Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 200894 |
| ensemblid | ENSG00000169379.17 |
| hgncid | 25419 |
| symbol | ARL13B |
| name | ADP ribosylation factor like GTPase 13B |
| refseq_nuc | NM_001174150.2 |
| refseq_prot | NP_001167621.1 |
| ensembl_nuc | ENST00000394222.8 |
| ensembl_prot | ENSP00000377769.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 93980155 |
| end | 94055678 |
| strand | + |
| ver | v1.2 |
| region | chr3:93980155-94055678 |
| region5000 | chr3:93975155-94060678 |
| regionname0 | ARL13B_chr3_93980155_94055678 |
| regionname5000 | ARL13B_chr3_93975155_94060678 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 428 | 219 | 64 | 45 | 70 | 8 | 30 | 55 | ARL13B_chr3_93975155_94060678 | ARL13B | MFSLM others(423): Show |
chr3 | 93975155 | 94060678 |
| a0002 | 0/0 | 428 | 23 | 1 | 4 | 12 | 2 | 4 | 8 | ARL13B_chr3_93975155_94060678 | ARL13B | MFSLM others(423): Show |
chr3 | 93975155 | 94060678 |
| a0003 | 0/0 | 284 | 17 | 6 | 7 | 1 | 0 | 3 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | MFSLM others(279): Show |
chr3 | 93975155 | 94060678 |
| a0004 | 0/0 | 428 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | MFSLM others(423): Show |
chr3 | 93975155 | 94060678 |
| a0005 | 0/0 | 428 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | MFSLM others(423): Show |
chr3 | 93975155 | 94060678 |
| a0006 | 0/0 | 428 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | MFSLM others(423): Show |
chr3 | 93975155 | 94060678 |
| a0007 | 0/0 | 428 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | MFSLM others(423): Show |
chr3 | 93975155 | 94060678 |
| a0008 | 0/0 | 428 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | MFSLM others(423): Show |
chr3 | 93975155 | 94060678 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1284 | 217 | 64 | 43 | 70 | 8 | 30 | ARL13B_chr3_93975155_94060678 | ARL13B | ATGTT others(1279): Show |
chr3 | 93975155 | 94060678 | ||
| a0001c0004 | 0/0 | 1284 | 2 | 0 | 2 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | ATGTT others(1279): Show |
chr3 | 93975155 | 94060678 | ||
| a0002c0002 | 0/0 | 1284 | 22 | 1 | 4 | 12 | 1 | 4 | ARL13B_chr3_93975155_94060678 | ARL13B | ATGTT others(1279): Show |
chr3 | 93975155 | 94060678 | ||
| a0002c0005 | 0/0 | 1284 | 1 | 0 | 0 | 0 | 1 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | ATGTT others(1279): Show |
chr3 | 93975155 | 94060678 | ||
| a0003c0003 | 0/0 | 1285 | 16 | 6 | 7 | 1 | 0 | 2 | ARL13B_chr3_93975155_94060678 | ARL13B | ATGTT others(1280): Show |
chr3 | 93975155 | 94060678 | ||
| a0003c0006 | 0/0 | 1285 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | ATGTT others(1280): Show |
chr3 | 93975155 | 94060678 | ||
| a0004c0008 | 0/0 | 1284 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | ATGTT others(1279): Show |
chr3 | 93975155 | 94060678 | ||
| a0005c0010 | 0/0 | 1284 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | ATGTT others(1279): Show |
chr3 | 93975155 | 94060678 | ||
| a0006c0007 | 0/0 | 1284 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | ATGTT others(1279): Show |
chr3 | 93975155 | 94060678 | ||
| a0007c0011 | 0/0 | 1284 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | ATGTT others(1279): Show |
chr3 | 93975155 | 94060678 | ||
| a0008c0009 | 0/0 | 1284 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | ATGTT others(1279): Show |
chr3 | 93975155 | 94060678 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3971 | 195 | 52 | 41 | 64 | 7 | 29 | ARL13B_chr3_93975155_94060678 | ARL13B | GCTTT others(3966): Show |
chr3 | 93975155 | 94060678 |
| a0001c0001t0002 | 0/0 | 3971 | 6 | 5 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | GCTTT others(3966): Show |
chr3 | 93975155 | 94060678 |
| a0001c0001t0003 | 0/0 | 3971 | 5 | 0 | 0 | 5 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | GCTTT others(3966): Show |
chr3 | 93975155 | 94060678 |
| a0001c0001t0004 | 0/0 | 3971 | 3 | 3 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | GCTTT others(3966): Show |
chr3 | 93975155 | 94060678 |
| a0001c0001t0005 | 0/0 | 3971 | 2 | 2 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | GCTTT others(3966): Show |
chr3 | 93975155 | 94060678 |
| a0001c0001t0006 | 0/0 | 3971 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | GCTTT others(3966): Show |
chr3 | 93975155 | 94060678 |
| a0001c0001t0009 | 0/0 | 3971 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | GCTTT others(3966): Show |
chr3 | 93975155 | 94060678 |
| a0001c0001t0010 | 0/0 | 3971 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | GCTTT others(3966): Show |
chr3 | 93975155 | 94060678 |
| a0001c0001t0011 | 0/0 | 3971 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | GCTTT others(3966): Show |
chr3 | 93975155 | 94060678 |
| a0001c0001t0013 | 0/0 | 3971 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | GCTTT others(3966): Show |
chr3 | 93975155 | 94060678 |
| a0001c0001t0014 | 0/0 | 3971 | 1 | 0 | 0 | 0 | 1 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | GCTTT others(3966): Show |
chr3 | 93975155 | 94060678 |
| a0001c0004t0001 | 0/0 | 3971 | 2 | 0 | 2 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | GCTTT others(3966): Show |
chr3 | 93975155 | 94060678 |
| a0002c0002t0001 | 0/0 | 3971 | 21 | 1 | 4 | 11 | 1 | 4 | ARL13B_chr3_93975155_94060678 | ARL13B | GCTTT others(3966): Show |
chr3 | 93975155 | 94060678 |
| a0002c0002t0007 | 0/0 | 3971 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | GCTTT others(3966): Show |
chr3 | 93975155 | 94060678 |
| a0002c0005t0001 | 0/0 | 3971 | 1 | 0 | 0 | 0 | 1 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | GCTTT others(3966): Show |
chr3 | 93975155 | 94060678 |
| a0003c0003t0001 | 0/0 | 3972 | 15 | 5 | 7 | 1 | 0 | 2 | ARL13B_chr3_93975155_94060678 | ARL13B | GCTTT others(3967): Show |
chr3 | 93975155 | 94060678 |
| a0003c0003t0006 | 0/0 | 3972 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | GCTTT others(3967): Show |
chr3 | 93975155 | 94060678 |
| a0003c0006t0001 | 0/0 | 3972 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | GCTTT others(3967): Show |
chr3 | 93975155 | 94060678 |
| a0004c0008t0012 | 0/0 | 3971 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | GCTTT others(3966): Show |
chr3 | 93975155 | 94060678 |
| a0005c0010t0001 | 0/0 | 3971 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | GCTTT others(3966): Show |
chr3 | 93975155 | 94060678 |
| a0006c0007t0001 | 0/0 | 3971 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | GCTTT others(3966): Show |
chr3 | 93975155 | 94060678 |
| a0007c0011t0008 | 0/0 | 3971 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | GCTTT others(3966): Show |
chr3 | 93975155 | 94060678 |
| a0008c0009t0001 | 0/0 | 3971 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | GCTTT others(3966): Show |
chr3 | 93975155 | 94060678 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0153 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0169 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0006g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0009g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0010g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0011g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0013g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0001t0014g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0004t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0001c0004t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0002c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0002c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0002c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0002c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0002c0002t0007g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0002c0005t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0003c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0003c0003t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0003c0003t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0003c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0003c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0003c0003t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0003c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0003c0003t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0003c0003t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0003c0003t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0003c0003t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0003c0003t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0003c0003t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0003c0003t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0003c0003t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0003c0003t0006g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0003c0006t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0004c0008t0012g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0005c0010t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0006c0007t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0007c0011t0008g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| a0008c0009t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0237 | EUR | GBR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0035 | EUR | GBR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | FIN | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | FIN | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG00438 | hp2 | a0003 | c0003 | t0001 | g0037 | EAS | CHS | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0131 | EAS | CHS | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG00621 | hp1 | a0002 | c0002 | t0001 | g0024 | EAS | CHS | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0174 | AMR | PUR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG00733 | hp2 | a0003 | c0003 | t0001 | g0089 | AMR | PUR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01074 | hp1 | a0001 | c0004 | t0001 | g0138 | AMR | PUR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01175 | hp1 | a0003 | c0003 | t0001 | g0222 | AMR | PUR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01175 | hp2 | a0003 | c0003 | t0001 | g0190 | AMR | PUR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0041 | AMR | CLM | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0040 | AMR | CLM | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0031 | AMR | CLM | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | CLM | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01433 | hp1 | a0003 | c0003 | t0001 | g0228 | AMR | CLM | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01433 | hp2 | a0003 | c0003 | t0001 | g0194 | AMR | CLM | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0125 | AMR | CLM | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0199 | EUR | IBS | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | IBS | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0240 | AFR | ACB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01928 | hp1 | a0003 | c0003 | t0001 | g0186 | AMR | PEL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PEL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | PEL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01952 | hp2 | a0003 | c0003 | t0001 | g0176 | AMR | PEL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02004 | hp2 | a0001 | c0004 | t0001 | g0067 | AMR | PEL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02015 | hp2 | a0001 | c0001 | t0003 | g0246 | EAS | KHV | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0140 | AFR | ACB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | KHV | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | ACB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | CDX | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CDX | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02258 | hp2 | a0001 | c0001 | t0002 | g0239 | AFR | ACB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02572 | hp2 | a0001 | c0001 | t0011 | g0227 | AFR | GWD | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02622 | hp1 | a0003 | c0003 | t0001 | g0145 | AFR | GWD | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0241 | AFR | GWD | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02683 | hp1 | a0002 | c0002 | t0001 | g0263 | SAS | PJL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02717 | hp2 | a0003 | c0003 | t0001 | g0207 | AFR | GWD | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0008 | SAS | PJL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02809 | hp1 | a0001 | c0001 | t0005 | g0058 | AFR | GWD | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | GWD | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03041 | hp2 | a0001 | c0001 | t0005 | g0057 | AFR | GWD | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ESN | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03209 | hp1 | a0003 | c0003 | t0001 | g0162 | AFR | MSL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | MSL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | MSL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0264 | AFR | MSL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0257 | SAS | PJL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03239 | hp2 | a0003 | c0003 | t0001 | g0172 | SAS | PJL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0141 | AFR | MSL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | MSL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0260 | AFR | MSL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03491 | hp1 | a0004 | c0008 | t0012 | g0136 | SAS | PJL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0261 | AFR | MSL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0133 | SAS | PJL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | STU | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | STU | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03831 | hp1 | a0003 | c0003 | t0001 | g0099 | SAS | BEB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | BEB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0135 | SAS | BEB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0217 | SAS | BEB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03927 | hp2 | a0003 | c0006 | t0001 | g0006 | SAS | BEB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | STU | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | STU | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | BEB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | STU | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG04199 | hp2 | a0001 | c0001 | t0010 | g0234 | SAS | STU | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | STU | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | STU | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | YRI | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18522 | hp2 | a0001 | c0001 | t0013 | g0002 | AFR | YRI | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | CHB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18906 | hp1 | a0003 | c0003 | t0006 | g0073 | AFR | YRI | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0163 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0027 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18978 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18982 | hp2 | a0002 | c0002 | t0007 | g0134 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18995 | hp1 | a0005 | c0010 | t0001 | g0054 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19009 | hp1 | a0001 | c0001 | t0009 | g0195 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19030 | hp2 | a0003 | c0003 | t0001 | g0238 | AFR | LWK | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19056 | hp1 | a0006 | c0007 | t0001 | g0028 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19070 | hp2 | a0007 | c0011 | t0008 | g0205 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | YRI | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA19240 | hp2 | a0003 | c0003 | t0001 | g0044 | AFR | YRI | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0151 | EUR | TSI | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA20752 | hp2 | a0002 | c0005 | t0001 | g0023 | EUR | TSI | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0039 | EUR | TSI | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA20805 | hp2 | a0001 | c0001 | t0014 | g0088 | EUR | TSI | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | GIH | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | GIH | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0142 | AFR | MSL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | USA | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA20300 | hp1 | a0008 | c0009 | t0001 | g0036 | AFR | USA | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | USA | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | LWK | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0169 | REF | REF | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0153 | REF | REF | ARL13B_chr3_93975155_94060678 | ARL13B | chr3 | 93975155 | 94060678 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:94003854 | A | G | 1 | a0007 | 1 | NA19070.hp2 | missense_variant | MODERATE | c.326A>G | p.Glu109Gly | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/10 | 595/3971 | 326/1287 | 109/428 | chr3 | 94003854 | |||
| chr3:94043038 | G | GA | 1 | a0003 | 17 | HG00438.hp2 HG00733.hp2 HG01175.hp1 others(14): Show |
frameshift_variant | HIGH | c.830dupA | p.Asn277fs | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/10 | 1100/3971 | 831/1287 | 277/428 | INFO_REALIGN_3_PRIME | chr3 | 94043038 | ||
| chr3:94043057 | G | A | 1 | a0006 | 1 | NA19056.hp1 | missense_variant | MODERATE | c.841G>A | p.Glu281Lys | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/10 | 1110/3971 | 841/1287 | 281/428 | chr3 | 94043057 | |||
| chr3:94049424 | C | G | 3 | a0002 a0003 a0006 |
25 | HG00558.hp2 HG00621.hp1 HG01256.hp1 others(22): Show |
missense_variant | MODERATE | c.1043C>G | p.Thr348Ser | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 8/10 | 1312/3971 | 1043/1287 | 348/428 | chr3 | 94049424 | |||
| chr3:94049471 | A | G | 1 | a0005 | 1 | NA18995.hp1 | missense_variant | MODERATE | c.1090A>G | p.Ile364Val | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 8/10 | 1359/3971 | 1090/1287 | 364/428 | chr3 | 94049471 | |||
| chr3:94049517 | C | T | 1 | a0008 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.1136C>T | p.Pro379Leu | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 8/10 | 1405/3971 | 1136/1287 | 379/428 | chr3 | 94049517 | |||
| chr3:94050868 | C | G | 1 | a0004 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.1186C>G | p.Pro396Ala | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 9/10 | 1455/3971 | 1186/1287 | 396/428 | chr3 | 94050868 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:93995919 | C | T | 1 | a0001c0004 | 2 | HG01074.hp1 HG02004.hp2 |
synonymous_variant | LOW | c.105C>T | p.Thr35Thr | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/10 | 374/3971 | 105/1287 | 35/428 | chr3 | 93995919 | |||
| chr3:94036572 | G | C | 1 | a0002c0005 | 1 | NA20752.hp2 | synonymous_variant | LOW | c.507G>C | p.Ser169Ser | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/10 | 776/3971 | 507/1287 | 169/428 | chr3 | 94036572 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:93980161 | C | T | 1 | a0001c0001t0014 | 1 | NA20805.hp2 | 5_prime_UTR_variant | MODIFIER | c.-263C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/10 | 263 | chr3 | 93980161 | ||||||
| chr3:93980167 | C | T | 2 | a0001c0001t0006 a0003c0003t0006 |
2 | HG00639.hp2 NA18906.hp1 |
5_prime_UTR_variant | MODIFIER | c.-257C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/10 | 257 | chr3 | 93980167 | ||||||
| chr3:93980190 | G | T | 1 | a0001c0001t0002 | 6 | HG01891.hp2 HG01952.hp1 HG02258.hp2 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-234G>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/10 | chr3 | 93980190 | |||||||
| chr3:93980408 | G | A | 1 | a0002c0002t0007 | 1 | NA18982.hp2 | 5_prime_UTR_variant | MODIFIER | c.-16G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/10 | 16 | chr3 | 93980408 | ||||||
| chr3:94053393 | T | G | 1 | a0007c0011t0008 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*130T>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 10/10 | 130 | chr3 | 94053393 | ||||||
| chr3:94053640 | T | A | 1 | a0001c0001t0009 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*377T>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 10/10 | 377 | chr3 | 94053640 | ||||||
| chr3:94053966 | C | T | 1 | a0001c0001t0003 | 5 | HG02015.hp2 NA18954.hp2 NA18957.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*703C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 10/10 | 703 | chr3 | 94053966 | ||||||
| chr3:94054326 | A | G | 1 | a0001c0001t0013 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1063A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 10/10 | 1063 | chr3 | 94054326 | ||||||
| chr3:94054399 | A | G | 1 | a0001c0001t0005 | 2 | HG02809.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1136A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 10/10 | 1136 | chr3 | 94054399 | ||||||
| chr3:94054968 | T | C | 1 | a0001c0001t0010 | 1 | HG04199.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1705T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 10/10 | 1705 | chr3 | 94054968 | ||||||
| chr3:94055409 | T | C | 1 | a0001c0001t0011 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2146T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 10/10 | 2146 | chr3 | 94055409 | ||||||
| chr3:94055560 | T | C | 1 | a0001c0001t0004 | 3 | HG02055.hp1 HG03453.hp2 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2297T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 10/10 | 2297 | chr3 | 94055560 | ||||||
| chr3:94055626 | C | G | 1 | a0004c0008t0012 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2363C>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 10/10 | 2363 | chr3 | 94055626 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:93980681 | A | G | 2 | a0001c0001t0001g0264 a0002c0002t0001g0263 |
2 | HG02683.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.59+199A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93980681 | |||||||
| chr3:93980726 | A | AGT | 27 | a0001c0001t0001g0229 a0001c0001t0001g0231 a0001c0001t0001g0232 others(24): Show |
27 | HG00140.hp1 HG00738.hp1 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.59+278_59+279dupTG | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 93980726 | ||||||
| chr3:93980726 | A | AGTGT | 8 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0256 others(5): Show |
8 | HG01884.hp1 HG02300.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.59+276_59+279dupTG others(2): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 93980726 | ||||||
| chr3:93980726 | A | AGTGTGTG others(3): Show |
1 | a0001c0001t0001g0262 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.59+270_59+279dupTG others(8): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 93980726 | ||||||
| chr3:93980726 | AGT | A | 55 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0010 others(52): Show |
55 | HG00140.hp2 HG00438.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.59+278_59+279delTG | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 93980726 | ||||||
| chr3:93980726 | AGTGT | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 |
3 | HG03471.hp2 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.59+276_59+279delTG others(2): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 93980726 | ||||||
| chr3:93980726 | AGTGTGTG others(7): Show |
A | 2 | a0001c0001t0001g0001 a0001c0001t0013g0002 |
2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.59+266_59+279delTG others(12): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 93980726 | ||||||
| chr3:93980944 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.59+462C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93980944 | |||||||
| chr3:93981070 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.59+588A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93981070 | |||||||
| chr3:93981145 | A | C | 2 | a0001c0001t0005g0057 a0001c0001t0005g0058 |
2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.59+663A>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93981145 | |||||||
| chr3:93981647 | C | G | 1 | a0001c0001t0001g0224 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.59+1165C>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93981647 | |||||||
| chr3:93981865 | C | CA | 87 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(84): Show |
87 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.59+1407dupA | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 93981865 | ||||||
| chr3:93981865 | C | CAA | 12 | a0001c0001t0001g0007 a0001c0001t0001g0059 a0001c0001t0001g0060 others(9): Show |
12 | HG00621.hp2 HG01358.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.59+1406_59+1407dup others(2): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 93981865 | ||||||
| chr3:93981886 | A | AG | 17 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0045 others(14): Show |
17 | HG00642.hp2 HG01109.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.59+1404_59+1405ins others(1): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93981886 | |||||||
| chr3:93981886 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.59+1404A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93981886 | |||||||
| chr3:93981890 | G | A | 1 | a0002c0002t0001g0130 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.59+1408G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93981890 | |||||||
| chr3:93981891 | A | G | 1 | a0002c0002t0001g0130 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.59+1409A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93981891 | |||||||
| chr3:93982208 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.59+1726A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93982208 | |||||||
| chr3:93982232 | T | G | 1 | a0002c0002t0001g0131 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.59+1750T>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93982232 | |||||||
| chr3:93982615 | T | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+2133T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93982615 | |||||||
| chr3:93982728 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.59+2246T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93982728 | |||||||
| chr3:93982818 | C | T | 3 | a0002c0002t0001g0039 a0002c0002t0001g0040 a0002c0002t0001g0041 |
3 | HG01256.hp1 HG01258.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.59+2336C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93982818 | |||||||
| chr3:93982983 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.59+2501T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93982983 | |||||||
| chr3:93983152 | C | T | 4 | a0002c0002t0001g0017 a0002c0002t0001g0039 a0002c0002t0001g0040 others(1): Show |
4 | HG01256.hp1 HG01258.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+2670C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93983152 | |||||||
| chr3:93983216 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.59+2734T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93983216 | |||||||
| chr3:93983492 | A | T | 1 | a0001c0001t0001g0219 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.59+3010A>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93983492 | |||||||
| chr3:93983529 | C | T | 1 | a0001c0001t0001g0016 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.59+3047C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93983529 | |||||||
| chr3:93983592 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.59+3110C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93983592 | |||||||
| chr3:93983701 | C | T | 2 | a0002c0002t0001g0040 a0002c0002t0001g0041 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.59+3219C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93983701 | |||||||
| chr3:93983776 | T | C | 24 | a0001c0001t0001g0009 a0002c0002t0001g0008 a0002c0002t0001g0017 others(21): Show |
24 | HG00558.hp2 HG00621.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.59+3294T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93983776 | |||||||
| chr3:93983806 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.59+3324G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93983806 | |||||||
| chr3:93983823 | T | C | 4 | a0001c0001t0002g0230 a0001c0001t0002g0239 a0001c0001t0002g0240 others(1): Show |
4 | HG01891.hp2 HG01952.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+3341T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93983823 | |||||||
| chr3:93983979 | A | G | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0253 |
3 | HG01168.hp1 HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.59+3497A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93983979 | |||||||
| chr3:93984121 | T | C | 1 | a0004c0008t0012g0136 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.59+3639T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93984121 | |||||||
| chr3:93984236 | A | G | 1 | a0001c0001t0001g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.59+3754A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93984236 | |||||||
| chr3:93984355 | TA | T | 209 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(206): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.59+3886delA | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 93984355 | ||||||
| chr3:93984442 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.59+3960C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93984442 | |||||||
| chr3:93984835 | C | G | 1 | a0001c0001t0001g0168 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.59+4353C>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93984835 | |||||||
| chr3:93985007 | C | CTCAA | 77 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(74): Show |
77 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.59+4551_59+4554dup others(4): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 93985007 | ||||||
| chr3:93985007 | CTCAATCA others(1): Show |
C | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0253 |
3 | HG01168.hp1 HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.59+4547_59+4554del others(8): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 93985007 | ||||||
| chr3:93985037 | A | C | 2 | a0001c0001t0001g0064 a0001c0001t0001g0129 |
2 | HG00621.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.59+4555A>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93985037 | |||||||
| chr3:93985154 | T | G | 1 | a0008c0009t0001g0036 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.59+4672T>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93985154 | |||||||
| chr3:93985267 | C | G | 1 | a0001c0001t0001g0167 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.59+4785C>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93985267 | |||||||
| chr3:93985293 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.59+4811C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93985293 | |||||||
| chr3:93985573 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.59+5091C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93985573 | |||||||
| chr3:93985822 | A | G | 6 | a0001c0001t0001g0038 a0001c0001t0001g0166 a0001c0001t0001g0206 others(3): Show |
6 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.59+5340A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93985822 | |||||||
| chr3:93986013 | C | G | 1 | a0001c0001t0001g0015 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.59+5531C>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93986013 | |||||||
| chr3:93986190 | G | A | 58 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(55): Show |
58 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.59+5708G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93986190 | |||||||
| chr3:93986242 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.59+5760A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93986242 | |||||||
| chr3:93986649 | C | T | 1 | a0002c0002t0001g0032 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.59+6167C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93986649 | |||||||
| chr3:93986766 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.59+6284C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93986766 | |||||||
| chr3:93987142 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.59+6660A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93987142 | |||||||
| chr3:93987157 | A | AT | 79 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(76): Show |
79 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.59+6689dupT | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 93987157 | ||||||
| chr3:93987370 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.59+6888T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93987370 | |||||||
| chr3:93987376 | A | C | 6 | a0001c0001t0002g0230 a0001c0001t0002g0239 a0001c0001t0002g0240 others(3): Show |
6 | HG01891.hp2 HG01952.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.59+6894A>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93987376 | |||||||
| chr3:93987425 | T | TGGAGTAT others(20): Show |
1 | a0001c0001t0001g0204 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.59+6945_59+6971dup others(27): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 93987425 | ||||||
| chr3:93987536 | T | G | 24 | a0001c0001t0001g0009 a0002c0002t0001g0008 a0002c0002t0001g0017 others(21): Show |
24 | HG00558.hp2 HG00621.hp1 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.59+7054T>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93987536 | |||||||
| chr3:93987563 | TTTTA | T | 4 | a0001c0001t0001g0077 a0001c0001t0001g0202 a0001c0001t0001g0203 others(1): Show |
4 | NA18943.hp2 NA18970.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+7085_59+7088del others(4): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 93987563 | ||||||
| chr3:93987573 | C | G | 1 | a0001c0001t0001g0016 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.59+7091C>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93987573 | |||||||
| chr3:93987573 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.59+7091C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93987573 | |||||||
| chr3:93987798 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0171 |
2 | NA18942.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.59+7316G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93987798 | |||||||
| chr3:93987821 | TA | T | 4 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0001g0209 others(1): Show |
4 | HG01884.hp2 HG02258.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.59+7341delA | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 93987821 | ||||||
| chr3:93988048 | G | A | 1 | a0001c0001t0001g0137 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.59+7566G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93988048 | |||||||
| chr3:93988080 | A | T | 1 | a0001c0001t0001g0252 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.59+7598A>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93988080 | |||||||
| chr3:93988171 | T | C | 1 | a0001c0001t0001g0242 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.59+7689T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93988171 | |||||||
| chr3:93988238 | G | GA | 6 | a0001c0001t0001g0016 a0001c0001t0001g0206 a0001c0001t0001g0211 others(3): Show |
6 | HG02258.hp1 HG02572.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.60-7621dupA | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 93988238 | ||||||
| chr3:93988238 | GA | G | 5 | a0001c0001t0003g0163 a0001c0001t0003g0164 a0001c0001t0003g0246 others(2): Show |
5 | HG02015.hp2 HG03927.hp2 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.60-7621delA | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 93988238 | ||||||
| chr3:93988599 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.60-7275A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93988599 | |||||||
| chr3:93988685 | C | T | 4 | a0001c0001t0002g0230 a0001c0001t0002g0239 a0001c0001t0002g0240 others(1): Show |
4 | HG01891.hp2 HG01952.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.60-7189C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93988685 | |||||||
| chr3:93988786 | A | AT | 60 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(57): Show |
60 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.60-7072dupT | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 93988786 | ||||||
| chr3:93988786 | A | T | 5 | a0001c0001t0001g0070 a0001c0001t0001g0159 a0001c0001t0001g0160 others(2): Show |
5 | HG02486.hp2 HG02723.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.60-7088A>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93988786 | |||||||
| chr3:93988786 | AT | A | 76 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(73): Show |
76 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.60-7072delT | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 93988786 | ||||||
| chr3:93989026 | A | T | 1 | a0001c0001t0003g0164 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.60-6848A>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93989026 | |||||||
| chr3:93989419 | T | A | 1 | a0001c0001t0001g0056 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.60-6455T>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93989419 | |||||||
| chr3:93989441 | C | T | 5 | a0001c0001t0001g0076 a0001c0001t0001g0200 a0001c0001t0001g0201 others(2): Show |
5 | NA18952.hp1 NA18962.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.60-6433C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93989441 | |||||||
| chr3:93989553 | T | TA | 5 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(2): Show |
5 | HG01109.hp2 HG03471.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.60-6319dupA | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 93989553 | ||||||
| chr3:93989555 | AT | A | 62 | a0001c0001t0001g0018 a0001c0001t0001g0066 a0001c0001t0001g0074 others(59): Show |
62 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.60-6302delT | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 93989555 | ||||||
| chr3:93989556 | T | A | 142 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0009 others(139): Show |
142 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.60-6318T>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93989556 | |||||||
| chr3:93989557 | T | A | 60 | a0001c0001t0001g0018 a0001c0001t0001g0074 a0001c0001t0001g0075 others(57): Show |
60 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.60-6317T>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93989557 | |||||||
| chr3:93989558 | T | A | 4 | a0001c0001t0001g0171 a0001c0001t0001g0199 a0001c0001t0001g0204 others(1): Show |
4 | HG01515.hp1 HG02698.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.60-6316T>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93989558 | |||||||
| chr3:93989561 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.60-6313T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93989561 | |||||||
| chr3:93989756 | A | C | 1 | a0001c0001t0001g0208 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.60-6118A>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93989756 | |||||||
| chr3:93989839 | T | C | 62 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(59): Show |
62 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.60-6035T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93989839 | |||||||
| chr3:93989994 | TTTTTGTT others(3): Show |
T | 2 | a0001c0001t0001g0087 a0003c0003t0001g0228 |
2 | HG01433.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.60-5861_60-5852del others(10): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 93989994 | ||||||
| chr3:93989998 | T | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.60-5876T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93989998 | |||||||
| chr3:93990374 | G | T | 1 | a0001c0001t0001g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.60-5500G>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93990374 | |||||||
| chr3:93991041 | T | C | 1 | a0001c0001t0001g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.60-4833T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93991041 | |||||||
| chr3:93991231 | A | G | 2 | a0001c0001t0001g0197 a0001c0001t0001g0198 |
2 | HG01261.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.60-4643A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93991231 | |||||||
| chr3:93991474 | A | C | 1 | a0001c0001t0001g0252 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.60-4400A>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93991474 | |||||||
| chr3:93991628 | C | T | 55 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(52): Show |
55 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(52): Show |
intron_variant | MODIFIER | c.60-4246C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93991628 | |||||||
| chr3:93991754 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.60-4120A>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93991754 | |||||||
| chr3:93992176 | A | T | 2 | a0001c0001t0005g0057 a0001c0001t0005g0058 |
2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.60-3698A>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93992176 | |||||||
| chr3:93992346 | A | G | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.60-3528A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93992346 | |||||||
| chr3:93992430 | T | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 |
3 | HG03471.hp2 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.60-3444T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93992430 | |||||||
| chr3:93992740 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.60-3134A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93992740 | |||||||
| chr3:93992944 | C | T | 4 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0001g0209 others(1): Show |
4 | HG01884.hp2 HG02258.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.60-2930C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93992944 | |||||||
| chr3:93992960 | T | C | 21 | a0001c0001t0001g0012 a0001c0001t0001g0060 a0001c0001t0001g0078 others(18): Show |
21 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.60-2914T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93992960 | |||||||
| chr3:93992967 | A | AT | 5 | a0001c0001t0001g0075 a0001c0001t0001g0080 a0001c0001t0001g0132 others(2): Show |
5 | HG01256.hp2 HG01934.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.60-2889dupT | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 93992967 | ||||||
| chr3:93992967 | A | T | 2 | a0001c0001t0003g0246 a0001c0001t0003g0251 |
2 | HG02015.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.60-2907A>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93992967 | |||||||
| chr3:93993149 | A | G | 31 | a0001c0001t0001g0009 a0001c0001t0001g0038 a0001c0001t0001g0166 others(28): Show |
31 | HG00558.hp2 HG00621.hp1 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.60-2725A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93993149 | |||||||
| chr3:93993575 | C | T | 25 | a0001c0001t0001g0009 a0002c0002t0001g0008 a0002c0002t0001g0017 others(22): Show |
25 | HG00558.hp2 HG00621.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.60-2299C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93993575 | |||||||
| chr3:93993787 | A | G | 25 | a0001c0001t0001g0009 a0002c0002t0001g0008 a0002c0002t0001g0017 others(22): Show |
25 | HG00558.hp2 HG00621.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.60-2087A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93993787 | |||||||
| chr3:93993827 | G | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0256 |
3 | HG02280.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.60-2047G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93993827 | |||||||
| chr3:93994379 | A | C | 1 | a0001c0001t0003g0071 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.60-1495A>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93994379 | |||||||
| chr3:93994433 | G | T | 4 | a0001c0001t0001g0034 a0001c0001t0001g0156 a0001c0001t0001g0264 others(1): Show |
4 | HG02896.hp1 HG03225.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.60-1441G>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93994433 | |||||||
| chr3:93994444 | C | T | 1 | a0001c0001t0001g0049 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.60-1430C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93994444 | |||||||
| chr3:93994497 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.60-1377G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93994497 | |||||||
| chr3:93994621 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.60-1253T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93994621 | |||||||
| chr3:93994711 | T | C | 1 | a0002c0002t0001g0133 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.60-1163T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93994711 | |||||||
| chr3:93994799 | A | AT | 6 | a0001c0001t0001g0034 a0001c0001t0001g0156 a0001c0001t0001g0252 others(3): Show |
6 | HG00639.hp2 HG02896.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.60-1062dupT | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr3 | 93994799 | ||||||
| chr3:93994883 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.60-991C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93994883 | |||||||
| chr3:93995331 | T | C | 3 | a0001c0001t0004g0140 a0001c0001t0004g0141 a0001c0001t0004g0142 |
3 | HG02055.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.60-543T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93995331 | |||||||
| chr3:93995729 | A | G | 1 | a0001c0001t0001g0009 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.60-145A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 1/9 | chr3 | 93995729 | |||||||
| chr3:93996095 | G | A | 1 | a0001c0001t0001g0016 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.130+151G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93996095 | |||||||
| chr3:93996186 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.130+242T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93996186 | |||||||
| chr3:93996344 | C | G | 1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.130+400C>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93996344 | |||||||
| chr3:93996433 | C | G | 1 | a0008c0009t0001g0036 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.130+489C>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93996433 | |||||||
| chr3:93996477 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.130+533C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93996477 | |||||||
| chr3:93996517 | CT | C | 6 | a0001c0001t0001g0078 a0001c0001t0001g0083 a0001c0001t0001g0101 others(3): Show |
6 | HG00280.hp2 HG01168.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.130+586delT | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr3 | 93996517 | ||||||
| chr3:93996669 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.130+725C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93996669 | |||||||
| chr3:93996670 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0264 |
2 | HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.130+726G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93996670 | |||||||
| chr3:93996718 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.130+774A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93996718 | |||||||
| chr3:93996797 | G | A | 6 | a0001c0001t0002g0230 a0001c0001t0002g0239 a0001c0001t0002g0240 others(3): Show |
6 | HG01891.hp2 HG01952.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.130+853G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93996797 | |||||||
| chr3:93996917 | C | T | 1 | a0001c0001t0009g0195 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.130+973C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93996917 | |||||||
| chr3:93997036 | T | C | 26 | a0001c0001t0001g0009 a0001c0001t0001g0213 a0002c0002t0001g0008 others(23): Show |
26 | HG00558.hp2 HG00621.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.130+1092T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93997036 | |||||||
| chr3:93997311 | G | T | 3 | a0001c0001t0001g0173 a0001c0001t0006g0174 a0003c0003t0006g0073 |
3 | HG00639.hp2 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.130+1367G>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93997311 | |||||||
| chr3:93997703 | G | C | 1 | a0001c0001t0001g0102 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.130+1759G>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93997703 | |||||||
| chr3:93997703 | G | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0083 |
3 | NA18966.hp2 NA18988.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.130+1759G>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93997703 | |||||||
| chr3:93997715 | G | T | 1 | a0001c0001t0001g0250 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.130+1771G>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93997715 | |||||||
| chr3:93997912 | C | T | 1 | a0004c0008t0012g0136 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.130+1968C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93997912 | |||||||
| chr3:93997913 | G | A | 66 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(63): Show |
66 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.130+1969G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93997913 | |||||||
| chr3:93997953 | T | G | 1 | a0001c0001t0001g0200 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.130+2009T>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93997953 | |||||||
| chr3:93998243 | T | G | 1 | a0001c0001t0001g0235 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.130+2299T>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93998243 | |||||||
| chr3:93998532 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.130+2588G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93998532 | |||||||
| chr3:93998608 | T | C | 1 | a0001c0001t0001g0049 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.130+2664T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93998608 | |||||||
| chr3:93998626 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0264 |
2 | HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.130+2682G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93998626 | |||||||
| chr3:93998925 | CT | C | 9 | a0001c0001t0001g0001 a0001c0001t0001g0021 a0001c0001t0001g0034 others(6): Show |
9 | HG00639.hp2 HG01515.hp1 HG02735.hp1 others(6): Show |
intron_variant | MODIFIER | c.130+2995delT | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr3 | 93998925 | ||||||
| chr3:93999085 | T | C | 2 | a0001c0001t0001g0018 a0001c0001t0001g0019 |
2 | HG02109.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.130+3141T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93999085 | |||||||
| chr3:93999087 | C | CTATT | 12 | a0001c0001t0001g0132 a0001c0001t0001g0189 a0001c0001t0001g0191 others(9): Show |
12 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(9): Show |
intron_variant | MODIFIER | c.130+3167_130+3170d others(6): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr3 | 93999087 | ||||||
| chr3:93999139 | C | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 |
3 | HG03471.hp2 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.130+3195C>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93999139 | |||||||
| chr3:93999293 | G | A | 1 | a0002c0002t0001g0125 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.130+3349G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93999293 | |||||||
| chr3:93999301 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.130+3357G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93999301 | |||||||
| chr3:93999333 | C | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0128 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.130+3389C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93999333 | |||||||
| chr3:93999375 | A | C | 4 | a0001c0001t0001g0173 a0001c0001t0006g0174 a0001c0001t0011g0227 others(1): Show |
4 | HG00639.hp2 HG02572.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+3431A>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93999375 | |||||||
| chr3:93999528 | C | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0155 |
2 | HG00621.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.130+3584C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93999528 | |||||||
| chr3:93999602 | C | T | 2 | a0001c0001t0002g0260 a0001c0001t0002g0261 |
2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.130+3658C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93999602 | |||||||
| chr3:93999793 | A | G | 1 | a0001c0001t0001g0250 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.130+3849A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93999793 | |||||||
| chr3:93999846 | T | G | 1 | a0003c0003t0001g0172 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.131-3813T>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93999846 | |||||||
| chr3:93999862 | C | T | 1 | a0008c0009t0001g0036 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.131-3797C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 93999862 | |||||||
| chr3:94000241 | T | G | 1 | a0001c0001t0001g0252 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.131-3418T>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 94000241 | |||||||
| chr3:94000401 | T | TC | 10 | a0001c0001t0001g0011 a0001c0001t0001g0082 a0001c0001t0001g0120 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.131-3257dupC | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr3 | 94000401 | ||||||
| chr3:94000426 | A | G | 1 | a0008c0009t0001g0036 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.131-3233A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 94000426 | |||||||
| chr3:94000639 | A | G | 1 | a0001c0001t0011g0227 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.131-3020A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 94000639 | |||||||
| chr3:94000747 | A | G | 1 | a0002c0002t0001g0031 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.131-2912A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 94000747 | |||||||
| chr3:94000996 | T | C | 3 | a0001c0001t0001g0173 a0001c0001t0006g0174 a0003c0003t0006g0073 |
3 | HG00639.hp2 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.131-2663T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 94000996 | |||||||
| chr3:94001040 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.131-2619A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 94001040 | |||||||
| chr3:94001532 | C | G | 1 | a0003c0003t0001g0099 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.131-2127C>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 94001532 | |||||||
| chr3:94001565 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.131-2094A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 94001565 | |||||||
| chr3:94002140 | G | T | 1 | a0001c0001t0002g0230 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.131-1519G>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 94002140 | |||||||
| chr3:94002247 | CT | C | 5 | a0001c0001t0001g0038 a0001c0001t0001g0206 a0001c0001t0001g0208 others(2): Show |
5 | HG01884.hp2 HG02258.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.131-1402delT | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr3 | 94002247 | ||||||
| chr3:94002405 | G | C | 2 | a0001c0001t0001g0139 a0001c0001t0001g0144 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.131-1254G>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 94002405 | |||||||
| chr3:94002433 | T | G | 4 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG03139.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-1226T>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 94002433 | |||||||
| chr3:94002676 | A | G | 25 | a0001c0001t0001g0009 a0002c0002t0001g0008 a0002c0002t0001g0017 others(22): Show |
25 | HG00558.hp2 HG00621.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.131-983A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 94002676 | |||||||
| chr3:94002939 | T | C | 71 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(68): Show |
71 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.131-720T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 94002939 | |||||||
| chr3:94003364 | A | G | 10 | a0001c0001t0001g0011 a0001c0001t0001g0082 a0001c0001t0001g0120 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.131-295A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 94003364 | |||||||
| chr3:94003537 | A | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0264 |
2 | HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.131-122A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 94003537 | |||||||
| chr3:94003581 | G | A | 4 | a0001c0001t0001g0077 a0001c0001t0001g0202 a0001c0001t0001g0203 others(1): Show |
4 | NA18943.hp2 NA18970.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-78G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 2/9 | chr3 | 94003581 | |||||||
| chr3:94004411 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.380+503G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94004411 | |||||||
| chr3:94004582 | T | C | 1 | a0001c0001t0001g0103 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.380+674T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94004582 | |||||||
| chr3:94004952 | G | C | 5 | a0001c0001t0001g0059 a0001c0001t0001g0080 a0001c0001t0001g0117 others(2): Show |
5 | HG01928.hp2 HG01934.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.380+1044G>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94004952 | |||||||
| chr3:94005108 | G | A | 63 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(60): Show |
63 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.380+1200G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94005108 | |||||||
| chr3:94005388 | C | T | 2 | a0002c0002t0001g0029 a0002c0002t0001g0030 |
2 | NA18978.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.380+1480C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94005388 | |||||||
| chr3:94005422 | T | G | 7 | a0001c0001t0001g0038 a0001c0001t0001g0166 a0001c0001t0001g0206 others(4): Show |
7 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.380+1514T>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94005422 | |||||||
| chr3:94005458 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.380+1550C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94005458 | |||||||
| chr3:94005572 | G | T | 1 | a0001c0001t0001g0033 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.380+1664G>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94005572 | |||||||
| chr3:94005659 | G | A | 2 | a0001c0001t0005g0057 a0001c0001t0005g0058 |
2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.380+1751G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94005659 | |||||||
| chr3:94005680 | T | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.380+1772T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94005680 | |||||||
| chr3:94005716 | G | T | 2 | a0001c0001t0001g0001 a0001c0001t0013g0002 |
2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.380+1808G>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94005716 | |||||||
| chr3:94005962 | A | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.380+2054A>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94005962 | |||||||
| chr3:94006022 | C | T | 3 | a0001c0001t0001g0082 a0001c0001t0001g0123 a0001c0001t0001g0126 |
3 | HG02109.hp2 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.380+2114C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94006022 | |||||||
| chr3:94006029 | G | A | 1 | a0001c0001t0001g0016 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.380+2121G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94006029 | |||||||
| chr3:94006432 | C | T | 1 | a0002c0002t0001g0130 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.380+2524C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94006432 | |||||||
| chr3:94006453 | C | T | 62 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(59): Show |
62 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.380+2545C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94006453 | |||||||
| chr3:94006671 | A | C | 1 | a0001c0001t0001g0199 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.380+2763A>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94006671 | |||||||
| chr3:94006701 | A | G | 1 | a0001c0001t0001g0016 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.380+2793A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94006701 | |||||||
| chr3:94006710 | T | C | 4 | a0001c0001t0001g0166 a0001c0001t0001g0206 a0001c0001t0001g0208 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.380+2802T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94006710 | |||||||
| chr3:94007079 | G | A | 2 | a0002c0002t0001g0133 a0002c0002t0001g0263 |
2 | HG02683.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.380+3171G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94007079 | |||||||
| chr3:94007189 | G | T | 2 | a0002c0002t0001g0031 a0006c0007t0001g0028 |
2 | HG01346.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.380+3281G>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94007189 | |||||||
| chr3:94007547 | C | T | 1 | a0004c0008t0012g0136 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.380+3639C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94007547 | |||||||
| chr3:94007614 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.380+3706C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94007614 | |||||||
| chr3:94007848 | A | G | 6 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0052 others(3): Show |
6 | HG02280.hp1 HG02809.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.380+3940A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94007848 | |||||||
| chr3:94007999 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.380+4091A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94007999 | |||||||
| chr3:94008424 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.380+4516T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94008424 | |||||||
| chr3:94008463 | A | G | 1 | a0001c0001t0001g0215 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.380+4555A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94008463 | |||||||
| chr3:94008485 | T | A | 1 | a0001c0001t0014g0088 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.380+4577T>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94008485 | |||||||
| chr3:94008507 | A | G | 1 | a0001c0001t0011g0227 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.380+4599A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94008507 | |||||||
| chr3:94008672 | TA | T | 3 | a0001c0001t0001g0206 a0001c0001t0001g0208 a0001c0001t0001g0209 |
3 | HG01884.hp2 HG02258.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.380+4768delA | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94008672 | ||||||
| chr3:94008788 | A | G | 1 | a0002c0002t0001g0135 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.380+4880A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94008788 | |||||||
| chr3:94008914 | G | C | 1 | a0001c0001t0001g0167 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.380+5006G>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94008914 | |||||||
| chr3:94009074 | A | AAGAT | 121 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0009 others(118): Show |
121 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.380+5212_380+5215d others(6): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94009074 | ||||||
| chr3:94009074 | A | AAGATAGA others(1): Show |
28 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0012 others(25): Show |
28 | HG00140.hp2 HG00738.hp2 HG01192.hp2 others(25): Show |
intron_variant | MODIFIER | c.380+5208_380+5215d others(10): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94009074 | ||||||
| chr3:94009074 | A | AAGATAGA others(5): Show |
13 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0104 others(10): Show |
13 | HG00642.hp2 HG00733.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.380+5204_380+5215d others(14): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94009074 | ||||||
| chr3:94009074 | A | AAGATAGA others(9): Show |
4 | a0001c0001t0001g0072 a0001c0001t0001g0189 a0001c0001t0006g0174 others(1): Show |
4 | HG00639.hp1 HG00639.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.380+5200_380+5215d others(18): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94009074 | ||||||
| chr3:94009074 | AAGAT | A | 13 | a0001c0001t0001g0065 a0001c0001t0001g0069 a0001c0001t0001g0077 others(10): Show |
13 | HG00280.hp2 HG00423.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.380+5212_380+5215d others(6): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94009074 | ||||||
| chr3:94009074 | AAGATAGA others(1): Show |
A | 8 | a0001c0001t0001g0185 a0001c0001t0001g0187 a0001c0001t0001g0188 others(5): Show |
8 | HG01358.hp1 HG01361.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.380+5208_380+5215d others(10): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94009074 | ||||||
| chr3:94009074 | AAGATAGA others(5): Show |
A | 2 | a0001c0001t0001g0262 a0002c0002t0001g0027 |
2 | NA18973.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.380+5204_380+5215d others(14): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94009074 | ||||||
| chr3:94009317 | A | G | 14 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0046 others(11): Show |
14 | HG00438.hp2 HG00642.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.380+5409A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94009317 | |||||||
| chr3:94009333 | G | T | 209 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(206): Show |
209 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.380+5425G>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94009333 | |||||||
| chr3:94009699 | T | C | 1 | a0003c0006t0001g0006 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.380+5791T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94009699 | |||||||
| chr3:94010156 | G | T | 1 | a0001c0001t0001g0098 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.380+6248G>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94010156 | |||||||
| chr3:94010315 | G | A | 1 | a0003c0003t0001g0037 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.380+6407G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94010315 | |||||||
| chr3:94010528 | C | T | 5 | a0001c0001t0001g0059 a0001c0001t0001g0080 a0001c0001t0001g0117 others(2): Show |
5 | HG01928.hp2 HG01934.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.380+6620C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94010528 | |||||||
| chr3:94010599 | A | G | 1 | a0002c0002t0001g0263 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.380+6691A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94010599 | |||||||
| chr3:94011061 | C | G | 1 | a0001c0001t0001g0170 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.380+7153C>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94011061 | |||||||
| chr3:94011149 | A | T | 1 | a0001c0001t0001g0252 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.380+7241A>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94011149 | |||||||
| chr3:94011448 | A | C | 212 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
212 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(209): Show |
intron_variant | MODIFIER | c.380+7540A>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94011448 | |||||||
| chr3:94011612 | C | T | 4 | a0001c0001t0001g0068 a0001c0001t0001g0137 a0001c0001t0001g0148 others(1): Show |
4 | HG00423.hp2 HG02083.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.380+7704C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94011612 | |||||||
| chr3:94011783 | A | C | 1 | a0001c0001t0001g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.380+7875A>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94011783 | |||||||
| chr3:94012044 | T | G | 1 | a0001c0001t0001g0247 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.380+8136T>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94012044 | |||||||
| chr3:94012086 | G | C | 5 | a0001c0001t0003g0071 a0001c0001t0003g0163 a0001c0001t0003g0164 others(2): Show |
5 | HG02015.hp2 NA18954.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.380+8178G>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94012086 | |||||||
| chr3:94012552 | A | G | 6 | a0001c0001t0001g0038 a0001c0001t0001g0166 a0001c0001t0001g0206 others(3): Show |
6 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.380+8644A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94012552 | |||||||
| chr3:94012951 | G | A | 71 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(68): Show |
71 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.380+9043G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94012951 | |||||||
| chr3:94013218 | G | A | 25 | a0001c0001t0001g0009 a0002c0002t0001g0008 a0002c0002t0001g0017 others(22): Show |
25 | HG00558.hp2 HG00621.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.380+9310G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94013218 | |||||||
| chr3:94013267 | T | C | 1 | a0001c0001t0001g0016 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.380+9359T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94013267 | |||||||
| chr3:94013638 | T | C | 3 | a0001c0001t0001g0177 a0001c0001t0001g0258 a0003c0003t0001g0176 |
3 | HG01496.hp2 HG01952.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.380+9730T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94013638 | |||||||
| chr3:94013720 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.380+9812C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94013720 | |||||||
| chr3:94014239 | T | C | 1 | a0002c0002t0001g0024 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.380+10331T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94014239 | |||||||
| chr3:94016132 | G | A | 1 | a0001c0001t0001g0149 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.380+12224G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94016132 | |||||||
| chr3:94016155 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.380+12247G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94016155 | |||||||
| chr3:94016179 | A | G | 25 | a0001c0001t0001g0009 a0002c0002t0001g0008 a0002c0002t0001g0017 others(22): Show |
25 | HG00558.hp2 HG00621.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.380+12271A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94016179 | |||||||
| chr3:94016464 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.380+12556G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94016464 | |||||||
| chr3:94016516 | A | G | 1 | a0001c0001t0011g0227 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.380+12608A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94016516 | |||||||
| chr3:94016649 | C | CT | 81 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(78): Show |
81 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.380+12755dupT | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94016649 | ||||||
| chr3:94016649 | C | T | 3 | a0001c0001t0001g0231 a0001c0001t0001g0242 a0001c0001t0001g0245 |
3 | NA18612.hp2 NA18942.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.380+12741C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94016649 | |||||||
| chr3:94017465 | T | C | 1 | a0002c0002t0001g0027 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.380+13557T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94017465 | |||||||
| chr3:94017809 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.380+13901C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94017809 | |||||||
| chr3:94017873 | G | A | 2 | a0001c0001t0005g0057 a0001c0001t0005g0058 |
2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.380+13965G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94017873 | |||||||
| chr3:94017994 | A | G | 1 | a0001c0001t0001g0059 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.380+14086A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94017994 | |||||||
| chr3:94018112 | G | A | 25 | a0001c0001t0001g0009 a0002c0002t0001g0008 a0002c0002t0001g0017 others(22): Show |
25 | HG00558.hp2 HG00621.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.380+14204G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94018112 | |||||||
| chr3:94018237 | A | G | 1 | a0003c0003t0001g0194 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.380+14329A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94018237 | |||||||
| chr3:94018290 | T | TGATAGA | 22 | a0001c0001t0001g0035 a0001c0001t0001g0066 a0001c0001t0001g0068 others(19): Show |
22 | HG00140.hp2 HG00423.hp2 HG01074.hp1 others(19): Show |
intron_variant | MODIFIER | c.380+14386_380+1439 others(10): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94018290 | ||||||
| chr3:94018593 | C | A | 5 | a0001c0001t0001g0139 a0001c0001t0001g0144 a0001c0001t0001g0158 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.380+14685C>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94018593 | |||||||
| chr3:94018603 | A | G | 2 | a0001c0001t0005g0057 a0001c0001t0005g0058 |
2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.380+14695A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94018603 | |||||||
| chr3:94018736 | C | T | 25 | a0001c0001t0001g0009 a0002c0002t0001g0008 a0002c0002t0001g0017 others(22): Show |
25 | HG00558.hp2 HG00621.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.380+14828C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94018736 | |||||||
| chr3:94018779 | T | G | 1 | a0001c0001t0001g0001 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.380+14871T>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94018779 | |||||||
| chr3:94018835 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.380+14927G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94018835 | |||||||
| chr3:94018870 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.380+14962A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94018870 | |||||||
| chr3:94018882 | C | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0212 |
2 | HG02602.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.380+14974C>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94018882 | |||||||
| chr3:94019159 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.380+15251C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94019159 | |||||||
| chr3:94019385 | T | G | 3 | a0001c0001t0001g0231 a0001c0001t0001g0242 a0001c0001t0001g0245 |
3 | NA18612.hp2 NA18942.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.380+15477T>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94019385 | |||||||
| chr3:94019457 | A | C | 1 | a0001c0001t0002g0230 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.380+15549A>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94019457 | |||||||
| chr3:94019484 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.380+15576C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94019484 | |||||||
| chr3:94019682 | C | T | 71 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(68): Show |
71 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.381-15649C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94019682 | |||||||
| chr3:94019705 | A | G | 27 | a0001c0001t0001g0009 a0001c0001t0001g0170 a0001c0001t0001g0171 others(24): Show |
27 | HG00558.hp2 HG00621.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.381-15626A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94019705 | |||||||
| chr3:94019816 | C | T | 1 | a0001c0001t0005g0058 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.381-15515C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94019816 | |||||||
| chr3:94019850 | A | G | 35 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(32): Show |
35 | HG00558.hp2 HG00621.hp1 HG01256.hp1 others(32): Show |
intron_variant | MODIFIER | c.381-15481A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94019850 | |||||||
| chr3:94019870 | G | A | 1 | a0004c0008t0012g0136 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.381-15461G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94019870 | |||||||
| chr3:94019882 | C | G | 1 | a0001c0001t0001g0048 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.381-15449C>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94019882 | |||||||
| chr3:94019898 | C | T | 1 | a0001c0001t0001g0100 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.381-15433C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94019898 | |||||||
| chr3:94020622 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.381-14709G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94020622 | |||||||
| chr3:94020637 | G | A | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0253 |
3 | HG01168.hp1 HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.381-14694G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94020637 | |||||||
| chr3:94020684 | T | C | 2 | a0002c0002t0001g0022 a0002c0002t0001g0025 |
2 | NA19009.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.381-14647T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94020684 | |||||||
| chr3:94020936 | C | T | 3 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 |
3 | HG00733.hp1 HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.381-14395C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94020936 | |||||||
| chr3:94021120 | A | G | 83 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(80): Show |
83 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.381-14211A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94021120 | |||||||
| chr3:94021182 | T | TTA | 37 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0082 others(34): Show |
37 | HG00558.hp2 HG00621.hp1 HG01256.hp1 others(34): Show |
intron_variant | MODIFIER | c.381-14132_381-1413 others(6): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94021182 | ||||||
| chr3:94021184 | A | T | 6 | a0001c0001t0001g0059 a0001c0001t0001g0080 a0001c0001t0001g0117 others(3): Show |
6 | HG01928.hp2 HG01934.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.381-14147A>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94021184 | |||||||
| chr3:94021220 | G | T | 1 | a0001c0001t0001g0112 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.381-14111G>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94021220 | |||||||
| chr3:94021429 | A | G | 1 | a0001c0001t0003g0071 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.381-13902A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94021429 | |||||||
| chr3:94021474 | T | C | 6 | a0001c0001t0002g0230 a0001c0001t0002g0239 a0001c0001t0002g0240 others(3): Show |
6 | HG01891.hp2 HG01952.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.381-13857T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94021474 | |||||||
| chr3:94021866 | A | G | 4 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.381-13465A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94021866 | |||||||
| chr3:94021968 | AC | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 |
3 | HG03471.hp2 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.381-13360delC | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94021968 | ||||||
| chr3:94021992 | C | T | 14 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0046 others(11): Show |
14 | HG00438.hp2 HG00642.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.381-13339C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94021992 | |||||||
| chr3:94022154 | G | A | 5 | a0001c0001t0001g0070 a0001c0001t0001g0159 a0001c0001t0001g0160 others(2): Show |
5 | HG02486.hp2 HG02723.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.381-13177G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94022154 | |||||||
| chr3:94022211 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.381-13120C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94022211 | |||||||
| chr3:94022475 | G | T | 71 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0012 others(68): Show |
71 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.381-12856G>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94022475 | |||||||
| chr3:94023606 | G | C | 81 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0011 others(78): Show |
81 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.381-11725G>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94023606 | |||||||
| chr3:94023694 | T | G | 1 | a0001c0001t0014g0088 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.381-11637T>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94023694 | |||||||
| chr3:94023752 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.381-11579A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94023752 | |||||||
| chr3:94023998 | T | C | 11 | a0001c0001t0001g0035 a0001c0001t0001g0066 a0001c0001t0001g0146 others(8): Show |
11 | HG00140.hp2 HG01074.hp1 HG02004.hp2 others(8): Show |
intron_variant | MODIFIER | c.381-11333T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94023998 | |||||||
| chr3:94024019 | A | C | 1 | a0001c0001t0001g0203 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.381-11312A>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94024019 | |||||||
| chr3:94024462 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.381-10869C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94024462 | |||||||
| chr3:94024654 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.381-10677C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94024654 | |||||||
| chr3:94024655 | G | A | 1 | a0003c0006t0001g0006 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.381-10676G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94024655 | |||||||
| chr3:94024996 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.381-10335T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94024996 | |||||||
| chr3:94025224 | T | TTTATTTA others(49): Show |
1 | a0001c0001t0001g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.381-10102_381-1010 others(60): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94025224 | ||||||
| chr3:94025264 | T | C | 1 | a0003c0003t0001g0207 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.381-10067T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94025264 | |||||||
| chr3:94025346 | A | T | 1 | a0001c0001t0001g0042 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.381-9985A>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94025346 | |||||||
| chr3:94025620 | A | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0212 |
2 | HG02602.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.381-9711A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94025620 | |||||||
| chr3:94025689 | G | A | 2 | a0002c0002t0001g0031 a0006c0007t0001g0028 |
2 | HG01346.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.381-9642G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94025689 | |||||||
| chr3:94025879 | A | T | 6 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0052 others(3): Show |
6 | HG02280.hp1 HG02809.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.381-9452A>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94025879 | |||||||
| chr3:94026021 | C | CT | 15 | a0001c0001t0001g0056 a0001c0001t0001g0075 a0001c0001t0001g0086 others(12): Show |
15 | HG01358.hp1 HG01361.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.381-9294dupT | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94026021 | ||||||
| chr3:94026021 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.381-9310C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94026021 | |||||||
| chr3:94026112 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 |
3 | HG03471.hp2 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.381-9219C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94026112 | |||||||
| chr3:94026202 | G | C | 2 | a0001c0001t0006g0174 a0003c0003t0006g0073 |
2 | HG00639.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.381-9129G>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94026202 | |||||||
| chr3:94026250 | T | A | 1 | a0001c0001t0001g0094 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.381-9081T>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94026250 | |||||||
| chr3:94026805 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.381-8526A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94026805 | |||||||
| chr3:94027090 | C | T | 1 | a0003c0003t0001g0190 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.381-8241C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94027090 | |||||||
| chr3:94027313 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.381-8018A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94027313 | |||||||
| chr3:94027397 | T | TA | 3 | a0001c0001t0001g0007 a0001c0001t0001g0105 a0001c0001t0001g0115 |
3 | HG01192.hp2 HG01358.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.381-7931dupA | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94027397 | ||||||
| chr3:94027496 | T | A | 3 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 |
3 | HG00733.hp1 HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.381-7835T>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94027496 | |||||||
| chr3:94028055 | G | A | 6 | a0001c0001t0001g0038 a0001c0001t0001g0166 a0001c0001t0001g0206 others(3): Show |
6 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.381-7276G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94028055 | |||||||
| chr3:94028129 | C | A | 1 | a0001c0001t0001g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.381-7202C>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94028129 | |||||||
| chr3:94028267 | C | G | 4 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0264 others(1): Show |
4 | HG02896.hp1 HG03225.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.381-7064C>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94028267 | |||||||
| chr3:94028311 | G | C | 2 | a0002c0002t0001g0008 a0002c0005t0001g0023 |
2 | HG02738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.381-7020G>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94028311 | |||||||
| chr3:94028403 | C | T | 2 | a0001c0001t0005g0057 a0001c0001t0005g0058 |
2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.381-6928C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94028403 | |||||||
| chr3:94029301 | C | CAT | 14 | a0001c0001t0001g0056 a0001c0001t0001g0062 a0001c0001t0001g0063 others(11): Show |
14 | HG00140.hp1 HG00621.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.381-5997_381-5996d others(4): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94029301 | ||||||
| chr3:94029301 | C | CATAT | 6 | a0001c0001t0001g0015 a0001c0001t0001g0079 a0001c0001t0001g0119 others(3): Show |
6 | HG01109.hp1 HG01261.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.381-5999_381-5996d others(6): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94029301 | ||||||
| chr3:94029301 | C | CATATAT | 8 | a0001c0001t0001g0059 a0001c0001t0001g0080 a0001c0001t0001g0090 others(5): Show |
8 | HG01928.hp2 HG01934.hp1 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.381-6001_381-5996d others(8): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94029301 | ||||||
| chr3:94029301 | C | CATATATA others(3): Show |
1 | a0001c0001t0011g0227 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.381-6005_381-5996d others(12): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94029301 | ||||||
| chr3:94029301 | CAT | C | 29 | a0001c0001t0001g0007 a0001c0001t0001g0035 a0001c0001t0001g0047 others(26): Show |
29 | HG00140.hp2 HG00423.hp2 HG00558.hp1 others(26): Show |
intron_variant | MODIFIER | c.381-5997_381-5996d others(4): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94029301 | ||||||
| chr3:94029301 | CATAT | C | 16 | a0001c0001t0001g0011 a0001c0001t0001g0018 a0001c0001t0001g0019 others(13): Show |
16 | HG00639.hp2 HG01891.hp2 HG01952.hp1 others(13): Show |
intron_variant | MODIFIER | c.381-5999_381-5996d others(6): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94029301 | ||||||
| chr3:94029301 | CATATAT | C | 6 | a0001c0001t0001g0173 a0001c0001t0001g0184 a0001c0001t0001g0253 others(3): Show |
6 | HG01168.hp1 HG03486.hp2 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.381-6001_381-5996d others(8): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94029301 | ||||||
| chr3:94029301 | CATATATA others(1): Show |
C | 6 | a0001c0001t0001g0166 a0001c0001t0001g0206 a0001c0001t0001g0208 others(3): Show |
6 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.381-6003_381-5996d others(10): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94029301 | ||||||
| chr3:94029324 | A | T | 1 | a0001c0001t0001g0034 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.381-6007A>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94029324 | |||||||
| chr3:94029328 | A | T | 24 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(21): Show |
24 | HG00438.hp2 HG00642.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.381-6003A>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94029328 | |||||||
| chr3:94029330 | A | T | 50 | a0001c0001t0001g0016 a0001c0001t0001g0074 a0001c0001t0001g0075 others(47): Show |
50 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.381-6001A>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94029330 | |||||||
| chr3:94029331 | TATATTTA | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0034 others(1): Show |
4 | HG02896.hp1 HG03471.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.381-5999_381-5993d others(9): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94029331 | |||||||
| chr3:94029332 | A | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0018 others(48): Show |
51 | HG00438.hp2 HG00621.hp1 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.381-5999A>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94029332 | |||||||
| chr3:94029332 | ATAT | A | 3 | a0001c0001t0001g0187 a0001c0001t0001g0256 a0001c0004t0001g0138 |
3 | HG01074.hp1 HG01361.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.381-5997_381-5995d others(5): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94029332 | ||||||
| chr3:94029332 | ATATT | A | 4 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0257 others(1): Show |
4 | HG01358.hp1 HG01928.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.381-5993_381-5990d others(6): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94029332 | ||||||
| chr3:94029333 | TA | T | 4 | a0001c0001t0001g0224 a0002c0002t0001g0031 a0002c0002t0001g0032 others(1): Show |
4 | HG00558.hp2 HG01346.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.381-5997delA | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94029333 | |||||||
| chr3:94029333 | TATTTA | T | 46 | a0001c0001t0001g0016 a0001c0001t0001g0074 a0001c0001t0001g0075 others(43): Show |
46 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.381-5997_381-5993d others(7): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94029333 | |||||||
| chr3:94029334 | A | ATATATAT others(6): Show |
1 | a0001c0001t0001g0157 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.381-5996_381-5995i others(15): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94029334 | ||||||
| chr3:94029334 | A | T | 4 | a0001c0001t0001g0139 a0001c0001t0001g0144 a0001c0001t0001g0156 others(1): Show |
4 | HG02717.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.381-5997A>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94029334 | |||||||
| chr3:94029335 | T | TA | 3 | a0001c0001t0001g0151 a0001c0001t0001g0245 a0001c0001t0003g0163 |
3 | NA18942.hp1 NA18957.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.381-5996_381-5995i others(3): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94029335 | |||||||
| chr3:94029335 | TTTA | T | 14 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0082 others(11): Show |
14 | HG01496.hp1 HG02071.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.381-5993_381-5991d others(5): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94029335 | ||||||
| chr3:94029336 | T | A | 11 | a0001c0001t0001g0069 a0001c0001t0001g0117 a0001c0001t0001g0143 others(8): Show |
11 | HG01258.hp1 HG02015.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.381-5995T>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94029336 | |||||||
| chr3:94029336 | TTA | T | 7 | a0001c0001t0001g0066 a0001c0001t0001g0155 a0001c0001t0001g0165 others(4): Show |
7 | HG00438.hp1 HG00621.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.381-5993_381-5992d others(4): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94029336 | ||||||
| chr3:94029337 | T | A | 3 | a0002c0002t0001g0031 a0002c0002t0001g0032 a0002c0002t0001g0131 |
3 | HG00558.hp2 HG01346.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.381-5994T>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94029337 | |||||||
| chr3:94029338 | A | T | 44 | a0001c0001t0001g0004 a0001c0001t0001g0035 a0001c0001t0001g0068 others(41): Show |
44 | HG00140.hp2 HG00423.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.381-5993A>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94029338 | |||||||
| chr3:94029339 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.381-5992T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94029339 | |||||||
| chr3:94029341 | T | A | 2 | a0001c0001t0001g0016 a0008c0009t0001g0036 |
2 | NA19043.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.381-5990T>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94029341 | |||||||
| chr3:94029342 | T | A | 21 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0045 others(18): Show |
21 | HG00438.hp2 HG00642.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.381-5989T>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94029342 | |||||||
| chr3:94029345 | T | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0056 a0001c0001t0001g0187 others(2): Show |
5 | HG01361.hp1 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.381-5986T>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94029345 | |||||||
| chr3:94029346 | T | A | 3 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0003c0003t0001g0186 |
3 | HG01358.hp1 HG01928.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.381-5985T>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94029346 | |||||||
| chr3:94029346 | TTTA | T | 6 | a0001c0001t0001g0247 a0001c0001t0001g0248 a0001c0001t0001g0252 others(3): Show |
6 | HG01891.hp2 HG02280.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.381-5982_381-5980d others(5): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94029346 | ||||||
| chr3:94029347 | T | A | 46 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 others(43): Show |
46 | HG00280.hp2 HG00733.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.381-5984T>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94029347 | |||||||
| chr3:94029347 | TTA | T | 8 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(5): Show |
8 | HG01106.hp1 HG01952.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.381-5982_381-5981d others(4): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94029347 | ||||||
| chr3:94029348 | T | A | 2 | a0001c0001t0001g0184 a0001c0001t0001g0253 |
2 | HG01168.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.381-5983T>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94029348 | |||||||
| chr3:94029349 | A | T | 155 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(152): Show |
155 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.381-5982A>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94029349 | |||||||
| chr3:94029349 | ATTT | A | 18 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0045 others(15): Show |
18 | HG00438.hp2 HG00642.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.381-5969_381-5967d others(5): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94029349 | ||||||
| chr3:94029350 | T | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0220 |
2 | HG04199.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.381-5981T>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94029350 | |||||||
| chr3:94029353 | T | A | 1 | a0001c0001t0001g0016 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.381-5978T>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94029353 | |||||||
| chr3:94029354 | T | A | 1 | a0001c0001t0001g0178 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.381-5977T>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94029354 | |||||||
| chr3:94029411 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.381-5920G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94029411 | |||||||
| chr3:94030174 | T | A | 2 | a0002c0002t0001g0026 a0002c0002t0001g0130 |
2 | NA18988.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.381-5157T>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94030174 | |||||||
| chr3:94030287 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.381-5044C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94030287 | |||||||
| chr3:94030392 | C | A | 1 | a0001c0001t0001g0179 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.381-4939C>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94030392 | |||||||
| chr3:94030393 | AT | A | 149 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(146): Show |
149 | HG00140.hp2 HG00280.hp2 HG00438.hp1 others(146): Show |
intron_variant | MODIFIER | c.381-4917delT | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94030393 | ||||||
| chr3:94030393 | ATT | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0043 others(4): Show |
7 | HG02809.hp2 HG02896.hp1 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.381-4918_381-4917d others(4): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94030393 | ||||||
| chr3:94030725 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.381-4606A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94030725 | |||||||
| chr3:94031240 | G | A | 1 | a0003c0003t0001g0207 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.381-4091G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94031240 | |||||||
| chr3:94031266 | C | T | 2 | a0001c0001t0001g0124 a0001c0001t0001g0128 |
2 | HG02622.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.381-4065C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94031266 | |||||||
| chr3:94031896 | A | G | 3 | a0001c0001t0001g0082 a0001c0001t0001g0123 a0001c0001t0001g0126 |
3 | HG02109.hp2 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.381-3435A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94031896 | |||||||
| chr3:94032097 | C | T | 61 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(58): Show |
61 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.381-3234C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94032097 | |||||||
| chr3:94032466 | A | G | 1 | a0001c0001t0001g0250 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.381-2865A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94032466 | |||||||
| chr3:94032739 | G | A | 8 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(5): Show |
8 | HG00642.hp2 HG01175.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.381-2592G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94032739 | |||||||
| chr3:94032765 | G | A | 1 | a0004c0008t0012g0136 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.381-2566G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94032765 | |||||||
| chr3:94032786 | G | A | 2 | a0001c0001t0001g0197 a0001c0001t0001g0198 |
2 | HG01261.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.381-2545G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94032786 | |||||||
| chr3:94033010 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.381-2321T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94033010 | |||||||
| chr3:94033382 | A | AT | 13 | a0001c0001t0001g0011 a0001c0001t0001g0047 a0001c0001t0001g0048 others(10): Show |
13 | HG00642.hp2 HG01884.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.381-1937dupT | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94033382 | ||||||
| chr3:94033685 | A | G | 18 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0045 others(15): Show |
18 | HG00438.hp2 HG00642.hp2 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.381-1646A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94033685 | |||||||
| chr3:94033789 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.381-1542C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94033789 | |||||||
| chr3:94033929 | A | C | 1 | a0002c0002t0001g0031 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.381-1402A>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94033929 | |||||||
| chr3:94034375 | C | A | 2 | a0002c0002t0001g0029 a0002c0002t0001g0030 |
2 | NA18978.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.381-956C>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94034375 | |||||||
| chr3:94034506 | AT | A | 23 | a0001c0001t0001g0011 a0001c0001t0001g0046 a0001c0001t0001g0047 others(20): Show |
23 | HG00642.hp2 HG01106.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.381-809delT | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94034506 | ||||||
| chr3:94034605 | T | G | 5 | a0001c0001t0001g0076 a0001c0001t0001g0200 a0001c0001t0001g0201 others(2): Show |
5 | NA18952.hp1 NA18962.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.381-726T>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94034605 | |||||||
| chr3:94034773 | A | ATTGATCT others(12): Show |
1 | a0001c0001t0001g0177 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.381-555_381-537dup others(19): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94034773 | ||||||
| chr3:94034843 | A | G | 1 | a0001c0004t0001g0138 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.381-488A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94034843 | |||||||
| chr3:94034944 | A | T | 1 | a0001c0001t0001g0033 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.381-387A>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94034944 | |||||||
| chr3:94034975 | T | C | 12 | a0001c0001t0001g0021 a0001c0001t0001g0069 a0001c0001t0001g0143 others(9): Show |
12 | HG00438.hp1 HG01258.hp1 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.381-356T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94034975 | |||||||
| chr3:94035026 | A | G | 1 | a0001c0004t0001g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.381-305A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94035026 | |||||||
| chr3:94035097 | C | T | 1 | a0001c0001t0001g0011 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.381-234C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94035097 | |||||||
| chr3:94035098 | G | A | 2 | a0001c0001t0001g0086 a0001c0001t0001g0111 |
2 | HG02698.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.381-233G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94035098 | |||||||
| chr3:94035236 | C | CA | 10 | a0001c0001t0001g0079 a0001c0001t0001g0156 a0001c0001t0001g0185 others(7): Show |
10 | HG00741.hp1 HG01175.hp2 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.381-77dupA | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr3 | 94035236 | ||||||
| chr3:94035258 | T | C | 2 | a0001c0001t0005g0057 a0001c0001t0005g0058 |
2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.381-73T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 3/9 | chr3 | 94035258 | |||||||
| chr3:94035442 | GT | G | 7 | a0001c0001t0001g0129 a0001c0001t0001g0143 a0001c0001t0001g0180 others(4): Show |
7 | HG00558.hp2 HG01106.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.486+22delT | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr3 | 94035442 | ||||||
| chr3:94035443 | T | G | 1 | a0002c0002t0001g0029 | 1 | NA18978.hp1 | splice_region_variant&intron_variant | LOW | c.486+7T>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 4/9 | chr3 | 94035443 | |||||||
| chr3:94035456 | T | A | 1 | a0001c0001t0001g0211 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.486+20T>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 4/9 | chr3 | 94035456 | |||||||
| chr3:94035705 | A | G | 1 | a0008c0009t0001g0036 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.486+269A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 4/9 | chr3 | 94035705 | |||||||
| chr3:94036925 | T | C | 1 | a0001c0001t0001g0016 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.689+171T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | chr3 | 94036925 | |||||||
| chr3:94036975 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.689+221G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | chr3 | 94036975 | |||||||
| chr3:94037403 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 |
3 | HG03471.hp2 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.689+649G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | chr3 | 94037403 | |||||||
| chr3:94037513 | C | T | 3 | a0001c0001t0001g0173 a0001c0001t0006g0174 a0003c0003t0006g0073 |
3 | HG00639.hp2 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.689+759C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | chr3 | 94037513 | |||||||
| chr3:94037558 | A | T | 1 | a0001c0001t0001g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.689+804A>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | chr3 | 94037558 | |||||||
| chr3:94037625 | T | G | 1 | a0001c0001t0001g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.689+871T>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | chr3 | 94037625 | |||||||
| chr3:94037626 | G | T | 1 | a0001c0001t0001g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.689+872G>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | chr3 | 94037626 | |||||||
| chr3:94037863 | C | T | 5 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0252 others(2): Show |
5 | HG02896.hp1 HG03195.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.689+1109C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | chr3 | 94037863 | |||||||
| chr3:94038091 | G | A | 1 | a0001c0001t0001g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.689+1337G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | chr3 | 94038091 | |||||||
| chr3:94038150 | C | A | 1 | a0001c0001t0001g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.689+1396C>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | chr3 | 94038150 | |||||||
| chr3:94038373 | A | C | 1 | a0001c0001t0001g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.690-1507A>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | chr3 | 94038373 | |||||||
| chr3:94038515 | C | CT | 34 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0043 others(31): Show |
34 | HG00423.hp1 HG01243.hp2 HG01433.hp2 others(31): Show |
intron_variant | MODIFIER | c.690-1340dupT | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr3 | 94038515 | ||||||
| chr3:94038515 | CT | C | 22 | a0001c0001t0001g0034 a0001c0001t0001g0042 a0001c0001t0001g0046 others(19): Show |
22 | HG00438.hp2 HG00642.hp1 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.690-1340delT | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr3 | 94038515 | ||||||
| chr3:94038617 | A | G | 1 | a0003c0006t0001g0006 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.690-1263A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | chr3 | 94038617 | |||||||
| chr3:94038627 | G | A | 1 | a0001c0001t0001g0151 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.690-1253G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | chr3 | 94038627 | |||||||
| chr3:94038701 | T | C | 1 | a0001c0001t0001g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.690-1179T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | chr3 | 94038701 | |||||||
| chr3:94038702 | C | G | 1 | a0001c0001t0001g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.690-1178C>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | chr3 | 94038702 | |||||||
| chr3:94038748 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.690-1132C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | chr3 | 94038748 | |||||||
| chr3:94038756 | C | A | 1 | a0001c0001t0001g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.690-1124C>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | chr3 | 94038756 | |||||||
| chr3:94038777 | T | A | 1 | a0005c0010t0001g0054 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.690-1103T>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | chr3 | 94038777 | |||||||
| chr3:94038895 | C | T | 2 | a0001c0001t0001g0001 a0001c0001t0013g0002 |
2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.690-985C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | chr3 | 94038895 | |||||||
| chr3:94038977 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.690-903T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | chr3 | 94038977 | |||||||
| chr3:94039047 | T | C | 1 | a0001c0001t0001g0106 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.690-833T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | chr3 | 94039047 | |||||||
| chr3:94039411 | AATGGCGT others(24): Show |
A | 1 | a0001c0001t0002g0241 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.690-468_690-438del others(31): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | chr3 | 94039411 | |||||||
| chr3:94039494 | C | T | 1 | a0001c0001t0001g0016 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.690-386C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | chr3 | 94039494 | |||||||
| chr3:94039499 | C | CA | 114 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(111): Show |
114 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.690-360dupA | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr3 | 94039499 | ||||||
| chr3:94039499 | C | CAA | 18 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0033 others(15): Show |
18 | HG01109.hp2 HG02080.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.690-361_690-360dup others(2): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr3 | 94039499 | ||||||
| chr3:94039806 | C | T | 1 | a0001c0004t0001g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.690-74C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 5/9 | chr3 | 94039806 | |||||||
| chr3:94040016 | G | A | 1 | a0001c0001t0001g0262 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.798+28G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 6/9 | chr3 | 94040016 | |||||||
| chr3:94040028 | A | G | 1 | a0001c0001t0001g0016 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.798+40A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 6/9 | chr3 | 94040028 | |||||||
| chr3:94040235 | A | G | 27 | a0001c0001t0001g0021 a0001c0001t0001g0069 a0001c0001t0001g0070 others(24): Show |
27 | HG00438.hp1 HG01243.hp1 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.798+247A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 6/9 | chr3 | 94040235 | |||||||
| chr3:94040349 | T | G | 3 | a0001c0001t0004g0140 a0001c0001t0004g0141 a0001c0001t0004g0142 |
3 | HG02055.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.798+361T>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 6/9 | chr3 | 94040349 | |||||||
| chr3:94040686 | G | GT | 9 | a0001c0001t0001g0007 a0001c0001t0001g0055 a0001c0001t0001g0061 others(6): Show |
9 | HG01358.hp2 HG01361.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.798+713dupT | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | 94040686 | ||||||
| chr3:94040686 | G | GTT | 6 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0156 others(3): Show |
6 | HG02896.hp1 HG03195.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.798+712_798+713dup others(2): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | 94040686 | ||||||
| chr3:94040772 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.798+784G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 6/9 | chr3 | 94040772 | |||||||
| chr3:94040803 | A | G | 2 | a0001c0001t0001g0050 a0008c0009t0001g0036 |
2 | NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.798+815A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 6/9 | chr3 | 94040803 | |||||||
| chr3:94040852 | T | G | 1 | a0001c0001t0002g0260 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.798+864T>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 6/9 | chr3 | 94040852 | |||||||
| chr3:94040873 | A | G | 1 | a0002c0002t0007g0134 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.798+885A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 6/9 | chr3 | 94040873 | |||||||
| chr3:94040881 | T | C | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0256 |
3 | HG02280.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.798+893T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 6/9 | chr3 | 94040881 | |||||||
| chr3:94040921 | A | G | 3 | a0001c0001t0001g0233 a0001c0001t0001g0236 a0001c0001t0001g0237 |
3 | HG00140.hp1 HG01109.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.798+933A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 6/9 | chr3 | 94040921 | |||||||
| chr3:94041080 | G | GT | 10 | a0001c0001t0001g0011 a0001c0001t0001g0115 a0001c0001t0001g0124 others(7): Show |
10 | HG01884.hp1 HG01978.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.798+1104dupT | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | 94041080 | ||||||
| chr3:94041500 | T | TTCAAAGC others(18): Show |
1 | a0001c0001t0001g0253 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.798+1513_799-1490d others(27): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | 94041500 | ||||||
| chr3:94041524 | A | T | 2 | a0001c0001t0001g0079 a0002c0002t0001g0008 |
2 | HG02738.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.799-1491A>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 6/9 | chr3 | 94041524 | |||||||
| chr3:94041951 | G | A | 53 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0035 others(50): Show |
53 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.799-1064G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 6/9 | chr3 | 94041951 | |||||||
| chr3:94041980 | T | C | 50 | a0001c0001t0001g0021 a0001c0001t0001g0033 a0001c0001t0001g0035 others(47): Show |
50 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(47): Show |
intron_variant | MODIFIER | c.799-1035T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 6/9 | chr3 | 94041980 | |||||||
| chr3:94042035 | C | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-980C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 6/9 | chr3 | 94042035 | |||||||
| chr3:94042048 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.799-967C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 6/9 | chr3 | 94042048 | |||||||
| chr3:94042256 | C | A | 1 | a0001c0001t0001g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.799-759C>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 6/9 | chr3 | 94042256 | |||||||
| chr3:94042350 | T | G | 2 | a0001c0001t0001g0001 a0001c0001t0013g0002 |
2 | HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.799-665T>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 6/9 | chr3 | 94042350 | |||||||
| chr3:94042366 | A | T | 5 | a0001c0001t0003g0071 a0001c0001t0003g0163 a0001c0001t0003g0164 others(2): Show |
5 | HG02015.hp2 NA18954.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.799-649A>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 6/9 | chr3 | 94042366 | |||||||
| chr3:94042636 | ATATATTT others(3): Show |
A | 1 | a0001c0001t0002g0241 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.799-375_799-366del others(10): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr3 | 94042636 | ||||||
| chr3:94042752 | G | A | 1 | a0001c0001t0001g0106 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.799-263G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 6/9 | chr3 | 94042752 | |||||||
| chr3:94042814 | C | T | 1 | a0003c0003t0001g0037 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.799-201C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 6/9 | chr3 | 94042814 | |||||||
| chr3:94043454 | TATAAGGA others(4): Show |
T | 1 | a0001c0001t0001g0181 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1024+216_1024+226d others(13): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043454 | ||||||
| chr3:94043496 | TTTGGGAT others(19): Show |
T | 1 | a0001c0001t0001g0218 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1024+258_1024+283d others(28): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043496 | ||||||
| chr3:94043502 | A | G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0156 others(3): Show |
6 | HG02896.hp1 HG03195.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1024+262A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043502 | |||||||
| chr3:94043535 | C | A | 62 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0019 others(59): Show |
62 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.1024+295C>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043535 | |||||||
| chr3:94043545 | C | CCCCCCTC others(358): Show |
1 | a0008c0009t0001g0036 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1024+306_1024+307i others(367): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCCCCTCC others(196): Show |
1 | a0001c0001t0001g0072 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1024+306_1024+307i others(205): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCCCCTCC others(157): Show |
1 | a0001c0001t0001g0019 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1024+306_1024+307i others(166): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCCCCTCC others(172): Show |
1 | a0003c0003t0001g0238 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1024+306_1024+307i others(181): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCCCCTCC others(166): Show |
1 | a0001c0001t0001g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1024+306_1024+307i others(175): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCCCCTCC others(170): Show |
1 | a0001c0001t0001g0020 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1024+306_1024+307i others(179): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(206): Show |
1 | a0001c0001t0001g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1024+312_1024+313i others(215): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(202): Show |
1 | a0001c0001t0001g0079 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(211): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(211): Show |
1 | a0001c0001t0001g0129 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(220): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(208): Show |
1 | a0001c0001t0001g0214 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(217): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(188): Show |
1 | a0001c0001t0001g0012 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(197): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(194): Show |
1 | a0001c0001t0001g0236 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(203): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(189): Show |
1 | a0001c0001t0001g0115 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(198): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(205): Show |
1 | a0001c0001t0001g0090 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(214): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(216): Show |
1 | a0001c0001t0001g0086 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(225): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(248): Show |
1 | a0001c0001t0001g0009 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(257): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(205): Show |
1 | a0001c0001t0001g0101 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(214): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(209): Show |
1 | a0001c0001t0001g0111 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(218): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(205): Show |
1 | a0001c0001t0001g0110 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(214): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(231): Show |
1 | a0001c0001t0001g0213 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(240): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(206): Show |
1 | a0001c0001t0001g0075 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(215): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(187): Show |
2 | a0001c0001t0001g0007 a0001c0001t0001g0105 |
2 | HG01192.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1024+318_1024+319i others(196): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(193): Show |
3 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0122 |
3 | HG00558.hp1 HG00642.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1024+318_1024+319i others(202): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(193): Show |
1 | a0003c0003t0001g0089 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(202): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(199): Show |
7 | a0001c0001t0001g0085 a0001c0001t0001g0091 a0001c0001t0001g0093 others(4): Show |
7 | HG00140.hp1 HG00280.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1024+318_1024+319i others(208): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(205): Show |
7 | a0001c0001t0001g0063 a0001c0001t0001g0065 a0001c0001t0001g0084 others(4): Show |
7 | HG00423.hp1 HG01071.hp2 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1024+318_1024+319i others(214): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(205): Show |
1 | a0003c0003t0001g0099 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(214): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(225): Show |
1 | a0001c0001t0014g0088 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(234): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(231): Show |
1 | a0001c0001t0001g0014 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(240): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(213): Show |
1 | a0001c0001t0010g0234 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(222): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(187): Show |
1 | a0001c0001t0001g0106 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(196): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(200): Show |
1 | a0001c0001t0001g0104 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(209): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(193): Show |
2 | a0001c0001t0001g0108 a0001c0001t0001g0119 |
2 | NA18983.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1024+318_1024+319i others(202): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(199): Show |
5 | a0001c0001t0001g0060 a0001c0001t0001g0064 a0001c0001t0001g0103 others(2): Show |
5 | HG00621.hp2 HG01934.hp2 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.1024+318_1024+319i others(208): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(211): Show |
1 | a0001c0001t0001g0109 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(220): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(192): Show |
1 | a0001c0001t0001g0081 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(201): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(193): Show |
2 | a0001c0001t0001g0102 a0001c0001t0001g0215 |
2 | NA18941.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1024+318_1024+319i others(202): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(225): Show |
2 | a0001c0001t0001g0127 a0001c0001t0001g0212 |
2 | HG02602.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.1024+318_1024+319i others(234): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(188): Show |
1 | a0003c0003t0001g0228 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(197): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(194): Show |
1 | a0001c0001t0001g0087 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(203): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(204): Show |
1 | a0001c0001t0001g0062 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(213): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(212): Show |
1 | a0001c0001t0001g0092 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(221): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(182): Show |
1 | a0001c0001t0001g0098 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(191): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(209): Show |
1 | a0001c0001t0001g0052 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(218): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(227): Show |
1 | a0001c0001t0001g0010 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(236): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(197): Show |
1 | a0001c0001t0001g0013 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(206): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(196): Show |
1 | a0001c0001t0001g0211 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(205): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCC others(221): Show |
1 | a0001c0001t0001g0235 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(230): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043545 | C | CCTCCCCT others(164): Show |
1 | a0002c0005t0001g0023 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1024+311_1024+312i others(173): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043545 | ||||||
| chr3:94043553 | T | TCCCCCTC others(206): Show |
1 | a0001c0001t0001g0078 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(215): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043553 | ||||||
| chr3:94043553 | T | TCCCCTCC others(232): Show |
1 | a0001c0001t0005g0058 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1024+317_1024+318i others(241): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043553 | ||||||
| chr3:94043553 | T | TCCCCTCC others(231): Show |
1 | a0001c0001t0005g0057 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1024+317_1024+318i others(240): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043553 | ||||||
| chr3:94043554 | C | CCCCCTCC others(98): Show |
2 | a0001c0001t0001g0068 a0001c0001t0001g0167 |
2 | HG00423.hp2 HG02083.hp2 |
intron_variant | MODIFIER | c.1024+318_1024+319i others(107): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043554 | ||||||
| chr3:94043554 | C | CCCCCTCC others(123): Show |
1 | a0001c0001t0001g0148 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(132): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043554 | ||||||
| chr3:94043554 | C | CCCCCTCC others(103): Show |
1 | a0001c0001t0001g0137 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(112): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043554 | ||||||
| chr3:94043554 | C | CCCCCTCC others(190): Show |
1 | a0001c0001t0001g0061 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(199): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043554 | ||||||
| chr3:94043558 | C | CCTCCCCC others(201): Show |
1 | a0001c0001t0001g0045 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1024+323_1024+324i others(210): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043558 | ||||||
| chr3:94043558 | C | CT | 6 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(3): Show |
6 | HG02055.hp2 HG02109.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1024+318_1024+319i others(3): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCACCC others(167): Show |
1 | a0002c0002t0001g0133 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(176): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCACCC others(166): Show |
1 | a0002c0002t0001g0263 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(175): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(328): Show |
1 | a0003c0003t0001g0190 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(337): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(344): Show |
1 | a0001c0001t0001g0181 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(353): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(233): Show |
1 | a0001c0001t0001g0080 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(242): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(279): Show |
1 | a0001c0001t0001g0210 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(288): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(173): Show |
1 | a0001c0001t0002g0241 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(182): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(144): Show |
2 | a0001c0001t0002g0239 a0001c0001t0002g0240 |
2 | HG01891.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.1024+318_1024+319i others(153): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(138): Show |
2 | a0001c0001t0002g0260 a0001c0001t0002g0261 |
2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1024+318_1024+319i others(147): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(138): Show |
1 | a0001c0001t0002g0230 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(147): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(239): Show |
1 | a0001c0001t0001g0218 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(248): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(192): Show |
1 | a0003c0003t0001g0145 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(201): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(333): Show |
1 | a0001c0001t0001g0198 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(342): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(314): Show |
1 | a0001c0001t0001g0197 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(323): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(113): Show |
1 | a0001c0001t0001g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(122): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(172): Show |
1 | a0001c0001t0001g0004 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(181): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(172): Show |
1 | a0001c0001t0001g0003 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(181): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(184): Show |
1 | a0001c0001t0001g0005 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(193): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(164): Show |
1 | a0001c0001t0001g0033 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(173): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(175): Show |
1 | a0002c0002t0001g0130 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(184): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(315): Show |
1 | a0001c0001t0001g0074 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(324): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(133): Show |
1 | a0001c0001t0011g0227 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(142): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(121): Show |
3 | a0001c0001t0001g0166 a0001c0001t0001g0208 a0001c0001t0001g0209 |
3 | HG01884.hp2 HG01891.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1024+318_1024+319i others(130): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(132): Show |
1 | a0003c0003t0001g0207 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(141): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(213): Show |
1 | a0001c0001t0001g0223 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(222): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(209): Show |
1 | a0001c0001t0001g0048 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(218): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(194): Show |
2 | a0003c0003t0001g0044 a0003c0003t0001g0222 |
2 | HG01175.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1024+318_1024+319i others(203): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(214): Show |
1 | a0001c0001t0001g0046 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(223): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(263): Show |
1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(272): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(213): Show |
1 | a0001c0001t0001g0047 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(222): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(167): Show |
1 | a0002c0002t0001g0125 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(176): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(195): Show |
1 | a0002c0002t0001g0040 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(204): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(194): Show |
2 | a0002c0002t0001g0039 a0002c0002t0001g0041 |
2 | HG01256.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1024+318_1024+319i others(203): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(320): Show |
1 | a0001c0001t0001g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(329): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(168): Show |
1 | a0003c0006t0001g0006 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(177): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(186): Show |
1 | a0002c0002t0001g0017 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(195): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(167): Show |
1 | a0002c0002t0001g0025 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(176): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(166): Show |
10 | a0002c0002t0001g0008 a0002c0002t0001g0024 a0002c0002t0001g0026 others(7): Show |
10 | HG00558.hp2 HG00621.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.1024+318_1024+319i others(175): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(180): Show |
3 | a0002c0002t0001g0031 a0002c0002t0001g0032 a0006c0007t0001g0028 |
3 | HG01346.hp1 HG02165.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1024+318_1024+319i others(189): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(165): Show |
1 | a0002c0002t0001g0022 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(174): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(182): Show |
1 | a0001c0001t0001g0252 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(191): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(188): Show |
1 | a0001c0001t0013g0002 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(197): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(195): Show |
1 | a0001c0001t0001g0156 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(204): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(194): Show |
2 | a0001c0001t0001g0034 a0001c0001t0001g0264 |
2 | HG02896.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1024+318_1024+319i others(203): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(322): Show |
1 | a0001c0001t0001g0193 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(331): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(323): Show |
1 | a0001c0001t0001g0177 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(332): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(313): Show |
1 | a0001c0001t0001g0076 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(322): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(301): Show |
1 | a0001c0001t0001g0262 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(310): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(313): Show |
2 | a0001c0001t0001g0201 a0001c0001t0001g0254 |
2 | HG03688.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.1024+318_1024+319i others(322): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(312): Show |
1 | a0001c0001t0001g0199 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(321): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(387): Show |
1 | a0001c0001t0001g0200 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(396): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(329): Show |
1 | a0001c0001t0001g0182 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(338): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(318): Show |
1 | a0001c0001t0009g0195 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(327): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(323): Show |
1 | a0001c0001t0001g0216 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(332): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(306): Show |
1 | a0003c0003t0001g0186 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(315): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(313): Show |
1 | a0001c0001t0001g0219 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(322): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(301): Show |
1 | a0001c0001t0001g0253 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(310): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(301): Show |
1 | a0001c0001t0001g0217 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(310): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(319): Show |
1 | a0001c0001t0001g0175 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(328): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(320): Show |
1 | a0001c0001t0001g0220 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(329): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(319): Show |
6 | a0001c0001t0001g0179 a0001c0001t0001g0191 a0001c0001t0001g0226 others(3): Show |
6 | HG00280.hp2 HG01192.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.1024+318_1024+319i others(328): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(318): Show |
1 | a0001c0001t0001g0187 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(327): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(318): Show |
1 | a0001c0001t0001g0171 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(327): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(310): Show |
1 | a0001c0001t0001g0259 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(319): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(251): Show |
1 | a0003c0003t0006g0073 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(260): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(312): Show |
1 | a0001c0001t0001g0170 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(321): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(224): Show |
1 | a0001c0001t0006g0174 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(233): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(312): Show |
1 | a0001c0001t0001g0188 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(321): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(325): Show |
1 | a0001c0001t0001g0185 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(334): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(215): Show |
1 | a0001c0001t0001g0196 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(224): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(326): Show |
1 | a0001c0001t0001g0189 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(335): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(319): Show |
1 | a0001c0001t0001g0183 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(328): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(317): Show |
2 | a0001c0001t0001g0232 a0001c0001t0001g0249 |
2 | HG00738.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1024+318_1024+319i others(326): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(325): Show |
2 | a0001c0001t0001g0180 a0001c0001t0001g0184 |
2 | NA18961.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1024+318_1024+319i others(334): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(330): Show |
1 | a0001c0001t0001g0132 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(339): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(359): Show |
1 | a0001c0001t0001g0015 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(368): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(181): Show |
1 | a0001c0001t0001g0001 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(190): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(242): Show |
1 | a0001c0001t0001g0016 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(251): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(232): Show |
1 | a0001c0001t0001g0059 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(241): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(219): Show |
1 | a0001c0001t0001g0100 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(228): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(231): Show |
1 | a0001c0001t0001g0118 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(240): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(207): Show |
1 | a0001c0001t0001g0117 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(216): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(174): Show |
3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0256 |
3 | HG02280.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1024+318_1024+319i others(183): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(178): Show |
1 | a0001c0001t0001g0255 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(187): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(185): Show |
1 | a0001c0001t0001g0011 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(194): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(176): Show |
1 | a0001c0001t0001g0124 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(185): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(157): Show |
1 | a0001c0001t0001g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(166): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(155): Show |
1 | a0001c0001t0001g0123 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(164): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(160): Show |
1 | a0001c0001t0001g0082 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(169): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(252): Show |
1 | a0001c0001t0001g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(261): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(319): Show |
1 | a0001c0001t0001g0202 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(328): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(318): Show |
1 | a0001c0001t0001g0077 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(327): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(318): Show |
1 | a0001c0001t0001g0203 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(327): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(324): Show |
1 | a0001c0001t0001g0204 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(333): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(211): Show |
3 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0248 |
3 | HG02280.hp1 HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1024+318_1024+319i others(220): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(210): Show |
1 | a0001c0001t0001g0053 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(219): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(212): Show |
1 | a0001c0001t0001g0247 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(221): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(224): Show |
1 | a0001c0001t0001g0173 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(233): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(312): Show |
1 | a0003c0003t0001g0172 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(321): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(165): Show |
1 | a0001c0001t0001g0128 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(174): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(168): Show |
2 | a0001c0001t0001g0069 a0001c0001t0001g0168 |
2 | HG02015.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.1024+318_1024+319i others(177): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(164): Show |
1 | a0001c0001t0001g0021 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(173): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(184): Show |
1 | a0001c0001t0001g0143 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(193): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(169): Show |
1 | a0001c0001t0001g0066 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(178): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(166): Show |
1 | a0001c0004t0001g0067 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(175): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(165): Show |
1 | a0001c0004t0001g0138 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(174): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(156): Show |
1 | a0001c0001t0004g0140 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(165): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(162): Show |
6 | a0001c0001t0001g0139 a0001c0001t0001g0144 a0001c0001t0001g0158 others(3): Show |
6 | HG01243.hp1 HG02717.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1024+318_1024+319i others(171): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(176): Show |
1 | a0001c0001t0001g0149 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(185): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(181): Show |
2 | a0001c0001t0001g0152 a0001c0001t0001g0155 |
2 | HG01258.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.1024+318_1024+319i others(190): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(158): Show |
1 | a0001c0001t0003g0071 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(167): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(181): Show |
1 | a0001c0001t0001g0147 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(190): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(176): Show |
1 | a0001c0001t0001g0225 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(185): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(154): Show |
2 | a0001c0001t0001g0150 a0001c0001t0001g0154 |
2 | HG03491.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1024+318_1024+319i others(163): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(168): Show |
11 | a0001c0001t0001g0035 a0001c0001t0001g0146 a0001c0001t0001g0151 others(8): Show |
11 | HG00140.hp2 HG00438.hp1 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.1024+318_1024+319i others(177): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(169): Show |
1 | a0001c0001t0003g0164 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(178): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(209): Show |
1 | a0003c0003t0001g0162 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(218): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(208): Show |
1 | a0001c0001t0001g0161 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(217): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(215): Show |
1 | a0001c0001t0001g0070 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(224): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(214): Show |
2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1024+318_1024+319i others(223): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(154): Show |
1 | a0001c0001t0001g0157 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(163): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(147): Show |
2 | a0001c0001t0004g0141 a0001c0001t0004g0142 |
2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1024+318_1024+319i others(156): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(179): Show |
1 | a0001c0001t0003g0163 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(188): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(253): Show |
1 | a0001c0001t0001g0231 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(262): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(191): Show |
1 | a0001c0001t0001g0042 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(200): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(192): Show |
1 | a0001c0001t0001g0049 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(201): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(202): Show |
1 | a0001c0001t0001g0055 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(211): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(214): Show |
1 | a0003c0003t0001g0037 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(223): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(197): Show |
1 | a0001c0001t0001g0221 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(206): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(210): Show |
1 | a0001c0001t0001g0056 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(219): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(312): Show |
1 | a0001c0001t0001g0178 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1024+318_1024+319i others(321): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | CTCCCCCC others(146): Show |
1 | a0001c0001t0001g0206 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1024+318_1024+319i others(155): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043558 | C | T | 2 | a0001c0001t0005g0057 a0001c0001t0005g0058 |
2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1024+318C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043558 | |||||||
| chr3:94043560 | T | C | 3 | a0001c0001t0001g0061 a0001c0001t0001g0082 a0001c0001t0001g0123 |
3 | HG02109.hp2 HG02897.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.1024+320T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043560 | |||||||
| chr3:94043561 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1024+321C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043561 | |||||||
| chr3:94043564 | T | C | 12 | a0001c0001t0001g0038 a0001c0001t0001g0043 a0001c0001t0001g0051 others(9): Show |
12 | HG00423.hp2 HG02083.hp2 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.1024+324T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043564 | |||||||
| chr3:94043566 | T | C | 4 | a0001c0001t0001g0068 a0001c0001t0001g0137 a0001c0001t0001g0148 others(1): Show |
4 | HG00423.hp2 HG02083.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024+326T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043566 | |||||||
| chr3:94043567 | T | C | 10 | a0001c0001t0001g0038 a0001c0001t0001g0043 a0001c0001t0001g0051 others(7): Show |
10 | HG02109.hp2 HG02280.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.1024+327T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043567 | |||||||
| chr3:94043571 | CT | C | 4 | a0001c0001t0001g0068 a0001c0001t0001g0137 a0001c0001t0001g0148 others(1): Show |
4 | HG00423.hp2 HG02083.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024+332delT | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043571 | |||||||
| chr3:94043574 | T | C | 2 | a0001c0001t0001g0082 a0001c0001t0001g0123 |
2 | HG02109.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1024+334T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043574 | |||||||
| chr3:94043578 | T | C | 1 | a0001c0001t0001g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1024+338T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043578 | |||||||
| chr3:94043580 | T | C | 5 | a0001c0001t0001g0068 a0001c0001t0001g0126 a0001c0001t0001g0137 others(2): Show |
5 | HG00423.hp2 HG02083.hp2 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.1024+340T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043580 | |||||||
| chr3:94043580 | TTC | T | 6 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0052 others(3): Show |
6 | HG02280.hp1 HG02809.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1024+341_1024+342d others(4): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043580 | |||||||
| chr3:94043581 | T | C | 6 | a0001c0001t0001g0068 a0001c0001t0001g0082 a0001c0001t0001g0123 others(3): Show |
6 | HG00423.hp2 HG02083.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.1024+341T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043581 | |||||||
| chr3:94043583 | C | CG | 4 | a0001c0001t0001g0068 a0001c0001t0001g0137 a0001c0001t0001g0148 others(1): Show |
4 | HG00423.hp2 HG02083.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024+343_1024+344i others(3): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043583 | |||||||
| chr3:94043586 | T | C | 4 | a0001c0001t0001g0068 a0001c0001t0001g0137 a0001c0001t0001g0148 others(1): Show |
4 | HG00423.hp2 HG02083.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024+346T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043586 | |||||||
| chr3:94043590 | T | C | 4 | a0001c0001t0001g0068 a0001c0001t0001g0137 a0001c0001t0001g0148 others(1): Show |
4 | HG00423.hp2 HG02083.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024+350T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043590 | |||||||
| chr3:94043592 | C | A | 1 | a0001c0001t0001g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1024+352C>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043592 | |||||||
| chr3:94043593 | C | G | 3 | a0001c0001t0001g0102 a0001c0001t0001g0129 a0001c0001t0001g0215 |
3 | NA18941.hp1 NA19011.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1024+353C>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043593 | |||||||
| chr3:94043594 | T | TCCCCCCT others(83): Show |
1 | a0001c0001t0001g0218 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1024+359_1024+360i others(92): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043594 | ||||||
| chr3:94043601 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1024+361C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043601 | |||||||
| chr3:94043606 | T | C | 1 | a0001c0001t0002g0241 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1024+366T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043606 | |||||||
| chr3:94043609 | C | A | 32 | a0001c0001t0001g0038 a0001c0001t0001g0166 a0001c0001t0001g0206 others(29): Show |
32 | HG00558.hp2 HG00621.hp1 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.1024+369C>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043609 | |||||||
| chr3:94043609 | C | CCTCCCCC others(3): Show |
1 | a0001c0001t0002g0241 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1024+370_1024+371i others(12): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043609 | ||||||
| chr3:94043613 | C | A | 1 | a0001c0001t0001g0218 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1024+373C>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043613 | |||||||
| chr3:94043620 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1024+380T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043620 | |||||||
| chr3:94043624 | C | CCCCCTCC others(77): Show |
1 | a0001c0001t0001g0192 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1024+387_1024+388i others(86): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043624 | ||||||
| chr3:94043653 | C | G | 1 | a0001c0001t0001g0177 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1024+413C>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043653 | |||||||
| chr3:94043658 | C | CCTTT | 5 | a0001c0001t0001g0059 a0001c0001t0001g0080 a0001c0001t0001g0100 others(2): Show |
5 | HG01928.hp2 HG01934.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.1024+437_1024+440d others(6): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94043658 | ||||||
| chr3:94043700 | G | A | 63 | a0001c0001t0001g0015 a0001c0001t0001g0043 a0001c0001t0001g0051 others(60): Show |
63 | HG00280.hp2 HG00639.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1024+460G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043700 | |||||||
| chr3:94043781 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1024+541C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043781 | |||||||
| chr3:94043850 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1024+610G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043850 | |||||||
| chr3:94043891 | T | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(193): Show |
196 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(193): Show |
intron_variant | MODIFIER | c.1024+651T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043891 | |||||||
| chr3:94043899 | C | T | 8 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(5): Show |
8 | HG00642.hp2 HG01175.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1024+659C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043899 | |||||||
| chr3:94043909 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(1): Show |
4 | HG03471.hp2 NA18906.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024+669C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043909 | |||||||
| chr3:94043957 | G | T | 1 | a0001c0001t0001g0253 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1024+717G>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94043957 | |||||||
| chr3:94044025 | G | A | 13 | a0001c0001t0001g0042 a0001c0001t0001g0045 a0001c0001t0001g0046 others(10): Show |
13 | HG00438.hp2 HG00642.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1024+785G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044025 | |||||||
| chr3:94044041 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1024+801C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044041 | |||||||
| chr3:94044076 | A | AC | 47 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(44): Show |
47 | HG00438.hp2 HG00621.hp1 HG00738.hp2 others(44): Show |
intron_variant | MODIFIER | c.1024+840dupC | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94044076 | ||||||
| chr3:94044080 | C | T | 1 | a0002c0002t0001g0030 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1024+840C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044080 | |||||||
| chr3:94044081 | G | A | 2 | a0001c0001t0001g0014 a0001c0001t0001g0116 |
2 | NA18612.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1024+841G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044081 | |||||||
| chr3:94044126 | G | T | 1 | a0001c0001t0001g0061 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1024+886G>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044126 | |||||||
| chr3:94044174 | C | T | 1 | a0001c0001t0011g0227 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1024+934C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044174 | |||||||
| chr3:94044301 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1024+1061G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044301 | |||||||
| chr3:94044330 | C | T | 1 | a0003c0003t0001g0207 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1024+1090C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044330 | |||||||
| chr3:94044337 | C | T | 25 | a0002c0002t0001g0008 a0002c0002t0001g0017 a0002c0002t0001g0022 others(22): Show |
25 | HG00558.hp2 HG00621.hp1 HG01256.hp1 others(22): Show |
intron_variant | MODIFIER | c.1024+1097C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044337 | |||||||
| chr3:94044341 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1024+1101C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044341 | |||||||
| chr3:94044345 | A | AC | 131 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0011 others(128): Show |
131 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.1024+1109dupC | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94044345 | ||||||
| chr3:94044345 | A | ACC | 6 | a0001c0001t0001g0045 a0001c0001t0001g0055 a0001c0001t0001g0083 others(3): Show |
6 | HG01243.hp2 HG02055.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1024+1108_1024+110 others(6): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94044345 | ||||||
| chr3:94044345 | A | C | 1 | a0001c0001t0001g0181 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1024+1105A>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044345 | |||||||
| chr3:94044381 | C | T | 6 | a0001c0001t0002g0230 a0001c0001t0002g0239 a0001c0001t0002g0240 others(3): Show |
6 | HG01891.hp2 HG01952.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.1024+1141C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044381 | |||||||
| chr3:94044385 | A | AC | 41 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0042 others(38): Show |
41 | HG00423.hp1 HG00438.hp2 HG00621.hp1 others(38): Show |
intron_variant | MODIFIER | c.1024+1149dupC | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94044385 | ||||||
| chr3:94044570 | G | T | 1 | a0001c0001t0001g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1024+1330G>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044570 | |||||||
| chr3:94044573 | A | AC | 18 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0042 others(15): Show |
18 | HG00423.hp1 HG00438.hp2 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.1024+1335dupC | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94044573 | ||||||
| chr3:94044613 | A | AC | 4 | a0001c0001t0001g0079 a0001c0001t0001g0177 a0001c0001t0001g0181 others(1): Show |
4 | HG00621.hp1 HG01496.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024+1376dupC | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94044613 | ||||||
| chr3:94044618 | G | A | 2 | a0001c0001t0005g0057 a0001c0001t0005g0058 |
2 | HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1024+1378G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044618 | |||||||
| chr3:94044636 | G | A | 3 | a0001c0001t0001g0045 a0003c0003t0001g0044 a0003c0003t0001g0222 |
3 | HG01175.hp1 HG02145.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1024+1396G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044636 | |||||||
| chr3:94044642 | G | GC | 3 | a0001c0001t0001g0109 a0001c0001t0001g0177 a0001c0001t0001g0245 |
3 | HG01496.hp2 NA18942.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1024+1405dupC | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94044642 | ||||||
| chr3:94044733 | G | A | 1 | a0001c0001t0003g0164 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1024+1493G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044733 | |||||||
| chr3:94044757 | G | GC | 4 | a0001c0001t0001g0059 a0001c0001t0001g0079 a0001c0001t0001g0114 others(1): Show |
4 | HG00423.hp1 HG01978.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024+1520dupC | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94044757 | ||||||
| chr3:94044760 | C | T | 3 | a0001c0001t0001g0177 a0001c0001t0001g0258 a0003c0003t0001g0176 |
3 | HG01496.hp2 HG01952.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1024+1520C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044760 | |||||||
| chr3:94044764 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1024+1524C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044764 | |||||||
| chr3:94044788 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1024+1548G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044788 | |||||||
| chr3:94044798 | G | A | 5 | a0001c0001t0003g0071 a0001c0001t0003g0163 a0001c0001t0003g0164 others(2): Show |
5 | HG02015.hp2 NA18954.hp2 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.1024+1558G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044798 | |||||||
| chr3:94044804 | G | A | 3 | a0001c0001t0004g0140 a0001c0001t0004g0141 a0001c0001t0004g0142 |
3 | HG02055.hp1 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1024+1564G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044804 | |||||||
| chr3:94044804 | G | C | 1 | a0001c0001t0001g0147 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1024+1564G>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044804 | |||||||
| chr3:94044808 | T | A | 1 | a0001c0001t0001g0147 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1024+1568T>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044808 | |||||||
| chr3:94044809 | C | A | 1 | a0001c0001t0001g0147 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1024+1569C>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044809 | |||||||
| chr3:94044819 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1024+1579G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044819 | |||||||
| chr3:94044841 | C | G | 1 | a0001c0001t0001g0147 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1024+1601C>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044841 | |||||||
| chr3:94044844 | G | A | 1 | a0001c0001t0001g0035 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1024+1604G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044844 | |||||||
| chr3:94044987 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1024+1747C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94044987 | |||||||
| chr3:94045080 | A | C | 1 | a0001c0001t0001g0083 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1024+1840A>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94045080 | |||||||
| chr3:94045255 | T | G | 1 | a0001c0001t0014g0088 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1024+2015T>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94045255 | |||||||
| chr3:94045287 | C | T | 4 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1024+2047C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94045287 | |||||||
| chr3:94045447 | TA | T | 16 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0043 others(13): Show |
16 | HG01071.hp1 HG01074.hp2 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.1024+2222delA | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94045447 | ||||||
| chr3:94045676 | G | C | 1 | a0001c0001t0001g0021 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1024+2436G>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94045676 | |||||||
| chr3:94045684 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1024+2444C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94045684 | |||||||
| chr3:94045943 | T | TC | 8 | a0001c0001t0001g0012 a0001c0001t0001g0085 a0001c0001t0001g0090 others(5): Show |
8 | HG00280.hp1 HG00642.hp1 HG00733.hp2 others(5): Show |
intron_variant | MODIFIER | c.1024+2705dupC | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94045943 | ||||||
| chr3:94045950 | C | CA | 43 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(40): Show |
43 | HG00438.hp1 HG00438.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.1024+2727dupA | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94045950 | ||||||
| chr3:94045962 | A | G | 17 | a0001c0001t0001g0076 a0001c0001t0001g0170 a0001c0001t0001g0171 others(14): Show |
17 | HG02083.hp1 NA18941.hp2 NA18942.hp2 others(14): Show |
intron_variant | MODIFIER | c.1024+2722A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94045962 | |||||||
| chr3:94045963 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1024+2723A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94045963 | |||||||
| chr3:94045968 | G | A | 15 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0132 others(12): Show |
15 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.1024+2728G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94045968 | |||||||
| chr3:94045968 | GA | G | 42 | a0001c0001t0001g0015 a0001c0001t0001g0076 a0001c0001t0001g0078 others(39): Show |
42 | HG00639.hp2 HG01168.hp1 HG01168.hp2 others(39): Show |
intron_variant | MODIFIER | c.1024+2738delA | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94045968 | ||||||
| chr3:94045969 | A | AG | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0198 others(1): Show |
4 | HG00741.hp1 HG01175.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024+2729_1024+273 others(5): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94045969 | |||||||
| chr3:94045969 | A | G | 12 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0132 others(9): Show |
12 | HG00280.hp2 HG00639.hp1 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.1024+2729A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94045969 | |||||||
| chr3:94046049 | A | T | 1 | a0003c0003t0001g0238 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1024+2809A>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94046049 | |||||||
| chr3:94046235 | C | A | 1 | a0001c0001t0001g0252 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1024+2995C>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94046235 | |||||||
| chr3:94046259 | A | G | 3 | a0001c0001t0001g0173 a0001c0001t0006g0174 a0003c0003t0006g0073 |
3 | HG00639.hp2 NA18906.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1024+3019A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94046259 | |||||||
| chr3:94046369 | CTTTATA | C | 10 | a0001c0001t0001g0011 a0001c0001t0001g0082 a0001c0001t0001g0120 others(7): Show |
10 | HG01884.hp1 HG02109.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1025-3029_1025-302 others(10): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94046369 | ||||||
| chr3:94046464 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1025-2942A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94046464 | |||||||
| chr3:94046596 | G | A | 4 | a0001c0001t0001g0166 a0001c0001t0001g0206 a0001c0001t0001g0208 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1025-2810G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94046596 | |||||||
| chr3:94046919 | G | A | 1 | a0001c0001t0001g0011 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1025-2487G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94046919 | |||||||
| chr3:94046996 | A | ACATTC | 4 | a0001c0001t0001g0077 a0001c0001t0001g0202 a0001c0001t0001g0203 others(1): Show |
4 | NA18943.hp2 NA18970.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025-2410_1025-240 others(9): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94046996 | |||||||
| chr3:94046997 | G | T | 4 | a0001c0001t0001g0077 a0001c0001t0001g0202 a0001c0001t0001g0203 others(1): Show |
4 | NA18943.hp2 NA18970.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025-2409G>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94046997 | |||||||
| chr3:94047000 | A | AGT | 4 | a0001c0001t0001g0077 a0001c0001t0001g0202 a0001c0001t0001g0203 others(1): Show |
4 | NA18943.hp2 NA18970.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025-2406_1025-240 others(6): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94047000 | |||||||
| chr3:94047003 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1025-2403T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94047003 | |||||||
| chr3:94047075 | G | A | 1 | a0001c0001t0013g0002 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1025-2331G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94047075 | |||||||
| chr3:94047132 | A | G | 4 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(1): Show |
4 | HG02055.hp2 HG02109.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025-2274A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94047132 | |||||||
| chr3:94047335 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1025-2071C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94047335 | |||||||
| chr3:94047999 | G | GAC | 33 | a0001c0001t0001g0045 a0001c0001t0001g0052 a0001c0001t0001g0055 others(30): Show |
33 | HG00140.hp1 HG00621.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1025-1370_1025-136 others(6): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94047999 | ||||||
| chr3:94047999 | GAC | G | 89 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(86): Show |
89 | HG00438.hp1 HG00558.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.1025-1370_1025-136 others(6): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94047999 | ||||||
| chr3:94047999 | GACAC | G | 6 | a0001c0001t0001g0034 a0001c0001t0001g0249 a0001c0001t0001g0255 others(3): Show |
6 | HG01071.hp1 HG01884.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1025-1372_1025-136 others(8): Show |
ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94047999 | ||||||
| chr3:94048037 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1025-1369C>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94048037 | |||||||
| chr3:94048401 | T | G | 1 | a0001c0001t0001g0009 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1025-1005T>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94048401 | |||||||
| chr3:94048761 | G | GT | 9 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0015 others(6): Show |
9 | HG01358.hp2 HG02809.hp1 HG03041.hp2 others(6): Show |
intron_variant | MODIFIER | c.1025-635dupT | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr3 | 94048761 | ||||||
| chr3:94049047 | T | C | 1 | a0002c0002t0001g0125 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1025-359T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94049047 | |||||||
| chr3:94049056 | T | G | 4 | a0001c0001t0001g0043 a0001c0001t0001g0051 a0001c0001t0001g0052 others(1): Show |
4 | HG03139.hp2 HG03195.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025-350T>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94049056 | |||||||
| chr3:94049261 | T | G | 6 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0156 others(3): Show |
6 | HG02896.hp1 HG03195.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1025-145T>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94049261 | |||||||
| chr3:94049276 | A | C | 1 | a0001c0001t0001g0020 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1025-130A>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94049276 | |||||||
| chr3:94049358 | G | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0072 a0001c0001t0001g0103 others(2): Show |
5 | HG02071.hp2 NA18970.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.1025-48G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 7/9 | chr3 | 94049358 | |||||||
| chr3:94049596 | G | C | 1 | a0001c0001t0001g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1141+74G>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 8/9 | chr3 | 94049596 | |||||||
| chr3:94049727 | A | G | 1 | a0001c0001t0001g0098 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1141+205A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 8/9 | chr3 | 94049727 | |||||||
| chr3:94049752 | A | G | 1 | a0001c0001t0001g0146 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1141+230A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 8/9 | chr3 | 94049752 | |||||||
| chr3:94049980 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1141+458G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 8/9 | chr3 | 94049980 | |||||||
| chr3:94049996 | C | CA | 21 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0021 others(18): Show |
21 | HG00438.hp1 HG01175.hp2 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1141+492dupA | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 94049996 | ||||||
| chr3:94050025 | G | A | 2 | a0001c0001t0006g0174 a0003c0003t0006g0073 |
2 | HG00639.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1141+503G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 8/9 | chr3 | 94050025 | |||||||
| chr3:94050166 | G | GA | 53 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0038 others(50): Show |
53 | HG00558.hp2 HG00621.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.1142-637dupA | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 94050166 | ||||||
| chr3:94050166 | GA | G | 7 | a0001c0001t0001g0078 a0001c0001t0001g0127 a0001c0001t0001g0212 others(4): Show |
7 | HG01168.hp2 HG02015.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.1142-637delA | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr3 | 94050166 | ||||||
| chr3:94050529 | T | G | 1 | a0001c0001t0001g0126 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1142-295T>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 8/9 | chr3 | 94050529 | |||||||
| chr3:94050976 | T | C | 1 | a0001c0001t0001g0046 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1210+84T>C | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 9/9 | chr3 | 94050976 | |||||||
| chr3:94051088 | A | G | 53 | a0001c0001t0001g0015 a0001c0001t0001g0074 a0001c0001t0001g0076 others(50): Show |
53 | HG00280.hp2 HG00639.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.1210+196A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 9/9 | chr3 | 94051088 | |||||||
| chr3:94051184 | AT | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0256 |
3 | HG02280.hp2 HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1210+293delT | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 9/9 | chr3 | 94051184 | |||||||
| chr3:94052096 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1211-1091G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 9/9 | chr3 | 94052096 | |||||||
| chr3:94052290 | G | A | 9 | a0001c0001t0001g0038 a0001c0001t0001g0166 a0001c0001t0001g0206 others(6): Show |
9 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1211-897G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 9/9 | chr3 | 94052290 | |||||||
| chr3:94052333 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1211-854A>G | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 9/9 | chr3 | 94052333 | |||||||
| chr3:94052565 | A | T | 1 | a0001c0001t0001g0085 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1211-622A>T | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 9/9 | chr3 | 94052565 | |||||||
| chr3:94052895 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1211-292G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 9/9 | chr3 | 94052895 | |||||||
| chr3:94053028 | G | A | 7 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0183 others(4): Show |
7 | HG02572.hp2 NA18954.hp1 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.1211-159G>A | ARL13B | ENSG00000169379.17 | transcript | ENST00000394222.8 | protein_coding | 9/9 | chr3 | 94053028 |