Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 57231 |
| ensemblid | ENSG00000135317.14 |
| hgncid | 14977 |
| symbol | SNX14 |
| name | sorting nexin 14 |
| refseq_nuc | NM_153816.6 |
| refseq_prot | NP_722523.1 |
| ensembl_nuc | ENST00000314673.8 |
| ensembl_prot | ENSP00000313121.3 |
| mane_status | MANE Select |
| chr | chr6 |
| start | 85505496 |
| end | 85593858 |
| strand | - |
| ver | v1.2 |
| region | chr6:85505496-85593858 |
| region5000 | chr6:85500496-85598858 |
| regionname0 | SNX14_chr6_85505496_85593858 |
| regionname5000 | SNX14_chr6_85500496_85598858 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 946 | 354 | 89 | 56 | 164 | 10 | 34 | 128 | SNX14_chr6_85500496_85598858 | SNX14 | MVPWV others(941): Show |
chr6 | 85500496 | 85598858 |
| a0002 | 0/1 | 946 | 5 | 0 | 2 | 0 | 2 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | MVPWV others(941): Show |
chr6 | 85500496 | 85598858 |
| a0003 | 0/0 | 946 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | MVPWV others(941): Show |
chr6 | 85500496 | 85598858 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2838 | 347 | 84 | 56 | 163 | 9 | 34 | SNX14_chr6_85500496_85598858 | SNX14 | ATGGT others(2833): Show |
chr6 | 85500496 | 85598858 | ||
| a0001c0003 | 0/0 | 2838 | 4 | 4 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | ATGGT others(2833): Show |
chr6 | 85500496 | 85598858 | ||
| a0001c0004 | 0/0 | 2838 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | ATGGT others(2833): Show |
chr6 | 85500496 | 85598858 | ||
| a0001c0005 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | ATGGT others(2833): Show |
chr6 | 85500496 | 85598858 | ||
| a0001c0007 | 0/0 | 2838 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | ATGGT others(2833): Show |
chr6 | 85500496 | 85598858 | ||
| a0002c0002 | 0/1 | 2838 | 5 | 0 | 2 | 0 | 2 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | ATGGT others(2833): Show |
chr6 | 85500496 | 85598858 | ||
| a0003c0006 | 0/0 | 2838 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | ATGGT others(2833): Show |
chr6 | 85500496 | 85598858 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3452 | 343 | 83 | 56 | 160 | 9 | 34 | SNX14_chr6_85500496_85598858 | SNX14 | CTCAG others(3447): Show |
chr6 | 85500496 | 85598858 |
| a0001c0001t0003 | 0/0 | 3452 | 2 | 0 | 0 | 2 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | CTCAG others(3447): Show |
chr6 | 85500496 | 85598858 |
| a0001c0001t0004 | 0/0 | 3452 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | CTCAG others(3447): Show |
chr6 | 85500496 | 85598858 |
| a0001c0001t0006 | 0/0 | 3452 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | CTCAG others(3447): Show |
chr6 | 85500496 | 85598858 |
| a0001c0003t0002 | 0/0 | 3452 | 4 | 4 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | CTCAG others(3447): Show |
chr6 | 85500496 | 85598858 |
| a0001c0004t0001 | 0/0 | 3452 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | CTCAG others(3447): Show |
chr6 | 85500496 | 85598858 |
| a0001c0005t0005 | 0/0 | 3452 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | CTCAG others(3447): Show |
chr6 | 85500496 | 85598858 |
| a0001c0007t0001 | 0/0 | 3452 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | CTCAG others(3447): Show |
chr6 | 85500496 | 85598858 |
| a0002c0002t0001 | 0/1 | 3452 | 5 | 0 | 2 | 0 | 2 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | CTCAG others(3447): Show |
chr6 | 85500496 | 85598858 |
| a0003c0006t0001 | 0/0 | 3452 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | CTCAG others(3447): Show |
chr6 | 85500496 | 85598858 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0166 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0001t0006g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0003t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0003t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0003t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0004t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0005t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0001c0007t0001g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0002c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0002c0002t0001g0285 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0002c0002t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0002c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| a0003c0006t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0318 | EUR | GBR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG00099 | hp2 | a0001 | c0007 | t0001 | g0346 | EUR | GBR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0338 | EUR | FIN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | FIN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | CHS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | CHS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0300 | EAS | CHS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | CHS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0339 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0345 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0297 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0304 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0343 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0012 | EUR | IBS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0141 | EUR | IBS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | IBS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0012 | EUR | IBS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0327 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CDX | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0341 | EAS | CDX | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02818 | hp1 | a0001 | c0003 | t0002 | g0035 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ESN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0331 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03041 | hp1 | a0001 | c0003 | t0002 | g0054 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03130 | hp2 | a0003 | c0006 | t0001 | g0049 | AFR | ESN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03209 | hp1 | a0001 | c0003 | t0002 | g0053 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03453 | hp2 | a0001 | c0003 | t0002 | g0036 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | STU | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | STU | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | BEB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | BEB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | BEB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | STU | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | STU | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | BEB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | STU | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | STU | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | STU | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | YRI | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | YRI | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | CHB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | CHB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | YRI | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | YRI | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18966 | hp1 | a0001 | c0004 | t0001 | g0243 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18991 | hp2 | a0001 | c0001 | t0006 | g0347 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0334 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | LWK | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | LWK | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | LWK | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | LWK | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19059 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | YRI | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | YRI | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | TSI | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0333 | EUR | TSI | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0326 | SAS | GIH | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | GIH | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03471 | hp1 | a0001 | c0005 | t0005 | g0026 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | USA | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | USA | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | USA | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | USA | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0285 | REF | REF | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0166 | REF | REF | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:85547145 | C | A | 1 | a0003 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.1075G>T | p.Ala359Ser | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/29 | 1215/3452 | 1075/2841 | 359/946 | chr6 | 85547145 | |||
| chr6:85547511 | T | G | 1 | a0002 | 4 | HG01168.hp1 HG01169.hp1 HG01515.hp1 others(1): Show |
missense_variant | MODERATE | c.907A>C | p.Ser303Arg | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 10/29 | 1047/3452 | 907/2841 | 303/946 | chr6 | 85547511 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:85514095 | C | T | 1 | a0001c0003 | 4 | HG02818.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
synonymous_variant | LOW | c.2532G>A | p.Leu844Leu | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 25/29 | 2672/3452 | 2532/2841 | 844/946 | chr6 | 85514095 | |||
| chr6:85565365 | A | G | 1 | a0001c0005 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.516T>C | p.Phe172Phe | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/29 | 656/3452 | 516/2841 | 172/946 | chr6 | 85565365 | |||
| chr6:85572158 | C | T | 1 | a0001c0004 | 1 | NA18966.hp1 | synonymous_variant | LOW | c.396G>A | p.Lys132Lys | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/29 | 536/3452 | 396/2841 | 132/946 | chr6 | 85572158 | |||
| chr6:85593710 | G | A | 1 | a0001c0007 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.9C>T | p.Pro3Pro | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/29 | 149/3452 | 9/2841 | 3/946 | chr6 | 85593710 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:85505625 | T | C | 1 | a0001c0001t0003 | 2 | HG00609.hp1 NA18981.hp1 |
3_prime_UTR_variant | MODIFIER | c.*342A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 29/29 | 342 | chr6 | 85505625 | ||||||
| chr6:85505630 | A | C | 1 | a0001c0005t0005 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*337T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 29/29 | 337 | chr6 | 85505630 | ||||||
| chr6:85505762 | G | A | 1 | a0001c0003t0002 | 4 | HG02818.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*205C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 29/29 | 205 | chr6 | 85505762 | ||||||
| chr6:85505953 | C | A | 1 | a0003c0006t0001 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 29/29 | 14 | chr6 | 85505953 | ||||||
| chr6:85593825 | G | A | 1 | a0001c0001t0006 | 1 | NA18991.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-107C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/29 | chr6 | 85593825 | |||||||
| chr6:85593829 | C | T | 1 | a0001c0001t0004 | 1 | NA18906.hp1 | 5_prime_UTR_variant | MODIFIER | c.-111G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/29 | 111 | chr6 | 85593829 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr6:85506048 | G | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0071 a0001c0001t0001g0170 others(5): Show |
9 | HG01175.hp1 HG01243.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.2803-43C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506048 | |||||||
| chr6:85506054 | T | C | 1 | a0003c0006t0001g0049 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2803-49A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506054 | |||||||
| chr6:85506126 | T | C | 1 | a0001c0001t0001g0337 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2803-121A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506126 | |||||||
| chr6:85506179 | C | T | 69 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0042 others(66): Show |
70 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.2803-174G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506179 | |||||||
| chr6:85506198 | T | C | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2803-193A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506198 | |||||||
| chr6:85506320 | A | AT | 11 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0059 others(8): Show |
11 | HG02109.hp1 HG02280.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2803-316dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506320 | |||||||
| chr6:85506320 | AT | A | 30 | a0001c0001t0001g0010 a0001c0001t0001g0122 a0001c0001t0001g0187 others(27): Show |
31 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.2803-316delA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506320 | |||||||
| chr6:85506374 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2803-369A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506374 | |||||||
| chr6:85506419 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2803-414G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506419 | |||||||
| chr6:85506450 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2803-445C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506450 | |||||||
| chr6:85506518 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2803-513C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506518 | |||||||
| chr6:85506563 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0150 |
2 | NA18961.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.2803-558C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506563 | |||||||
| chr6:85506598 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2803-593C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506598 | |||||||
| chr6:85506674 | G | A | 1 | a0001c0001t0001g0343 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2802+559C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506674 | |||||||
| chr6:85506899 | C | T | 7 | a0001c0001t0001g0051 a0001c0001t0001g0187 a0001c0001t0001g0188 others(4): Show |
7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2802+334G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506899 | |||||||
| chr6:85506907 | A | G | 26 | a0001c0001t0001g0010 a0001c0001t0001g0256 a0001c0001t0001g0258 others(23): Show |
27 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.2802+326T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506907 | |||||||
| chr6:85506928 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2802+305C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506928 | |||||||
| chr6:85507166 | C | A | 1 | a0001c0001t0001g0186 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2802+67G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85507166 | |||||||
| chr6:85507361 | A | G | 8 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0020 others(5): Show |
9 | HG01884.hp2 HG02559.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2746-72T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 27/28 | chr6 | 85507361 | |||||||
| chr6:85507372 | T | C | 8 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0020 others(5): Show |
9 | HG01884.hp2 HG02559.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2746-83A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 27/28 | chr6 | 85507372 | |||||||
| chr6:85507730 | G | T | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(277): Show |
289 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.2745+238C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 27/28 | chr6 | 85507730 | |||||||
| chr6:85507742 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2745+226T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 27/28 | chr6 | 85507742 | |||||||
| chr6:85507797 | T | A | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2745+171A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 27/28 | chr6 | 85507797 | |||||||
| chr6:85507884 | T | C | 1 | a0001c0001t0001g0341 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2745+84A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 27/28 | chr6 | 85507884 | |||||||
| chr6:85507915 | C | A | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2745+53G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 27/28 | chr6 | 85507915 | |||||||
| chr6:85507915 | C | T | 4 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0059 others(1): Show |
4 | HG02647.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2745+53G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 27/28 | chr6 | 85507915 | |||||||
| chr6:85508098 | T | G | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2654-39A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85508098 | |||||||
| chr6:85508320 | T | TA | 16 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0020 others(13): Show |
17 | HG01884.hp2 HG02148.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.2654-262dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85508320 | |||||||
| chr6:85508534 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2654-475A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85508534 | |||||||
| chr6:85508549 | T | C | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2654-490A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85508549 | |||||||
| chr6:85508638 | G | C | 1 | a0001c0001t0001g0321 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2654-579C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85508638 | |||||||
| chr6:85508642 | C | CAAACCAA others(3): Show |
1 | a0001c0001t0001g0321 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2654-584_2654-583i others(12): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85508642 | |||||||
| chr6:85508696 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2654-637T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85508696 | |||||||
| chr6:85508711 | A | G | 1 | a0001c0001t0001g0299 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2654-652T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85508711 | |||||||
| chr6:85508716 | G | C | 1 | a0001c0001t0001g0326 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2654-657C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85508716 | |||||||
| chr6:85508772 | A | G | 1 | a0001c0001t0001g0330 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2654-713T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85508772 | |||||||
| chr6:85508927 | C | G | 4 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0059 others(1): Show |
4 | HG02647.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2654-868G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85508927 | |||||||
| chr6:85508959 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2654-900C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85508959 | |||||||
| chr6:85509032 | T | C | 2 | a0001c0001t0001g0176 a0001c0001t0001g0345 |
2 | HG01069.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.2654-973A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85509032 | |||||||
| chr6:85509336 | T | TA | 29 | a0001c0001t0001g0010 a0001c0001t0001g0256 a0001c0001t0001g0257 others(26): Show |
30 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.2654-1278dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85509336 | |||||||
| chr6:85509452 | C | G | 1 | a0001c0001t0001g0141 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2654-1393G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85509452 | |||||||
| chr6:85509494 | T | TTCTG | 230 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(227): Show |
237 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.2654-1439_2654-143 others(8): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85509494 | |||||||
| chr6:85509598 | T | C | 4 | a0001c0001t0001g0253 a0001c0001t0001g0257 a0001c0001t0001g0273 others(1): Show |
4 | HG02280.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2654-1539A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85509598 | |||||||
| chr6:85509769 | A | G | 8 | a0001c0001t0001g0051 a0001c0001t0001g0187 a0001c0001t0001g0188 others(5): Show |
8 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2654-1710T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85509769 | |||||||
| chr6:85509841 | C | T | 26 | a0001c0001t0001g0010 a0001c0001t0001g0256 a0001c0001t0001g0258 others(23): Show |
27 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.2654-1782G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85509841 | |||||||
| chr6:85510021 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2654-1962A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85510021 | |||||||
| chr6:85510090 | T | G | 1 | a0001c0001t0001g0138 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2654-2031A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85510090 | |||||||
| chr6:85510379 | T | G | 11 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0051 others(8): Show |
11 | HG02109.hp1 HG02145.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2654-2320A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85510379 | |||||||
| chr6:85510534 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2654-2475C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85510534 | |||||||
| chr6:85510645 | G | A | 9 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(6): Show |
9 | HG00741.hp1 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2654-2586C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85510645 | |||||||
| chr6:85510666 | T | C | 1 | a0001c0001t0001g0208 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2654-2607A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85510666 | |||||||
| chr6:85510728 | C | G | 1 | a0001c0001t0001g0059 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2654-2669G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85510728 | |||||||
| chr6:85510795 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2654-2736A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85510795 | |||||||
| chr6:85510823 | T | C | 8 | a0001c0001t0001g0008 a0001c0001t0001g0071 a0001c0001t0001g0170 others(5): Show |
9 | HG01175.hp1 HG01243.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.2654-2764A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85510823 | |||||||
| chr6:85511000 | T | C | 25 | a0001c0001t0001g0011 a0001c0001t0001g0289 a0001c0001t0001g0290 others(22): Show |
26 | HG02027.hp1 HG02083.hp2 HG02523.hp1 others(23): Show |
intron_variant | MODIFIER | c.2653+2800A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511000 | |||||||
| chr6:85511005 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2653+2795C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511005 | |||||||
| chr6:85511189 | AT | A | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.2653+2610delA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511189 | |||||||
| chr6:85511210 | C | T | 25 | a0001c0001t0001g0009 a0001c0001t0001g0043 a0001c0001t0001g0044 others(22): Show |
26 | HG00423.hp1 HG01255.hp2 HG01928.hp1 others(23): Show |
intron_variant | MODIFIER | c.2653+2590G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511210 | |||||||
| chr6:85511402 | A | G | 1 | a0001c0001t0001g0264 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2653+2398T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511402 | |||||||
| chr6:85511536 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2653+2264C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511536 | |||||||
| chr6:85511603 | A | G | 9 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(6): Show |
9 | HG00741.hp1 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2653+2197T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511603 | |||||||
| chr6:85511749 | T | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG02451.hp2 HG02886.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2653+2051A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511749 | |||||||
| chr6:85511768 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2653+2032G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511768 | |||||||
| chr6:85511795 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2653+2005C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511795 | |||||||
| chr6:85511854 | A | C | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(78): Show |
84 | HG00408.hp2 HG00423.hp1 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.2653+1946T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511854 | |||||||
| chr6:85511868 | A | T | 157 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
164 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.2653+1932T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511868 | |||||||
| chr6:85511969 | AG | A | 13 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0047 others(10): Show |
13 | HG01884.hp2 HG01891.hp2 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.2653+1830delC | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511969 | |||||||
| chr6:85511984 | T | G | 1 | a0001c0001t0001g0018 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2653+1816A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511984 | |||||||
| chr6:85512034 | C | G | 6 | a0001c0001t0001g0016 a0001c0001t0001g0058 a0001c0001t0001g0059 others(3): Show |
6 | HG02615.hp1 HG02647.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2653+1766G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512034 | |||||||
| chr6:85512049 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2653+1751A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512049 | |||||||
| chr6:85512053 | C | T | 205 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(202): Show |
209 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(206): Show |
intron_variant | MODIFIER | c.2653+1747G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512053 | |||||||
| chr6:85512215 | G | A | 6 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0182 others(3): Show |
6 | HG02257.hp2 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2653+1585C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512215 | |||||||
| chr6:85512225 | A | G | 58 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(55): Show |
58 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.2653+1575T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512225 | |||||||
| chr6:85512230 | G | A | 4 | a0001c0003t0002g0035 a0001c0003t0002g0036 a0001c0003t0002g0053 others(1): Show |
4 | HG02818.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2653+1570C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512230 | |||||||
| chr6:85512308 | T | G | 4 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0217 others(1): Show |
4 | HG01358.hp2 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2653+1492A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512308 | |||||||
| chr6:85512350 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2653+1450C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512350 | |||||||
| chr6:85512420 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2653+1380C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512420 | |||||||
| chr6:85512557 | G | C | 1 | a0001c0001t0001g0181 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2653+1243C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512557 | |||||||
| chr6:85512621 | CA | C | 253 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(250): Show |
262 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.2653+1178delT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512621 | |||||||
| chr6:85512621 | CAA | C | 7 | a0001c0001t0001g0019 a0001c0001t0001g0039 a0001c0001t0001g0138 others(4): Show |
7 | HG01069.hp1 HG01168.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.2653+1177_2653+117 others(6): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512621 | |||||||
| chr6:85512645 | G | T | 1 | a0001c0001t0001g0342 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.2653+1155C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512645 | |||||||
| chr6:85512660 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2653+1140C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512660 | |||||||
| chr6:85512673 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2653+1127A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512673 | |||||||
| chr6:85512884 | T | C | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.2653+916A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512884 | |||||||
| chr6:85513079 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2653+721G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85513079 | |||||||
| chr6:85513202 | C | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | HG02451.hp2 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2653+598G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85513202 | |||||||
| chr6:85513309 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2653+491T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85513309 | |||||||
| chr6:85513500 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2653+300C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85513500 | |||||||
| chr6:85513558 | T | A | 1 | a0001c0001t0001g0139 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2653+242A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85513558 | |||||||
| chr6:85513574 | G | GAATGCCC others(21): Show |
1 | a0001c0001t0001g0139 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2653+225_2653+226i others(30): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85513574 | |||||||
| chr6:85513595 | G | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0021 others(5): Show |
8 | HG01884.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.2653+205C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85513595 | |||||||
| chr6:85513598 | T | C | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.2653+202A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85513598 | |||||||
| chr6:85513737 | T | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2653+63A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85513737 | |||||||
| chr6:85513753 | C | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0038 others(10): Show |
15 | HG00735.hp1 HG01106.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.2653+47G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85513753 | |||||||
| chr6:85513754 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2653+46C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85513754 | |||||||
| chr6:85513914 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.2558-19T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 25/28 | chr6 | 85513914 | |||||||
| chr6:85514335 | T | G | 158 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(155): Show |
165 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.2393-101A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 24/28 | chr6 | 85514335 | |||||||
| chr6:85514748 | A | G | 1 | a0001c0003t0002g0053 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2269-119T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85514748 | |||||||
| chr6:85514794 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2269-165G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85514794 | |||||||
| chr6:85514796 | G | A | 4 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0051 others(1): Show |
4 | HG02145.hp2 HG02486.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2269-167C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85514796 | |||||||
| chr6:85515021 | T | C | 7 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(4): Show |
7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2269-392A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515021 | |||||||
| chr6:85515068 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2269-439G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515068 | |||||||
| chr6:85515177 | G | A | 27 | a0001c0001t0001g0010 a0001c0001t0001g0256 a0001c0001t0001g0257 others(24): Show |
28 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.2269-548C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515177 | |||||||
| chr6:85515216 | G | A | 4 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0059 others(1): Show |
4 | HG02647.hp2 HG03209.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2269-587C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515216 | |||||||
| chr6:85515234 | T | G | 1 | a0001c0001t0001g0301 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2269-605A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515234 | |||||||
| chr6:85515250 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2269-621C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515250 | |||||||
| chr6:85515262 | C | CA | 44 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0029 others(41): Show |
44 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.2269-634dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515262 | |||||||
| chr6:85515262 | C | CAA | 32 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0052 others(29): Show |
33 | HG00544.hp2 HG01109.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.2269-635_2269-634d others(4): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515262 | |||||||
| chr6:85515262 | C | CAAA | 32 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0042 others(29): Show |
33 | HG00408.hp2 HG00735.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.2269-636_2269-634d others(5): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515262 | |||||||
| chr6:85515262 | C | CAAAA | 12 | a0001c0001t0001g0045 a0001c0001t0001g0202 a0001c0001t0001g0203 others(9): Show |
12 | HG00423.hp1 HG01928.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.2269-637_2269-634d others(6): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515262 | |||||||
| chr6:85515262 | CA | C | 8 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0047 others(5): Show |
8 | HG01975.hp2 HG02109.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2269-634delT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515262 | |||||||
| chr6:85515268 | A | AC | 7 | a0001c0001t0001g0010 a0001c0001t0001g0259 a0001c0001t0001g0281 others(4): Show |
8 | HG01109.hp2 HG02818.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.2269-640_2269-639i others(3): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515268 | |||||||
| chr6:85515273 | A | AC | 23 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(20): Show |
23 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.2269-645_2269-644i others(3): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515273 | |||||||
| chr6:85515273 | A | C | 7 | a0001c0001t0001g0010 a0001c0001t0001g0259 a0001c0001t0001g0281 others(4): Show |
8 | HG01109.hp2 HG02818.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.2269-644T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515273 | |||||||
| chr6:85515278 | A | C | 5 | a0001c0001t0001g0272 a0001c0003t0002g0035 a0001c0003t0002g0036 others(2): Show |
5 | HG02818.hp1 HG03041.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2269-649T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515278 | |||||||
| chr6:85515342 | G | A | 68 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0042 others(65): Show |
69 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.2269-713C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515342 | |||||||
| chr6:85515551 | G | A | 1 | a0001c0001t0001g0309 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2269-922C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515551 | |||||||
| chr6:85515575 | T | C | 3 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0057 |
3 | HG02145.hp2 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2269-946A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515575 | |||||||
| chr6:85515897 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2269-1268T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515897 | |||||||
| chr6:85515953 | G | A | 47 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(44): Show |
51 | HG00609.hp2 HG00735.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.2269-1324C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515953 | |||||||
| chr6:85516021 | T | C | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(277): Show |
289 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.2269-1392A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85516021 | |||||||
| chr6:85516061 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2269-1432A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85516061 | |||||||
| chr6:85516414 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2268+1342A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85516414 | |||||||
| chr6:85516508 | A | C | 1 | a0001c0001t0004g0013 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2268+1248T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85516508 | |||||||
| chr6:85516584 | A | G | 1 | a0001c0001t0001g0136 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2268+1172T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85516584 | |||||||
| chr6:85516585 | TTATAGGC others(2): Show |
T | 3 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 |
3 | HG02818.hp2 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2268+1162_2268+117 others(13): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85516585 | |||||||
| chr6:85516630 | A | ACC | 7 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(4): Show |
7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2268+1125_2268+112 others(6): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85516630 | |||||||
| chr6:85516632 | C | CT | 36 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0021 others(33): Show |
36 | HG00423.hp1 HG01496.hp1 HG01515.hp2 others(33): Show |
intron_variant | MODIFIER | c.2268+1123dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85516632 | |||||||
| chr6:85516632 | C | T | 7 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(4): Show |
7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2268+1124G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85516632 | |||||||
| chr6:85516632 | CTTTT | C | 30 | a0001c0001t0001g0010 a0001c0001t0001g0256 a0001c0001t0001g0257 others(27): Show |
31 | HG00423.hp2 HG01070.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.2268+1120_2268+112 others(8): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85516632 | |||||||
| chr6:85516632 | CTTTTTTT others(7): Show |
C | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2268+1110_2268+112 others(18): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85516632 | |||||||
| chr6:85516763 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2268+993C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85516763 | |||||||
| chr6:85516897 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2268+859G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85516897 | |||||||
| chr6:85517175 | A | T | 1 | a0001c0001t0001g0329 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2268+581T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85517175 | |||||||
| chr6:85517265 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2268+491G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85517265 | |||||||
| chr6:85517426 | C | A | 1 | a0001c0001t0001g0070 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2268+330G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85517426 | |||||||
| chr6:85517516 | A | T | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2268+240T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85517516 | |||||||
| chr6:85517725 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0059 |
3 | HG02647.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2268+31G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85517725 | |||||||
| chr6:85518161 | A | G | 8 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0021 others(5): Show |
8 | HG01884.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.2108-113T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85518161 | |||||||
| chr6:85518174 | T | C | 1 | a0001c0001t0001g0211 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2108-126A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85518174 | |||||||
| chr6:85518314 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2108-266T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85518314 | |||||||
| chr6:85518391 | G | A | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(182): Show |
192 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.2108-343C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85518391 | |||||||
| chr6:85518442 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2108-394C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85518442 | |||||||
| chr6:85518763 | A | G | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.2108-715T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85518763 | |||||||
| chr6:85518787 | T | C | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | HG02451.hp2 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2108-739A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85518787 | |||||||
| chr6:85518953 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2108-905C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85518953 | |||||||
| chr6:85519002 | G | C | 1 | a0001c0001t0001g0097 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2108-954C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519002 | |||||||
| chr6:85519023 | A | G | 27 | a0001c0001t0001g0010 a0001c0001t0001g0256 a0001c0001t0001g0257 others(24): Show |
28 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.2108-975T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519023 | |||||||
| chr6:85519123 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2108-1075T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519123 | |||||||
| chr6:85519371 | C | T | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2108-1323G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519371 | |||||||
| chr6:85519471 | T | G | 1 | a0003c0006t0001g0049 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2108-1423A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519471 | |||||||
| chr6:85519482 | G | T | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2108-1434C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519482 | |||||||
| chr6:85519491 | G | A | 47 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(44): Show |
51 | HG00609.hp2 HG00735.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.2108-1443C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519491 | |||||||
| chr6:85519502 | CCTGTAGT others(24): Show |
C | 1 | a0001c0001t0001g0020 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2108-1485_2108-145 others(35): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519502 | |||||||
| chr6:85519561 | T | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0052 |
3 | HG02895.hp2 HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2108-1513A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519561 | |||||||
| chr6:85519595 | G | T | 2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2108-1547C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519595 | |||||||
| chr6:85519651 | C | A | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(277): Show |
289 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.2108-1603G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519651 | |||||||
| chr6:85519712 | T | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2108-1664A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519712 | |||||||
| chr6:85519794 | G | A | 31 | a0001c0001t0001g0010 a0001c0001t0001g0256 a0001c0001t0001g0257 others(28): Show |
32 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.2108-1746C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519794 | |||||||
| chr6:85519862 | C | T | 68 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0042 others(65): Show |
69 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.2108-1814G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519862 | |||||||
| chr6:85519885 | A | C | 2 | a0001c0001t0001g0239 a0001c0004t0001g0243 |
2 | NA18966.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.2108-1837T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519885 | |||||||
| chr6:85519889 | C | CA | 5 | a0001c0001t0001g0017 a0001c0001t0001g0198 a0001c0001t0001g0199 others(2): Show |
5 | HG01358.hp2 HG02896.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2108-1842dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519889 | |||||||
| chr6:85519933 | T | C | 8 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0021 others(5): Show |
8 | HG01884.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.2108-1885A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519933 | |||||||
| chr6:85519962 | A | G | 15 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0287 others(12): Show |
17 | HG00597.hp2 HG00609.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.2108-1914T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519962 | |||||||
| chr6:85520015 | C | CAGT | 12 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(9): Show |
12 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.2108-1970_2108-196 others(7): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85520015 | |||||||
| chr6:85520120 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2108-2072C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85520120 | |||||||
| chr6:85520211 | T | A | 1 | a0001c0001t0001g0136 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2108-2163A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85520211 | |||||||
| chr6:85520545 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2108-2497T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85520545 | |||||||
| chr6:85520748 | C | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0052 a0001c0001t0001g0055 others(2): Show |
6 | HG02559.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2108-2700G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85520748 | |||||||
| chr6:85520808 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2108-2760T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85520808 | |||||||
| chr6:85521254 | G | T | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2108-3206C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85521254 | |||||||
| chr6:85521347 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2108-3299C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85521347 | |||||||
| chr6:85521444 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2108-3396C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85521444 | |||||||
| chr6:85521495 | T | A | 2 | a0001c0001t0001g0048 a0001c0001t0001g0057 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2108-3447A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85521495 | |||||||
| chr6:85521561 | A | G | 1 | a0001c0001t0001g0085 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2108-3513T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85521561 | |||||||
| chr6:85521646 | A | C | 1 | a0001c0001t0004g0013 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2108-3598T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85521646 | |||||||
| chr6:85521782 | T | C | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0182 others(4): Show |
7 | HG02257.hp2 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2108-3734A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85521782 | |||||||
| chr6:85521800 | C | A | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2108-3752G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85521800 | |||||||
| chr6:85521897 | C | T | 5 | a0001c0001t0001g0142 a0001c0001t0001g0154 a0001c0001t0001g0157 others(2): Show |
5 | HG03471.hp1 NA18967.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.2108-3849G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85521897 | |||||||
| chr6:85522003 | T | A | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(277): Show |
289 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.2108-3955A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85522003 | |||||||
| chr6:85522136 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2107+3990C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85522136 | |||||||
| chr6:85522369 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2107+3757C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85522369 | |||||||
| chr6:85522401 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2107+3725C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85522401 | |||||||
| chr6:85522515 | G | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0052 a0001c0001t0001g0055 others(2): Show |
6 | HG02559.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2107+3611C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85522515 | |||||||
| chr6:85522645 | T | A | 1 | a0001c0001t0001g0268 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2107+3481A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85522645 | |||||||
| chr6:85522714 | A | G | 3 | a0001c0001t0001g0037 a0001c0001t0001g0100 a0001c0001t0001g0101 |
3 | HG02280.hp1 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2107+3412T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85522714 | |||||||
| chr6:85522825 | A | G | 31 | a0001c0001t0001g0010 a0001c0001t0001g0256 a0001c0001t0001g0257 others(28): Show |
32 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.2107+3301T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85522825 | |||||||
| chr6:85522836 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2107+3290T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85522836 | |||||||
| chr6:85522908 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2107+3218A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85522908 | |||||||
| chr6:85522916 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2107+3210G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85522916 | |||||||
| chr6:85522940 | A | G | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2107+3186T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85522940 | |||||||
| chr6:85522992 | G | A | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.2107+3134C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85522992 | |||||||
| chr6:85523001 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2107+3125C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85523001 | |||||||
| chr6:85523100 | T | C | 1 | a0001c0001t0001g0296 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2107+3026A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85523100 | |||||||
| chr6:85523679 | T | C | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(277): Show |
289 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.2107+2447A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85523679 | |||||||
| chr6:85523846 | G | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0292 others(4): Show |
9 | NA18944.hp1 NA18952.hp1 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.2107+2280C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85523846 | |||||||
| chr6:85523949 | T | C | 4 | a0001c0001t0001g0324 a0001c0001t0001g0325 a0001c0001t0001g0327 others(1): Show |
4 | HG00544.hp2 HG02132.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.2107+2177A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85523949 | |||||||
| chr6:85524071 | A | C | 71 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0042 others(68): Show |
72 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.2107+2055T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85524071 | |||||||
| chr6:85524117 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2107+2009C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85524117 | |||||||
| chr6:85524190 | A | AAAAG | 9 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(6): Show |
9 | HG02109.hp1 HG02129.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.2107+1932_2107+193 others(8): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85524190 | |||||||
| chr6:85524190 | AAAAGAAA others(1): Show |
A | 4 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(1): Show |
4 | HG01256.hp1 HG01258.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.2107+1928_2107+193 others(12): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85524190 | |||||||
| chr6:85524255 | T | C | 1 | a0001c0001t0001g0234 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2107+1871A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85524255 | |||||||
| chr6:85524261 | C | G | 1 | a0001c0001t0001g0230 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2107+1865G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85524261 | |||||||
| chr6:85524352 | A | G | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(277): Show |
289 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.2107+1774T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85524352 | |||||||
| chr6:85524666 | C | T | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.2107+1460G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85524666 | |||||||
| chr6:85524698 | C | A | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
4 | HG02109.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2107+1428G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85524698 | |||||||
| chr6:85524754 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2107+1372T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85524754 | |||||||
| chr6:85524785 | G | GA | 12 | a0001c0001t0001g0030 a0001c0001t0001g0057 a0001c0001t0001g0062 others(9): Show |
12 | HG00423.hp2 HG02074.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2107+1340dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85524785 | |||||||
| chr6:85524785 | GA | G | 78 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(75): Show |
79 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.2107+1340delT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85524785 | |||||||
| chr6:85524956 | T | A | 1 | a0001c0001t0001g0230 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2107+1170A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85524956 | |||||||
| chr6:85525047 | A | G | 1 | a0001c0001t0001g0247 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2107+1079T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85525047 | |||||||
| chr6:85525117 | C | T | 41 | a0001c0001t0001g0008 a0001c0001t0001g0062 a0001c0001t0001g0063 others(38): Show |
42 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.2107+1009G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85525117 | |||||||
| chr6:85525170 | A | C | 3 | a0001c0001t0001g0124 a0001c0001t0001g0138 a0001c0001t0001g0181 |
3 | HG01243.hp2 HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2107+956T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85525170 | |||||||
| chr6:85525257 | C | A | 6 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(3): Show |
6 | HG01169.hp2 HG01261.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.2107+869G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85525257 | |||||||
| chr6:85525286 | T | C | 1 | a0001c0001t0001g0268 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2107+840A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85525286 | |||||||
| chr6:85525370 | A | G | 68 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0042 others(65): Show |
69 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.2107+756T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85525370 | |||||||
| chr6:85525401 | A | G | 5 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
5 | HG02647.hp2 HG03130.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2107+725T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85525401 | |||||||
| chr6:85525434 | T | C | 2 | a0001c0001t0001g0326 a0001c0001t0001g0335 |
2 | HG06807.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2107+692A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85525434 | |||||||
| chr6:85525663 | C | T | 1 | a0001c0001t0001g0223 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2107+463G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85525663 | |||||||
| chr6:85525693 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2107+433A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85525693 | |||||||
| chr6:85525989 | G | A | 1 | a0001c0001t0001g0244 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2107+137C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85525989 | |||||||
| chr6:85526284 | G | T | 1 | a0001c0001t0001g0125 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1996-47C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85526284 | |||||||
| chr6:85526396 | T | C | 1 | a0001c0001t0001g0227 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1996-159A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85526396 | |||||||
| chr6:85526438 | G | A | 2 | a0001c0001t0001g0195 a0001c0001t0001g0200 |
2 | HG03017.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1996-201C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85526438 | |||||||
| chr6:85526470 | C | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
199 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.1996-233G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85526470 | |||||||
| chr6:85526508 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1996-271G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85526508 | |||||||
| chr6:85526685 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1996-448C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85526685 | |||||||
| chr6:85526793 | G | C | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1996-556C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85526793 | |||||||
| chr6:85526797 | C | A | 1 | a0001c0001t0001g0235 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1996-560G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85526797 | |||||||
| chr6:85526898 | G | A | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1996-661C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85526898 | |||||||
| chr6:85527034 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0020 |
2 | HG01884.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1996-797C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85527034 | |||||||
| chr6:85527395 | A | G | 2 | a0001c0003t0002g0035 a0001c0003t0002g0053 |
2 | HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1995+867T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85527395 | |||||||
| chr6:85527397 | A | AT | 186 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(183): Show |
191 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.1995+864dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85527397 | |||||||
| chr6:85527398 | T | TA | 94 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(91): Show |
98 | HG00609.hp2 HG00735.hp1 HG01070.hp1 others(95): Show |
intron_variant | MODIFIER | c.1995+863_1995+864i others(3): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85527398 | |||||||
| chr6:85527399 | T | A | 1 | a0001c0001t0001g0327 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1995+863A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85527399 | |||||||
| chr6:85527400 | T | A | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1995+862A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85527400 | |||||||
| chr6:85527477 | G | C | 2 | a0001c0001t0001g0048 a0001c0001t0001g0057 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1995+785C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85527477 | |||||||
| chr6:85527556 | T | C | 8 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0021 others(5): Show |
8 | HG01884.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1995+706A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85527556 | |||||||
| chr6:85527576 | A | C | 1 | a0003c0006t0001g0049 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1995+686T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85527576 | |||||||
| chr6:85527638 | T | C | 1 | a0001c0001t0001g0200 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1995+624A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85527638 | |||||||
| chr6:85527652 | A | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(2): Show |
5 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1995+610T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85527652 | |||||||
| chr6:85527705 | A | G | 1 | a0001c0001t0001g0113 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1995+557T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85527705 | |||||||
| chr6:85527962 | T | C | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1995+300A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85527962 | |||||||
| chr6:85528079 | A | G | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(277): Show |
289 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.1995+183T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85528079 | |||||||
| chr6:85528081 | G | A | 3 | a0001c0001t0001g0051 a0001c0001t0001g0187 a0001c0001t0001g0188 |
3 | HG02559.hp2 HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1995+181C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85528081 | |||||||
| chr6:85528143 | A | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0040 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1995+119T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85528143 | |||||||
| chr6:85528384 | G | T | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1895-22C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 19/28 | chr6 | 85528384 | |||||||
| chr6:85528749 | T | C | 4 | a0001c0001t0001g0002 a0001c0001t0001g0052 a0001c0001t0001g0055 others(1): Show |
5 | HG02647.hp1 HG02895.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1895-387A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 19/28 | chr6 | 85528749 | |||||||
| chr6:85528831 | C | T | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1895-469G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 19/28 | chr6 | 85528831 | |||||||
| chr6:85528914 | TG | T | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1895-553delC | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 19/28 | chr6 | 85528914 | |||||||
| chr6:85528947 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1895-585C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 19/28 | chr6 | 85528947 | |||||||
| chr6:85528991 | G | T | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1895-629C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 19/28 | chr6 | 85528991 | |||||||
| chr6:85529053 | A | G | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1895-691T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 19/28 | chr6 | 85529053 | |||||||
| chr6:85529086 | C | A | 1 | a0001c0001t0001g0204 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1895-724G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 19/28 | chr6 | 85529086 | |||||||
| chr6:85529233 | C | T | 1 | a0001c0004t0001g0243 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1895-871G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 19/28 | chr6 | 85529233 | |||||||
| chr6:85529568 | G | C | 1 | a0001c0001t0001g0331 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1894+624C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 19/28 | chr6 | 85529568 | |||||||
| chr6:85529575 | A | G | 1 | a0003c0006t0001g0049 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1894+617T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 19/28 | chr6 | 85529575 | |||||||
| chr6:85530149 | C | T | 4 | a0001c0003t0002g0035 a0001c0003t0002g0036 a0001c0003t0002g0053 others(1): Show |
4 | HG02818.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1894+43G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 19/28 | chr6 | 85530149 | |||||||
| chr6:85530290 | C | T | 3 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0240 |
3 | HG03492.hp1 HG03704.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1811-15G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85530290 | |||||||
| chr6:85530348 | T | C | 1 | a0001c0001t0001g0336 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1811-73A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85530348 | |||||||
| chr6:85530429 | G | A | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1811-154C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85530429 | |||||||
| chr6:85530504 | G | C | 67 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0042 others(64): Show |
68 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.1811-229C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85530504 | |||||||
| chr6:85530555 | G | T | 1 | a0001c0001t0001g0072 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1811-280C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85530555 | |||||||
| chr6:85530601 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0059 |
3 | HG02647.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1811-326G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85530601 | |||||||
| chr6:85530644 | C | CA | 23 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(20): Show |
24 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1811-370dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85530644 | |||||||
| chr6:85530910 | G | GT | 68 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0042 others(65): Show |
69 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.1811-636dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85530910 | |||||||
| chr6:85531233 | A | G | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(277): Show |
289 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.1811-958T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85531233 | |||||||
| chr6:85531460 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1811-1185T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85531460 | |||||||
| chr6:85531720 | A | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG01433.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1811-1445T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85531720 | |||||||
| chr6:85531795 | G | T | 1 | a0001c0001t0001g0086 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1811-1520C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85531795 | |||||||
| chr6:85531875 | A | T | 1 | a0001c0001t0001g0177 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1811-1600T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85531875 | |||||||
| chr6:85531883 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1811-1608G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85531883 | |||||||
| chr6:85532033 | G | GA | 249 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
257 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.1810+1565dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85532033 | |||||||
| chr6:85532117 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1810+1482A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85532117 | |||||||
| chr6:85532176 | T | C | 260 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(257): Show |
268 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.1810+1423A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85532176 | |||||||
| chr6:85532300 | T | A | 1 | a0001c0001t0001g0109 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1810+1299A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85532300 | |||||||
| chr6:85532593 | A | C | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1810+1006T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85532593 | |||||||
| chr6:85532700 | C | T | 1 | a0001c0001t0001g0345 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1810+899G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85532700 | |||||||
| chr6:85532713 | T | TAATTTGA others(330): Show |
1 | a0001c0001t0001g0240 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1810+885_1810+886i others(339): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85532713 | |||||||
| chr6:85533233 | C | T | 4 | a0001c0001t0001g0002 a0001c0001t0001g0052 a0001c0001t0001g0055 others(1): Show |
5 | HG02647.hp1 HG02895.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1810+366G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85533233 | |||||||
| chr6:85533250 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1810+349A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85533250 | |||||||
| chr6:85533265 | T | A | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1810+334A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85533265 | |||||||
| chr6:85533345 | T | C | 3 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0059 |
3 | HG02647.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1810+254A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85533345 | |||||||
| chr6:85533496 | A | G | 1 | a0001c0001t0001g0200 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1810+103T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85533496 | |||||||
| chr6:85533869 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1609-69T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85533869 | |||||||
| chr6:85534036 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1609-236G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85534036 | |||||||
| chr6:85534138 | C | G | 7 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(4): Show |
7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1609-338G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85534138 | |||||||
| chr6:85534186 | C | T | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1609-386G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85534186 | |||||||
| chr6:85534189 | G | T | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1609-389C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85534189 | |||||||
| chr6:85534317 | T | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0052 a0001c0001t0001g0055 others(2): Show |
6 | HG02559.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1609-517A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85534317 | |||||||
| chr6:85534469 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1609-669C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85534469 | |||||||
| chr6:85534785 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1609-985A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85534785 | |||||||
| chr6:85534831 | G | GT | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(141): Show |
150 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.1609-1032dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85534831 | |||||||
| chr6:85534831 | G | GTT | 185 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(182): Show |
192 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.1609-1033_1609-103 others(6): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85534831 | |||||||
| chr6:85534831 | G | GTTT | 13 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(10): Show |
13 | HG00741.hp1 HG01496.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1609-1034_1609-103 others(7): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85534831 | |||||||
| chr6:85534849 | A | T | 3 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 |
3 | HG02258.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1609-1049T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85534849 | |||||||
| chr6:85534913 | T | C | 1 | a0003c0006t0001g0049 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1609-1113A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85534913 | |||||||
| chr6:85534937 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1609-1137T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85534937 | |||||||
| chr6:85535012 | C | T | 1 | a0001c0001t0001g0317 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1609-1212G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535012 | |||||||
| chr6:85535028 | C | CT | 31 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0256 others(28): Show |
32 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.1609-1229dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535028 | |||||||
| chr6:85535028 | CT | C | 154 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(151): Show |
160 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1609-1229delA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535028 | |||||||
| chr6:85535031 | T | C | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1609-1231A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535031 | |||||||
| chr6:85535130 | C | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
199 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.1609-1330G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535130 | |||||||
| chr6:85535252 | C | A | 1 | a0001c0001t0001g0200 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1609-1452G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535252 | |||||||
| chr6:85535497 | C | T | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
199 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.1608+1295G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535497 | |||||||
| chr6:85535500 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1608+1292G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535500 | |||||||
| chr6:85535537 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1608+1255C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535537 | |||||||
| chr6:85535589 | A | G | 1 | a0001c0001t0001g0338 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1608+1203T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535589 | |||||||
| chr6:85535604 | C | CA | 76 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0043 others(73): Show |
78 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.1608+1187dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535604 | |||||||
| chr6:85535604 | C | CAA | 6 | a0001c0001t0001g0017 a0001c0001t0001g0042 a0001c0001t0001g0047 others(3): Show |
6 | HG02135.hp2 HG03453.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1608+1186_1608+118 others(6): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535604 | |||||||
| chr6:85535604 | CA | C | 167 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(164): Show |
173 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.1608+1187delT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535604 | |||||||
| chr6:85535604 | CAA | C | 26 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0019 others(23): Show |
26 | HG00099.hp2 HG01070.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.1608+1186_1608+118 others(6): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535604 | |||||||
| chr6:85535873 | C | T | 1 | a0001c0007t0001g0346 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1608+919G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535873 | |||||||
| chr6:85535908 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1608+884C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535908 | |||||||
| chr6:85535999 | A | C | 1 | a0001c0001t0001g0096 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1608+793T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535999 | |||||||
| chr6:85536092 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1608+700G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85536092 | |||||||
| chr6:85536267 | T | C | 1 | a0001c0001t0001g0213 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1608+525A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85536267 | |||||||
| chr6:85536287 | A | G | 1 | a0001c0001t0001g0329 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1608+505T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85536287 | |||||||
| chr6:85536682 | A | G | 3 | a0001c0001t0001g0124 a0001c0001t0001g0138 a0001c0001t0001g0181 |
3 | HG01243.hp2 HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1608+110T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85536682 | |||||||
| chr6:85536991 | C | A | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1476-67G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85536991 | |||||||
| chr6:85536998 | T | TA | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(277): Show |
289 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.1476-75dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85536998 | |||||||
| chr6:85537073 | G | C | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1476-149C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85537073 | |||||||
| chr6:85537212 | A | C | 1 | a0001c0001t0001g0048 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1476-288T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85537212 | |||||||
| chr6:85537349 | G | GA | 7 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0059 others(4): Show |
7 | HG02257.hp2 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1476-426dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85537349 | |||||||
| chr6:85537579 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1476-655T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85537579 | |||||||
| chr6:85537706 | T | C | 1 | a0003c0006t0001g0049 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1476-782A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85537706 | |||||||
| chr6:85537927 | G | C | 9 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(6): Show |
9 | HG00741.hp1 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1475+911C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85537927 | |||||||
| chr6:85537934 | T | G | 1 | a0001c0001t0001g0197 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1475+904A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85537934 | |||||||
| chr6:85537962 | C | A | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1475+876G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85537962 | |||||||
| chr6:85537988 | T | C | 1 | a0001c0007t0001g0346 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1475+850A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85537988 | |||||||
| chr6:85538041 | T | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
199 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.1475+797A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85538041 | |||||||
| chr6:85538081 | T | C | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1475+757A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85538081 | |||||||
| chr6:85538155 | T | C | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1475+683A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85538155 | |||||||
| chr6:85538224 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1475+614C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85538224 | |||||||
| chr6:85538269 | G | GT | 11 | a0001c0001t0001g0008 a0001c0001t0001g0071 a0001c0001t0001g0093 others(8): Show |
12 | HG00099.hp2 HG01069.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1475+568dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85538269 | |||||||
| chr6:85538329 | A | T | 1 | a0001c0001t0006g0347 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1475+509T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85538329 | |||||||
| chr6:85538330 | C | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0232 |
2 | HG00735.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1475+508G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85538330 | |||||||
| chr6:85538448 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1475+390T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85538448 | |||||||
| chr6:85538459 | G | A | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1475+379C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85538459 | |||||||
| chr6:85538491 | A | T | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1475+347T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85538491 | |||||||
| chr6:85538582 | A | G | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1475+256T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85538582 | |||||||
| chr6:85538667 | T | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1475+171A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85538667 | |||||||
| chr6:85538742 | T | C | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(277): Show |
289 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.1475+96A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85538742 | |||||||
| chr6:85539128 | G | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0059 |
3 | HG02647.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1449-264C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539128 | |||||||
| chr6:85539353 | G | C | 3 | a0001c0001t0001g0107 a0001c0001t0001g0120 a0001c0001t0001g0121 |
3 | HG01975.hp2 HG02004.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1449-489C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539353 | |||||||
| chr6:85539385 | A | T | 1 | a0001c0001t0001g0171 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1449-521T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539385 | |||||||
| chr6:85539560 | A | G | 2 | a0001c0001t0001g0314 a0001c0001t0001g0315 |
2 | HG02027.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1449-696T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539560 | |||||||
| chr6:85539935 | T | TTTTTA | 24 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0048 others(21): Show |
24 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1449-1076_1449-107 others(9): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539935 | |||||||
| chr6:85539935 | T | TTTTTATT others(3): Show |
14 | a0001c0001t0001g0037 a0001c0001t0001g0057 a0001c0001t0001g0058 others(11): Show |
14 | HG02083.hp1 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1449-1081_1449-107 others(14): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539935 | |||||||
| chr6:85539935 | T | TTTTTATT others(8): Show |
15 | a0001c0001t0001g0047 a0001c0001t0001g0051 a0001c0001t0001g0055 others(12): Show |
15 | HG00609.hp2 HG01081.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1449-1086_1449-107 others(19): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539935 | |||||||
| chr6:85539935 | T | TTTTTATT others(13): Show |
31 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0016 others(28): Show |
33 | HG00099.hp2 HG00280.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1449-1091_1449-107 others(24): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539935 | |||||||
| chr6:85539935 | T | TTTTTATT others(18): Show |
72 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(69): Show |
74 | HG00408.hp1 HG00597.hp1 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.1449-1096_1449-107 others(29): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539935 | |||||||
| chr6:85539935 | T | TTTTTATT others(23): Show |
17 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0028 others(14): Show |
18 | HG01175.hp1 HG01243.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.1449-1101_1449-107 others(34): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539935 | |||||||
| chr6:85539935 | T | TTTTTATT others(28): Show |
5 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0129 others(2): Show |
7 | HG01516.hp1 HG01517.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.1449-1106_1449-107 others(39): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539935 | |||||||
| chr6:85539935 | T | TTTTTATT others(33): Show |
1 | a0001c0001t0001g0136 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1449-1111_1449-107 others(44): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539935 | |||||||
| chr6:85539935 | TTTTTA | T | 5 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(2): Show |
5 | HG01358.hp2 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1449-1076_1449-107 others(9): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539935 | |||||||
| chr6:85539935 | TTTTTATT others(3): Show |
T | 42 | a0001c0001t0001g0010 a0001c0001t0001g0018 a0001c0001t0001g0020 others(39): Show |
43 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.1449-1081_1449-107 others(14): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539935 | |||||||
| chr6:85539976 | T | TTTTATTT others(8): Show |
1 | a0001c0001t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1449-1113_1449-111 others(19): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539976 | |||||||
| chr6:85539989 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1449-1125C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539989 | |||||||
| chr6:85540116 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1449-1252G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540116 | |||||||
| chr6:85540253 | C | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1449-1389G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540253 | |||||||
| chr6:85540254 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1449-1390C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540254 | |||||||
| chr6:85540338 | C | A | 1 | a0001c0001t0001g0330 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1449-1474G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540338 | |||||||
| chr6:85540342 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1449-1478C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540342 | |||||||
| chr6:85540383 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1449-1519C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540383 | |||||||
| chr6:85540479 | A | G | 3 | a0001c0001t0001g0312 a0001c0001t0003g0300 a0001c0001t0003g0313 |
3 | HG00609.hp1 NA18981.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1448+1506T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540479 | |||||||
| chr6:85540609 | C | T | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0182 others(4): Show |
7 | HG02257.hp2 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1448+1376G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540609 | |||||||
| chr6:85540707 | G | C | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1448+1278C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540707 | |||||||
| chr6:85540712 | G | A | 31 | a0001c0001t0001g0010 a0001c0001t0001g0256 a0001c0001t0001g0257 others(28): Show |
32 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.1448+1273C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540712 | |||||||
| chr6:85540804 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1448+1181A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540804 | |||||||
| chr6:85540805 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1448+1180G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540805 | |||||||
| chr6:85540896 | T | G | 2 | a0001c0001t0001g0237 a0001c0001t0001g0240 |
2 | HG03704.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1448+1089A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540896 | |||||||
| chr6:85540996 | C | CT | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1448+988dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540996 | |||||||
| chr6:85540996 | CT | C | 7 | a0001c0001t0001g0128 a0001c0001t0001g0176 a0001c0001t0001g0279 others(4): Show |
7 | HG01069.hp2 HG01070.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.1448+988delA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540996 | |||||||
| chr6:85541070 | T | C | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG00280.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1448+915A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85541070 | |||||||
| chr6:85541405 | T | C | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1448+580A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85541405 | |||||||
| chr6:85541600 | G | T | 1 | a0001c0001t0004g0013 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1448+385C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85541600 | |||||||
| chr6:85542445 | A | G | 3 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 |
3 | HG02258.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1390-402T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 14/28 | chr6 | 85542445 | |||||||
| chr6:85542488 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1390-445C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 14/28 | chr6 | 85542488 | |||||||
| chr6:85542605 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1390-562C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 14/28 | chr6 | 85542605 | |||||||
| chr6:85542636 | C | T | 36 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0040 others(33): Show |
37 | HG00408.hp1 HG00597.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1389+546G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 14/28 | chr6 | 85542636 | |||||||
| chr6:85542673 | C | T | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1389+509G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 14/28 | chr6 | 85542673 | |||||||
| chr6:85542690 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1389+492C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 14/28 | chr6 | 85542690 | |||||||
| chr6:85542732 | G | A | 2 | a0001c0001t0001g0253 a0001c0001t0001g0335 |
2 | HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1389+450C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 14/28 | chr6 | 85542732 | |||||||
| chr6:85542956 | T | C | 68 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0042 others(65): Show |
69 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.1389+226A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 14/28 | chr6 | 85542956 | |||||||
| chr6:85543023 | C | T | 4 | a0001c0001t0001g0002 a0001c0001t0001g0052 a0001c0001t0001g0055 others(1): Show |
5 | HG02647.hp1 HG02895.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1389+159G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 14/28 | chr6 | 85543023 | |||||||
| chr6:85543879 | C | T | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1109-119G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85543879 | |||||||
| chr6:85543883 | T | C | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1109-123A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85543883 | |||||||
| chr6:85544370 | G | A | 1 | a0001c0001t0001g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1109-610C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85544370 | |||||||
| chr6:85544546 | C | G | 1 | a0001c0001t0001g0309 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1109-786G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85544546 | |||||||
| chr6:85544588 | C | T | 37 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0040 others(34): Show |
38 | HG00408.hp1 HG00597.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1109-828G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85544588 | |||||||
| chr6:85544685 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1109-925G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85544685 | |||||||
| chr6:85544744 | A | G | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1109-984T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85544744 | |||||||
| chr6:85544804 | T | C | 47 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(44): Show |
51 | HG00609.hp2 HG00735.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.1109-1044A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85544804 | |||||||
| chr6:85544832 | T | C | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1109-1072A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85544832 | |||||||
| chr6:85544969 | G | C | 1 | a0001c0001t0001g0336 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1109-1209C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85544969 | |||||||
| chr6:85545123 | C | G | 1 | a0001c0001t0001g0095 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1109-1363G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85545123 | |||||||
| chr6:85545351 | A | T | 1 | a0001c0001t0001g0246 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1109-1591T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85545351 | |||||||
| chr6:85545435 | CAGAT | C | 9 | a0001c0001t0001g0256 a0001c0001t0001g0260 a0001c0001t0001g0261 others(6): Show |
9 | HG00423.hp2 HG00544.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1108+1673_1108+167 others(8): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85545435 | |||||||
| chr6:85545644 | T | C | 7 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(4): Show |
7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1108+1468A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85545644 | |||||||
| chr6:85545769 | C | T | 2 | a0001c0001t0001g0196 a0001c0001t0001g0206 |
2 | HG00408.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1108+1343G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85545769 | |||||||
| chr6:85545831 | G | A | 1 | a0001c0001t0001g0332 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1108+1281C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85545831 | |||||||
| chr6:85545937 | C | G | 1 | a0001c0001t0001g0296 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1108+1175G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85545937 | |||||||
| chr6:85545939 | T | C | 1 | a0001c0001t0001g0296 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1108+1173A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85545939 | |||||||
| chr6:85545940 | C | T | 1 | a0001c0001t0001g0296 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1108+1172G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85545940 | |||||||
| chr6:85545943 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1108+1169C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85545943 | |||||||
| chr6:85546095 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1108+1017T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85546095 | |||||||
| chr6:85546181 | G | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0021 others(5): Show |
8 | HG01884.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1108+931C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85546181 | |||||||
| chr6:85546191 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0020 |
2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1108+921T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85546191 | |||||||
| chr6:85546340 | A | T | 1 | a0001c0001t0001g0047 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1108+772T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85546340 | |||||||
| chr6:85546502 | G | C | 1 | a0001c0001t0001g0064 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1108+610C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85546502 | |||||||
| chr6:85546526 | T | A | 1 | a0001c0001t0001g0193 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1108+586A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85546526 | |||||||
| chr6:85546689 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0020 |
2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1108+423C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85546689 | |||||||
| chr6:85546732 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0059 |
3 | HG02647.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1108+380C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85546732 | |||||||
| chr6:85546753 | G | A | 1 | a0001c0001t0001g0214 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1108+359C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85546753 | |||||||
| chr6:85546965 | C | CA | 47 | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0022 others(44): Show |
48 | HG00544.hp1 HG01070.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.1108+146dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85546965 | |||||||
| chr6:85547065 | T | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0022 |
2 | HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1108+47A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85547065 | |||||||
| chr6:85547231 | A | T | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | splice_region_variant&intron_variant | LOW | c.994-5T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 11/28 | chr6 | 85547231 | |||||||
| chr6:85547817 | C | A | 144 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(141): Show |
150 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.868-267G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 9/28 | chr6 | 85547817 | |||||||
| chr6:85548072 | G | A | 3 | a0001c0001t0001g0107 a0001c0001t0001g0120 a0001c0001t0001g0121 |
3 | HG01975.hp2 HG02004.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.867+229C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 9/28 | chr6 | 85548072 | |||||||
| chr6:85548088 | G | A | 1 | a0001c0001t0001g0341 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.867+213C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 9/28 | chr6 | 85548088 | |||||||
| chr6:85548156 | A | C | 31 | a0001c0001t0001g0010 a0001c0001t0001g0256 a0001c0001t0001g0257 others(28): Show |
32 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.867+145T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 9/28 | chr6 | 85548156 | |||||||
| chr6:85548787 | T | A | 6 | a0001c0001t0001g0256 a0001c0001t0001g0263 a0001c0001t0001g0264 others(3): Show |
6 | HG00544.hp1 NA18948.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.792-411A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 8/28 | chr6 | 85548787 | |||||||
| chr6:85548839 | T | C | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(277): Show |
289 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.792-463A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 8/28 | chr6 | 85548839 | |||||||
| chr6:85548896 | G | A | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.792-520C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 8/28 | chr6 | 85548896 | |||||||
| chr6:85548982 | A | C | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0137 |
3 | HG00609.hp2 HG02155.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.792-606T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 8/28 | chr6 | 85548982 | |||||||
| chr6:85548988 | AG | A | 278 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(275): Show |
286 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.792-613delC | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 8/28 | chr6 | 85548988 | |||||||
| chr6:85548989 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.792-613C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 8/28 | chr6 | 85548989 | |||||||
| chr6:85548993 | G | A | 9 | a0001c0001t0001g0008 a0001c0001t0001g0071 a0001c0001t0001g0170 others(6): Show |
10 | HG01175.hp1 HG01243.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.792-617C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 8/28 | chr6 | 85548993 | |||||||
| chr6:85549118 | C | T | 31 | a0001c0001t0001g0010 a0001c0001t0001g0256 a0001c0001t0001g0257 others(28): Show |
32 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.791+605G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 8/28 | chr6 | 85549118 | |||||||
| chr6:85549310 | T | A | 1 | a0001c0001t0001g0180 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.791+413A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 8/28 | chr6 | 85549310 | |||||||
| chr6:85549424 | A | G | 3 | a0001c0001t0001g0236 a0001c0001t0001g0237 a0001c0001t0001g0240 |
3 | HG03492.hp1 HG03704.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.791+299T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 8/28 | chr6 | 85549424 | |||||||
| chr6:85549487 | A | G | 7 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(4): Show |
7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.791+236T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 8/28 | chr6 | 85549487 | |||||||
| chr6:85549595 | A | T | 4 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0217 others(1): Show |
4 | HG01358.hp2 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.791+128T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 8/28 | chr6 | 85549595 | |||||||
| chr6:85549627 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.791+96T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 8/28 | chr6 | 85549627 | |||||||
| chr6:85550067 | C | A | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.635-188G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85550067 | |||||||
| chr6:85550438 | A | C | 1 | a0001c0001t0001g0010 | 2 | HG01109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.635-559T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85550438 | |||||||
| chr6:85550644 | G | A | 1 | a0001c0001t0001g0290 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.635-765C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85550644 | |||||||
| chr6:85550788 | C | CT | 10 | a0001c0001t0001g0256 a0001c0001t0001g0260 a0001c0001t0001g0263 others(7): Show |
10 | HG00609.hp1 HG02074.hp1 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.635-910dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85550788 | |||||||
| chr6:85551038 | C | T | 31 | a0001c0001t0001g0010 a0001c0001t0001g0256 a0001c0001t0001g0257 others(28): Show |
32 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.635-1159G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85551038 | |||||||
| chr6:85551103 | G | T | 6 | a0001c0001t0001g0256 a0001c0001t0001g0263 a0001c0001t0001g0264 others(3): Show |
6 | HG00544.hp1 NA18948.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.635-1224C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85551103 | |||||||
| chr6:85551172 | T | A | 1 | a0001c0001t0001g0333 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.635-1293A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85551172 | |||||||
| chr6:85551414 | C | A | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.635-1535G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85551414 | |||||||
| chr6:85551513 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0178 |
3 | HG01175.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.635-1634A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85551513 | |||||||
| chr6:85551563 | T | C | 1 | a0001c0001t0001g0038 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.635-1684A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85551563 | |||||||
| chr6:85551668 | C | T | 68 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0042 others(65): Show |
69 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.635-1789G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85551668 | |||||||
| chr6:85551924 | T | C | 1 | a0001c0001t0001g0016 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.635-2045A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85551924 | |||||||
| chr6:85551949 | A | G | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.635-2070T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85551949 | |||||||
| chr6:85552031 | T | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG01433.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.635-2152A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85552031 | |||||||
| chr6:85552032 | C | CT | 100 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0018 others(97): Show |
101 | HG00408.hp2 HG00597.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.635-2154dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85552032 | |||||||
| chr6:85552032 | C | CTT | 9 | a0001c0001t0001g0143 a0001c0001t0001g0145 a0001c0001t0001g0146 others(6): Show |
9 | HG00423.hp1 HG02027.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.635-2155_635-2154d others(4): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85552032 | |||||||
| chr6:85552032 | CT | C | 15 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0047 others(12): Show |
17 | HG00099.hp2 HG00735.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.635-2154delA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85552032 | |||||||
| chr6:85552119 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG01928.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.635-2240G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85552119 | |||||||
| chr6:85552152 | T | C | 3 | a0001c0001t0001g0260 a0001c0001t0001g0261 a0001c0001t0001g0262 |
3 | HG00423.hp2 HG02074.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.635-2273A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85552152 | |||||||
| chr6:85552194 | A | G | 342 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(339): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(352): Show |
intron_variant | MODIFIER | c.635-2315T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85552194 | |||||||
| chr6:85552288 | G | A | 5 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(2): Show |
5 | HG01256.hp1 HG01258.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.635-2409C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85552288 | |||||||
| chr6:85552534 | A | C | 2 | a0001c0001t0001g0310 a0001c0001t0001g0311 |
2 | NA18946.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.635-2655T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85552534 | |||||||
| chr6:85552591 | T | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0052 a0001c0001t0001g0055 others(2): Show |
6 | HG02559.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.635-2712A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85552591 | |||||||
| chr6:85553009 | A | G | 68 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0042 others(65): Show |
69 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.635-3130T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85553009 | |||||||
| chr6:85553090 | G | T | 1 | a0001c0001t0001g0072 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.635-3211C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85553090 | |||||||
| chr6:85553491 | A | C | 1 | a0001c0001t0001g0231 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.635-3612T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85553491 | |||||||
| chr6:85553587 | A | G | 3 | a0001c0001t0001g0124 a0001c0001t0001g0138 a0001c0001t0001g0181 |
3 | HG01243.hp2 HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.635-3708T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85553587 | |||||||
| chr6:85553593 | G | C | 1 | a0001c0001t0001g0288 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.635-3714C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85553593 | |||||||
| chr6:85553647 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.635-3768C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85553647 | |||||||
| chr6:85553786 | C | CA | 157 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(154): Show |
163 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.635-3908dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85553786 | |||||||
| chr6:85553830 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.635-3951A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85553830 | |||||||
| chr6:85553837 | T | C | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.635-3958A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85553837 | |||||||
| chr6:85553911 | C | G | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.635-4032G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85553911 | |||||||
| chr6:85553918 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.635-4039A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85553918 | |||||||
| chr6:85554050 | G | C | 1 | a0001c0001t0001g0122 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.634+3926C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85554050 | |||||||
| chr6:85554210 | T | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0046 |
2 | HG01928.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.634+3766A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85554210 | |||||||
| chr6:85554222 | T | TTA | 11 | a0001c0001t0001g0085 a0001c0001t0001g0180 a0001c0001t0001g0224 others(8): Show |
11 | HG01256.hp2 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.634+3752_634+3753d others(4): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85554222 | |||||||
| chr6:85554297 | T | TACACACA others(15): Show |
7 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0292 others(4): Show |
9 | NA18944.hp1 NA18952.hp1 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.634+3657_634+3678d others(24): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85554297 | |||||||
| chr6:85554367 | C | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG01433.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.634+3609G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85554367 | |||||||
| chr6:85554656 | T | G | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
199 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.634+3320A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85554656 | |||||||
| chr6:85554683 | T | G | 1 | a0001c0001t0001g0141 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.634+3293A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85554683 | |||||||
| chr6:85554964 | GCACATGC others(3): Show |
G | 1 | a0001c0001t0001g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.634+3002_634+3011d others(12): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85554964 | |||||||
| chr6:85555335 | T | C | 2 | a0001c0001t0001g0182 a0001c0001t0001g0185 |
2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.634+2641A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85555335 | |||||||
| chr6:85555367 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.634+2609C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85555367 | |||||||
| chr6:85555484 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.634+2492C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85555484 | |||||||
| chr6:85555646 | T | C | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.634+2330A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85555646 | |||||||
| chr6:85555755 | C | A | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.634+2221G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85555755 | |||||||
| chr6:85555994 | A | AT | 3 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0057 |
3 | HG02145.hp2 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.634+1981dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85555994 | |||||||
| chr6:85556114 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.634+1862C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85556114 | |||||||
| chr6:85556227 | G | A | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.634+1749C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85556227 | |||||||
| chr6:85556310 | T | C | 1 | a0001c0001t0001g0010 | 2 | HG01109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.634+1666A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85556310 | |||||||
| chr6:85556410 | A | T | 1 | a0001c0003t0002g0035 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.634+1566T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85556410 | |||||||
| chr6:85556411 | A | T | 30 | a0001c0001t0001g0010 a0001c0001t0001g0256 a0001c0001t0001g0257 others(27): Show |
31 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.634+1565T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85556411 | |||||||
| chr6:85556415 | G | T | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(277): Show |
289 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.634+1561C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85556415 | |||||||
| chr6:85556472 | C | CT | 239 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(236): Show |
247 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.634+1503dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85556472 | |||||||
| chr6:85556764 | T | G | 31 | a0001c0001t0001g0010 a0001c0001t0001g0256 a0001c0001t0001g0257 others(28): Show |
32 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.634+1212A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85556764 | |||||||
| chr6:85556933 | C | T | 41 | a0001c0001t0001g0008 a0001c0001t0001g0062 a0001c0001t0001g0063 others(38): Show |
42 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.634+1043G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85556933 | |||||||
| chr6:85557216 | G | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0052 a0001c0001t0001g0055 others(1): Show |
5 | HG02647.hp1 HG02895.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.634+760C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85557216 | |||||||
| chr6:85557396 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.634+580C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85557396 | |||||||
| chr6:85557409 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG01433.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.634+567A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85557409 | |||||||
| chr6:85557661 | C | T | 1 | a0001c0001t0001g0264 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.634+315G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85557661 | |||||||
| chr6:85557691 | A | T | 1 | a0001c0001t0001g0308 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.634+285T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85557691 | |||||||
| chr6:85558072 | C | T | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.550-12G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85558072 | |||||||
| chr6:85558302 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.550-242T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85558302 | |||||||
| chr6:85558325 | G | T | 1 | a0001c0001t0001g0266 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.550-265C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85558325 | |||||||
| chr6:85558408 | A | G | 4 | a0001c0003t0002g0035 a0001c0003t0002g0036 a0001c0003t0002g0053 others(1): Show |
4 | HG02818.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.550-348T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85558408 | |||||||
| chr6:85558430 | C | A | 1 | a0001c0001t0001g0219 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.550-370G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85558430 | |||||||
| chr6:85558535 | C | T | 1 | a0001c0001t0001g0258 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.550-475G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85558535 | |||||||
| chr6:85558555 | G | A | 10 | a0001c0001t0001g0006 a0001c0001t0001g0129 a0001c0001t0001g0130 others(7): Show |
11 | HG00609.hp2 HG02040.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.550-495C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85558555 | |||||||
| chr6:85558588 | G | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0052 |
3 | HG02895.hp2 HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.550-528C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85558588 | |||||||
| chr6:85558606 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.550-546G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85558606 | |||||||
| chr6:85558618 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.550-558G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85558618 | |||||||
| chr6:85558653 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.550-593C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85558653 | |||||||
| chr6:85558936 | GA | G | 279 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(276): Show |
288 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.550-877delT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85558936 | |||||||
| chr6:85559008 | G | A | 10 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.550-948C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85559008 | |||||||
| chr6:85559321 | C | T | 47 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(44): Show |
51 | HG00609.hp2 HG00735.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.550-1261G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85559321 | |||||||
| chr6:85559374 | A | G | 2 | a0001c0001t0001g0237 a0001c0001t0001g0240 |
2 | HG03704.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.550-1314T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85559374 | |||||||
| chr6:85559413 | A | T | 2 | a0001c0001t0001g0143 a0001c0001t0001g0144 |
2 | HG00597.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.550-1353T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85559413 | |||||||
| chr6:85559437 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.550-1377A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85559437 | |||||||
| chr6:85559475 | A | G | 1 | a0001c0001t0001g0089 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.550-1415T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85559475 | |||||||
| chr6:85559654 | T | A | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
4 | HG02109.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.550-1594A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85559654 | |||||||
| chr6:85559694 | G | A | 1 | a0001c0001t0001g0342 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.550-1634C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85559694 | |||||||
| chr6:85559913 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.550-1853C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85559913 | |||||||
| chr6:85560201 | T | C | 1 | a0001c0001t0001g0200 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.550-2141A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85560201 | |||||||
| chr6:85560494 | G | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0170 a0001c0001t0001g0171 others(7): Show |
11 | HG00099.hp2 HG01069.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.550-2434C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85560494 | |||||||
| chr6:85560803 | G | A | 5 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0051 others(2): Show |
5 | HG02145.hp2 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.550-2743C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85560803 | |||||||
| chr6:85560818 | G | C | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.550-2758C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85560818 | |||||||
| chr6:85561033 | TA | T | 7 | a0001c0001t0001g0018 a0001c0001t0001g0240 a0001c0001t0001g0254 others(4): Show |
7 | HG02523.hp1 HG02895.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.550-2974delT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85561033 | |||||||
| chr6:85561052 | G | C | 1 | a0001c0001t0001g0075 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.550-2992C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85561052 | |||||||
| chr6:85561240 | C | T | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.550-3180G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85561240 | |||||||
| chr6:85561471 | A | G | 3 | a0001c0001t0001g0106 a0001c0001t0001g0123 a0001c0001t0001g0128 |
3 | HG01070.hp1 HG01071.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.550-3411T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85561471 | |||||||
| chr6:85561472 | A | C | 2 | a0001c0001t0001g0094 a0001c0001t0001g0255 |
2 | NA19006.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.550-3412T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85561472 | |||||||
| chr6:85561711 | G | A | 3 | a0001c0001t0001g0069 a0001c0001t0001g0087 a0001c0001t0001g0088 |
3 | NA18959.hp2 NA18971.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.549+3621C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85561711 | |||||||
| chr6:85561808 | T | G | 72 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0017 others(69): Show |
74 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.549+3524A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85561808 | |||||||
| chr6:85561818 | CTTTTTTG | C | 8 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0102 others(5): Show |
8 | HG02257.hp2 HG02717.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.549+3507_549+3513d others(9): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85561818 | |||||||
| chr6:85561825 | G | GT | 13 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0047 others(10): Show |
13 | HG01109.hp2 HG01243.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.549+3506dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85561825 | |||||||
| chr6:85562103 | G | A | 25 | a0001c0001t0001g0010 a0001c0001t0001g0257 a0001c0001t0001g0258 others(22): Show |
26 | HG00423.hp2 HG01070.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.549+3229C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85562103 | |||||||
| chr6:85562118 | T | A | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.549+3214A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85562118 | |||||||
| chr6:85562193 | G | A | 7 | a0001c0001t0001g0239 a0001c0001t0001g0241 a0001c0001t0001g0242 others(4): Show |
7 | NA18952.hp2 NA18966.hp1 NA19055.hp2 others(4): Show |
intron_variant | MODIFIER | c.549+3139C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85562193 | |||||||
| chr6:85562454 | G | A | 5 | a0001c0001t0001g0096 a0001c0001t0001g0182 a0001c0001t0001g0184 others(2): Show |
5 | HG02257.hp2 HG02723.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.549+2878C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85562454 | |||||||
| chr6:85562582 | C | CT | 191 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(188): Show |
196 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.549+2749dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85562582 | |||||||
| chr6:85562582 | C | CTT | 29 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0022 others(26): Show |
29 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.549+2748_549+2749d others(4): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85562582 | |||||||
| chr6:85562582 | CTTT | C | 7 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(4): Show |
7 | HG01168.hp2 HG02109.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.549+2747_549+2749d others(5): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85562582 | |||||||
| chr6:85562582 | CTTTTTTT | C | 44 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(41): Show |
48 | HG00609.hp2 HG00735.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.549+2743_549+2749d others(9): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85562582 | |||||||
| chr6:85562606 | A | C | 5 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0059 others(2): Show |
5 | HG02647.hp2 HG03130.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.549+2726T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85562606 | |||||||
| chr6:85562658 | C | T | 25 | a0001c0001t0001g0010 a0001c0001t0001g0257 a0001c0001t0001g0258 others(22): Show |
26 | HG00423.hp2 HG01070.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.549+2674G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85562658 | |||||||
| chr6:85562755 | A | G | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.549+2577T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85562755 | |||||||
| chr6:85562857 | T | C | 1 | a0001c0003t0002g0053 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.549+2475A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85562857 | |||||||
| chr6:85562920 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.549+2412G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85562920 | |||||||
| chr6:85563297 | A | G | 1 | a0003c0006t0001g0049 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.549+2035T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85563297 | |||||||
| chr6:85563541 | G | A | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.549+1791C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85563541 | |||||||
| chr6:85563626 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.549+1706G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85563626 | |||||||
| chr6:85563627 | G | T | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.549+1705C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85563627 | |||||||
| chr6:85563682 | C | A | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
4 | HG02109.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.549+1650G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85563682 | |||||||
| chr6:85563684 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.549+1648G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85563684 | |||||||
| chr6:85563920 | C | A | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
4 | HG02109.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.549+1412G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85563920 | |||||||
| chr6:85564039 | A | G | 280 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(277): Show |
289 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.549+1293T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85564039 | |||||||
| chr6:85564341 | C | T | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.549+991G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85564341 | |||||||
| chr6:85564614 | G | A | 3 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0057 |
3 | HG02145.hp2 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.549+718C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85564614 | |||||||
| chr6:85564737 | C | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0059 |
3 | HG02647.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.549+595G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85564737 | |||||||
| chr6:85564807 | G | A | 78 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0017 others(75): Show |
80 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.549+525C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85564807 | |||||||
| chr6:85564849 | C | T | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.549+483G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85564849 | |||||||
| chr6:85564921 | G | A | 1 | a0001c0001t0001g0222 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.549+411C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85564921 | |||||||
| chr6:85564947 | C | T | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.549+385G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85564947 | |||||||
| chr6:85564951 | T | C | 2 | a0001c0003t0002g0036 a0001c0003t0002g0054 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.549+381A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85564951 | |||||||
| chr6:85564987 | T | TA | 15 | a0001c0001t0001g0010 a0001c0001t0001g0191 a0001c0001t0001g0257 others(12): Show |
16 | HG00423.hp2 HG01109.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.549+344dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85564987 | |||||||
| chr6:85565063 | G | C | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.549+269C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85565063 | |||||||
| chr6:85565111 | T | TAACA | 193 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
200 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.549+220_549+221ins others(4): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85565111 | |||||||
| chr6:85565663 | A | T | 1 | a0001c0001t0001g0050 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.462-244T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85565663 | |||||||
| chr6:85565762 | C | G | 1 | a0001c0001t0001g0269 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.462-343G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85565762 | |||||||
| chr6:85565771 | T | G | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.462-352A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85565771 | |||||||
| chr6:85566031 | T | C | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.462-612A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85566031 | |||||||
| chr6:85566178 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.462-759C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85566178 | |||||||
| chr6:85566239 | C | G | 1 | a0001c0001t0001g0020 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.462-820G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85566239 | |||||||
| chr6:85566298 | C | G | 1 | a0001c0001t0001g0228 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.462-879G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85566298 | |||||||
| chr6:85566448 | A | G | 4 | a0001c0001t0001g0002 a0001c0001t0001g0052 a0001c0001t0001g0055 others(1): Show |
5 | HG02647.hp1 HG02895.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.462-1029T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85566448 | |||||||
| chr6:85566570 | C | T | 31 | a0001c0001t0001g0010 a0001c0001t0001g0256 a0001c0001t0001g0257 others(28): Show |
32 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.461+964G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85566570 | |||||||
| chr6:85566653 | G | A | 21 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(18): Show |
21 | HG00735.hp2 HG01168.hp2 HG02818.hp2 others(18): Show |
intron_variant | MODIFIER | c.461+881C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85566653 | |||||||
| chr6:85566729 | A | G | 1 | a0001c0001t0001g0236 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.461+805T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85566729 | |||||||
| chr6:85566748 | T | A | 2 | a0001c0001t0001g0076 a0001c0001t0001g0077 |
2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.461+786A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85566748 | |||||||
| chr6:85566748 | T | C | 4 | a0001c0001t0001g0002 a0001c0001t0001g0052 a0001c0001t0001g0055 others(1): Show |
5 | HG02647.hp1 HG02895.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.461+786A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85566748 | |||||||
| chr6:85566916 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.461+618A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85566916 | |||||||
| chr6:85566950 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.461+584C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85566950 | |||||||
| chr6:85566986 | A | G | 27 | a0001c0001t0001g0010 a0001c0001t0001g0256 a0001c0001t0001g0257 others(24): Show |
28 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.461+548T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85566986 | |||||||
| chr6:85567123 | C | T | 27 | a0001c0001t0001g0010 a0001c0001t0001g0256 a0001c0001t0001g0257 others(24): Show |
28 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.461+411G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85567123 | |||||||
| chr6:85567135 | A | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG00280.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.461+399T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85567135 | |||||||
| chr6:85567351 | CA | C | 67 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0042 others(64): Show |
68 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.461+182delT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85567351 | |||||||
| chr6:85567402 | T | C | 3 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 |
3 | HG02818.hp2 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.461+132A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85567402 | |||||||
| chr6:85567437 | A | G | 2 | a0002c0002t0001g0297 a0002c0002t0001g0304 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.461+97T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85567437 | |||||||
| chr6:85567654 | T | C | 1 | a0003c0006t0001g0049 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.418-77A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85567654 | |||||||
| chr6:85567679 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.418-102T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85567679 | |||||||
| chr6:85567704 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.418-127C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85567704 | |||||||
| chr6:85567874 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.418-297A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85567874 | |||||||
| chr6:85567900 | T | C | 2 | a0001c0001t0001g0123 a0001c0001t0001g0128 |
2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.418-323A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85567900 | |||||||
| chr6:85567957 | T | C | 7 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0140 others(4): Show |
7 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.418-380A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85567957 | |||||||
| chr6:85568102 | A | AAAAATTC others(7): Show |
9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.418-539_418-526dup others(14): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85568102 | |||||||
| chr6:85568225 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.418-648G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85568225 | |||||||
| chr6:85568464 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0059 |
3 | HG02647.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.418-887C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85568464 | |||||||
| chr6:85568548 | C | T | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.418-971G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85568548 | |||||||
| chr6:85568575 | A | G | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.418-998T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85568575 | |||||||
| chr6:85568585 | C | T | 1 | a0001c0001t0001g0303 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.418-1008G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85568585 | |||||||
| chr6:85568586 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.418-1009C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85568586 | |||||||
| chr6:85568698 | A | G | 1 | a0001c0001t0001g0245 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.418-1121T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85568698 | |||||||
| chr6:85568729 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.418-1152A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85568729 | |||||||
| chr6:85568973 | T | C | 197 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(194): Show |
204 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.418-1396A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85568973 | |||||||
| chr6:85568974 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.418-1397A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85568974 | |||||||
| chr6:85569006 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.418-1429G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85569006 | |||||||
| chr6:85569037 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.418-1460G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85569037 | |||||||
| chr6:85569103 | T | C | 3 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 |
3 | HG02258.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.418-1526A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85569103 | |||||||
| chr6:85569408 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.418-1831G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85569408 | |||||||
| chr6:85569409 | A | T | 7 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(4): Show |
7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.418-1832T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85569409 | |||||||
| chr6:85569523 | G | A | 2 | a0001c0003t0002g0036 a0001c0003t0002g0054 |
2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.418-1946C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85569523 | |||||||
| chr6:85569699 | T | C | 3 | a0001c0001t0001g0124 a0001c0001t0001g0138 a0001c0001t0001g0181 |
3 | HG01243.hp2 HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.418-2122A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85569699 | |||||||
| chr6:85569755 | C | T | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG00280.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.418-2178G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85569755 | |||||||
| chr6:85569786 | T | C | 1 | a0001c0001t0001g0291 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.418-2209A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85569786 | |||||||
| chr6:85570019 | C | T | 121 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(118): Show |
126 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(123): Show |
intron_variant | MODIFIER | c.417+2118G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85570019 | |||||||
| chr6:85570333 | TG | T | 199 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(196): Show |
206 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.417+1803delC | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85570333 | |||||||
| chr6:85570416 | T | C | 1 | a0001c0001t0001g0245 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.417+1721A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85570416 | |||||||
| chr6:85570537 | T | C | 1 | a0001c0001t0001g0090 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.417+1600A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85570537 | |||||||
| chr6:85570580 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0059 |
3 | HG02647.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.417+1557G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85570580 | |||||||
| chr6:85570597 | A | AT | 7 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(4): Show |
7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.417+1539dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85570597 | |||||||
| chr6:85570604 | C | A | 1 | a0001c0001t0001g0259 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.417+1533G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85570604 | |||||||
| chr6:85570621 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.417+1516C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85570621 | |||||||
| chr6:85570668 | T | C | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG01433.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.417+1469A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85570668 | |||||||
| chr6:85570670 | T | C | 2 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.417+1467A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85570670 | |||||||
| chr6:85570675 | A | C | 1 | a0001c0001t0001g0020 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.417+1462T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85570675 | |||||||
| chr6:85571091 | G | A | 3 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0057 |
3 | HG02145.hp2 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.417+1046C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85571091 | |||||||
| chr6:85571157 | G | A | 199 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(196): Show |
206 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.417+980C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85571157 | |||||||
| chr6:85571211 | T | C | 1 | a0001c0001t0001g0127 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.417+926A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85571211 | |||||||
| chr6:85571216 | C | T | 11 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 others(8): Show |
11 | HG00642.hp2 HG01169.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.417+921G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85571216 | |||||||
| chr6:85571220 | C | A | 1 | a0001c0001t0001g0046 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.417+917G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85571220 | |||||||
| chr6:85571232 | C | T | 1 | a0001c0001t0001g0069 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.417+905G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85571232 | |||||||
| chr6:85571359 | C | CA | 10 | a0001c0001t0001g0002 a0001c0001t0001g0052 a0001c0001t0001g0055 others(7): Show |
11 | HG00544.hp1 HG02040.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.417+777dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85571359 | |||||||
| chr6:85571536 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.417+601C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85571536 | |||||||
| chr6:85571742 | C | T | 4 | a0001c0003t0002g0035 a0001c0003t0002g0036 a0001c0003t0002g0053 others(1): Show |
4 | HG02818.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.417+395G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85571742 | |||||||
| chr6:85571819 | C | A | 1 | a0001c0001t0001g0270 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.417+318G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85571819 | |||||||
| chr6:85571864 | G | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0052 a0001c0001t0001g0055 others(1): Show |
5 | HG02647.hp1 HG02895.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.417+273C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85571864 | |||||||
| chr6:85572058 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.417+79A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85572058 | |||||||
| chr6:85572262 | T | C | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.338+36A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 3/28 | chr6 | 85572262 | |||||||
| chr6:85572542 | A | T | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.262-168T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85572542 | |||||||
| chr6:85572560 | A | AAAATACC | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.262-193_262-187dup others(7): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85572560 | |||||||
| chr6:85572725 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.262-351C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85572725 | |||||||
| chr6:85572740 | T | A | 8 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0021 others(5): Show |
8 | HG01884.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.262-366A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85572740 | |||||||
| chr6:85572865 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.262-491C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85572865 | |||||||
| chr6:85573060 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.262-686C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85573060 | |||||||
| chr6:85573348 | C | A | 1 | a0001c0001t0001g0057 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.261+910G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85573348 | |||||||
| chr6:85573372 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0090 |
2 | NA18973.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.261+886A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85573372 | |||||||
| chr6:85573798 | A | G | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.261+460T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85573798 | |||||||
| chr6:85573857 | G | C | 199 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(196): Show |
206 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.261+401C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85573857 | |||||||
| chr6:85574059 | TATA | T | 150 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(147): Show |
156 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.261+196_261+198del others(3): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85574059 | |||||||
| chr6:85574080 | T | C | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.261+178A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85574080 | |||||||
| chr6:85574100 | G | A | 3 | a0001c0001t0001g0227 a0001c0001t0001g0247 a0001c0001t0001g0248 |
3 | HG01109.hp1 HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.261+158C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85574100 | |||||||
| chr6:85574119 | C | A | 1 | a0001c0001t0001g0162 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.261+139G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85574119 | |||||||
| chr6:85574119 | C | CA | 238 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(235): Show |
248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.261+138dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85574119 | |||||||
| chr6:85574119 | C | CAA | 18 | a0001c0001t0001g0006 a0001c0001t0001g0129 a0001c0001t0001g0130 others(15): Show |
19 | HG00609.hp2 HG02040.hp1 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.261+137_261+138dup others(2): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85574119 | |||||||
| chr6:85574123 | A | C | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.261+135T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85574123 | |||||||
| chr6:85574131 | AGAG | A | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.261+124_261+126del others(3): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85574131 | |||||||
| chr6:85574383 | AAAAT | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 |
3 | HG01258.hp1 HG02055.hp2 HG02145.hp1 |
splice_region_variant&intron_variant | LOW | c.141-9_141-6delATTT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85574383 | |||||||
| chr6:85574437 | C | T | 7 | a0001c0001t0001g0017 a0001c0001t0001g0187 a0001c0001t0001g0188 others(4): Show |
7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.141-59G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85574437 | |||||||
| chr6:85574506 | GATTA | G | 6 | a0001c0001t0001g0037 a0001c0001t0001g0097 a0001c0001t0001g0098 others(3): Show |
6 | HG02280.hp1 HG02615.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.141-132_141-129del others(4): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85574506 | |||||||
| chr6:85574583 | A | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0104 |
2 | NA18941.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.141-205T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85574583 | |||||||
| chr6:85574618 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.141-240G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85574618 | |||||||
| chr6:85574646 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.141-268G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85574646 | |||||||
| chr6:85574794 | TAGTCTCT others(52): Show |
T | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.141-475_141-417del others(59): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85574794 | |||||||
| chr6:85574885 | C | T | 4 | a0001c0003t0002g0035 a0001c0003t0002g0036 a0001c0003t0002g0053 others(1): Show |
4 | HG02818.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-507G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85574885 | |||||||
| chr6:85574953 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.141-575C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85574953 | |||||||
| chr6:85574962 | G | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0170 a0001c0001t0001g0171 others(5): Show |
9 | HG01175.hp1 HG01243.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.141-584C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85574962 | |||||||
| chr6:85575108 | C | T | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.141-730G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85575108 | |||||||
| chr6:85575138 | TA | T | 4 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0059 others(1): Show |
4 | HG02647.hp2 HG03209.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-761delT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85575138 | |||||||
| chr6:85575236 | A | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0052 a0001c0001t0001g0055 others(2): Show |
6 | HG02559.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.141-858T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85575236 | |||||||
| chr6:85575741 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.141-1363C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85575741 | |||||||
| chr6:85575867 | T | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0052 a0001c0001t0001g0055 others(2): Show |
6 | HG02559.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.141-1489A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85575867 | |||||||
| chr6:85576258 | T | C | 1 | a0001c0001t0001g0018 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.141-1880A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85576258 | |||||||
| chr6:85576345 | A | G | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.141-1967T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85576345 | |||||||
| chr6:85576364 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.141-1986C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85576364 | |||||||
| chr6:85576520 | CA | C | 31 | a0001c0001t0001g0010 a0001c0001t0001g0256 a0001c0001t0001g0257 others(28): Show |
32 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.141-2143delT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85576520 | |||||||
| chr6:85576631 | C | T | 2 | a0001c0001t0001g0140 a0001c0001t0001g0165 |
2 | HG02451.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.141-2253G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85576631 | |||||||
| chr6:85576849 | T | C | 1 | a0001c0001t0001g0163 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.141-2471A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85576849 | |||||||
| chr6:85576879 | A | T | 1 | a0001c0001t0001g0042 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.141-2501T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85576879 | |||||||
| chr6:85576944 | G | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0067 |
3 | HG01257.hp1 HG01258.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.141-2566C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85576944 | |||||||
| chr6:85576978 | A | G | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.141-2600T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85576978 | |||||||
| chr6:85577287 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.141-2909C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85577287 | |||||||
| chr6:85577411 | C | A | 160 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(157): Show |
166 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.141-3033G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85577411 | |||||||
| chr6:85577711 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.141-3333A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85577711 | |||||||
| chr6:85578023 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.141-3645C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85578023 | |||||||
| chr6:85578150 | G | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0052 a0001c0001t0001g0055 others(2): Show |
6 | HG02559.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.141-3772C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85578150 | |||||||
| chr6:85578185 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.141-3807C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85578185 | |||||||
| chr6:85578330 | T | C | 1 | a0003c0006t0001g0049 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.141-3952A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85578330 | |||||||
| chr6:85578641 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.141-4263A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85578641 | |||||||
| chr6:85578858 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.141-4480C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85578858 | |||||||
| chr6:85578874 | G | A | 4 | a0001c0001t0001g0002 a0001c0001t0001g0052 a0001c0001t0001g0055 others(1): Show |
5 | HG02647.hp1 HG02895.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.141-4496C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85578874 | |||||||
| chr6:85578995 | G | A | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.141-4617C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85578995 | |||||||
| chr6:85579080 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.141-4702C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85579080 | |||||||
| chr6:85579203 | T | A | 31 | a0001c0001t0001g0010 a0001c0001t0001g0256 a0001c0001t0001g0257 others(28): Show |
32 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.141-4825A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85579203 | |||||||
| chr6:85579385 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.141-5007G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85579385 | |||||||
| chr6:85579459 | C | T | 3 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0057 |
3 | HG02145.hp2 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.141-5081G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85579459 | |||||||
| chr6:85579598 | G | C | 7 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(4): Show |
7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.141-5220C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85579598 | |||||||
| chr6:85579671 | G | A | 1 | a0003c0006t0001g0049 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.141-5293C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85579671 | |||||||
| chr6:85579697 | A | G | 342 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(339): Show |
355 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(352): Show |
intron_variant | MODIFIER | c.141-5319T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85579697 | |||||||
| chr6:85579705 | G | A | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | NA18952.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.141-5327C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85579705 | |||||||
| chr6:85579739 | C | T | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.141-5361G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85579739 | |||||||
| chr6:85579955 | C | T | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
220 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.141-5577G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85579955 | |||||||
| chr6:85579972 | C | A | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.141-5594G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85579972 | |||||||
| chr6:85580028 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.141-5650C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85580028 | |||||||
| chr6:85580081 | T | C | 1 | a0001c0001t0001g0228 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.141-5703A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85580081 | |||||||
| chr6:85580294 | G | A | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.141-5916C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85580294 | |||||||
| chr6:85580462 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.141-6084T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85580462 | |||||||
| chr6:85580606 | C | T | 14 | a0001c0001t0001g0256 a0001c0001t0001g0260 a0001c0001t0001g0261 others(11): Show |
14 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.141-6228G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85580606 | |||||||
| chr6:85580648 | A | G | 1 | a0001c0001t0001g0296 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.141-6270T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85580648 | |||||||
| chr6:85580925 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.141-6547A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85580925 | |||||||
| chr6:85581275 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.141-6897C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85581275 | |||||||
| chr6:85581352 | G | A | 10 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(7): Show |
10 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.141-6974C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85581352 | |||||||
| chr6:85581597 | A | G | 3 | a0001c0001t0001g0286 a0001c0001t0001g0293 a0001c0001t0001g0294 |
3 | HG03704.hp1 HG03831.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.141-7219T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85581597 | |||||||
| chr6:85581731 | T | C | 1 | a0001c0001t0001g0139 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.141-7353A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85581731 | |||||||
| chr6:85581752 | A | T | 3 | a0001c0001t0001g0287 a0001c0001t0001g0288 a0001c0001t0001g0295 |
3 | HG00597.hp2 NA18998.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.141-7374T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85581752 | |||||||
| chr6:85582193 | T | C | 31 | a0001c0001t0001g0010 a0001c0001t0001g0256 a0001c0001t0001g0257 others(28): Show |
32 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.141-7815A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85582193 | |||||||
| chr6:85582217 | G | A | 151 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(148): Show |
157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.141-7839C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85582217 | |||||||
| chr6:85582628 | T | G | 3 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0059 |
3 | HG02647.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.141-8250A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85582628 | |||||||
| chr6:85583007 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.141-8629C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85583007 | |||||||
| chr6:85583040 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.141-8662G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85583040 | |||||||
| chr6:85583056 | A | G | 3 | a0001c0001t0001g0258 a0001c0001t0001g0259 a0001c0001t0001g0279 |
3 | HG02258.hp2 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.141-8678T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85583056 | |||||||
| chr6:85583069 | C | T | 3 | a0001c0001t0001g0286 a0001c0001t0001g0293 a0001c0001t0001g0294 |
3 | HG03704.hp1 HG03831.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.141-8691G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85583069 | |||||||
| chr6:85583079 | C | T | 7 | a0001c0001t0001g0037 a0001c0001t0001g0097 a0001c0001t0001g0098 others(4): Show |
7 | HG02280.hp1 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.141-8701G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85583079 | |||||||
| chr6:85583305 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.141-8927A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85583305 | |||||||
| chr6:85583509 | T | C | 37 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0040 others(34): Show |
38 | HG00408.hp1 HG00597.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.141-9131A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85583509 | |||||||
| chr6:85583605 | T | C | 1 | a0001c0001t0001g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.141-9227A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85583605 | |||||||
| chr6:85583777 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.141-9399C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85583777 | |||||||
| chr6:85583783 | G | C | 2 | a0001c0001t0001g0048 a0001c0001t0001g0057 |
2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.141-9405C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85583783 | |||||||
| chr6:85583802 | C | A | 68 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0042 others(65): Show |
69 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.141-9424G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85583802 | |||||||
| chr6:85584065 | A | G | 4 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(1): Show |
4 | HG01256.hp1 HG01258.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.140+9514T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85584065 | |||||||
| chr6:85584175 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.140+9404A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85584175 | |||||||
| chr6:85584330 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.140+9249G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85584330 | |||||||
| chr6:85584397 | T | G | 1 | a0001c0001t0001g0239 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.140+9182A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85584397 | |||||||
| chr6:85584400 | G | A | 1 | a0001c0001t0001g0239 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.140+9179C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85584400 | |||||||
| chr6:85584885 | A | C | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.140+8694T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85584885 | |||||||
| chr6:85585229 | C | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(62): Show |
69 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.140+8350G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585229 | |||||||
| chr6:85585292 | G | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0052 a0001c0001t0001g0055 others(2): Show |
6 | HG02559.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.140+8287C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585292 | |||||||
| chr6:85585365 | C | T | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.140+8214G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585365 | |||||||
| chr6:85585391 | A | C | 3 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0057 |
3 | HG02145.hp2 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.140+8188T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585391 | |||||||
| chr6:85585461 | A | G | 1 | a0001c0001t0001g0343 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.140+8118T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585461 | |||||||
| chr6:85585680 | ACTAT | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(62): Show |
69 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.140+7895_140+7898d others(6): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585680 | |||||||
| chr6:85585711 | C | T | 288 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(285): Show |
300 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(297): Show |
intron_variant | MODIFIER | c.140+7868G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585711 | |||||||
| chr6:85585855 | T | G | 1 | a0001c0001t0001g0093 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.140+7724A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585855 | |||||||
| chr6:85585908 | C | A | 10 | a0001c0001t0001g0008 a0001c0001t0001g0170 a0001c0001t0001g0171 others(7): Show |
11 | HG00099.hp2 HG01069.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.140+7671G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585908 | |||||||
| chr6:85585939 | T | C | 3 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0059 |
3 | HG02647.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.140+7640A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585939 | |||||||
| chr6:85585982 | C | T | 1 | a0001c0001t0006g0347 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.140+7597G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585982 | |||||||
| chr6:85585990 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0059 |
3 | HG02647.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.140+7589C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585990 | |||||||
| chr6:85585990 | G | GA | 8 | a0001c0001t0001g0061 a0001c0001t0001g0177 a0001c0001t0001g0178 others(5): Show |
8 | HG00544.hp1 HG01175.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.140+7588dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585990 | |||||||
| chr6:85585990 | GA | G | 10 | a0001c0001t0001g0002 a0001c0001t0001g0051 a0001c0001t0001g0052 others(7): Show |
11 | HG02559.hp1 HG02647.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.140+7588delT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585990 | |||||||
| chr6:85586007 | A | C | 1 | a0001c0001t0001g0021 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.140+7572T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85586007 | |||||||
| chr6:85586140 | C | A | 69 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(66): Show |
73 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.140+7439G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85586140 | |||||||
| chr6:85586274 | G | C | 1 | a0001c0001t0001g0341 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.140+7305C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85586274 | |||||||
| chr6:85586315 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.140+7264C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85586315 | |||||||
| chr6:85586613 | C | T | 1 | a0001c0001t0001g0292 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.140+6966G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85586613 | |||||||
| chr6:85586662 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.140+6917G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85586662 | |||||||
| chr6:85586728 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.140+6851C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85586728 | |||||||
| chr6:85587070 | G | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(62): Show |
69 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.140+6509C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85587070 | |||||||
| chr6:85587146 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.140+6433G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85587146 | |||||||
| chr6:85587207 | CA | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(144): Show |
153 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.140+6371delT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85587207 | |||||||
| chr6:85587364 | T | C | 5 | a0001c0001t0001g0002 a0001c0001t0001g0052 a0001c0001t0001g0055 others(2): Show |
6 | HG02559.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.140+6215A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85587364 | |||||||
| chr6:85587659 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.140+5920C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85587659 | |||||||
| chr6:85587762 | TTAAA | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0050 others(6): Show |
10 | HG02145.hp2 HG02486.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.140+5813_140+5816d others(6): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85587762 | |||||||
| chr6:85587839 | A | G | 3 | a0001c0001t0001g0048 a0001c0001t0001g0050 a0001c0001t0001g0057 |
3 | HG02145.hp2 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.140+5740T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85587839 | |||||||
| chr6:85587908 | C | G | 68 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0042 others(65): Show |
69 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.140+5671G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85587908 | |||||||
| chr6:85588001 | A | G | 29 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 others(26): Show |
29 | HG00642.hp2 HG01169.hp2 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.140+5578T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85588001 | |||||||
| chr6:85588345 | A | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(191): Show |
201 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.140+5234T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85588345 | |||||||
| chr6:85588401 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.140+5178C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85588401 | |||||||
| chr6:85588438 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.140+5141C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85588438 | |||||||
| chr6:85588440 | G | A | 2 | a0001c0001t0001g0017 a0001c0001t0001g0253 |
2 | HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.140+5139C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85588440 | |||||||
| chr6:85588453 | T | G | 1 | a0001c0001t0001g0018 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.140+5126A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85588453 | |||||||
| chr6:85588575 | C | CTAAATAA others(1): Show |
10 | a0001c0001t0001g0047 a0001c0001t0001g0187 a0001c0001t0001g0188 others(7): Show |
10 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.140+4996_140+5003d others(10): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85588575 | |||||||
| chr6:85588575 | C | CTAAATAA others(5): Show |
115 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0011 others(112): Show |
120 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.140+4992_140+5003d others(14): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85588575 | |||||||
| chr6:85588575 | C | CTAAATAA others(9): Show |
36 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0019 others(33): Show |
37 | HG00735.hp2 HG01168.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.140+4988_140+5003d others(18): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85588575 | |||||||
| chr6:85588575 | C | CTAAATAA others(13): Show |
4 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0193 others(1): Show |
4 | HG02647.hp1 HG03654.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.140+4984_140+5003d others(22): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85588575 | |||||||
| chr6:85588575 | C | CTAAATAA others(17): Show |
1 | a0001c0001t0001g0195 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.140+4980_140+5003d others(26): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85588575 | |||||||
| chr6:85588780 | A | G | 2 | a0001c0001t0001g0004 a0001c0001t0001g0067 |
3 | HG01257.hp1 HG01258.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.140+4799T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85588780 | |||||||
| chr6:85588799 | T | C | 6 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(3): Show |
6 | HG03017.hp1 HG03492.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.140+4780A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85588799 | |||||||
| chr6:85589051 | C | T | 1 | a0001c0003t0002g0035 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.140+4528G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85589051 | |||||||
| chr6:85589052 | G | A | 1 | a0001c0007t0001g0346 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.140+4527C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85589052 | |||||||
| chr6:85589139 | C | T | 1 | a0001c0001t0001g0014 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.140+4440G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85589139 | |||||||
| chr6:85589143 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.140+4436C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85589143 | |||||||
| chr6:85589225 | C | CT | 10 | a0001c0001t0001g0042 a0001c0001t0001g0048 a0001c0001t0001g0057 others(7): Show |
10 | HG01358.hp2 HG02129.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.140+4353dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85589225 | |||||||
| chr6:85589225 | CT | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(83): Show |
90 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(87): Show |
intron_variant | MODIFIER | c.140+4353delA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85589225 | |||||||
| chr6:85589287 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.140+4292C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85589287 | |||||||
| chr6:85589365 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.140+4214G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85589365 | |||||||
| chr6:85589474 | T | G | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | HG02451.hp2 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.140+4105A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85589474 | |||||||
| chr6:85589475 | C | T | 3 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | HG02451.hp2 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.140+4104G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85589475 | |||||||
| chr6:85589750 | A | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.140+3829T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85589750 | |||||||
| chr6:85589808 | A | G | 1 | a0001c0001t0001g0286 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.140+3771T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85589808 | |||||||
| chr6:85589981 | G | A | 3 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0059 |
3 | HG02647.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.140+3598C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85589981 | |||||||
| chr6:85590078 | A | T | 1 | a0001c0001t0001g0003 | 2 | HG00735.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.140+3501T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85590078 | |||||||
| chr6:85590142 | A | C | 1 | a0001c0001t0001g0197 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.140+3437T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85590142 | |||||||
| chr6:85590230 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.140+3349T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85590230 | |||||||
| chr6:85590263 | T | C | 1 | a0001c0001t0001g0342 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.140+3316A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85590263 | |||||||
| chr6:85590440 | C | A | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.140+3139G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85590440 | |||||||
| chr6:85590569 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.140+3010G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85590569 | |||||||
| chr6:85590701 | G | A | 6 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0001g0244 others(3): Show |
6 | NA18952.hp2 NA18966.hp1 NA19056.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+2878C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85590701 | |||||||
| chr6:85590784 | T | C | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.140+2795A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85590784 | |||||||
| chr6:85591026 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.140+2553G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85591026 | |||||||
| chr6:85591070 | T | C | 3 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 |
3 | HG02258.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.140+2509A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85591070 | |||||||
| chr6:85591112 | C | T | 3 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 |
3 | HG03017.hp1 HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.140+2467G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85591112 | |||||||
| chr6:85591133 | A | G | 68 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0042 others(65): Show |
69 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.140+2446T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85591133 | |||||||
| chr6:85591220 | CTG | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(191): Show |
201 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.140+2357_140+2358d others(4): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85591220 | |||||||
| chr6:85591388 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.140+2191T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85591388 | |||||||
| chr6:85591692 | G | A | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.140+1887C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85591692 | |||||||
| chr6:85591707 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.140+1872A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85591707 | |||||||
| chr6:85591887 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.140+1692G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85591887 | |||||||
| chr6:85591896 | C | G | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.140+1683G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85591896 | |||||||
| chr6:85592115 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.140+1464T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85592115 | |||||||
| chr6:85592151 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.140+1428G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85592151 | |||||||
| chr6:85592302 | C | G | 68 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0042 others(65): Show |
69 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.140+1277G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85592302 | |||||||
| chr6:85592316 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(185): Show |
195 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.140+1263T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85592316 | |||||||
| chr6:85592619 | T | C | 27 | a0001c0001t0001g0010 a0001c0001t0001g0256 a0001c0001t0001g0257 others(24): Show |
28 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.140+960A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85592619 | |||||||
| chr6:85592644 | G | A | 6 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 others(3): Show |
6 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+935C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85592644 | |||||||
| chr6:85592742 | C | A | 1 | a0001c0001t0001g0343 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.140+837G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85592742 | |||||||
| chr6:85592803 | A | C | 1 | a0001c0001t0001g0041 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.140+776T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85592803 | |||||||
| chr6:85592825 | T | TA | 100 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0017 others(97): Show |
102 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.140+753dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85592825 | |||||||
| chr6:85592825 | TA | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(67): Show |
74 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.140+753delT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85592825 | |||||||
| chr6:85592963 | G | A | 2 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.140+616C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85592963 | |||||||
| chr6:85593016 | A | T | 8 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(5): Show |
8 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.140+563T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85593016 | |||||||
| chr6:85593091 | G | T | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.140+488C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85593091 | |||||||
| chr6:85593364 | C | T | 1 | a0001c0005t0005g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.140+215G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85593364 | |||||||
| chr6:85593373 | G | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0014 others(62): Show |
69 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.140+206C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85593373 | |||||||
| chr6:85593426 | C | G | 9 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(6): Show |
9 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.140+153G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85593426 | |||||||
| chr6:85593456 | C | T | 1 | a0001c0001t0001g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.140+123G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85593456 | |||||||
| chr6:85593522 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0016 |
2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.140+57G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85593522 | |||||||
| chr6:85593567 | C | G | 1 | a0001c0001t0001g0014 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.140+12G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85593567 |