Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79501 |
| ensemblid | ENSG00000186092.7 |
| hgncid | 14825 |
| symbol | OR4F5 |
| name | olfactory receptor family 4 subfamily F member 5 |
| refseq_nuc | NM_001005484.2 |
| refseq_prot | NP_001005484.2 |
| ensembl_nuc | ENST00000641515.2 |
| ensembl_prot | ENSP00000493376.2 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 65419 |
| end | 71585 |
| strand | + |
| ver | v1.2 |
| region | chr1:65419-71585 |
| region5000 | chr1:60419-76585 |
| regionname0 | OR4F5_chr1_65419_71585 |
| regionname5000 | OR4F5_chr1_60419_76585 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 326 | 105 | 8 | 12 | 76 | 1 | 8 | 69 | OR4F5_chr1_60419_76585 | OR4F5 | MKKVT others(321): Show |
chr1 | 60419 | 76585 |
| a0002 | 0/0 | 239 | 42 | 1 | 6 | 35 | 0 | 0 | 33 | OR4F5_chr1_60419_76585 | OR4F5 | MKKVT others(234): Show |
chr1 | 60419 | 76585 |
| a0003 | 0/0 | 326 | 25 | 5 | 3 | 8 | 3 | 6 | 7 | OR4F5_chr1_60419_76585 | OR4F5 | MKKVT others(321): Show |
chr1 | 60419 | 76585 |
| a0004 | 0/0 | 326 | 19 | 11 | 5 | 0 | 1 | 2 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | MKKVT others(321): Show |
chr1 | 60419 | 76585 |
| a0005 | 1/0 | 326 | 15 | 12 | 1 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | MKKVT others(321): Show |
chr1 | 60419 | 76585 |
| a0006 | 0/0 | 326 | 3 | 0 | 1 | 0 | 0 | 2 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | MKKVT others(321): Show |
chr1 | 60419 | 76585 |
| a0007 | 0/0 | 326 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | MKKVT others(321): Show |
chr1 | 60419 | 76585 |
| a0008 | 0/0 | 326 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | MKKVT others(321): Show |
chr1 | 60419 | 76585 |
| a0009 | 0/0 | 326 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | MKKVT others(321): Show |
chr1 | 60419 | 76585 |
| a0010 | 0/0 | 326 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | MKKVT others(321): Show |
chr1 | 60419 | 76585 |
| a0011 | 0/0 | 273 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | OR4F5_chr1_60419_76585 | OR4F5 | MKKVT others(268): Show |
chr1 | 60419 | 76585 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 978 | 90 | 6 | 10 | 67 | 1 | 6 | OR4F5_chr1_60419_76585 | OR4F5 | ATGAA others(973): Show |
chr1 | 60419 | 76585 | ||
| a0001c0006 | 0/0 | 978 | 10 | 0 | 1 | 7 | 0 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | ATGAA others(973): Show |
chr1 | 60419 | 76585 | ||
| a0001c0009 | 0/0 | 978 | 2 | 2 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | ATGAA others(973): Show |
chr1 | 60419 | 76585 | ||
| a0001c0012 | 0/0 | 978 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | ATGAA others(973): Show |
chr1 | 60419 | 76585 | ||
| a0001c0018 | 0/0 | 978 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | ATGAA others(973): Show |
chr1 | 60419 | 76585 | ||
| a0001c0019 | 0/0 | 978 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | ATGAA others(973): Show |
chr1 | 60419 | 76585 | ||
| a0002c0002 | 0/0 | 978 | 41 | 1 | 5 | 35 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | ATGAA others(973): Show |
chr1 | 60419 | 76585 | ||
| a0002c0014 | 0/0 | 978 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | ATGAA others(973): Show |
chr1 | 60419 | 76585 | ||
| a0003c0004 | 0/0 | 978 | 15 | 5 | 3 | 0 | 3 | 4 | OR4F5_chr1_60419_76585 | OR4F5 | ATGAA others(973): Show |
chr1 | 60419 | 76585 | ||
| a0003c0007 | 0/0 | 978 | 9 | 0 | 0 | 8 | 0 | 1 | OR4F5_chr1_60419_76585 | OR4F5 | ATGAA others(973): Show |
chr1 | 60419 | 76585 | ||
| a0003c0013 | 0/0 | 978 | 1 | 0 | 0 | 0 | 0 | 1 | OR4F5_chr1_60419_76585 | OR4F5 | ATGAA others(973): Show |
chr1 | 60419 | 76585 | ||
| a0004c0003 | 0/0 | 978 | 18 | 10 | 5 | 0 | 1 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | ATGAA others(973): Show |
chr1 | 60419 | 76585 | ||
| a0004c0011 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | ATGAA others(973): Show |
chr1 | 60419 | 76585 | ||
| a0005c0005 | 1/0 | 978 | 15 | 12 | 1 | 0 | 1 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | ATGAA others(973): Show |
chr1 | 60419 | 76585 | ||
| a0006c0008 | 0/0 | 978 | 3 | 0 | 1 | 0 | 0 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | ATGAA others(973): Show |
chr1 | 60419 | 76585 | ||
| a0007c0010 | 0/0 | 978 | 2 | 0 | 0 | 2 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | ATGAA others(973): Show |
chr1 | 60419 | 76585 | ||
| a0008c0015 | 0/0 | 978 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | ATGAA others(973): Show |
chr1 | 60419 | 76585 | ||
| a0009c0020 | 0/0 | 978 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | ATGAA others(973): Show |
chr1 | 60419 | 76585 | ||
| a0010c0017 | 0/0 | 978 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | ATGAA others(973): Show |
chr1 | 60419 | 76585 | ||
| a0011c0016 | 0/0 | 978 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | ATGAA others(973): Show |
chr1 | 60419 | 76585 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2618 | 89 | 6 | 10 | 66 | 1 | 6 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2613): Show |
chr1 | 60419 | 76585 |
| a0001c0001t0013 | 0/0 | 2618 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2613): Show |
chr1 | 60419 | 76585 |
| a0001c0006t0002 | 0/0 | 2618 | 8 | 0 | 1 | 5 | 0 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2613): Show |
chr1 | 60419 | 76585 |
| a0001c0006t0006 | 0/0 | 2618 | 2 | 0 | 0 | 2 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2613): Show |
chr1 | 60419 | 76585 |
| a0001c0009t0007 | 0/0 | 2618 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2613): Show |
chr1 | 60419 | 76585 |
| a0001c0009t0008 | 0/0 | 2618 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2613): Show |
chr1 | 60419 | 76585 |
| a0001c0012t0001 | 0/0 | 2618 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2613): Show |
chr1 | 60419 | 76585 |
| a0001c0018t0001 | 0/0 | 2618 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2613): Show |
chr1 | 60419 | 76585 |
| a0001c0019t0001 | 0/0 | 2618 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2613): Show |
chr1 | 60419 | 76585 |
| a0002c0002t0002 | 0/0 | 2618 | 40 | 1 | 5 | 34 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2613): Show |
chr1 | 60419 | 76585 |
| a0002c0002t0012 | 0/0 | 2617 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2612): Show |
chr1 | 60419 | 76585 |
| a0002c0014t0002 | 0/0 | 2618 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2613): Show |
chr1 | 60419 | 76585 |
| a0003c0004t0003 | 0/0 | 2618 | 15 | 5 | 3 | 0 | 3 | 4 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2613): Show |
chr1 | 60419 | 76585 |
| a0003c0007t0003 | 0/0 | 2618 | 9 | 0 | 0 | 8 | 0 | 1 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2613): Show |
chr1 | 60419 | 76585 |
| a0003c0013t0014 | 0/0 | 2618 | 1 | 0 | 0 | 0 | 0 | 1 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2613): Show |
chr1 | 60419 | 76585 |
| a0004c0003t0002 | 0/0 | 2618 | 8 | 3 | 2 | 0 | 1 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2613): Show |
chr1 | 60419 | 76585 |
| a0004c0003t0004 | 0/0 | 2618 | 8 | 6 | 2 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2613): Show |
chr1 | 60419 | 76585 |
| a0004c0003t0009 | 0/0 | 2618 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2613): Show |
chr1 | 60419 | 76585 |
| a0004c0003t0010 | 0/0 | 2618 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2613): Show |
chr1 | 60419 | 76585 |
| a0004c0011t0003 | 0/0 | 2618 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2613): Show |
chr1 | 60419 | 76585 |
| a0005c0005t0001 | 1/0 | 2618 | 13 | 12 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2613): Show |
chr1 | 60419 | 76585 |
| a0005c0005t0005 | 0/0 | 2617 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2612): Show |
chr1 | 60419 | 76585 |
| a0005c0005t0011 | 0/0 | 2618 | 1 | 0 | 0 | 0 | 1 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2613): Show |
chr1 | 60419 | 76585 |
| a0006c0008t0005 | 0/0 | 2617 | 3 | 0 | 1 | 0 | 0 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2612): Show |
chr1 | 60419 | 76585 |
| a0007c0010t0001 | 0/0 | 2618 | 2 | 0 | 0 | 2 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2613): Show |
chr1 | 60419 | 76585 |
| a0008c0015t0001 | 0/0 | 2618 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2613): Show |
chr1 | 60419 | 76585 |
| a0009c0020t0001 | 0/0 | 2618 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2613): Show |
chr1 | 60419 | 76585 |
| a0010c0017t0002 | 0/0 | 2618 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2613): Show |
chr1 | 60419 | 76585 |
| a0011c0016t0002 | 0/0 | 2618 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | CCCAG others(2613): Show |
chr1 | 60419 | 76585 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 70 | 2 | 10 | 51 | 1 | 6 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0001c0001t0001g0017 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0001c0001t0013g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0001c0006t0002g0003 | 0/0 | 8 | 0 | 1 | 5 | 0 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0001c0006t0006g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0001c0009t0007g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0001c0009t0008g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0001c0012t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0001c0018t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0001c0019t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0002c0002t0002g0002 | 0/0 | 32 | 0 | 3 | 29 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0002c0002t0002g0008 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0002c0002t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0002c0002t0012g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0002c0014t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0003c0004t0003g0009 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0003c0004t0003g0012 | 0/0 | 3 | 2 | 0 | 0 | 1 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0003c0004t0003g0013 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0003c0004t0003g0019 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0003c0004t0003g0020 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0003c0004t0003g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0003c0007t0003g0005 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0003c0007t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0003c0013t0014g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0004c0003t0002g0004 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0004c0003t0002g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0004c0003t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0004c0003t0002g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0004c0003t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0004c0003t0004g0010 | 0/0 | 5 | 3 | 2 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0004c0003t0004g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0004c0003t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0004c0003t0009g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0004c0003t0010g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0004c0011t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0005c0005t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0005c0005t0001g0007 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0005c0005t0001g0011 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0005c0005t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0005c0005t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0005c0005t0005g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0005c0005t0011g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0006c0008t0005g0004 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0006c0008t0005g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0007c0010t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0008c0015t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0009c0020t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0010c0017t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| a0011c0016t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0004 | t0003 | g0019 | EUR | GBR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG00099 | hp2 | a0005 | c0005 | t0011 | g0016 | EUR | GBR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG00544 | hp1 | a0003 | c0007 | t0003 | g0005 | EAS | CHS | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG00639 | hp1 | a0002 | c0014 | t0002 | g0042 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG00642 | hp1 | a0005 | c0005 | t0005 | g0004 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG00738 | hp1 | a0001 | c0012 | t0001 | g0001 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG00741 | hp1 | a0008 | c0015 | t0001 | g0004 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG00741 | hp2 | a0003 | c0004 | t0003 | g0020 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG01106 | hp1 | a0004 | c0003 | t0002 | g0004 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG01106 | hp2 | a0004 | c0003 | t0002 | g0023 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG01109 | hp2 | a0004 | c0003 | t0004 | g0010 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG01167 | hp2 | a0003 | c0004 | t0003 | g0046 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG01243 | hp2 | a0004 | c0003 | t0010 | g0004 | AMR | PUR | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG01433 | hp1 | a0006 | c0008 | t0005 | g0034 | AMR | CLM | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG01433 | hp2 | a0004 | c0003 | t0004 | g0010 | AMR | CLM | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG01496 | hp2 | a0003 | c0004 | t0003 | g0009 | AMR | CLM | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG01515 | hp1 | a0004 | c0003 | t0002 | g0004 | EUR | IBS | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG01515 | hp2 | a0003 | c0004 | t0003 | g0019 | EUR | IBS | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG01891 | hp1 | a0005 | c0005 | t0001 | g0007 | AFR | ACB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG01891 | hp2 | a0003 | c0004 | t0003 | g0012 | AFR | ACB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG01928 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG01928 | hp2 | a0009 | c0020 | t0001 | g0041 | AMR | PEL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PEL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0008 | AMR | PEL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02083 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02145 | hp1 | a0005 | c0005 | t0001 | g0016 | AFR | ACB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02145 | hp2 | a0003 | c0004 | t0003 | g0009 | AFR | ACB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02148 | hp1 | a0001 | c0006 | t0002 | g0003 | AMR | PEL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02257 | hp1 | a0004 | c0011 | t0003 | g0009 | AFR | ACB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02257 | hp2 | a0005 | c0005 | t0001 | g0007 | AFR | ACB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02280 | hp1 | a0010 | c0017 | t0002 | g0022 | AFR | ACB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02293 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02523 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02572 | hp1 | a0005 | c0005 | t0001 | g0011 | AFR | GWD | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02572 | hp2 | a0003 | c0004 | t0003 | g0009 | AFR | GWD | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02615 | hp1 | a0004 | c0003 | t0009 | g0036 | AFR | GWD | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02615 | hp2 | a0004 | c0003 | t0004 | g0021 | AFR | GWD | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02622 | hp1 | a0005 | c0005 | t0001 | g0007 | AFR | GWD | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02622 | hp2 | a0004 | c0003 | t0004 | g0021 | AFR | GWD | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02630 | hp1 | a0005 | c0005 | t0001 | g0004 | AFR | GWD | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02630 | hp2 | a0005 | c0005 | t0001 | g0007 | AFR | GWD | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02738 | hp1 | a0001 | c0006 | t0002 | g0003 | SAS | PJL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02738 | hp2 | a0003 | c0004 | t0003 | g0020 | SAS | PJL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0025 | AFR | GWD | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02886 | hp2 | a0005 | c0005 | t0001 | g0007 | AFR | GWD | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02976 | hp1 | a0004 | c0003 | t0004 | g0047 | AFR | ESN | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02976 | hp2 | a0004 | c0003 | t0004 | g0010 | AFR | ESN | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG03017 | hp2 | a0001 | c0006 | t0002 | g0003 | SAS | PJL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG03098 | hp1 | a0001 | c0009 | t0008 | g0014 | AFR | MSL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG03098 | hp2 | a0004 | c0003 | t0004 | g0010 | AFR | MSL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG03139 | hp1 | a0005 | c0005 | t0001 | g0007 | AFR | ESN | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG03139 | hp2 | a0003 | c0004 | t0003 | g0009 | AFR | ESN | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG03195 | hp1 | a0004 | c0003 | t0004 | g0010 | AFR | ESN | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG03195 | hp2 | a0001 | c0009 | t0007 | g0035 | AFR | ESN | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG03239 | hp2 | a0003 | c0004 | t0003 | g0013 | SAS | PJL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG03486 | hp1 | a0005 | c0005 | t0001 | g0011 | AFR | MSL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | MSL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG03490 | hp1 | a0003 | c0007 | t0003 | g0045 | SAS | PJL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG03490 | hp2 | a0003 | c0004 | t0003 | g0013 | SAS | PJL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG03491 | hp1 | a0006 | c0008 | t0005 | g0004 | SAS | PJL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG03492 | hp1 | a0003 | c0004 | t0003 | g0013 | SAS | PJL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG03492 | hp2 | a0006 | c0008 | t0005 | g0004 | SAS | PJL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG03540 | hp1 | a0004 | c0003 | t0002 | g0015 | AFR | GWD | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG03540 | hp2 | a0005 | c0005 | t0001 | g0026 | AFR | GWD | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG03579 | hp2 | a0004 | c0003 | t0002 | g0024 | AFR | MSL | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG03831 | hp1 | a0004 | c0003 | t0002 | g0018 | SAS | BEB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG04184 | hp2 | a0003 | c0013 | t0014 | g0043 | SAS | BEB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18939 | hp1 | a0003 | c0007 | t0003 | g0005 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18939 | hp2 | a0001 | c0018 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18952 | hp1 | a0003 | c0007 | t0003 | g0005 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18956 | hp2 | a0001 | c0001 | t0013 | g0044 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18957 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18959 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18966 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18967 | hp1 | a0002 | c0002 | t0012 | g0039 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18968 | hp1 | a0007 | c0010 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18971 | hp1 | a0001 | c0006 | t0002 | g0003 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18974 | hp2 | a0001 | c0006 | t0002 | g0003 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18975 | hp2 | a0001 | c0006 | t0002 | g0003 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18979 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18987 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18987 | hp2 | a0007 | c0010 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18991 | hp1 | a0001 | c0006 | t0006 | g0003 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18998 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18998 | hp2 | a0001 | c0006 | t0002 | g0003 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19003 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19004 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19005 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19007 | hp2 | a0011 | c0016 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19011 | hp2 | a0003 | c0007 | t0003 | g0005 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19043 | hp1 | a0005 | c0005 | t0001 | g0011 | AFR | LWK | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19043 | hp2 | a0003 | c0004 | t0003 | g0012 | AFR | LWK | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19062 | hp1 | a0003 | c0007 | t0003 | g0005 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19067 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19070 | hp1 | a0003 | c0007 | t0003 | g0005 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19072 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19077 | hp2 | a0001 | c0006 | t0006 | g0003 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19078 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19078 | hp2 | a0001 | c0019 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19081 | hp1 | a0001 | c0006 | t0002 | g0003 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19082 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19083 | hp1 | a0003 | c0007 | t0003 | g0005 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19085 | hp2 | a0003 | c0007 | t0003 | g0005 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA20752 | hp1 | a0003 | c0004 | t0003 | g0012 | EUR | TSI | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA20905 | hp1 | a0004 | c0003 | t0002 | g0018 | SAS | GIH | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| HG02559 | hp2 | a0004 | c0003 | t0002 | g0015 | AFR | ACB | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| homoSapiens | grch38p0 | a0005 | c0005 | t0001 | g0011 | REF | REF | OR4F5_chr1_60419_76585 | OR4F5 | chr1 | 60419 | 76585 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:69134 | A | G | 1 | a0009 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.107A>G | p.Glu36Gly | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 167/2618 | 107/981 | 36/326 | chr1 | 69134 | |||
| chr1:69284 | C | T | 1 | a0010 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.257C>T | p.Ser86Phe | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 317/2618 | 257/981 | 86/326 | chr1 | 69284 | |||
| chr1:69355 | G | T | 1 | a0009 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.328G>T | p.Gly110Cys | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 388/2618 | 328/981 | 110/326 | chr1 | 69355 | |||
| chr1:69446 | T | C | 1 | a0011 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.419T>C | p.Ile140Thr | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 479/2618 | 419/981 | 140/326 | chr1 | 69446 | |||
| chr1:69448 | T | C | 1 | a0011 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.421T>C | p.Cys141Arg | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 481/2618 | 421/981 | 141/326 | chr1 | 69448 | |||
| chr1:69451 | A | G | 1 | a0011 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.424A>G | p.Lys142Glu | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 484/2618 | 424/981 | 142/326 | chr1 | 69451 | |||
| chr1:69452 | A | T | 1 | a0011 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.425A>T | p.Lys142Met | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 485/2618 | 425/981 | 142/326 | chr1 | 69452 | |||
| chr1:69454 | C | T | 1 | a0011 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.427C>T | p.Pro143Ser | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 487/2618 | 427/981 | 143/326 | chr1 | 69454 | |||
| chr1:69455 | C | T | 1 | a0011 | 1 | NA19007.hp2 | missense_variant | MODERATE | c.428C>T | p.Pro143Leu | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 488/2618 | 428/981 | 143/326 | chr1 | 69455 | |||
| chr1:69511 | A | G | 10 | a0001 a0002 a0003 others(7): Show |
200 | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(197): Show |
missense_variant | MODERATE | c.484A>G | p.Thr162Ala | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 544/2618 | 484/981 | 162/326 | chr1 | 69511 | |||
| chr1:69569 | T | C | 5 | a0002 a0003 a0004 others(2): Show |
88 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(85): Show |
missense_variant | MODERATE | c.542T>C | p.Leu181Pro | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 602/2618 | 542/981 | 181/326 | chr1 | 69569 | |||
| chr1:69590 | T | A | 1 | a0009 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.563T>A | p.Val188Asp | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 623/2618 | 563/981 | 188/326 | chr1 | 69590 | |||
| chr1:69610 | C | T | 1 | a0007 | 2 | NA18968.hp1 NA18987.hp2 |
missense_variant | MODERATE | c.583C>T | p.Leu195Phe | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 643/2618 | 583/981 | 195/326 | chr1 | 69610 | |||
| chr1:69745 | C | T | 1 | a0002 | 1 | HG00639.hp1 | stop_gained | HIGH | c.718C>T | p.Gln240* | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 778/2618 | 718/981 | 240/326 | chr1 | 69745 | |||
| chr1:69761 | A | T | 1 | a0006 | 3 | HG01433.hp1 HG03491.hp1 HG03492.hp2 |
missense_variant | MODERATE | c.734A>T | p.Asp245Val | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 794/2618 | 734/981 | 245/326 | chr1 | 69761 | |||
| chr1:69849 | G | A | 2 | a0002 a0011 |
42 | HG01928.hp1 HG01981.hp1 HG01993.hp1 others(39): Show |
stop_gained | HIGH | c.822G>A | p.Trp274* | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 882/2618 | 822/981 | 274/326 | chr1 | 69849 | |||
| chr1:69899 | T | A | 1 | a0008 | 1 | HG00741.hp1 | missense_variant | MODERATE | c.872T>A | p.Val291Glu | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 932/2618 | 872/981 | 291/326 | chr1 | 69899 | |||
| chr1:69968 | A | G | 1 | a0003 | 25 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(22): Show |
missense_variant | MODERATE | c.941A>G | p.Gln314Arg | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 1001/2618 | 941/981 | 314/326 | chr1 | 69968 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:69063 | T | C | 3 | a0003c0004 a0003c0007 a0004c0011 |
25 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(22): Show |
synonymous_variant | LOW | c.36T>C | p.Asn12Asn | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 96/2618 | 36/981 | 12/326 | chr1 | 69063 | |||
| chr1:69081 | G | C | 1 | a0001c0012 | 1 | HG00738.hp1 | synonymous_variant | LOW | c.54G>C | p.Thr18Thr | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 114/2618 | 54/981 | 18/326 | chr1 | 69081 | |||
| chr1:69270 | A | G | 6 | a0001c0001 a0001c0012 a0001c0018 others(3): Show |
98 | HG00544.hp2 HG00639.hp2 HG00642.hp2 others(95): Show |
synonymous_variant | LOW | c.243A>G | p.Ser81Ser | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 303/2618 | 243/981 | 81/326 | chr1 | 69270 | |||
| chr1:69369 | G | A | 2 | a0003c0004 a0004c0011 |
16 | HG00099.hp1 HG00741.hp2 HG01167.hp2 others(13): Show |
synonymous_variant | LOW | c.342G>A | p.Gln114Gln | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 402/2618 | 342/981 | 114/326 | chr1 | 69369 | |||
| chr1:69441 | A | C | 1 | a0011c0016 | 1 | NA19007.hp2 | synonymous_variant | LOW | c.414A>C | p.Ile138Ile | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 474/2618 | 414/981 | 138/326 | chr1 | 69441 | |||
| chr1:69450 | C | T | 1 | a0011c0016 | 1 | NA19007.hp2 | synonymous_variant | LOW | c.423C>T | p.Cys141Cys | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 483/2618 | 423/981 | 141/326 | chr1 | 69450 | |||
| chr1:69453 | G | A | 9 | a0001c0006 a0002c0002 a0002c0014 others(6): Show |
97 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(94): Show |
synonymous_variant | LOW | c.426G>A | p.Lys142Lys | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 486/2618 | 426/981 | 142/326 | chr1 | 69453 | |||
| chr1:69534 | T | C | 1 | a0001c0018 | 1 | NA18939.hp2 | synonymous_variant | LOW | c.507T>C | p.His169His | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 567/2618 | 507/981 | 169/326 | chr1 | 69534 | |||
| chr1:69552 | G | C | 10 | a0001c0006 a0002c0002 a0002c0014 others(7): Show |
98 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(95): Show |
synonymous_variant | LOW | c.525G>C | p.Ala175Ala | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 585/2618 | 525/981 | 175/326 | chr1 | 69552 | |||
| chr1:69735 | A | G | 1 | a0003c0007 | 9 | HG00544.hp1 HG03490.hp1 NA18939.hp1 others(6): Show |
synonymous_variant | LOW | c.708A>G | p.Leu236Leu | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 768/2618 | 708/981 | 236/326 | chr1 | 69735 | |||
| chr1:69876 | A | G | 1 | a0001c0019 | 1 | NA19078.hp2 | synonymous_variant | LOW | c.849A>G | p.Lys283Lys | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 909/2618 | 849/981 | 283/326 | chr1 | 69876 | |||
| chr1:69897 | T | C | 7 | a0001c0001 a0001c0012 a0001c0018 others(4): Show |
99 | HG00544.hp2 HG00639.hp2 HG00642.hp2 others(96): Show |
synonymous_variant | LOW | c.870T>C | p.Ser290Ser | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 930/2618 | 870/981 | 290/326 | chr1 | 69897 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:65529 | C | T | 5 | a0001c0001t0013 a0003c0004t0003 a0003c0007t0003 others(2): Show |
27 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(24): Show |
5_prime_UTR_variant | MODIFIER | c.-36C>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/3 | 36 | chr1 | 65529 | ||||||
| chr1:65552 | G | A | 4 | a0001c0001t0013 a0003c0004t0003 a0003c0007t0003 others(1): Show |
26 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(23): Show |
5_prime_UTR_variant | MODIFIER | c.-13G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/3 | 13 | chr1 | 65552 | ||||||
| chr1:70246 | A | G | 1 | a0003c0013t0014 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*238A>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 238 | chr1 | 70246 | ||||||
| chr1:70300 | C | T | 4 | a0003c0004t0003 a0003c0007t0003 a0003c0013t0014 others(1): Show |
26 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*292C>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 292 | chr1 | 70300 | ||||||
| chr1:70302 | C | T | 1 | a0003c0013t0014 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*294C>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 294 | chr1 | 70302 | ||||||
| chr1:70317 | G | A | 1 | a0001c0009t0007 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*309G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 309 | chr1 | 70317 | ||||||
| chr1:70351 | TA | T | 3 | a0002c0002t0012 a0005c0005t0005 a0006c0008t0005 |
5 | HG00642.hp1 HG01433.hp1 HG03491.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*352delA | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 352 | INFO_REALIGN_3_PRIME | chr1 | 70351 | |||||
| chr1:70352 | A | T | 1 | a0001c0001t0001 | 2 | HG01109.hp1 HG01243.hp1 |
3_prime_UTR_variant | MODIFIER | c.*344A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 344 | chr1 | 70352 | ||||||
| chr1:70499 | C | T | 3 | a0003c0004t0003 a0003c0007t0003 a0004c0011t0003 |
25 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*491C>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 491 | chr1 | 70499 | ||||||
| chr1:70534 | T | C | 1 | a0001c0006t0006 | 2 | NA18991.hp1 NA19077.hp2 |
3_prime_UTR_variant | MODIFIER | c.*526T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 526 | chr1 | 70534 | ||||||
| chr1:70594 | G | C | 1 | a0001c0009t0008 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*586G>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 586 | chr1 | 70594 | ||||||
| chr1:70604 | G | A | 15 | a0001c0006t0002 a0001c0006t0006 a0002c0002t0002 others(12): Show |
98 | HG00099.hp1 HG00544.hp1 HG00639.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*596G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 596 | chr1 | 70604 | ||||||
| chr1:70806 | G | A | 1 | a0004c0003t0009 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*798G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 798 | chr1 | 70806 | ||||||
| chr1:70917 | C | T | 2 | a0004c0003t0004 a0004c0003t0010 |
9 | HG01109.hp2 HG01243.hp2 HG01433.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*909C>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 909 | chr1 | 70917 | ||||||
| chr1:71192 | A | G | 1 | a0003c0013t0014 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1184A>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 1184 | chr1 | 71192 | ||||||
| chr1:71298 | G | A | 1 | a0005c0005t0011 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1290G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 1290 | chr1 | 71298 | ||||||
| chr1:71381 | T | C | 3 | a0003c0004t0003 a0003c0007t0003 a0004c0011t0003 |
25 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1373T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 1373 | chr1 | 71381 | ||||||
| chr1:71449 | G | C | 1 | a0004c0003t0010 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1441G>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 3/3 | 1441 | chr1 | 71449 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:65451 | A | G | 3 | a0004c0003t0004g0010 a0004c0003t0004g0021 a0004c0003t0004g0047 |
8 | HG01109.hp2 HG01433.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-46+18A>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 1/2 | chr1 | 65451 | |||||||
| chr1:65591 | C | T | 11 | a0001c0001t0013g0044 a0003c0004t0003g0009 a0003c0004t0003g0012 others(8): Show |
27 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.9+18C>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 65591 | |||||||
| chr1:65649 | G | A | 1 | a0003c0013t0014g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.9+76G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 65649 | |||||||
| chr1:65745 | A | G | 11 | a0001c0001t0013g0044 a0003c0004t0003g0009 a0003c0004t0003g0012 others(8): Show |
27 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.9+172A>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 65745 | |||||||
| chr1:65797 | T | C | 11 | a0001c0001t0013g0044 a0003c0004t0003g0009 a0003c0004t0003g0012 others(8): Show |
27 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.9+224T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 65797 | |||||||
| chr1:65872 | T | G | 1 | a0003c0013t0014g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.9+299T>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 65872 | |||||||
| chr1:65898 | T | C | 2 | a0001c0001t0001g0014 a0001c0009t0008g0014 |
2 | HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.9+325T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 65898 | |||||||
| chr1:65974 | A | G | 1 | a0002c0014t0002g0042 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.9+401A>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 65974 | |||||||
| chr1:66008 | C | G | 11 | a0001c0001t0013g0044 a0003c0004t0003g0009 a0003c0004t0003g0012 others(8): Show |
27 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.9+435C>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66008 | |||||||
| chr1:66131 | C | G | 1 | a0009c0020t0001g0041 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.9+558C>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66131 | |||||||
| chr1:66160 | T | TTA | 1 | a0001c0001t0001g0006 | 7 | NA18962.hp2 NA18979.hp2 NA19005.hp1 others(4): Show |
intron_variant | MODIFIER | c.9+601_9+602dupAT | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66160 | ||||||
| chr1:66162 | A | T | 11 | a0001c0001t0013g0044 a0003c0004t0003g0009 a0003c0004t0003g0012 others(8): Show |
27 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.9+589A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66162 | |||||||
| chr1:66176 | T | A | 5 | a0002c0014t0002g0042 a0004c0003t0002g0015 a0004c0003t0002g0023 others(2): Show |
6 | HG00639.hp1 HG01106.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.9+603T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66176 | |||||||
| chr1:66214 | A | T | 1 | a0001c0001t0001g0040 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.9+641A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66214 | |||||||
| chr1:66217 | T | C | 1 | a0002c0002t0002g0025 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.9+644T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66217 | |||||||
| chr1:66218 | A | T | 1 | a0002c0002t0002g0025 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.9+645A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66218 | |||||||
| chr1:66219 | A | T | 5 | a0002c0002t0002g0002 a0002c0002t0002g0008 a0002c0002t0002g0038 others(2): Show |
41 | HG01928.hp1 HG01981.hp1 HG01993.hp1 others(38): Show |
intron_variant | MODIFIER | c.9+646A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66219 | |||||||
| chr1:66220 | TATATATT others(37): Show |
T | 1 | a0002c0002t0002g0038 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.9+653_9+696delTTAT others(40): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66220 | ||||||
| chr1:66221 | A | AT | 7 | a0003c0004t0003g0009 a0003c0004t0003g0012 a0003c0004t0003g0013 others(4): Show |
16 | HG00099.hp1 HG00741.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.9+649dupT | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66221 | ||||||
| chr1:66221 | ATATATTA others(49): Show |
A | 1 | a0004c0003t0002g0024 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.9+667_9+722delTTAT others(52): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66221 | ||||||
| chr1:66222 | T | TTATATAT others(205): Show |
1 | a0003c0004t0003g0046 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.9+649_9+650insTATA others(208): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66222 | |||||||
| chr1:66224 | TATTATAT others(44): Show |
T | 1 | a0004c0003t0002g0004 | 2 | HG01106.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.9+659_9+709delAATA others(47): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66224 | ||||||
| chr1:66225 | A | T | 1 | a0002c0002t0002g0025 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.9+652A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66225 | |||||||
| chr1:66225 | AT | A | 10 | a0001c0001t0013g0044 a0003c0004t0003g0009 a0003c0004t0003g0012 others(7): Show |
26 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.9+654delT | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66225 | ||||||
| chr1:66226 | T | A | 1 | a0004c0003t0009g0036 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.9+653T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66226 | |||||||
| chr1:66227 | T | A | 1 | a0003c0004t0003g0046 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.9+654T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66227 | |||||||
| chr1:66231 | TAATATAT others(34): Show |
T | 2 | a0001c0006t0002g0003 a0001c0006t0006g0003 |
10 | HG02148.hp1 HG02738.hp1 HG03017.hp2 others(7): Show |
intron_variant | MODIFIER | c.9+659_9+699delAATA others(37): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66231 | |||||||
| chr1:66233 | A | T | 1 | a0002c0002t0002g0025 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.9+660A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66233 | |||||||
| chr1:66236 | T | C | 1 | a0002c0002t0002g0025 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.9+663T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66236 | |||||||
| chr1:66238 | T | A | 1 | a0001c0001t0001g0001 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.9+665T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66238 | |||||||
| chr1:66238 | TATTATAT others(30): Show |
T | 14 | a0002c0002t0002g0002 a0002c0002t0002g0008 a0002c0002t0012g0039 others(11): Show |
56 | HG00639.hp1 HG01106.hp2 HG01109.hp2 others(53): Show |
intron_variant | MODIFIER | c.9+710_9+746delTATA others(33): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66238 | ||||||
| chr1:66240 | T | A | 1 | a0009c0020t0001g0041 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.9+667T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66240 | |||||||
| chr1:66244 | AT | A | 2 | a0002c0002t0002g0025 a0009c0020t0001g0041 |
2 | HG01928.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.9+673delT | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66244 | ||||||
| chr1:66246 | T | A | 1 | a0009c0020t0001g0041 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.9+673T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66246 | |||||||
| chr1:66249 | A | ATATATAA others(170): Show |
1 | a0003c0007t0003g0005 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.9+678_9+679insTATA others(173): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66249 | ||||||
| chr1:66249 | A | ATATATAA others(172): Show |
2 | a0001c0001t0013g0044 a0003c0007t0003g0005 |
7 | HG00544.hp1 NA18939.hp1 NA18956.hp2 others(4): Show |
intron_variant | MODIFIER | c.9+678_9+679insTATA others(175): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66249 | ||||||
| chr1:66249 | A | ATATATAA others(186): Show |
1 | a0003c0007t0003g0045 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.9+678_9+679insTATA others(189): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66249 | ||||||
| chr1:66249 | A | ATATATAA others(206): Show |
1 | a0003c0004t0003g0020 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.9+678_9+679insTATA others(209): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66249 | ||||||
| chr1:66249 | A | ATATATTA others(188): Show |
1 | a0003c0004t0003g0020 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.9+678_9+679insTATT others(191): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66249 | ||||||
| chr1:66249 | A | ATATATTA others(208): Show |
1 | a0003c0004t0003g0012 | 2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.9+678_9+679insTATT others(211): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66249 | ||||||
| chr1:66249 | A | ATATATTA others(205): Show |
1 | a0003c0004t0003g0019 | 2 | HG00099.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.9+678_9+679insTATT others(208): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66249 | ||||||
| chr1:66249 | A | ATATATTA others(206): Show |
2 | a0003c0004t0003g0009 a0003c0004t0003g0012 |
2 | HG02145.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.9+678_9+679insTATT others(209): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66249 | ||||||
| chr1:66249 | A | ATATATTA others(215): Show |
2 | a0003c0004t0003g0013 a0004c0011t0003g0009 |
3 | HG02257.hp1 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.9+678_9+679insTATT others(218): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66249 | ||||||
| chr1:66249 | A | ATATATTA others(215): Show |
1 | a0003c0004t0003g0013 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.9+678_9+679insTATT others(218): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66249 | ||||||
| chr1:66249 | A | ATATATTA others(224): Show |
1 | a0003c0004t0003g0009 | 2 | HG01496.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.9+678_9+679insTATT others(227): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66249 | ||||||
| chr1:66249 | A | ATATATTA others(242): Show |
1 | a0003c0004t0003g0009 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.9+678_9+679insTATT others(245): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66249 | ||||||
| chr1:66252 | A | ATATATAT others(168): Show |
1 | a0003c0007t0003g0005 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.9+685_9+686insTATA others(171): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66252 | ||||||
| chr1:66252 | A | T | 9 | a0001c0001t0013g0044 a0003c0004t0003g0009 a0003c0004t0003g0012 others(6): Show |
24 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.9+679A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66252 | |||||||
| chr1:66258 | A | G | 1 | a0003c0004t0003g0046 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.9+685A>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66258 | |||||||
| chr1:66258 | A | T | 1 | a0009c0020t0001g0041 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.9+685A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66258 | |||||||
| chr1:66258 | AATATAAA others(50): Show |
A | 1 | a0004c0003t0004g0010 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.9+702_9+758delAATT others(53): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66258 | ||||||
| chr1:66259 | A | T | 1 | a0002c0002t0002g0025 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.9+686A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66259 | |||||||
| chr1:66264 | A | ATAT | 9 | a0001c0001t0013g0044 a0003c0004t0003g0009 a0003c0004t0003g0012 others(6): Show |
25 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.9+691_9+692insTAT | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66264 | |||||||
| chr1:66264 | A | ATATATTA others(243): Show |
1 | a0003c0013t0014g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.9+691_9+692insTATA others(246): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66264 | |||||||
| chr1:66275 | A | T | 6 | a0001c0006t0002g0003 a0001c0006t0006g0003 a0002c0002t0002g0025 others(3): Show |
14 | HG01167.hp2 HG01928.hp2 HG02148.hp1 others(11): Show |
intron_variant | MODIFIER | c.9+702A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66275 | |||||||
| chr1:66276 | A | T | 10 | a0001c0001t0013g0044 a0003c0004t0003g0009 a0003c0004t0003g0012 others(7): Show |
26 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.9+703A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66276 | |||||||
| chr1:66277 | T | A | 10 | a0001c0001t0013g0044 a0003c0004t0003g0009 a0003c0004t0003g0012 others(7): Show |
26 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.9+704T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66277 | |||||||
| chr1:66279 | A | T | 2 | a0003c0004t0003g0046 a0009c0020t0001g0041 |
2 | HG01167.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.9+706A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66279 | |||||||
| chr1:66289 | AT | A | 10 | a0001c0001t0013g0044 a0003c0004t0003g0009 a0003c0004t0003g0012 others(7): Show |
26 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.9+717delT | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66289 | |||||||
| chr1:66294 | T | A | 2 | a0003c0004t0003g0046 a0009c0020t0001g0041 |
2 | HG01167.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.9+721T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66294 | |||||||
| chr1:66295 | A | T | 2 | a0003c0004t0003g0046 a0009c0020t0001g0041 |
2 | HG01167.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.9+722A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66295 | |||||||
| chr1:66300 | A | ATAT | 10 | a0001c0001t0013g0044 a0003c0004t0003g0009 a0003c0004t0003g0012 others(7): Show |
26 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.9+727_9+728insTAT | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66300 | |||||||
| chr1:66300 | A | ATTATATA others(5): Show |
1 | a0009c0020t0001g0041 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.9+727_9+728insTTAT others(8): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66300 | |||||||
| chr1:66301 | A | T | 1 | a0003c0007t0003g0045 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.9+728A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66301 | |||||||
| chr1:66312 | A | T | 11 | a0001c0001t0013g0044 a0003c0004t0003g0009 a0003c0004t0003g0012 others(8): Show |
27 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.9+739A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66312 | |||||||
| chr1:66320 | A | T | 1 | a0001c0001t0001g0037 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.9+747A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66320 | |||||||
| chr1:66321 | A | ATATAATA others(24): Show |
1 | a0001c0001t0001g0037 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.9+748_9+749insTATA others(27): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66321 | |||||||
| chr1:66325 | TAATATAT others(95): Show |
T | 2 | a0005c0005t0001g0016 a0005c0005t0011g0016 |
2 | HG00099.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.9+763_9+864del | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66325 | ||||||
| chr1:66331 | A | C | 5 | a0002c0014t0002g0042 a0004c0003t0002g0015 a0004c0003t0002g0023 others(2): Show |
6 | HG00639.hp1 HG01106.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.9+758A>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66331 | |||||||
| chr1:66335 | T | A | 2 | a0003c0004t0003g0046 a0009c0020t0001g0041 |
2 | HG01167.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.9+762T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66335 | |||||||
| chr1:66336 | T | A | 1 | a0003c0004t0003g0046 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.9+763T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66336 | |||||||
| chr1:66339 | T | TAATATAT others(41): Show |
1 | a0003c0004t0003g0046 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.9+766_9+767insAATA others(44): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66339 | |||||||
| chr1:66339 | T | TCATATAA others(2): Show |
3 | a0001c0001t0013g0044 a0003c0007t0003g0005 a0003c0007t0003g0045 |
10 | HG00544.hp1 HG03490.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.9+766_9+767insCATA others(5): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66339 | |||||||
| chr1:66339 | T | TCATATAA others(7): Show |
6 | a0003c0004t0003g0009 a0003c0004t0003g0012 a0003c0004t0003g0013 others(3): Show |
15 | HG00099.hp1 HG00741.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.9+766_9+767insCATA others(10): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66339 | |||||||
| chr1:66356 | T | A | 10 | a0001c0001t0013g0044 a0003c0004t0003g0009 a0003c0004t0003g0012 others(7): Show |
26 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.9+783T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66356 | |||||||
| chr1:66356 | T | TATAATAT others(7): Show |
1 | a0003c0013t0014g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.9+785_9+786insAATA others(10): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66356 | ||||||
| chr1:66364 | AAATATAA others(14): Show |
A | 1 | a0004c0003t0002g0004 | 2 | HG01106.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.9+805_9+825delAATT others(17): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66364 | ||||||
| chr1:66370 | A | ATTATTAT others(159): Show |
1 | a0009c0020t0001g0041 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.9+797_9+798insTTAT others(162): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66370 | |||||||
| chr1:66377 | A | ATTT | 11 | a0001c0001t0013g0044 a0003c0004t0003g0009 a0003c0004t0003g0012 others(8): Show |
27 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.9+804_9+805insTTT | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66377 | |||||||
| chr1:66378 | A | T | 12 | a0001c0001t0013g0044 a0003c0004t0003g0009 a0003c0004t0003g0012 others(9): Show |
28 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.9+805A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66378 | |||||||
| chr1:66381 | T | A | 4 | a0004c0003t0004g0010 a0004c0003t0004g0021 a0004c0003t0004g0047 others(1): Show |
9 | HG01109.hp2 HG01243.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.9+808T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66381 | |||||||
| chr1:66381 | TATATA | T | 3 | a0001c0001t0001g0014 a0001c0009t0008g0014 a0004c0003t0002g0023 |
3 | HG01106.hp2 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.9+819_9+823delATAT others(1): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66381 | ||||||
| chr1:66430 | T | A | 1 | a0005c0005t0001g0026 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.9+857T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66430 | |||||||
| chr1:66434 | T | A | 1 | a0001c0001t0001g0027 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.9+861T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66434 | |||||||
| chr1:66435 | A | T | 1 | a0001c0001t0001g0027 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.9+862A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66435 | |||||||
| chr1:66435 | ATT | A | 5 | a0002c0014t0002g0042 a0004c0003t0002g0015 a0004c0003t0002g0023 others(2): Show |
6 | HG00639.hp1 HG01106.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.9+863_9+864delTT | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66435 | |||||||
| chr1:66436 | T | A | 1 | a0001c0001t0001g0027 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.9+863T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66436 | |||||||
| chr1:66438 | ATATTATA others(12): Show |
A | 1 | a0001c0001t0001g0028 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.9+884_9+902delTTAT others(15): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66438 | ||||||
| chr1:66442 | T | A | 1 | a0009c0020t0001g0041 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.9+869T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66442 | |||||||
| chr1:66442 | T | TCTATATA | 11 | a0001c0001t0013g0044 a0003c0004t0003g0009 a0003c0004t0003g0012 others(8): Show |
27 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.9+869_9+870insCTAT others(3): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66442 | |||||||
| chr1:66457 | T | A | 4 | a0004c0003t0004g0010 a0004c0003t0004g0021 a0004c0003t0004g0047 others(1): Show |
9 | HG01109.hp2 HG01243.hp2 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.9+884T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66457 | |||||||
| chr1:66461 | T | A | 1 | a0001c0001t0001g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.9+888T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66461 | |||||||
| chr1:66461 | T | TATATAAT others(39): Show |
1 | a0001c0001t0001g0033 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.9+933_9+934insAATA others(42): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66461 | ||||||
| chr1:66466 | A | G | 2 | a0001c0001t0001g0014 a0001c0009t0008g0014 |
2 | HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.9+893A>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66466 | |||||||
| chr1:66479 | TATTTATA others(1): Show |
T | 2 | a0004c0003t0002g0018 a0004c0003t0009g0036 |
3 | HG02615.hp1 HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.9+908_9+915delTTTA others(4): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66479 | ||||||
| chr1:66480 | AT | A | 3 | a0001c0001t0013g0044 a0003c0007t0003g0005 a0003c0007t0003g0045 |
10 | HG00544.hp1 HG03490.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.9+910delT | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66480 | ||||||
| chr1:66481 | T | TTATAGAA others(75): Show |
1 | a0009c0020t0001g0041 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.9+909_9+910insATAG others(78): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66481 | ||||||
| chr1:66488 | A | T | 2 | a0004c0003t0002g0018 a0004c0003t0009g0036 |
3 | HG02615.hp1 HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.9+915A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66488 | |||||||
| chr1:66502 | T | G | 1 | a0004c0003t0009g0036 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.9+929T>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66502 | |||||||
| chr1:66507 | T | A | 16 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0017 others(13): Show |
93 | HG00544.hp2 HG00639.hp2 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.9+934T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66507 | |||||||
| chr1:66521 | T | TATATA | 11 | a0001c0001t0013g0044 a0003c0004t0003g0009 a0003c0004t0003g0012 others(8): Show |
27 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.9+954_9+958dupATAT others(1): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66521 | ||||||
| chr1:66525 | T | A | 1 | a0001c0001t0001g0017 | 2 | HG02280.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.9+952T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66525 | |||||||
| chr1:66572 | G | GTACTATA others(5): Show |
10 | a0001c0001t0013g0044 a0003c0004t0003g0009 a0003c0004t0003g0012 others(7): Show |
25 | HG00544.hp1 HG00741.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.9+1001_9+1002insCT others(10): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66572 | ||||||
| chr1:66572 | GTA | G | 1 | a0003c0004t0003g0019 | 2 | HG00099.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.9+1002_9+1003delTA | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66572 | ||||||
| chr1:66577 | A | AATATATT | 10 | a0001c0001t0013g0044 a0003c0004t0003g0009 a0003c0004t0003g0012 others(7): Show |
25 | HG00544.hp1 HG00741.hp2 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.9+1004_9+1005insAT others(5): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66577 | |||||||
| chr1:66577 | A | C | 1 | a0003c0004t0003g0019 | 2 | HG00099.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.9+1004A>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66577 | |||||||
| chr1:66598 | T | A | 1 | a0006c0008t0005g0034 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.9+1025T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66598 | |||||||
| chr1:66598 | T | TTATATAT others(10): Show |
1 | a0010c0017t0002g0022 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.9+1039_9+1055dupAA others(15): Show |
OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr1 | 66598 | ||||||
| chr1:66605 | T | A | 3 | a0001c0001t0013g0044 a0003c0007t0003g0005 a0003c0007t0003g0045 |
10 | HG00544.hp1 HG03490.hp1 NA18939.hp1 others(7): Show |
intron_variant | MODIFIER | c.9+1032T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66605 | |||||||
| chr1:66667 | T | C | 1 | a0002c0002t0012g0039 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.9+1094T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66667 | |||||||
| chr1:66668 | G | A | 1 | a0002c0002t0012g0039 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.9+1095G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66668 | |||||||
| chr1:66669 | A | C | 1 | a0002c0002t0012g0039 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.9+1096A>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66669 | |||||||
| chr1:66670 | A | T | 1 | a0002c0002t0012g0039 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.9+1097A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66670 | |||||||
| chr1:66675 | T | G | 1 | a0002c0002t0012g0039 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.9+1102T>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66675 | |||||||
| chr1:66677 | T | G | 1 | a0002c0002t0012g0039 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.9+1104T>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66677 | |||||||
| chr1:66678 | A | T | 1 | a0002c0002t0012g0039 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.9+1105A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66678 | |||||||
| chr1:66679 | C | T | 1 | a0002c0002t0012g0039 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.9+1106C>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66679 | |||||||
| chr1:66737 | G | A | 1 | a0009c0020t0001g0041 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.9+1164G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66737 | |||||||
| chr1:66795 | T | A | 11 | a0001c0001t0013g0044 a0003c0004t0003g0009 a0003c0004t0003g0012 others(8): Show |
26 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.9+1222T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66795 | |||||||
| chr1:66814 | A | G | 11 | a0001c0001t0013g0044 a0003c0004t0003g0009 a0003c0004t0003g0012 others(8): Show |
27 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.9+1241A>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66814 | |||||||
| chr1:66861 | C | T | 5 | a0002c0014t0002g0042 a0004c0003t0002g0015 a0004c0003t0002g0023 others(2): Show |
6 | HG00639.hp1 HG01106.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.9+1288C>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66861 | |||||||
| chr1:66876 | T | G | 8 | a0002c0002t0002g0002 a0002c0002t0002g0008 a0002c0002t0002g0025 others(5): Show |
45 | HG01928.hp1 HG01981.hp1 HG01993.hp1 others(42): Show |
intron_variant | MODIFIER | c.9+1303T>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 66876 | |||||||
| chr1:67181 | A | G | 5 | a0002c0014t0002g0042 a0004c0003t0002g0015 a0004c0003t0002g0023 others(2): Show |
6 | HG00639.hp1 HG01106.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.9+1608A>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67181 | |||||||
| chr1:67184 | G | A | 2 | a0003c0013t0014g0043 a0009c0020t0001g0041 |
2 | HG01928.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.9+1611G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67184 | |||||||
| chr1:67223 | C | A | 1 | a0009c0020t0001g0041 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.9+1650C>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67223 | |||||||
| chr1:67224 | G | A | 1 | a0004c0003t0004g0021 | 2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.9+1651G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67224 | |||||||
| chr1:67242 | A | C | 12 | a0001c0001t0013g0044 a0003c0004t0003g0009 a0003c0004t0003g0012 others(9): Show |
28 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.9+1669A>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67242 | |||||||
| chr1:67314 | A | C | 1 | a0003c0013t0014g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10-1723A>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67314 | |||||||
| chr1:67400 | G | A | 1 | a0003c0013t0014g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10-1637G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67400 | |||||||
| chr1:67437 | A | T | 1 | a0001c0001t0001g0032 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.10-1600A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67437 | |||||||
| chr1:67448 | T | A | 10 | a0001c0001t0013g0044 a0003c0004t0003g0009 a0003c0004t0003g0012 others(7): Show |
26 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.10-1589T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67448 | |||||||
| chr1:67598 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.10-1439G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67598 | |||||||
| chr1:67605 | T | C | 12 | a0001c0001t0013g0044 a0003c0004t0003g0009 a0003c0004t0003g0012 others(9): Show |
28 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.10-1432T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67605 | |||||||
| chr1:67631 | G | C | 1 | a0004c0003t0002g0023 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.10-1406G>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67631 | |||||||
| chr1:67711 | C | T | 2 | a0005c0005t0001g0007 a0005c0005t0001g0026 |
7 | HG01891.hp1 HG02257.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.10-1326C>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67711 | |||||||
| chr1:67744 | G | A | 3 | a0003c0004t0003g0019 a0003c0004t0003g0020 a0003c0004t0003g0046 |
5 | HG00099.hp1 HG00741.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.10-1293G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67744 | |||||||
| chr1:67861 | G | A | 1 | a0003c0004t0003g0012 | 3 | HG01891.hp2 NA19043.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.10-1176G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67861 | |||||||
| chr1:67897 | GAGTTAAA others(429): Show |
G | 1 | a0003c0013t0014g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10-1139_10-704del | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67897 | |||||||
| chr1:67942 | A | C | 2 | a0001c0001t0001g0014 a0001c0009t0008g0014 |
2 | HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.10-1095A>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 67942 | |||||||
| chr1:68082 | T | C | 2 | a0006c0008t0005g0004 a0006c0008t0005g0034 |
3 | HG01433.hp1 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.10-955T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68082 | |||||||
| chr1:68120 | G | T | 1 | a0001c0001t0001g0031 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.10-917G>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68120 | |||||||
| chr1:68179 | A | T | 6 | a0002c0002t0002g0002 a0002c0002t0002g0008 a0002c0002t0002g0025 others(3): Show |
42 | HG01928.hp1 HG01981.hp1 HG01993.hp1 others(39): Show |
intron_variant | MODIFIER | c.10-858A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68179 | |||||||
| chr1:68306 | C | T | 10 | a0003c0004t0003g0009 a0003c0004t0003g0012 a0003c0004t0003g0013 others(7): Show |
26 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.10-731C>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68306 | |||||||
| chr1:68316 | T | C | 1 | a0009c0020t0001g0041 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.10-721T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68316 | |||||||
| chr1:68334 | T | C | 1 | a0003c0013t0014g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10-703T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68334 | |||||||
| chr1:68336 | A | C | 1 | a0003c0013t0014g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10-701A>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68336 | |||||||
| chr1:68338 | T | C | 1 | a0003c0013t0014g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10-699T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68338 | |||||||
| chr1:68340 | G | C | 1 | a0003c0013t0014g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10-697G>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68340 | |||||||
| chr1:68341 | G | C | 1 | a0003c0013t0014g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10-696G>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68341 | |||||||
| chr1:68347 | T | A | 1 | a0003c0013t0014g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10-690T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68347 | |||||||
| chr1:68387 | G | C | 9 | a0003c0004t0003g0009 a0003c0004t0003g0012 a0003c0004t0003g0013 others(6): Show |
25 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.10-650G>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68387 | |||||||
| chr1:68407 | A | G | 9 | a0003c0004t0003g0009 a0003c0004t0003g0012 a0003c0004t0003g0013 others(6): Show |
25 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.10-630A>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68407 | |||||||
| chr1:68547 | T | C | 10 | a0003c0004t0003g0009 a0003c0004t0003g0012 a0003c0004t0003g0013 others(7): Show |
26 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.10-490T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68547 | |||||||
| chr1:68555 | T | C | 3 | a0003c0004t0003g0019 a0003c0004t0003g0020 a0003c0004t0003g0046 |
5 | HG00099.hp1 HG00741.hp2 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.10-482T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68555 | |||||||
| chr1:68562 | T | G | 1 | a0003c0004t0003g0013 | 3 | HG03239.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.10-475T>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68562 | |||||||
| chr1:68596 | T | C | 1 | a0004c0003t0002g0024 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.10-441T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68596 | |||||||
| chr1:68596 | T | G | 1 | a0002c0002t0002g0008 | 6 | HG01981.hp1 HG01993.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.10-441T>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68596 | |||||||
| chr1:68616 | T | C | 1 | a0003c0013t0014g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10-421T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68616 | |||||||
| chr1:68635 | A | G | 1 | a0001c0001t0001g0031 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.10-402A>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68635 | |||||||
| chr1:68749 | A | G | 1 | a0004c0003t0004g0047 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.10-288A>G | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68749 | |||||||
| chr1:68777 | C | T | 1 | a0002c0014t0002g0042 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.10-260C>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68777 | |||||||
| chr1:68849 | C | T | 1 | a0003c0013t0014g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10-188C>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68849 | |||||||
| chr1:68889 | C | T | 1 | a0001c0009t0007g0035 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.10-148C>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68889 | |||||||
| chr1:68894 | T | C | 1 | a0003c0013t0014g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10-143T>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68894 | |||||||
| chr1:68896 | G | A | 60 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0014 others(57): Show |
211 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(208): Show |
intron_variant | MODIFIER | c.10-141G>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68896 | |||||||
| chr1:68905 | T | A | 2 | a0003c0007t0003g0005 a0003c0007t0003g0045 |
9 | HG00544.hp1 HG03490.hp1 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.10-132T>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68905 | |||||||
| chr1:68934 | A | C | 9 | a0003c0004t0003g0009 a0003c0004t0003g0012 a0003c0004t0003g0013 others(6): Show |
25 | HG00099.hp1 HG00544.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.10-103A>C | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68934 | |||||||
| chr1:68945 | A | T | 1 | a0003c0013t0014g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.10-92A>T | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 68945 | |||||||
| chr1:69008 | C | A | 1 | a0009c0020t0001g0041 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.10-29C>A | OR4F5 | ENSG00000186092.7 | transcript | ENST00000641515.2 | protein_coding | 2/2 | chr1 | 69008 |