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.2424+1136C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077898 | |||||||
| chr9:123077933 | A | G | 14 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0201 others(11): Show |
14 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.2424+1171A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123077933 | |||||||
| chr9:123078159 | T | C | 1 | a0001c0001t0042g0147 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2424+1397T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123078159 | |||||||
| chr9:123078439 | T | C | 67 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0085 others(64): Show |
67 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.2424+1677T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123078439 | |||||||
| chr9:123078483 | T | G | 1 | a0001c0001t0001g0087 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2424+1721T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123078483 | |||||||
| chr9:123078684 | C | A | 1 | a0001c0001t0002g0254 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.2424+1922C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123078684 | |||||||
| chr9:123078706 | A | G | 1 | a0001c0001t0024g0067 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2424+1944A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123078706 | |||||||
| chr9:123078759 | C | A | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2424+1997C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123078759 | |||||||
| chr9:123078902 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2424+2140C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123078902 | |||||||
| chr9:123079055 | T | C | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.2424+2293T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123079055 | |||||||
| chr9:123079221 | GTTT | G | 82 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(79): Show |
82 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.2424+2464_2424+246 others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123079221 | ||||||
| chr9:123079239 | G | T | 2 | a0001c0001t0006g0088 a0001c0001t0006g0089 |
2 | HG01109.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.2424+2477G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123079239 | |||||||
| chr9:123079239 | GT | G | 9 | a0001c0001t0005g0239 a0001c0001t0005g0240 a0001c0001t0005g0241 others(6): Show |
9 | HG01109.hp1 HG02818.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.2424+2495delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123079239 | ||||||
| chr9:123079239 | GTTT | G | 81 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(78): Show |
81 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.2424+2493_2424+249 others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123079239 | ||||||
| chr9:123079242 | T | TTG | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.2424+2481_2424+248 others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123079242 | ||||||
| chr9:123079244 | T | G | 81 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0085 others(78): Show |
81 | HG00558.hp2 HG00621.hp1 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.2424+2482T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123079244 | |||||||
| chr9:123079247 | T | G | 4 | a0001c0001t0003g0211 a0001c0001t0019g0227 a0001c0001t0019g0231 others(1): Show |
4 | HG01070.hp1 NA18956.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.2424+2485T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123079247 | |||||||
| chr9:123079248 | T | G | 1 | a0001c0001t0007g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2424+2486T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123079248 | |||||||
| chr9:123079249 | T | G | 2 | a0001c0001t0001g0124 a0001c0001t0020g0114 |
2 | HG02165.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.2424+2487T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123079249 | |||||||
| chr9:123079252 | T | G | 1 | a0001c0001t0003g0211 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2424+2490T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123079252 | |||||||
| chr9:123079263 | A | C | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.2424+2501A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123079263 | |||||||
| chr9:123079534 | C | G | 1 | a0001c0001t0006g0077 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.2424+2772C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123079534 | |||||||
| chr9:123079859 | C | T | 1 | a0001c0001t0046g0190 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2424+3097C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123079859 | |||||||
| chr9:123079968 | C | T | 1 | a0001c0001t0001g0002 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2424+3206C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123079968 | |||||||
| chr9:123080177 | A | G | 133 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(130): Show |
133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.2424+3415A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123080177 | |||||||
| chr9:123080198 | T | C | 29 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(26): Show |
29 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.2424+3436T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123080198 | |||||||
| chr9:123080495 | G | T | 1 | a0001c0001t0006g0060 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2424+3733G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123080495 | |||||||
| chr9:123080761 | A | G | 134 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(131): Show |
134 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
intron_variant | MODIFIER | c.2424+3999A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123080761 | |||||||
| chr9:123080795 | A | G | 3 | a0001c0001t0002g0171 a0001c0001t0014g0189 a0001c0001t0014g0208 |
3 | HG00280.hp2 HG00642.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.2424+4033A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123080795 | |||||||
| chr9:123080890 | A | G | 3 | a0001c0001t0003g0181 a0001c0001t0003g0211 a0001c0001t0030g0210 |
3 | HG01070.hp1 HG01993.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.2424+4128A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123080890 | |||||||
| chr9:123081515 | C | G | 4 | a0001c0001t0005g0240 a0001c0001t0005g0245 a0001c0001t0005g0246 others(1): Show |
4 | HG02055.hp2 HG02886.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2424+4753C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123081515 | |||||||
| chr9:123081533 | C | T | 2 | a0001c0001t0001g0237 a0001c0001t0001g0253 |
2 | HG02056.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.2424+4771C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123081533 | |||||||
| chr9:123081565 | T | G | 1 | a0001c0001t0001g0144 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2424+4803T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123081565 | |||||||
| chr9:123081614 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2424+4852T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123081614 | |||||||
| chr9:123081817 | C | T | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.2424+5055C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123081817 | |||||||
| chr9:123081841 | A | G | 1 | a0001c0001t0055g0065 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2424+5079A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123081841 | |||||||
| chr9:123081874 | C | T | 3 | a0001c0001t0012g0084 a0001c0001t0012g0116 a0001c0001t0012g0120 |
3 | HG00558.hp2 HG02027.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.2424+5112C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123081874 | |||||||
| chr9:123081946 | G | A | 7 | a0001c0001t0005g0239 a0001c0001t0005g0241 a0001c0001t0005g0242 others(4): Show |
7 | HG01109.hp1 HG02818.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2424+5184G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123081946 | |||||||
| chr9:123082247 | A | T | 245 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.2424+5485A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123082247 | |||||||
| chr9:123082282 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2424+5520G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123082282 | |||||||
| chr9:123082303 | G | A | 10 | a0001c0001t0003g0179 a0001c0001t0003g0182 a0001c0001t0003g0213 others(7): Show |
10 | HG00099.hp1 HG00733.hp2 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.2424+5541G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123082303 | |||||||
| chr9:123082701 | A | T | 135 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.2424+5939A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123082701 | |||||||
| chr9:123082706 | G | T | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2424+5944G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123082706 | |||||||
| chr9:123082727 | G | GA | 245 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.2424+5966dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123082727 | ||||||
| chr9:123082750 | T | A | 1 | a0001c0001t0005g0241 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2424+5988T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123082750 | |||||||
| chr9:123082913 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2424+6151C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123082913 | |||||||
| chr9:123082930 | G | A | 104 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(101): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.2424+6168G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123082930 | |||||||
| chr9:123082969 | C | T | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2424+6207C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123082969 | |||||||
| chr9:123083028 | A | G | 104 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(101): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.2424+6266A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123083028 | |||||||
| chr9:123083505 | T | A | 1 | a0001c0001t0002g0178 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2425-6253T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123083505 | |||||||
| chr9:123083842 | C | T | 2 | a0001c0001t0002g0166 a0001c0001t0002g0220 |
2 | HG00099.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.2425-5916C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123083842 | |||||||
| chr9:123084117 | T | C | 2 | a0001c0002t0023g0032 a0001c0002t0023g0044 |
2 | NA18949.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.2425-5641T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123084117 | |||||||
| chr9:123084409 | C | T | 1 | a0002c0003t0011g0079 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2425-5349C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123084409 | |||||||
| chr9:123084452 | G | A | 1 | a0001c0001t0045g0130 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2425-5306G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123084452 | |||||||
| chr9:123084683 | G | A | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.2425-5075G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123084683 | |||||||
| chr9:123084817 | T | C | 3 | a0001c0001t0002g0223 a0001c0001t0002g0224 a0001c0001t0002g0232 |
3 | HG00741.hp1 HG01258.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.2425-4941T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123084817 | |||||||
| chr9:123084991 | A | G | 2 | a0001c0001t0024g0067 a0001c0001t0055g0065 |
2 | HG02970.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2425-4767A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123084991 | |||||||
| chr9:123085102 | A | T | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2425-4656A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123085102 | |||||||
| chr9:123085170 | G | A | 1 | a0001c0007t0025g0035 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2425-4588G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123085170 | |||||||
| chr9:123085181 | A | G | 7 | a0001c0001t0006g0077 a0002c0003t0011g0062 a0002c0003t0011g0074 others(4): Show |
7 | HG00544.hp1 HG02155.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.2425-4577A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123085181 | |||||||
| chr9:123085409 | C | T | 6 | a0001c0001t0010g0003 a0001c0001t0010g0004 a0001c0001t0010g0005 others(3): Show |
6 | HG02129.hp1 NA18970.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.2425-4349C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123085409 | |||||||
| chr9:123085488 | T | C | 3 | a0001c0001t0002g0223 a0001c0001t0002g0224 a0001c0001t0002g0232 |
3 | HG00741.hp1 HG01258.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.2425-4270T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123085488 | |||||||
| chr9:123085612 | G | T | 1 | a0001c0001t0001g0086 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.2425-4146G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123085612 | |||||||
| chr9:123085613 | C | T | 8 | a0001c0001t0001g0086 a0001c0001t0002g0169 a0001c0001t0002g0188 others(5): Show |
8 | HG00558.hp1 HG02040.hp1 HG02071.hp2 others(5): Show |
intron_variant | MODIFIER | c.2425-4145C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123085613 | |||||||
| chr9:123085615 | G | A | 2 | a0001c0001t0002g0172 a0001c0001t0002g0207 |
2 | HG01952.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2425-4143G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123085615 | |||||||
| chr9:123085664 | G | A | 1 | a0001c0001t0013g0198 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2425-4094G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123085664 | |||||||
| chr9:123085710 | C | A | 2 | a0001c0002t0023g0032 a0001c0002t0023g0044 |
2 | NA18949.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.2425-4048C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123085710 | |||||||
| chr9:123085742 | T | G | 135 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.2425-4016T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123085742 | |||||||
| chr9:123085760 | G | A | 245 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(242): Show |
246 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(243): Show |
intron_variant | MODIFIER | c.2425-3998G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123085760 | |||||||
| chr9:123085869 | A | G | 2 | a0001c0001t0002g0185 a0001c0001t0002g0186 |
2 | HG02280.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2425-3889A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123085869 | |||||||
| chr9:123085931 | ATTTG | A | 4 | a0001c0001t0001g0064 a0001c0001t0024g0066 a0001c0001t0024g0067 others(1): Show |
4 | HG02109.hp2 HG02970.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2425-3823_2425-382 others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123085931 | ||||||
| chr9:123086203 | G | A | 135 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(132): Show |
135 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.2425-3555G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123086203 | |||||||
| chr9:123086429 | C | T | 1 | a0001c0001t0016g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2425-3329C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123086429 | |||||||
| chr9:123086621 | C | A | 217 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(214): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(215): Show |
intron_variant | MODIFIER | c.2425-3137C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123086621 | |||||||
| chr9:123086631 | C | G | 1 | a0001c0001t0001g0119 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.2425-3127C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123086631 | |||||||
| chr9:123086906 | C | G | 1 | a0001c0001t0012g0084 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2425-2852C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123086906 | |||||||
| chr9:123087231 | A | G | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2425-2527A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123087231 | |||||||
| chr9:123087413 | A | G | 13 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0069 others(10): Show |
14 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.2425-2345A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123087413 | |||||||
| chr9:123087430 | G | C | 1 | a0001c0001t0001g0064 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2425-2328G>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123087430 | |||||||
| chr9:123087523 | C | G | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2425-2235C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123087523 | |||||||
| chr9:123087617 | C | T | 110 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(107): Show |
111 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.2425-2141C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123087617 | |||||||
| chr9:123087638 | C | A | 1 | a0001c0001t0001g0137 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2425-2120C>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123087638 | |||||||
| chr9:123087992 | T | C | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.2425-1766T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123087992 | |||||||
| chr9:123088042 | C | CT | 31 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(28): Show |
31 | HG00639.hp1 HG01069.hp2 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.2425-1703dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123088042 | ||||||
| chr9:123088302 | G | A | 26 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0002g0177 others(23): Show |
26 | HG00558.hp1 HG00597.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.2425-1456G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123088302 | |||||||
| chr9:123088594 | G | A | 2 | a0001c0001t0001g0110 a0001c0001t0001g0123 |
2 | NA18970.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.2425-1164G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123088594 | |||||||
| chr9:123088804 | G | T | 12 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0069 others(9): Show |
13 | HG00323.hp1 HG00738.hp2 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.2425-954G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123088804 | |||||||
| chr9:123088924 | A | G | 4 | a0002c0003t0011g0062 a0002c0003t0011g0074 a0002c0003t0011g0078 others(1): Show |
4 | HG00544.hp1 HG02155.hp1 NA18944.hp2 others(1): Show |
intron_variant | MODIFIER | c.2425-834A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123088924 | |||||||
| chr9:123088935 | A | C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | NA18973.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2425-823A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123088935 | |||||||
| chr9:123089034 | A | T | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.2425-724A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123089034 | |||||||
| chr9:123089081 | AAG | A | 80 | a0001c0001t0002g0159 a0001c0001t0002g0161 a0001c0001t0002g0163 others(77): Show |
80 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.2425-673_2425-672d others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr9 | 123089081 | ||||||
| chr9:123089157 | A | T | 27 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(24): Show |
27 | HG01069.hp2 HG01167.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.2425-601A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123089157 | |||||||
| chr9:123089232 | G | T | 2 | a0001c0001t0008g0098 a0001c0001t0016g0071 |
2 | HG02818.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2425-526G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 19/25 | chr9 | 123089232 | |||||||
| chr9:123089909 | C | T | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.2517+59C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 20/25 | chr9 | 123089909 | |||||||
| chr9:123090574 | C | G | 3 | a0001c0001t0001g0237 a0001c0001t0001g0238 a0001c0001t0001g0253 |
3 | HG02056.hp2 HG02132.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.2628+189C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123090574 | |||||||
| chr9:123090589 | T | G | 3 | a0001c0001t0018g0026 a0001c0001t0018g0249 a0001c0001t0018g0251 |
3 | HG01243.hp1 HG02717.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2628+204T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123090589 | |||||||
| chr9:123090924 | C | T | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2628+539C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123090924 | |||||||
| chr9:123090925 | T | G | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2628+540T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123090925 | |||||||
| chr9:123091047 | A | G | 1 | a0001c0001t0017g0191 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.2628+662A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123091047 | |||||||
| chr9:123091259 | GT | G | 32 | a0001c0001t0005g0239 a0001c0001t0005g0240 a0001c0001t0005g0241 others(29): Show |
32 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.2628+876delT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr9 | 123091259 | ||||||
| chr9:123091414 | A | G | 1 | a0001c0001t0006g0088 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2628+1029A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123091414 | |||||||
| chr9:123091578 | C | G | 1 | a0001c0002t0056g0047 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2628+1193C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123091578 | |||||||
| chr9:123091637 | A | C | 1 | a0001c0001t0001g0153 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2628+1252A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123091637 | |||||||
| chr9:123092036 | G | A | 83 | a0001c0001t0002g0111 a0001c0001t0002g0159 a0001c0001t0002g0161 others(80): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.2628+1651G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123092036 | |||||||
| chr9:123092038 | A | G | 10 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0069 others(7): Show |
11 | HG00323.hp1 HG00738.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.2628+1653A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123092038 | |||||||
| chr9:123092079 | C | G | 1 | a0001c0001t0003g0214 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2628+1694C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123092079 | |||||||
| chr9:123092086 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2628+1701G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123092086 | |||||||
| chr9:123092204 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2628+1819C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123092204 | |||||||
| chr9:123092560 | C | CT | 40 | a0001c0001t0002g0159 a0001c0001t0004g0009 a0001c0001t0004g0010 others(37): Show |
40 | HG00639.hp1 HG01069.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.2628+2184dupT | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr9 | 123092560 | ||||||
| chr9:123092586 | T | A | 1 | a0001c0001t0002g0163 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2628+2201T>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123092586 | |||||||
| chr9:123092592 | G | A | 32 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(29): Show |
32 | HG01069.hp2 HG01099.hp2 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.2628+2207G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123092592 | |||||||
| chr9:123092643 | A | ATG | 81 | a0001c0001t0002g0111 a0001c0001t0002g0159 a0001c0001t0002g0161 others(78): Show |
81 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.2628+2259_2628+226 others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr9 | 123092643 | ||||||
| chr9:123093002 | T | G | 1 | a0001c0001t0002g0111 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2628+2617T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123093002 | |||||||
| chr9:123093236 | T | G | 1 | a0001c0001t0047g0199 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.2628+2851T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123093236 | |||||||
| chr9:123093410 | C | G | 3 | a0001c0001t0006g0068 a0001c0001t0016g0071 a0001c0001t0016g0073 |
3 | HG01099.hp2 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.2628+3025C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123093410 | |||||||
| chr9:123093432 | C | T | 94 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(91): Show |
95 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.2628+3047C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123093432 | |||||||
| chr9:123093501 | A | C | 248 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(245): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.2628+3116A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123093501 | |||||||
| chr9:123093546 | T | G | 3 | a0001c0001t0002g0163 a0001c0001t0002g0166 a0001c0001t0002g0220 |
3 | HG00099.hp2 HG01934.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2628+3161T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123093546 | |||||||
| chr9:123093961 | A | G | 83 | a0001c0001t0002g0111 a0001c0001t0002g0159 a0001c0001t0002g0161 others(80): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.2628+3576A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123093961 | |||||||
| chr9:123094180 | C | G | 1 | a0001c0001t0003g0219 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2629-3561C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123094180 | |||||||
| chr9:123094255 | T | C | 1 | a0001c0001t0042g0147 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2629-3486T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123094255 | |||||||
| chr9:123094451 | T | C | 151 | a0001c0001t0002g0111 a0001c0001t0002g0159 a0001c0001t0002g0161 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.2629-3290T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123094451 | |||||||
| chr9:123094456 | C | T | 1 | a0001c0001t0002g0165 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2629-3285C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123094456 | |||||||
| chr9:123094549 | T | G | 3 | a0001c0001t0024g0066 a0001c0001t0024g0067 a0001c0001t0055g0065 |
3 | HG02109.hp2 HG02970.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2629-3192T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123094549 | |||||||
| chr9:123094586 | T | C | 3 | a0001c0001t0006g0088 a0001c0001t0006g0089 a0001c0001t0006g0090 |
3 | HG01109.hp2 HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.2629-3155T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123094586 | |||||||
| chr9:123094659 | G | A | 246 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(243): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.2629-3082G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123094659 | |||||||
| chr9:123094753 | G | A | 85 | a0001c0001t0001g0085 a0001c0001t0001g0128 a0001c0001t0002g0111 others(82): Show |
85 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.2629-2988G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123094753 | |||||||
| chr9:123094819 | A | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0134 |
2 | NA20300.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2629-2922A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123094819 | |||||||
| chr9:123095226 | C | CA | 11 | a0001c0001t0004g0015 a0001c0001t0007g0014 a0001c0001t0007g0020 others(8): Show |
11 | HG00639.hp1 HG01069.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2629-2490dupA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr9 | 123095226 | ||||||
| chr9:123095226 | CA | C | 83 | a0001c0001t0001g0064 a0001c0001t0001g0086 a0001c0001t0001g0102 others(80): Show |
83 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(80): Show |
intron_variant | MODIFIER | c.2629-2490delA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr9 | 123095226 | ||||||
| chr9:123095226 | CAA | C | 85 | a0001c0001t0001g0063 a0001c0001t0001g0083 a0001c0001t0001g0085 others(82): Show |
85 | HG00544.hp1 HG00673.hp2 HG00733.hp1 others(82): Show |
intron_variant | MODIFIER | c.2629-2491_2629-249 others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr9 | 123095226 | ||||||
| chr9:123095226 | CAAA | C | 28 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0070 others(25): Show |
29 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.2629-2492_2629-249 others(7): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr9 | 123095226 | ||||||
| chr9:123095308 | T | C | 22 | a0001c0002t0009g0033 a0001c0002t0009g0034 a0001c0002t0009g0036 others(19): Show |
22 | HG00280.hp1 HG00323.hp2 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.2629-2433T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123095308 | |||||||
| chr9:123095497 | C | G | 1 | a0001c0001t0001g0153 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2629-2244C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123095497 | |||||||
| chr9:123095624 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0113 |
2 | NA18973.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.2629-2117C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123095624 | |||||||
| chr9:123095642 | T | C | 37 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(34): Show |
37 | HG00639.hp1 HG01069.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.2629-2099T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123095642 | |||||||
| chr9:123095665 | G | A | 7 | a0001c0001t0006g0077 a0002c0003t0011g0062 a0002c0003t0011g0074 others(4): Show |
7 | HG00544.hp1 HG02155.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.2629-2076G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123095665 | |||||||
| chr9:123095708 | GA | G | 10 | a0001c0001t0004g0100 a0001c0001t0006g0077 a0001c0001t0007g0025 others(7): Show |
10 | HG00544.hp1 HG02155.hp1 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.2629-2019delA | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr9 | 123095708 | ||||||
| chr9:123095775 | G | A | 2 | a0001c0001t0002g0184 a0001c0001t0002g0254 |
2 | HG00597.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.2629-1966G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123095775 | |||||||
| chr9:123096076 | T | G | 3 | a0001c0001t0002g0223 a0001c0001t0002g0224 a0001c0001t0002g0232 |
3 | HG00741.hp1 HG01258.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.2629-1665T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123096076 | |||||||
| chr9:123096239 | C | CATTTTGG others(66): Show |
8 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
8 | HG01081.hp1 HG01106.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.2629-1441_2629-144 others(77): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | INFO_REALIGN_3_PRIME | chr9 | 123096239 | ||||||
| chr9:123096315 | C | G | 81 | a0001c0001t0002g0111 a0001c0001t0002g0159 a0001c0001t0002g0161 others(78): Show |
81 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.2629-1426C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123096315 | |||||||
| chr9:123096351 | T | G | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2629-1390T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123096351 | |||||||
| chr9:123096500 | G | T | 3 | a0001c0001t0007g0014 a0001c0001t0007g0019 a0001c0001t0007g0020 |
3 | HG02280.hp1 HG02896.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2629-1241G>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123096500 | |||||||
| chr9:123096600 | G | A | 2 | a0001c0001t0004g0016 a0001c0001t0004g0018 |
2 | HG02965.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2629-1141G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123096600 | |||||||
| chr9:123096631 | C | T | 1 | a0001c0001t0018g0251 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2629-1110C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123096631 | |||||||
| chr9:123096726 | G | A | 1 | a0001c0001t0003g0181 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2629-1015G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123096726 | |||||||
| chr9:123096734 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2629-1007A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123096734 | |||||||
| chr9:123096772 | A | T | 14 | a0001c0001t0002g0171 a0001c0001t0002g0172 a0001c0001t0002g0201 others(11): Show |
14 | HG00280.hp2 HG00639.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.2629-969A>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123096772 | |||||||
| chr9:123096940 | A | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0121 |
2 | HG02129.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.2629-801A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123096940 | |||||||
| chr9:123097166 | C | G | 81 | a0001c0001t0002g0111 a0001c0001t0002g0159 a0001c0001t0002g0161 others(78): Show |
81 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.2629-575C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 21/25 | chr9 | 123097166 | |||||||
| chr9:123097943 | C | G | 2 | a0001c0001t0007g0053 a0001c0001t0007g0256 |
2 | HG03579.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2733+98C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 22/25 | chr9 | 123097943 | |||||||
| chr9:123098299 | T | C | 248 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(245): Show |
249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.2734-416T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 22/25 | chr9 | 123098299 | |||||||
| chr9:123098303 | A | G | 246 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(243): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.2734-412A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 22/25 | chr9 | 123098303 | |||||||
| chr9:123098310 | G | A | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2734-405G>A | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 22/25 | chr9 | 123098310 | |||||||
| chr9:123098999 | C | G | 5 | a0001c0001t0010g0004 a0001c0001t0010g0005 a0001c0001t0010g0006 others(2): Show |
5 | NA18970.hp2 NA18979.hp2 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.2817+201C>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 23/25 | chr9 | 123098999 | |||||||
| chr9:123099416 | T | C | 122 | a0001c0001t0002g0111 a0001c0001t0002g0159 a0001c0001t0002g0161 others(119): Show |
122 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.2818-62T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 23/25 | chr9 | 123099416 | |||||||
| chr9:123099462 | A | C | 52 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0083 others(49): Show |
52 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.2818-16A>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 23/25 | chr9 | 123099462 | |||||||
| chr9:123099584 | A | G | 2 | a0001c0002t0009g0036 a0001c0002t0009g0037 |
2 | NA18952.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2889+35A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | chr9 | 123099584 | |||||||
| chr9:123099609 | A | G | 147 | a0001c0001t0002g0111 a0001c0001t0002g0159 a0001c0001t0002g0161 others(144): Show |
147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.2889+60A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | chr9 | 123099609 | |||||||
| chr9:123099819 | C | T | 2 | a0001c0001t0005g0239 a0001c0001t0005g0248 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2889+270C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | chr9 | 123099819 | |||||||
| chr9:123100383 | A | ATG | 17 | a0001c0001t0001g0083 a0001c0001t0001g0107 a0001c0001t0001g0123 others(14): Show |
17 | HG01361.hp1 HG01943.hp1 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.2889+888_2889+889d others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 123100383 | ||||||
| chr9:123100383 | A | ATGTG | 5 | a0001c0001t0001g0122 a0001c0001t0001g0257 a0001c0001t0004g0030 others(2): Show |
5 | HG01952.hp1 HG02055.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.2889+886_2889+889d others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 123100383 | ||||||
| chr9:123100383 | A | ATGTGTG | 3 | a0001c0001t0001g0087 a0001c0001t0001g0139 a0001c0001t0006g0061 |
3 | HG00673.hp2 HG01106.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.2889+884_2889+889d others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 123100383 | ||||||
| chr9:123100383 | A | ATGTGTGT others(3): Show |
4 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0001t0028g0252 others(1): Show |
4 | HG01081.hp1 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.2889+880_2889+889d others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 123100383 | ||||||
| chr9:123100383 | A | G | 1 | a0001c0001t0018g0026 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2889+834A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | chr9 | 123100383 | |||||||
| chr9:123100383 | ATG | A | 43 | a0001c0001t0001g0063 a0001c0001t0001g0102 a0001c0001t0001g0104 others(40): Show |
43 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.2889+888_2889+889d others(4): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 123100383 | ||||||
| chr9:123100383 | ATGTG | A | 26 | a0001c0001t0001g0059 a0001c0001t0001g0072 a0001c0001t0001g0121 others(23): Show |
27 | HG00544.hp1 HG00558.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.2889+886_2889+889d others(6): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 123100383 | ||||||
| chr9:123100383 | ATGTGTG | A | 16 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0105 others(13): Show |
16 | HG01496.hp1 HG02055.hp2 HG02723.hp1 others(13): Show |
intron_variant | MODIFIER | c.2889+884_2889+889d others(8): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 123100383 | ||||||
| chr9:123100383 | ATGTGTGT others(1): Show |
A | 8 | a0001c0001t0001g0103 a0001c0001t0005g0240 a0001c0001t0005g0246 others(5): Show |
8 | HG00280.hp2 HG01099.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.2889+882_2889+889d others(10): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 123100383 | ||||||
| chr9:123100383 | ATGTGTGT others(3): Show |
A | 14 | a0001c0001t0002g0185 a0001c0001t0002g0186 a0001c0001t0002g0192 others(11): Show |
14 | HG00741.hp1 HG01258.hp1 HG02155.hp1 others(11): Show |
intron_variant | MODIFIER | c.2889+880_2889+889d others(12): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 123100383 | ||||||
| chr9:123100383 | ATGTGTGT others(5): Show |
A | 8 | a0001c0001t0001g0002 a0001c0001t0002g0209 a0001c0001t0003g0182 others(5): Show |
8 | HG01106.hp1 HG01167.hp2 HG02056.hp1 others(5): Show |
intron_variant | MODIFIER | c.2889+878_2889+889d others(14): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 123100383 | ||||||
| chr9:123100383 | ATGTGTGT others(7): Show |
A | 62 | a0001c0001t0002g0111 a0001c0001t0002g0159 a0001c0001t0002g0161 others(59): Show |
62 | HG00099.hp1 HG00099.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.2889+876_2889+889d others(16): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 123100383 | ||||||
| chr9:123100383 | ATGTGTGT others(9): Show |
A | 4 | a0001c0001t0001g0101 a0001c0001t0002g0212 a0001c0001t0003g0181 others(1): Show |
4 | HG00621.hp2 HG01069.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.2889+874_2889+889d others(18): Show |
RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr9 | 123100383 | ||||||
| chr9:123100508 | C | T | 1 | a0001c0001t0016g0054 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2889+959C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | chr9 | 123100508 | |||||||
| chr9:123100665 | C | T | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2890-901C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | chr9 | 123100665 | |||||||
| chr9:123101071 | A | G | 121 | a0001c0001t0001g0002 a0001c0001t0001g0059 a0001c0001t0001g0063 others(118): Show |
122 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.2890-495A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 24/25 | chr9 | 123101071 | |||||||
| chr9:123101784 | A | G | 1 | a0001c0001t0003g0162 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3087+21A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 25/25 | chr9 | 123101784 | |||||||
| chr9:123101795 | C | T | 1 | a0001c0001t0007g0053 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3087+32C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 25/25 | chr9 | 123101795 | |||||||
| chr9:123101814 | T | G | 37 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(34): Show |
37 | HG00639.hp1 HG01069.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.3087+51T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 25/25 | chr9 | 123101814 | |||||||
| chr9:123101838 | C | T | 3 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02258.hp2 HG02486.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.3087+75C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 25/25 | chr9 | 123101838 | |||||||
| chr9:123101915 | T | C | 1 | a0001c0001t0004g0027 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3087+152T>C | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 25/25 | chr9 | 123101915 | |||||||
| chr9:123102213 | T | G | 37 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0011 others(34): Show |
37 | HG00639.hp1 HG01069.hp2 HG01099.hp2 others(34): Show |
intron_variant | MODIFIER | c.3087+450T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 25/25 | chr9 | 123102213 | |||||||
| chr9:123102410 | C | T | 1 | a0001c0001t0033g0023 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3087+647C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 25/25 | chr9 | 123102410 | |||||||
| chr9:123102457 | A | G | 1 | a0001c0001t0001g0117 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.3088-634A>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 25/25 | chr9 | 123102457 | |||||||
| chr9:123102470 | T | G | 2 | a0001c0001t0039g0234 a0001c0001t0048g0233 |
2 | HG00639.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.3088-621T>G | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 25/25 | chr9 | 123102470 | |||||||
| chr9:123102989 | C | T | 1 | a0001c0001t0004g0009 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.3088-102C>T | RABGAP1 | ENSG00000011454.18 | transcript | ENST00000373647.9 | protein_coding | 25/25 | chr9 | 123102989 |