Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 346562 |
| ensemblid | ENSG00000214415.4 |
| hgncid | 22800 |
| symbol | GNAT3 |
| name | G protein subunit alpha transducin 3 |
| refseq_nuc | NM_001102386.3 |
| refseq_prot | NP_001095856.1 |
| ensembl_nuc | ENST00000398291.4 |
| ensembl_prot | ENSP00000381339.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 80458635 |
| end | 80512064 |
| strand | - |
| ver | v1.2 |
| region | chr7:80458635-80512064 |
| region5000 | chr7:80453635-80517064 |
| regionname0 | GNAT3_chr7_80458635_80512064 |
| regionname5000 | GNAT3_chr7_80453635_80517064 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 354 | 329 | 88 | 62 | 129 | 14 | 34 | 95 | GNAT3_chr7_80453635_80517064 | GNAT3 | MGSGI others(349): Show |
chr7 | 80453635 | 80517064 |
| a0002 | 0/0 | 354 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | MGSGI others(349): Show |
chr7 | 80453635 | 80517064 |
| a0003 | 0/0 | 354 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | MGSGI others(349): Show |
chr7 | 80453635 | 80517064 |
| a0004 | 0/0 | 354 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | MGSGI others(349): Show |
chr7 | 80453635 | 80517064 |
| a0005 | 0/0 | 354 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | MGSGI others(349): Show |
chr7 | 80453635 | 80517064 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1062 | 180 | 40 | 25 | 95 | 3 | 17 | GNAT3_chr7_80453635_80517064 | GNAT3 | ATGGG others(1057): Show |
chr7 | 80453635 | 80517064 | ||
| a0001c0002 | 1/1 | 1062 | 147 | 48 | 37 | 33 | 10 | 17 | GNAT3_chr7_80453635_80517064 | GNAT3 | ATGGG others(1057): Show |
chr7 | 80453635 | 80517064 | ||
| a0001c0004 | 0/0 | 1062 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | ATGGG others(1057): Show |
chr7 | 80453635 | 80517064 | ||
| a0001c0006 | 0/0 | 1062 | 1 | 0 | 0 | 0 | 1 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | ATGGG others(1057): Show |
chr7 | 80453635 | 80517064 | ||
| a0002c0003 | 0/0 | 1062 | 2 | 2 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | ATGGG others(1057): Show |
chr7 | 80453635 | 80517064 | ||
| a0003c0005 | 0/0 | 1062 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | ATGGG others(1057): Show |
chr7 | 80453635 | 80517064 | ||
| a0004c0008 | 0/0 | 1062 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | ATGGG others(1057): Show |
chr7 | 80453635 | 80517064 | ||
| a0005c0007 | 0/0 | 1062 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | ATGGG others(1057): Show |
chr7 | 80453635 | 80517064 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1239 | 176 | 36 | 25 | 95 | 3 | 17 | GNAT3_chr7_80453635_80517064 | GNAT3 | AGAAT others(1234): Show |
chr7 | 80453635 | 80517064 |
| a0001c0001t0003 | 0/0 | 1237 | 4 | 4 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | AGAAT others(1232): Show |
chr7 | 80453635 | 80517064 |
| a0001c0002t0001 | 0/0 | 1239 | 2 | 0 | 2 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | AGAAT others(1234): Show |
chr7 | 80453635 | 80517064 |
| a0001c0002t0002 | 1/1 | 1239 | 145 | 48 | 35 | 33 | 10 | 17 | GNAT3_chr7_80453635_80517064 | GNAT3 | AGAAT others(1234): Show |
chr7 | 80453635 | 80517064 |
| a0001c0004t0001 | 0/0 | 1239 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | AGAAT others(1234): Show |
chr7 | 80453635 | 80517064 |
| a0001c0006t0002 | 0/0 | 1239 | 1 | 0 | 0 | 0 | 1 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | AGAAT others(1234): Show |
chr7 | 80453635 | 80517064 |
| a0002c0003t0001 | 0/0 | 1239 | 2 | 2 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | AGAAT others(1234): Show |
chr7 | 80453635 | 80517064 |
| a0003c0005t0002 | 0/0 | 1239 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | AGAAT others(1234): Show |
chr7 | 80453635 | 80517064 |
| a0004c0008t0001 | 0/0 | 1239 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | AGAAT others(1234): Show |
chr7 | 80453635 | 80517064 |
| a0005c0007t0001 | 0/0 | 1239 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | AGAAT others(1234): Show |
chr7 | 80453635 | 80517064 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0029 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0003g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0001t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0020 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0073 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0261 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0002t0002g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0004t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0001c0006t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0002c0003t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0002c0003t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0003c0005t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0004c0008t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| a0005c0007t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0006 | t0002 | g0264 | EUR | GBR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG00099 | hp2 | a0001 | c0002 | t0002 | g0054 | EUR | GBR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG00280 | hp1 | a0001 | c0002 | t0002 | g0079 | EUR | FIN | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0145 | EUR | FIN | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG00597 | hp2 | a0001 | c0002 | t0002 | g0271 | EAS | CHS | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | CHS | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG00621 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | CHS | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG00639 | hp1 | a0001 | c0002 | t0001 | g0036 | AMR | PUR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG00642 | hp1 | a0001 | c0002 | t0002 | g0152 | AMR | PUR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG00642 | hp2 | a0001 | c0002 | t0002 | g0053 | AMR | PUR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | CHS | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG00735 | hp1 | a0001 | c0002 | t0002 | g0169 | AMR | PUR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0185 | AMR | PUR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG00738 | hp1 | a0001 | c0002 | t0002 | g0269 | AMR | PUR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG00738 | hp2 | a0001 | c0002 | t0002 | g0149 | AMR | PUR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG00741 | hp1 | a0001 | c0002 | t0002 | g0074 | AMR | PUR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG00741 | hp2 | a0001 | c0002 | t0002 | g0078 | AMR | PUR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01071 | hp1 | a0001 | c0002 | t0002 | g0173 | AMR | PUR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01081 | hp2 | a0001 | c0002 | t0002 | g0030 | AMR | PUR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0199 | AMR | PUR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0280 | AMR | PUR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0172 | AMR | PUR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0064 | AMR | PUR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0076 | AMR | PUR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01169 | hp2 | a0001 | c0002 | t0002 | g0077 | AMR | PUR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PUR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01243 | hp2 | a0001 | c0002 | t0002 | g0201 | AMR | PUR | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01255 | hp1 | a0001 | c0002 | t0002 | g0207 | AMR | CLM | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0055 | AMR | CLM | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01257 | hp2 | a0001 | c0002 | t0002 | g0022 | AMR | CLM | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0022 | AMR | CLM | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0217 | AMR | CLM | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0160 | AMR | CLM | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01358 | hp2 | a0001 | c0002 | t0002 | g0061 | AMR | CLM | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01361 | hp1 | a0001 | c0002 | t0002 | g0259 | AMR | CLM | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01361 | hp2 | a0001 | c0002 | t0002 | g0268 | AMR | CLM | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0176 | AMR | CLM | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01496 | hp1 | a0001 | c0002 | t0002 | g0063 | AMR | CLM | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0282 | AMR | CLM | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0272 | EUR | IBS | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01515 | hp2 | a0001 | c0002 | t0002 | g0164 | EUR | IBS | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01516 | hp2 | a0001 | c0002 | t0002 | g0244 | EUR | IBS | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01517 | hp2 | a0001 | c0002 | t0002 | g0163 | EUR | IBS | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0006 | AFR | ACB | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01934 | hp2 | a0001 | c0002 | t0002 | g0246 | AMR | PEL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PEL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01981 | hp2 | a0001 | c0002 | t0002 | g0008 | AMR | PEL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02015 | hp1 | a0001 | c0004 | t0001 | g0033 | EAS | KHV | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02055 | hp2 | a0001 | c0002 | t0002 | g0041 | AFR | ACB | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02056 | hp1 | a0001 | c0002 | t0002 | g0254 | EAS | KHV | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02074 | hp1 | a0001 | c0002 | t0002 | g0255 | EAS | KHV | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | KHV | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02148 | hp2 | a0001 | c0002 | t0002 | g0062 | AMR | PEL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02155 | hp1 | a0001 | c0002 | t0002 | g0212 | EAS | CDX | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CDX | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02165 | hp1 | a0001 | c0002 | t0002 | g0015 | EAS | CDX | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02165 | hp2 | a0001 | c0002 | t0002 | g0283 | EAS | CDX | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02257 | hp1 | a0001 | c0002 | t0002 | g0249 | AFR | ACB | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0202 | AFR | ACB | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02273 | hp1 | a0001 | c0002 | t0002 | g0258 | AMR | PEL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02293 | hp1 | a0001 | c0002 | t0002 | g0008 | AMR | PEL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02602 | hp1 | a0001 | c0002 | t0002 | g0267 | SAS | PJL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02615 | hp1 | a0001 | c0002 | t0002 | g0289 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02615 | hp2 | a0002 | c0003 | t0001 | g0284 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02622 | hp2 | a0003 | c0005 | t0002 | g0226 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02647 | hp2 | a0001 | c0002 | t0002 | g0019 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0210 | SAS | PJL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0020 | SAS | PJL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02717 | hp1 | a0001 | c0002 | t0002 | g0224 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0024 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0203 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02818 | hp1 | a0001 | c0002 | t0002 | g0188 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0040 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0032 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0039 | AFR | ESN | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02922 | hp2 | a0001 | c0002 | t0002 | g0211 | AFR | ESN | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0006 | AFR | ESN | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ESN | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | ESN | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02976 | hp1 | a0001 | c0002 | t0002 | g0168 | AFR | ESN | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03017 | hp1 | a0001 | c0002 | t0002 | g0129 | SAS | PJL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03041 | hp1 | a0001 | c0002 | t0002 | g0228 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03041 | hp2 | a0001 | c0002 | t0002 | g0024 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0189 | AFR | MSL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03098 | hp2 | a0001 | c0002 | t0002 | g0250 | AFR | MSL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03130 | hp1 | a0002 | c0003 | t0001 | g0285 | AFR | ESN | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03139 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | ESN | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ESN | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03195 | hp1 | a0001 | c0002 | t0002 | g0197 | AFR | ESN | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0206 | AFR | ESN | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | MSL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0019 | AFR | MSL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0165 | AFR | MSL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | MSL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03239 | hp1 | a0001 | c0002 | t0002 | g0171 | SAS | PJL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03239 | hp2 | a0001 | c0002 | t0002 | g0030 | SAS | PJL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0069 | AFR | MSL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0190 | AFR | MSL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0222 | AFR | MSL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03491 | hp1 | a0001 | c0002 | t0002 | g0095 | SAS | PJL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03491 | hp2 | a0001 | c0002 | t0002 | g0209 | SAS | PJL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03492 | hp1 | a0001 | c0002 | t0002 | g0208 | SAS | PJL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03516 | hp1 | a0001 | c0002 | t0002 | g0179 | AFR | ESN | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0006 | AFR | ESN | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0051 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03540 | hp2 | a0001 | c0002 | t0002 | g0020 | AFR | GWD | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03579 | hp1 | a0001 | c0002 | t0002 | g0080 | AFR | MSL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03654 | hp2 | a0001 | c0002 | t0002 | g0178 | SAS | PJL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03669 | hp1 | a0001 | c0002 | t0002 | g0167 | SAS | PJL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03704 | hp1 | a0001 | c0002 | t0002 | g0183 | SAS | PJL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03704 | hp2 | a0001 | c0002 | t0002 | g0101 | SAS | PJL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | BEB | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0279 | SAS | BEB | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | BEB | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03927 | hp1 | a0001 | c0002 | t0002 | g0263 | SAS | BEB | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | STU | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | STU | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG04204 | hp1 | a0001 | c0002 | t0002 | g0275 | SAS | STU | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | STU | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18522 | hp1 | a0001 | c0002 | t0002 | g0002 | AFR | YRI | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | YRI | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHB | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18612 | hp2 | a0001 | c0002 | t0002 | g0253 | EAS | CHB | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHB | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHB | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18906 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | YRI | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18906 | hp2 | a0001 | c0002 | t0002 | g0286 | AFR | YRI | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18943 | hp1 | a0001 | c0002 | t0002 | g0266 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18947 | hp1 | a0001 | c0002 | t0002 | g0241 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18948 | hp2 | a0001 | c0002 | t0002 | g0097 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18953 | hp1 | a0001 | c0002 | t0002 | g0082 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0270 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18966 | hp1 | a0001 | c0002 | t0002 | g0118 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18969 | hp1 | a0001 | c0002 | t0002 | g0247 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18974 | hp2 | a0001 | c0002 | t0002 | g0240 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18979 | hp1 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18981 | hp1 | a0001 | c0002 | t0002 | g0278 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18982 | hp1 | a0001 | c0002 | t0002 | g0144 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18985 | hp2 | a0001 | c0002 | t0002 | g0242 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18992 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19000 | hp2 | a0001 | c0002 | t0002 | g0281 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0239 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19005 | hp1 | a0001 | c0002 | t0002 | g0028 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19006 | hp2 | a0001 | c0002 | t0002 | g0016 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19012 | hp2 | a0001 | c0002 | t0002 | g0182 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | LWK | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0287 | AFR | LWK | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | LWK | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | LWK | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19063 | hp1 | a0001 | c0002 | t0002 | g0277 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19067 | hp1 | a0001 | c0002 | t0002 | g0257 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0083 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19070 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0213 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19091 | hp1 | a0004 | c0008 | t0001 | g0295 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19091 | hp2 | a0001 | c0002 | t0002 | g0005 | EAS | JPT | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19240 | hp1 | a0005 | c0007 | t0001 | g0294 | AFR | YRI | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | YRI | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA20129 | hp1 | a0001 | c0002 | t0002 | g0136 | AFR | ASW | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0026 | AFR | ASW | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA20752 | hp1 | a0001 | c0002 | t0002 | g0075 | EUR | TSI | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA20752 | hp2 | a0001 | c0002 | t0002 | g0276 | EUR | TSI | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA20805 | hp1 | a0001 | c0002 | t0002 | g0265 | EUR | TSI | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0057 | EUR | TSI | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA20905 | hp1 | a0001 | c0002 | t0002 | g0052 | SAS | GIH | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | GIH | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01123 | hp1 | a0001 | c0002 | t0002 | g0151 | AMR | CLM | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG01123 | hp2 | a0001 | c0002 | t0002 | g0070 | AMR | CLM | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ACB | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG02559 | hp2 | a0001 | c0002 | t0002 | g0180 | AFR | ACB | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03471 | hp1 | a0001 | c0002 | t0002 | g0026 | AFR | MSL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0050 | AFR | MSL | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA20300 | hp1 | a0001 | c0002 | t0002 | g0252 | AFR | USA | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0090 | AFR | USA | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0047 | AFR | LWK | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| NA21309 | hp2 | a0001 | c0002 | t0002 | g0225 | AFR | LWK | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| homoSapiens | chm13v2 | a0001 | c0002 | t0002 | g0073 | REF | REF | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0002 | g0261 | REF | REF | GNAT3_chr7_80453635_80517064 | GNAT3 | chr7 | 80453635 | 80517064 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:80458698 | C | A | 1 | a0002 | 2 | HG02615.hp2 HG03130.hp1 |
missense_variant | MODERATE | c.1038G>T | p.Glu346Asp | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 8/8 | 1176/1239 | 1038/1065 | 346/354 | chr7 | 80458698 | |||
| chr7:80478988 | C | T | 1 | a0003 | 1 | HG02622.hp2 | missense_variant | MODERATE | c.314G>A | p.Arg105Gln | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/8 | 452/1239 | 314/1065 | 105/354 | chr7 | 80478988 | |||
| chr7:80511850 | T | C | 1 | a0005 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.77A>G | p.Asp26Gly | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/8 | 215/1239 | 77/1065 | 26/354 | chr7 | 80511850 | |||
| chr7:80511876 | T | G | 1 | a0004 | 1 | NA19091.hp1 | missense_variant | MODERATE | c.51A>C | p.Lys17Asn | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/8 | 189/1239 | 51/1065 | 17/354 | chr7 | 80511876 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:80458722 | T | C | 1 | a0001c0006 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.1014A>G | p.Ala338Ala | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 8/8 | 1152/1239 | 1014/1065 | 338/354 | chr7 | 80458722 | |||
| chr7:80458725 | G | A | 5 | a0001c0001 a0001c0004 a0002c0003 others(2): Show |
185 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(182): Show |
synonymous_variant | LOW | c.1011C>T | p.Asp337Asp | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 8/8 | 1149/1239 | 1011/1065 | 337/354 | chr7 | 80458725 | |||
| chr7:80478861 | C | T | 1 | a0001c0004 | 1 | HG02015.hp1 | synonymous_variant | LOW | c.441G>A | p.Gln147Gln | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/8 | 579/1239 | 441/1065 | 147/354 | chr7 | 80478861 | |||
| chr7:80511894 | C | T | 1 | a0001c0004 | 1 | HG02015.hp1 | synonymous_variant | LOW | c.33G>A | p.Glu11Glu | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/8 | 171/1239 | 33/1065 | 11/354 | chr7 | 80511894 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:80458665 | A | G | 7 | a0001c0001t0001 a0001c0001t0003 a0001c0002t0001 others(4): Show |
187 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(184): Show |
3_prime_UTR_variant | MODIFIER | c.*6T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 8/8 | 6 | chr7 | 80458665 | ||||||
| chr7:80511952 | TTA | T | 1 | a0001c0001t0003 | 4 | HG02895.hp2 HG02897.hp1 HG03225.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-28_-27delTA | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/8 | 27 | chr7 | 80511952 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:80458996 | T | C | 107 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(104): Show |
119 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.875-135A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80458996 | |||||||
| chr7:80459040 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(53): Show |
65 | HG00639.hp2 HG00673.hp1 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.875-179C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80459040 | |||||||
| chr7:80459241 | A | T | 1 | a0001c0001t0003g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.875-380T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80459241 | |||||||
| chr7:80459276 | A | G | 108 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(105): Show |
120 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.875-415T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80459276 | |||||||
| chr7:80459345 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0248 |
2 | HG03834.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.875-484C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80459345 | |||||||
| chr7:80459355 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.875-494G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80459355 | |||||||
| chr7:80460009 | C | T | 28 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0044 others(25): Show |
33 | HG01243.hp1 HG02027.hp1 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.875-1148G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80460009 | |||||||
| chr7:80460046 | T | C | 1 | a0001c0002t0002g0182 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.875-1185A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80460046 | |||||||
| chr7:80460148 | A | C | 107 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(104): Show |
119 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.875-1287T>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80460148 | |||||||
| chr7:80460200 | C | CT | 166 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(163): Show |
187 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.875-1340_875-1339i others(3): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80460200 | |||||||
| chr7:80460220 | G | T | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | NA18995.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.875-1359C>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80460220 | |||||||
| chr7:80460233 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.875-1372C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80460233 | |||||||
| chr7:80460340 | G | A | 2 | a0001c0002t0002g0003 a0001c0002t0002g0197 |
4 | HG02970.hp2 HG03195.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.875-1479C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80460340 | |||||||
| chr7:80460364 | C | T | 39 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0043 others(36): Show |
46 | HG00673.hp1 HG00673.hp2 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.875-1503G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80460364 | |||||||
| chr7:80460474 | C | T | 4 | a0001c0001t0001g0187 a0001c0001t0001g0288 a0002c0003t0001g0284 others(1): Show |
4 | HG01891.hp2 HG02109.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.875-1613G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80460474 | |||||||
| chr7:80460550 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.874+1609G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80460550 | |||||||
| chr7:80460563 | C | T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0238 |
2 | HG02630.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.874+1596G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80460563 | |||||||
| chr7:80460750 | G | GA | 108 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(105): Show |
120 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(117): Show |
intron_variant | MODIFIER | c.874+1408dupT | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80460750 | |||||||
| chr7:80460763 | A | G | 4 | a0001c0001t0001g0187 a0001c0001t0001g0288 a0002c0003t0001g0284 others(1): Show |
4 | HG01891.hp2 HG02109.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.874+1396T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80460763 | |||||||
| chr7:80460990 | A | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0230 others(6): Show |
11 | HG00673.hp1 HG00673.hp2 HG03834.hp2 others(8): Show |
intron_variant | MODIFIER | c.874+1169T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80460990 | |||||||
| chr7:80461025 | A | ATAT | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(194): Show |
222 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.874+1133_874+1134i others(5): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80461025 | |||||||
| chr7:80461187 | T | C | 109 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(106): Show |
121 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.874+972A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80461187 | |||||||
| chr7:80461207 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.874+952G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80461207 | |||||||
| chr7:80461246 | T | C | 1 | a0001c0002t0002g0252 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.874+913A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80461246 | |||||||
| chr7:80461314 | A | G | 8 | a0001c0002t0002g0002 a0001c0002t0002g0039 a0001c0002t0002g0040 others(5): Show |
10 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.874+845T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80461314 | |||||||
| chr7:80461401 | T | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0227 |
3 | HG02818.hp2 HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.874+758A>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80461401 | |||||||
| chr7:80461428 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.874+731G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80461428 | |||||||
| chr7:80461506 | C | T | 5 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0223 others(2): Show |
6 | HG02145.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.874+653G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80461506 | |||||||
| chr7:80461585 | A | AAAAT | 107 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(104): Show |
119 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.874+570_874+573dup others(4): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80461585 | |||||||
| chr7:80461660 | GCTGA | G | 4 | a0001c0001t0001g0187 a0001c0001t0001g0288 a0002c0003t0001g0284 others(1): Show |
4 | HG01891.hp2 HG02109.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.874+495_874+498del others(4): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80461660 | |||||||
| chr7:80461986 | G | A | 41 | a0001c0001t0001g0001 a0001c0001t0001g0027 a0001c0001t0001g0042 others(38): Show |
48 | HG00639.hp2 HG01243.hp1 HG01433.hp2 others(45): Show |
intron_variant | MODIFIER | c.874+173C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 7/7 | chr7 | 80461986 | |||||||
| chr7:80462476 | T | C | 1 | a0001c0001t0001g0096 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.720+26A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 6/7 | chr7 | 80462476 | |||||||
| chr7:80462653 | A | G | 2 | a0001c0001t0003g0007 a0001c0001t0003g0032 |
3 | HG02895.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.591-22T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80462653 | |||||||
| chr7:80462665 | G | A | 122 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(119): Show |
136 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.591-34C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80462665 | |||||||
| chr7:80462725 | C | A | 125 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(122): Show |
139 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.591-94G>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80462725 | |||||||
| chr7:80462780 | G | C | 1 | a0001c0001t0001g0108 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.591-149C>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80462780 | |||||||
| chr7:80462803 | A | G | 2 | a0001c0002t0001g0036 a0001c0002t0001g0199 |
2 | HG00639.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.591-172T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80462803 | |||||||
| chr7:80462814 | A | G | 107 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(104): Show |
119 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.591-183T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80462814 | |||||||
| chr7:80462977 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.591-346G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80462977 | |||||||
| chr7:80462994 | G | C | 14 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0124 others(11): Show |
16 | HG00639.hp1 HG00673.hp1 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.591-363C>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80462994 | |||||||
| chr7:80463329 | T | A | 5 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0223 others(2): Show |
6 | HG02145.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.591-698A>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80463329 | |||||||
| chr7:80463376 | A | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0124 others(9): Show |
14 | HG00673.hp1 HG00673.hp2 HG03834.hp1 others(11): Show |
intron_variant | MODIFIER | c.591-745T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80463376 | |||||||
| chr7:80463596 | T | G | 14 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0124 others(11): Show |
16 | HG00639.hp1 HG00673.hp1 HG00673.hp2 others(13): Show |
intron_variant | MODIFIER | c.591-965A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80463596 | |||||||
| chr7:80463603 | A | T | 28 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0044 others(25): Show |
33 | HG01243.hp1 HG02027.hp1 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.591-972T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80463603 | |||||||
| chr7:80463636 | A | G | 9 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0230 others(6): Show |
11 | HG00673.hp1 HG00673.hp2 HG03834.hp2 others(8): Show |
intron_variant | MODIFIER | c.591-1005T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80463636 | |||||||
| chr7:80463810 | C | A | 5 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0223 others(2): Show |
6 | HG02145.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.591-1179G>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80463810 | |||||||
| chr7:80463894 | T | C | 2 | a0001c0001t0001g0187 a0001c0001t0001g0288 |
2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.591-1263A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80463894 | |||||||
| chr7:80463983 | A | G | 125 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(122): Show |
139 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(136): Show |
intron_variant | MODIFIER | c.591-1352T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80463983 | |||||||
| chr7:80464070 | C | T | 1 | a0001c0002t0002g0064 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.591-1439G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80464070 | |||||||
| chr7:80464145 | T | A | 1 | a0001c0001t0001g0096 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.591-1514A>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80464145 | |||||||
| chr7:80464166 | C | A | 104 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(101): Show |
116 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.591-1535G>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80464166 | |||||||
| chr7:80464168 | ATAT | A | 104 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(101): Show |
116 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.591-1540_591-1538d others(5): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80464168 | |||||||
| chr7:80464691 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.591-2060G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80464691 | |||||||
| chr7:80464945 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.591-2314T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80464945 | |||||||
| chr7:80465207 | A | C | 13 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0124 others(10): Show |
15 | HG00673.hp1 HG00673.hp2 HG03834.hp1 others(12): Show |
intron_variant | MODIFIER | c.591-2576T>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80465207 | |||||||
| chr7:80465291 | A | G | 111 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(108): Show |
123 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.591-2660T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80465291 | |||||||
| chr7:80465544 | G | A | 1 | a0001c0002t0002g0173 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.591-2913C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80465544 | |||||||
| chr7:80465565 | A | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0243 |
2 | HG02129.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.591-2934T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80465565 | |||||||
| chr7:80465601 | G | C | 1 | a0001c0001t0001g0128 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.591-2970C>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80465601 | |||||||
| chr7:80465612 | T | C | 21 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0039 others(18): Show |
25 | HG00280.hp1 HG00642.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.591-2981A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80465612 | |||||||
| chr7:80465624 | G | A | 1 | a0001c0002t0001g0036 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.591-2993C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80465624 | |||||||
| chr7:80465814 | A | T | 2 | a0002c0003t0001g0284 a0002c0003t0001g0285 |
2 | HG02615.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.591-3183T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80465814 | |||||||
| chr7:80465825 | T | G | 5 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0223 others(2): Show |
6 | HG02145.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.591-3194A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80465825 | |||||||
| chr7:80465886 | T | C | 1 | a0001c0001t0001g0196 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.591-3255A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80465886 | |||||||
| chr7:80466043 | A | T | 104 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(101): Show |
116 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.591-3412T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80466043 | |||||||
| chr7:80466098 | A | T | 104 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(101): Show |
116 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.591-3467T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80466098 | |||||||
| chr7:80466107 | C | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | NA18995.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.591-3476G>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80466107 | |||||||
| chr7:80466221 | A | C | 10 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0230 others(7): Show |
12 | HG00673.hp1 HG00673.hp2 HG03834.hp2 others(9): Show |
intron_variant | MODIFIER | c.591-3590T>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80466221 | |||||||
| chr7:80466228 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.591-3597C>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80466228 | |||||||
| chr7:80466325 | A | G | 10 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0230 others(7): Show |
12 | HG00673.hp1 HG00673.hp2 HG03834.hp2 others(9): Show |
intron_variant | MODIFIER | c.591-3694T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80466325 | |||||||
| chr7:80466379 | T | G | 1 | a0001c0002t0002g0253 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.591-3748A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80466379 | |||||||
| chr7:80466439 | C | T | 5 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0223 others(2): Show |
6 | HG02145.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.591-3808G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80466439 | |||||||
| chr7:80466615 | T | C | 1 | a0001c0001t0003g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.591-3984A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80466615 | |||||||
| chr7:80466773 | A | G | 4 | a0001c0001t0001g0187 a0001c0001t0001g0288 a0002c0003t0001g0284 others(1): Show |
4 | HG01891.hp2 HG02109.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.591-4142T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80466773 | |||||||
| chr7:80466881 | A | G | 4 | a0001c0001t0001g0194 a0001c0001t0001g0205 a0001c0001t0001g0214 others(1): Show |
4 | NA19012.hp1 NA19064.hp1 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.591-4250T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80466881 | |||||||
| chr7:80467039 | A | T | 15 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0124 others(12): Show |
17 | HG00639.hp1 HG00673.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.591-4408T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80467039 | |||||||
| chr7:80467066 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0227 |
3 | HG02818.hp2 HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.591-4435G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80467066 | |||||||
| chr7:80467091 | C | T | 1 | a0001c0004t0001g0033 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.591-4460G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80467091 | |||||||
| chr7:80467249 | A | G | 1 | a0001c0001t0003g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.591-4618T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80467249 | |||||||
| chr7:80467283 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0248 |
2 | HG03834.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.591-4652C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80467283 | |||||||
| chr7:80467346 | G | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0230 others(12): Show |
18 | HG00673.hp1 HG00673.hp2 HG02056.hp1 others(15): Show |
intron_variant | MODIFIER | c.591-4715C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80467346 | |||||||
| chr7:80467347 | T | A | 1 | a0001c0002t0002g0080 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.591-4716A>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80467347 | |||||||
| chr7:80467377 | A | T | 1 | a0001c0002t0001g0036 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.591-4746T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80467377 | |||||||
| chr7:80467398 | A | G | 3 | a0001c0002t0002g0201 a0001c0002t0002g0202 a0001c0002t0002g0203 |
3 | HG01243.hp2 HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.591-4767T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80467398 | |||||||
| chr7:80467423 | C | G | 1 | a0001c0002t0002g0265 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.591-4792G>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80467423 | |||||||
| chr7:80467662 | C | T | 5 | a0001c0002t0002g0015 a0001c0002t0002g0239 a0001c0002t0002g0240 others(2): Show |
6 | HG00621.hp1 HG02165.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.591-5031G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80467662 | |||||||
| chr7:80467700 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.591-5069T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80467700 | |||||||
| chr7:80467776 | G | A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0230 others(8): Show |
13 | HG00673.hp1 HG00673.hp2 HG03834.hp2 others(10): Show |
intron_variant | MODIFIER | c.591-5145C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80467776 | |||||||
| chr7:80467807 | T | C | 2 | a0001c0001t0001g0056 a0001c0001t0001g0248 |
2 | HG03834.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.591-5176A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80467807 | |||||||
| chr7:80467958 | G | T | 28 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0044 others(25): Show |
33 | HG01243.hp1 HG02027.hp1 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.591-5327C>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80467958 | |||||||
| chr7:80467985 | A | C | 2 | a0001c0001t0001g0056 a0001c0001t0001g0248 |
2 | HG03834.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.591-5354T>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80467985 | |||||||
| chr7:80468003 | C | A | 11 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0230 others(8): Show |
13 | HG00673.hp1 HG00673.hp2 HG03834.hp2 others(10): Show |
intron_variant | MODIFIER | c.591-5372G>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80468003 | |||||||
| chr7:80468044 | G | A | 2 | a0001c0001t0001g0056 a0001c0001t0001g0248 |
2 | HG03834.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.591-5413C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80468044 | |||||||
| chr7:80468224 | G | A | 14 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0124 others(11): Show |
16 | HG00673.hp1 HG00673.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.591-5593C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80468224 | |||||||
| chr7:80468260 | A | G | 110 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(107): Show |
122 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(119): Show |
intron_variant | MODIFIER | c.591-5629T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80468260 | |||||||
| chr7:80468290 | GATT | G | 103 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(100): Show |
115 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.591-5662_591-5660d others(5): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80468290 | |||||||
| chr7:80468541 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.590+5710A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80468541 | |||||||
| chr7:80468616 | C | G | 2 | a0001c0002t0002g0206 a0001c0002t0002g0228 |
2 | HG03041.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.590+5635G>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80468616 | |||||||
| chr7:80468774 | A | T | 1 | a0001c0002t0002g0252 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.590+5477T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80468774 | |||||||
| chr7:80469023 | T | C | 1 | a0001c0002t0002g0082 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.590+5228A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80469023 | |||||||
| chr7:80469171 | C | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(183): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.590+5080G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80469171 | |||||||
| chr7:80469208 | C | T | 5 | a0001c0002t0002g0005 a0001c0002t0002g0247 a0001c0002t0002g0277 others(2): Show |
7 | HG00609.hp2 NA18969.hp1 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.590+5043G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80469208 | |||||||
| chr7:80469252 | T | C | 28 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0044 others(25): Show |
33 | HG01243.hp1 HG02027.hp1 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.590+4999A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80469252 | |||||||
| chr7:80469548 | C | T | 119 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(116): Show |
133 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.590+4703G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80469548 | |||||||
| chr7:80469617 | T | C | 1 | a0001c0001t0001g0100 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.590+4634A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80469617 | |||||||
| chr7:80469768 | A | C | 10 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0230 others(7): Show |
12 | HG00673.hp1 HG00673.hp2 HG03834.hp2 others(9): Show |
intron_variant | MODIFIER | c.590+4483T>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80469768 | |||||||
| chr7:80469985 | G | C | 1 | a0001c0002t0002g0228 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.590+4266C>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80469985 | |||||||
| chr7:80469992 | A | G | 14 | a0001c0001t0001g0004 a0001c0001t0001g0056 a0001c0001t0001g0124 others(11): Show |
16 | HG00673.hp1 HG00673.hp2 HG01099.hp1 others(13): Show |
intron_variant | MODIFIER | c.590+4259T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80469992 | |||||||
| chr7:80470198 | T | G | 1 | a0001c0001t0001g0128 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.590+4053A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80470198 | |||||||
| chr7:80470227 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.590+4024A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80470227 | |||||||
| chr7:80470275 | G | A | 1 | a0001c0002t0002g0160 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.590+3976C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80470275 | |||||||
| chr7:80470411 | G | A | 103 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(100): Show |
115 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.590+3840C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80470411 | |||||||
| chr7:80470519 | C | A | 1 | a0001c0001t0001g0056 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.590+3732G>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80470519 | |||||||
| chr7:80470679 | C | G | 102 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(99): Show |
114 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(111): Show |
intron_variant | MODIFIER | c.590+3572G>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80470679 | |||||||
| chr7:80470968 | C | T | 10 | a0001c0001t0001g0004 a0001c0001t0001g0124 a0001c0001t0001g0230 others(7): Show |
12 | HG00673.hp1 HG00673.hp2 HG03834.hp2 others(9): Show |
intron_variant | MODIFIER | c.590+3283G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80470968 | |||||||
| chr7:80471008 | G | T | 1 | a0001c0001t0001g0256 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.590+3243C>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80471008 | |||||||
| chr7:80471235 | T | C | 4 | a0001c0001t0001g0056 a0001c0001t0001g0248 a0001c0002t0002g0052 others(1): Show |
4 | HG02683.hp1 HG03834.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.590+3016A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80471235 | |||||||
| chr7:80471252 | C | T | 247 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(244): Show |
278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.590+2999G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80471252 | |||||||
| chr7:80471263 | G | A | 1 | a0001c0002t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.590+2988C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80471263 | |||||||
| chr7:80471301 | A | C | 1 | a0001c0001t0001g0231 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.590+2950T>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80471301 | |||||||
| chr7:80471313 | T | C | 1 | a0001c0001t0001g0231 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.590+2938A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80471313 | |||||||
| chr7:80471390 | C | T | 290 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(287): Show |
329 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(326): Show |
intron_variant | MODIFIER | c.590+2861G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80471390 | |||||||
| chr7:80471409 | A | G | 8 | a0001c0002t0002g0002 a0001c0002t0002g0039 a0001c0002t0002g0040 others(5): Show |
10 | HG02055.hp2 HG02257.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.590+2842T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80471409 | |||||||
| chr7:80471412 | AT | A | 4 | a0001c0001t0001g0056 a0001c0001t0001g0248 a0001c0002t0002g0052 others(1): Show |
4 | HG02683.hp1 HG03834.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.590+2838delA | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80471412 | |||||||
| chr7:80471471 | A | T | 1 | a0001c0001t0003g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.590+2780T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80471471 | |||||||
| chr7:80471573 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.590+2678C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80471573 | |||||||
| chr7:80471607 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.590+2644G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80471607 | |||||||
| chr7:80471653 | C | A | 31 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0181 others(28): Show |
39 | HG00673.hp1 HG01123.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.590+2598G>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80471653 | |||||||
| chr7:80471841 | C | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0230 a0001c0001t0001g0231 others(6): Show |
11 | HG00673.hp1 HG03834.hp2 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.590+2410G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80471841 | |||||||
| chr7:80471897 | G | A | 18 | a0001c0001t0001g0004 a0001c0001t0001g0187 a0001c0001t0001g0230 others(15): Show |
21 | HG00673.hp1 HG01891.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.590+2354C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80471897 | |||||||
| chr7:80471981 | TTACTC | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0230 a0001c0001t0001g0231 others(6): Show |
11 | HG00673.hp1 HG03834.hp2 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.590+2265_590+2269d others(7): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80471981 | |||||||
| chr7:80472227 | C | T | 9 | a0001c0001t0001g0187 a0001c0001t0001g0223 a0001c0001t0003g0031 others(6): Show |
9 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.590+2024G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80472227 | |||||||
| chr7:80472306 | G | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0230 a0001c0001t0001g0231 others(6): Show |
11 | HG00673.hp1 HG03834.hp2 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.590+1945C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80472306 | |||||||
| chr7:80472332 | G | A | 8 | a0001c0001t0001g0042 a0001c0001t0001g0218 a0001c0001t0001g0219 others(5): Show |
8 | HG00639.hp2 HG01243.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.590+1919C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80472332 | |||||||
| chr7:80472379 | G | GCAGTGTA others(15): Show |
1 | a0001c0002t0002g0061 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.590+1871_590+1872i others(24): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80472379 | |||||||
| chr7:80472427 | T | C | 131 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0029 others(128): Show |
149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.590+1824A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80472427 | |||||||
| chr7:80472519 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.590+1732C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80472519 | |||||||
| chr7:80472836 | A | T | 28 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0187 others(25): Show |
30 | HG00639.hp2 HG00673.hp1 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.590+1415T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80472836 | |||||||
| chr7:80472839 | T | G | 2 | a0001c0001t0001g0248 a0001c0002t0002g0210 |
2 | HG02683.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.590+1412A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80472839 | |||||||
| chr7:80472877 | T | C | 32 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0187 others(29): Show |
35 | HG00639.hp2 HG00673.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.590+1374A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80472877 | |||||||
| chr7:80472917 | C | T | 11 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(8): Show |
13 | HG02055.hp1 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.590+1334G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80472917 | |||||||
| chr7:80473004 | G | A | 2 | a0001c0002t0002g0006 a0001c0002t0002g0244 |
4 | HG01516.hp2 HG01891.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.590+1247C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80473004 | |||||||
| chr7:80473282 | C | G | 3 | a0001c0002t0002g0286 a0002c0003t0001g0284 a0002c0003t0001g0285 |
3 | HG02615.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.590+969G>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80473282 | |||||||
| chr7:80473283 | G | A | 29 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0187 others(26): Show |
31 | HG00639.hp2 HG00673.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.590+968C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80473283 | |||||||
| chr7:80473389 | A | C | 5 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0220 others(2): Show |
5 | HG02630.hp1 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.590+862T>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80473389 | |||||||
| chr7:80473426 | A | C | 1 | a0001c0002t0002g0212 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.590+825T>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80473426 | |||||||
| chr7:80473498 | CAA | C | 11 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(8): Show |
13 | HG02055.hp1 HG02559.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.590+751_590+752del others(2): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80473498 | |||||||
| chr7:80473505 | A | G | 2 | a0001c0001t0001g0248 a0001c0002t0002g0210 |
2 | HG02683.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.590+746T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80473505 | |||||||
| chr7:80473525 | TATTG | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0230 a0001c0001t0001g0231 others(6): Show |
11 | HG00673.hp1 HG03834.hp2 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.590+722_590+725del others(4): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80473525 | |||||||
| chr7:80473568 | A | G | 2 | a0001c0001t0001g0130 a0001c0001t0001g0139 |
2 | NA18946.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.590+683T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80473568 | |||||||
| chr7:80473669 | T | C | 1 | a0001c0002t0002g0228 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.590+582A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80473669 | |||||||
| chr7:80473940 | T | C | 2 | a0001c0001t0001g0248 a0001c0002t0002g0210 |
2 | HG02683.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.590+311A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80473940 | |||||||
| chr7:80474084 | A | G | 9 | a0001c0001t0001g0004 a0001c0001t0001g0230 a0001c0001t0001g0231 others(6): Show |
11 | HG00673.hp1 HG03834.hp2 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.590+167T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80474084 | |||||||
| chr7:80474186 | C | G | 1 | a0001c0001t0001g0142 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.590+65G>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80474186 | |||||||
| chr7:80474208 | A | G | 1 | a0001c0002t0002g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.590+43T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80474208 | |||||||
| chr7:80474240 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.590+11A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 5/7 | chr7 | 80474240 | |||||||
| chr7:80474462 | C | CAT | 18 | a0001c0001t0001g0034 a0001c0001t0001g0042 a0001c0001t0001g0187 others(15): Show |
18 | HG00639.hp2 HG01243.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.462-85_462-84dupAT | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80474462 | |||||||
| chr7:80474548 | T | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0042 others(30): Show |
36 | HG00639.hp2 HG00673.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.462-169A>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80474548 | |||||||
| chr7:80474554 | G | T | 33 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0042 others(30): Show |
36 | HG00639.hp2 HG00673.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.462-175C>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80474554 | |||||||
| chr7:80474578 | C | T | 1 | a0001c0002t0002g0006 | 3 | HG01891.hp1 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.462-199G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80474578 | |||||||
| chr7:80474758 | G | A | 1 | a0001c0002t0002g0283 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.462-379C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80474758 | |||||||
| chr7:80474789 | C | T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0191 a0001c0001t0001g0192 others(10): Show |
18 | HG02027.hp1 HG02083.hp2 HG02132.hp1 others(15): Show |
intron_variant | MODIFIER | c.462-410G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80474789 | |||||||
| chr7:80474844 | C | T | 18 | a0001c0001t0001g0034 a0001c0001t0001g0042 a0001c0001t0001g0187 others(15): Show |
18 | HG00639.hp2 HG01243.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.462-465G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80474844 | |||||||
| chr7:80474951 | A | G | 1 | a0001c0002t0002g0118 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.462-572T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80474951 | |||||||
| chr7:80475011 | A | G | 11 | a0001c0001t0001g0004 a0001c0001t0001g0230 a0001c0001t0001g0231 others(8): Show |
13 | HG00673.hp1 HG02683.hp1 HG03834.hp1 others(10): Show |
intron_variant | MODIFIER | c.462-632T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80475011 | |||||||
| chr7:80475024 | C | T | 4 | a0001c0001t0001g0288 a0001c0001t0003g0007 a0001c0001t0003g0032 others(1): Show |
5 | HG02109.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.462-645G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80475024 | |||||||
| chr7:80475103 | C | T | 7 | a0001c0001t0001g0042 a0001c0001t0001g0218 a0001c0001t0001g0219 others(4): Show |
7 | HG00639.hp2 HG01243.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.462-724G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80475103 | |||||||
| chr7:80475119 | A | G | 20 | a0001c0001t0001g0029 a0001c0001t0001g0143 a0001c0001t0001g0251 others(17): Show |
22 | HG00099.hp1 HG00738.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.462-740T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80475119 | |||||||
| chr7:80475233 | A | G | 100 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0029 others(97): Show |
113 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.462-854T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80475233 | |||||||
| chr7:80475361 | TA | T | 16 | a0001c0001t0001g0042 a0001c0001t0001g0107 a0001c0001t0001g0218 others(13): Show |
16 | HG00639.hp2 HG01243.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.462-983delT | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80475361 | |||||||
| chr7:80475361 | TAA | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0230 a0001c0001t0001g0231 others(8): Show |
13 | HG00673.hp1 HG02683.hp1 HG03834.hp1 others(10): Show |
intron_variant | MODIFIER | c.462-984_462-983del others(2): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80475361 | |||||||
| chr7:80475372 | A | G | 1 | a0001c0002t0002g0286 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.462-993T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80475372 | |||||||
| chr7:80475437 | C | A | 1 | a0001c0001t0001g0130 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.462-1058G>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80475437 | |||||||
| chr7:80475462 | A | G | 1 | a0001c0002t0002g0286 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.462-1083T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80475462 | |||||||
| chr7:80475484 | C | T | 2 | a0001c0001t0001g0248 a0001c0002t0002g0210 |
2 | HG02683.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.462-1105G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80475484 | |||||||
| chr7:80475575 | C | T | 31 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(28): Show |
37 | HG00099.hp2 HG00642.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.462-1196G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80475575 | |||||||
| chr7:80476037 | T | C | 4 | a0001c0002t0002g0002 a0001c0002t0002g0039 a0001c0002t0002g0040 others(1): Show |
6 | HG02055.hp2 HG02258.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.462-1658A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80476037 | |||||||
| chr7:80476052 | G | A | 1 | a0001c0001t0001g0110 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.462-1673C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80476052 | |||||||
| chr7:80476185 | A | G | 1 | a0001c0001t0003g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.462-1806T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80476185 | |||||||
| chr7:80476329 | A | T | 31 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(28): Show |
37 | HG00099.hp2 HG00642.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.462-1950T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80476329 | |||||||
| chr7:80476409 | T | C | 18 | a0001c0001t0001g0034 a0001c0001t0001g0042 a0001c0001t0001g0187 others(15): Show |
18 | HG00639.hp2 HG01243.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.462-2030A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80476409 | |||||||
| chr7:80476496 | G | A | 1 | a0001c0002t0002g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.462-2117C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80476496 | |||||||
| chr7:80476499 | A | G | 5 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0220 others(2): Show |
5 | HG02630.hp1 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.462-2120T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80476499 | |||||||
| chr7:80476523 | A | G | 2 | a0001c0001t0001g0248 a0001c0002t0002g0210 |
2 | HG02683.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.462-2144T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80476523 | |||||||
| chr7:80476857 | GA | G | 3 | a0001c0002t0002g0002 a0001c0002t0002g0041 a0001c0002t0002g0286 |
5 | HG02055.hp2 HG02258.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.461+1983delT | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80476857 | |||||||
| chr7:80476938 | T | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0034 others(77): Show |
94 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.461+1903A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80476938 | |||||||
| chr7:80477165 | C | T | 1 | a0001c0002t0002g0228 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.461+1676G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80477165 | |||||||
| chr7:80477198 | A | G | 5 | a0001c0001t0001g0048 a0001c0001t0001g0288 a0001c0001t0003g0007 others(2): Show |
6 | HG02109.hp1 HG02109.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.461+1643T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80477198 | |||||||
| chr7:80477412 | G | C | 5 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0220 others(2): Show |
5 | HG02630.hp1 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.461+1429C>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80477412 | |||||||
| chr7:80477507 | A | C | 1 | a0001c0002t0002g0271 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.461+1334T>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80477507 | |||||||
| chr7:80477641 | G | A | 2 | a0001c0001t0001g0248 a0001c0002t0002g0210 |
2 | HG02683.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.461+1200C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80477641 | |||||||
| chr7:80477927 | T | A | 1 | a0001c0002t0002g0190 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.461+914A>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80477927 | |||||||
| chr7:80478005 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.461+836G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80478005 | |||||||
| chr7:80478018 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.461+823G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80478018 | |||||||
| chr7:80478116 | A | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(84): Show |
103 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.461+725T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80478116 | |||||||
| chr7:80478190 | C | A | 2 | a0001c0001t0001g0046 a0005c0007t0001g0294 |
2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.461+651G>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80478190 | |||||||
| chr7:80478404 | G | A | 3 | a0001c0002t0002g0064 a0001c0002t0002g0163 a0001c0002t0002g0164 |
3 | HG01168.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.461+437C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80478404 | |||||||
| chr7:80478482 | G | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(83): Show |
102 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.461+359C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80478482 | |||||||
| chr7:80478490 | T | A | 29 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0042 others(26): Show |
31 | HG00639.hp2 HG00673.hp1 HG01243.hp1 others(28): Show |
intron_variant | MODIFIER | c.461+351A>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80478490 | |||||||
| chr7:80478516 | G | A | 1 | a0001c0002t0002g0052 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.461+325C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80478516 | |||||||
| chr7:80478586 | A | T | 1 | a0001c0002t0002g0006 | 3 | HG01891.hp1 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.461+255T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80478586 | |||||||
| chr7:80478800 | A | C | 1 | a0001c0002t0002g0006 | 3 | HG01891.hp1 HG02965.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.461+41T>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 4/7 | chr7 | 80478800 | |||||||
| chr7:80479128 | T | C | 1 | a0001c0002t0002g0144 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.304-130A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80479128 | |||||||
| chr7:80479198 | C | G | 1 | a0001c0001t0001g0034 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.304-200G>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80479198 | |||||||
| chr7:80479212 | T | C | 78 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0042 others(75): Show |
92 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.304-214A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80479212 | |||||||
| chr7:80479215 | TATGTG | T | 4 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0001g0227 others(1): Show |
7 | HG01891.hp1 HG02818.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.304-222_304-218del others(5): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80479215 | |||||||
| chr7:80479223 | G | T | 1 | a0001c0001t0001g0089 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.304-225C>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80479223 | |||||||
| chr7:80479245 | T | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0186 |
3 | HG01943.hp2 HG02273.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.304-247A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80479245 | |||||||
| chr7:80479353 | G | A | 1 | a0001c0001t0001g0256 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.304-355C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80479353 | |||||||
| chr7:80479457 | C | T | 9 | a0001c0001t0001g0187 a0001c0001t0001g0193 a0001c0001t0001g0223 others(6): Show |
9 | HG01261.hp1 HG01891.hp2 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.304-459G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80479457 | |||||||
| chr7:80479511 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.304-513C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80479511 | |||||||
| chr7:80479523 | C | T | 19 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0191 others(16): Show |
25 | HG01123.hp1 HG02027.hp1 HG02083.hp2 others(22): Show |
intron_variant | MODIFIER | c.304-525G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80479523 | |||||||
| chr7:80479710 | C | CA | 36 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0013 others(33): Show |
48 | HG00642.hp1 HG01081.hp1 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.304-713dupT | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80479710 | |||||||
| chr7:80479710 | C | CAA | 32 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(29): Show |
37 | HG00099.hp2 HG00642.hp2 HG01081.hp2 others(34): Show |
intron_variant | MODIFIER | c.304-714_304-713dup others(2): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80479710 | |||||||
| chr7:80479710 | CA | C | 30 | a0001c0001t0001g0042 a0001c0001t0001g0093 a0001c0001t0001g0107 others(27): Show |
31 | HG00280.hp1 HG00639.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.304-713delT | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80479710 | |||||||
| chr7:80479798 | TG | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0191 a0001c0001t0001g0192 others(12): Show |
20 | HG01123.hp1 HG02027.hp1 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.304-801delC | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80479798 | |||||||
| chr7:80479812 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.304-814G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80479812 | |||||||
| chr7:80480050 | T | C | 1 | a0001c0001t0001g0126 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.304-1052A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80480050 | |||||||
| chr7:80480097 | A | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0042 others(45): Show |
56 | HG00639.hp2 HG00673.hp1 HG01123.hp1 others(53): Show |
intron_variant | MODIFIER | c.304-1099T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80480097 | |||||||
| chr7:80480189 | C | T | 20 | a0001c0001t0001g0056 a0001c0001t0001g0198 a0001c0002t0001g0199 others(17): Show |
24 | HG00099.hp2 HG00642.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.304-1191G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80480189 | |||||||
| chr7:80480242 | CAATTTAC others(3): Show |
C | 3 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0181 |
3 | HG02602.hp2 HG03017.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.304-1254_304-1245d others(12): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80480242 | |||||||
| chr7:80480251 | A | G | 19 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0218 others(16): Show |
21 | HG00639.hp2 HG00673.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.304-1253T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80480251 | |||||||
| chr7:80480511 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.304-1513G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80480511 | |||||||
| chr7:80480522 | A | G | 79 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0042 others(76): Show |
93 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.304-1524T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80480522 | |||||||
| chr7:80480621 | T | A | 1 | a0001c0001t0001g0175 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.304-1623A>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80480621 | |||||||
| chr7:80480854 | G | A | 1 | a0001c0002t0002g0022 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.304-1856C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80480854 | |||||||
| chr7:80480959 | C | T | 1 | a0001c0002t0002g0272 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.304-1961G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80480959 | |||||||
| chr7:80481115 | T | C | 2 | a0001c0001t0001g0114 a0001c0001t0001g0128 |
2 | NA18962.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.304-2117A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80481115 | |||||||
| chr7:80481221 | G | A | 9 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0001g0215 others(6): Show |
12 | HG01891.hp1 HG02630.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.304-2223C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80481221 | |||||||
| chr7:80481785 | T | G | 30 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(27): Show |
35 | HG00099.hp2 HG00642.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.304-2787A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80481785 | |||||||
| chr7:80481919 | A | T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0191 a0001c0001t0001g0192 others(14): Show |
23 | HG01123.hp1 HG02083.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.304-2921T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80481919 | |||||||
| chr7:80482152 | T | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0230 a0001c0001t0001g0231 others(8): Show |
13 | HG00673.hp1 HG02683.hp1 HG03834.hp1 others(10): Show |
intron_variant | MODIFIER | c.304-3154A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80482152 | |||||||
| chr7:80482157 | C | G | 2 | a0001c0001t0001g0248 a0001c0002t0002g0210 |
2 | HG02683.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.304-3159G>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80482157 | |||||||
| chr7:80482295 | G | T | 3 | a0001c0002t0002g0286 a0002c0003t0001g0284 a0002c0003t0001g0285 |
3 | HG02615.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.304-3297C>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80482295 | |||||||
| chr7:80482403 | T | C | 5 | a0001c0002t0002g0005 a0001c0002t0002g0247 a0001c0002t0002g0277 others(2): Show |
7 | HG00609.hp2 NA18969.hp1 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.304-3405A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80482403 | |||||||
| chr7:80482481 | T | G | 9 | a0001c0001t0001g0004 a0001c0001t0001g0230 a0001c0001t0001g0231 others(6): Show |
11 | HG00673.hp1 HG03834.hp2 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.304-3483A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80482481 | |||||||
| chr7:80482492 | T | G | 20 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0001g0043 others(17): Show |
25 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(22): Show |
intron_variant | MODIFIER | c.304-3494A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80482492 | |||||||
| chr7:80482537 | G | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0230 a0001c0001t0001g0231 others(6): Show |
11 | HG00673.hp1 HG03834.hp2 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.304-3539C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80482537 | |||||||
| chr7:80482684 | T | C | 19 | a0001c0001t0001g0056 a0001c0001t0001g0198 a0001c0002t0001g0199 others(16): Show |
22 | HG00099.hp2 HG00642.hp2 HG01099.hp1 others(19): Show |
intron_variant | MODIFIER | c.304-3686A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80482684 | |||||||
| chr7:80482689 | A | AT | 5 | a0001c0001t0001g0158 a0001c0001t0001g0288 a0001c0001t0003g0007 others(2): Show |
6 | HG01261.hp2 HG02109.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-3692dupA | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80482689 | |||||||
| chr7:80482689 | AT | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0009 others(176): Show |
208 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.304-3692delA | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80482689 | |||||||
| chr7:80482689 | ATT | A | 17 | a0001c0001t0001g0113 a0001c0001t0001g0150 a0001c0001t0001g0215 others(14): Show |
18 | HG01515.hp1 HG02129.hp1 HG02630.hp1 others(15): Show |
intron_variant | MODIFIER | c.304-3693_304-3692d others(4): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80482689 | |||||||
| chr7:80482689 | ATTT | A | 12 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(9): Show |
16 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.304-3694_304-3692d others(5): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80482689 | |||||||
| chr7:80482752 | C | T | 4 | a0001c0002t0002g0026 a0001c0002t0002g0188 a0001c0002t0002g0189 others(1): Show |
5 | HG02818.hp1 HG03098.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.304-3754G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80482752 | |||||||
| chr7:80482914 | C | G | 1 | a0001c0002t0002g0267 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.304-3916G>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80482914 | |||||||
| chr7:80482951 | C | A | 10 | a0001c0001t0001g0034 a0001c0001t0001g0187 a0001c0001t0001g0223 others(7): Show |
10 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.304-3953G>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80482951 | |||||||
| chr7:80482960 | C | T | 19 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(16): Show |
24 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(21): Show |
intron_variant | MODIFIER | c.304-3962G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80482960 | |||||||
| chr7:80483029 | C | T | 1 | a0001c0001t0001g0138 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.304-4031G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80483029 | |||||||
| chr7:80483030 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.304-4032C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80483030 | |||||||
| chr7:80483106 | A | G | 8 | a0001c0001t0001g0056 a0001c0002t0002g0003 a0001c0002t0002g0052 others(5): Show |
10 | HG00099.hp2 HG00642.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.304-4108T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80483106 | |||||||
| chr7:80483149 | T | C | 19 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(16): Show |
24 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(21): Show |
intron_variant | MODIFIER | c.304-4151A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80483149 | |||||||
| chr7:80483670 | A | G | 1 | a0001c0002t0002g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.304-4672T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80483670 | |||||||
| chr7:80483763 | C | T | 3 | a0001c0002t0002g0201 a0001c0002t0002g0202 a0001c0002t0002g0203 |
3 | HG01243.hp2 HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.304-4765G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80483763 | |||||||
| chr7:80483765 | C | G | 4 | a0001c0001t0001g0288 a0001c0001t0003g0007 a0001c0001t0003g0032 others(1): Show |
5 | HG02109.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.304-4767G>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80483765 | |||||||
| chr7:80483782 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.303+4753G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80483782 | |||||||
| chr7:80483898 | A | G | 1 | a0001c0001t0003g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.303+4637T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80483898 | |||||||
| chr7:80483912 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.303+4623G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80483912 | |||||||
| chr7:80484010 | A | C | 1 | a0001c0002t0002g0057 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.303+4525T>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80484010 | |||||||
| chr7:80484102 | G | A | 4 | a0001c0001t0001g0288 a0001c0001t0003g0007 a0001c0001t0003g0032 others(1): Show |
5 | HG02109.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.303+4433C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80484102 | |||||||
| chr7:80484398 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.303+4137C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80484398 | |||||||
| chr7:80484516 | A | G | 2 | a0001c0001t0001g0248 a0001c0002t0002g0210 |
2 | HG02683.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.303+4019T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80484516 | |||||||
| chr7:80484525 | C | T | 6 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0065 others(3): Show |
8 | HG01256.hp2 HG01258.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.303+4010G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80484525 | |||||||
| chr7:80484548 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.303+3987A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80484548 | |||||||
| chr7:80484699 | T | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0227 |
3 | HG02818.hp2 HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.303+3836A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80484699 | |||||||
| chr7:80484745 | T | C | 12 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(9): Show |
16 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.303+3790A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80484745 | |||||||
| chr7:80484760 | A | G | 10 | a0001c0001t0001g0034 a0001c0001t0001g0187 a0001c0001t0001g0223 others(7): Show |
10 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.303+3775T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80484760 | |||||||
| chr7:80484878 | T | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0230 a0001c0001t0001g0231 others(5): Show |
10 | HG00673.hp1 HG03834.hp2 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.303+3657A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80484878 | |||||||
| chr7:80485118 | G | A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0034 others(40): Show |
51 | HG00673.hp1 HG01261.hp1 HG01891.hp1 others(48): Show |
intron_variant | MODIFIER | c.303+3417C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80485118 | |||||||
| chr7:80485170 | G | GT | 89 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0029 others(86): Show |
102 | HG00099.hp1 HG00597.hp2 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.303+3364dupA | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80485170 | |||||||
| chr7:80485170 | GT | G | 48 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0034 others(45): Show |
56 | HG00673.hp1 HG01261.hp1 HG01515.hp2 others(53): Show |
intron_variant | MODIFIER | c.303+3364delA | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80485170 | |||||||
| chr7:80485172 | T | G | 1 | a0001c0002t0002g0228 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.303+3363A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80485172 | |||||||
| chr7:80485288 | A | T | 2 | a0001c0002t0002g0206 a0001c0002t0002g0287 |
2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.303+3247T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80485288 | |||||||
| chr7:80485291 | A | G | 29 | a0001c0001t0001g0027 a0001c0001t0001g0034 a0001c0001t0001g0043 others(26): Show |
34 | HG01261.hp1 HG01891.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.303+3244T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80485291 | |||||||
| chr7:80485326 | C | G | 2 | a0001c0001t0001g0027 a0001c0001t0001g0227 |
3 | HG02818.hp2 HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.303+3209G>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80485326 | |||||||
| chr7:80485327 | T | C | 28 | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0018 others(25): Show |
31 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.303+3208A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80485327 | |||||||
| chr7:80485548 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0181 |
2 | HG02602.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.303+2987G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80485548 | |||||||
| chr7:80485622 | C | T | 1 | a0001c0002t0002g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.303+2913G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80485622 | |||||||
| chr7:80485804 | T | C | 1 | a0001c0002t0002g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.303+2731A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80485804 | |||||||
| chr7:80486101 | T | G | 1 | a0001c0001t0001g0125 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.303+2434A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80486101 | |||||||
| chr7:80486150 | C | G | 13 | a0001c0001t0001g0004 a0001c0001t0001g0230 a0001c0001t0001g0231 others(10): Show |
16 | HG00673.hp1 HG02109.hp1 HG02895.hp2 others(13): Show |
intron_variant | MODIFIER | c.303+2385G>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80486150 | |||||||
| chr7:80486172 | A | T | 1 | a0001c0002t0002g0169 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.303+2363T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80486172 | |||||||
| chr7:80486371 | G | T | 1 | a0001c0001t0001g0092 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.303+2164C>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80486371 | |||||||
| chr7:80486386 | T | A | 7 | a0001c0001t0001g0042 a0001c0001t0001g0218 a0001c0001t0001g0219 others(4): Show |
7 | HG00639.hp2 HG01243.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.303+2149A>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80486386 | |||||||
| chr7:80486610 | AT | A | 28 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(25): Show |
33 | HG01261.hp1 HG01891.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.303+1924delA | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80486610 | |||||||
| chr7:80486632 | C | CT | 8 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0001c0001t0001g0111 others(5): Show |
8 | HG00423.hp2 HG01358.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.303+1902dupA | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80486632 | |||||||
| chr7:80486632 | CT | C | 34 | a0001c0001t0001g0025 a0001c0001t0001g0038 a0001c0001t0001g0042 others(31): Show |
41 | HG00639.hp2 HG01081.hp1 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.303+1902delA | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80486632 | |||||||
| chr7:80486632 | CTT | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(47): Show |
60 | HG00099.hp2 HG00642.hp2 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.303+1901_303+1902d others(4): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80486632 | |||||||
| chr7:80486738 | A | C | 3 | a0001c0002t0002g0206 a0001c0002t0002g0211 a0001c0002t0002g0287 |
3 | HG02922.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.303+1797T>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80486738 | |||||||
| chr7:80486738 | A | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(78): Show |
97 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.303+1797T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80486738 | |||||||
| chr7:80486802 | G | A | 1 | a0001c0002t0002g0178 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.303+1733C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80486802 | |||||||
| chr7:80486819 | T | G | 9 | a0001c0001t0001g0017 a0001c0001t0001g0067 a0001c0001t0001g0145 others(6): Show |
10 | HG00280.hp2 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.303+1716A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80486819 | |||||||
| chr7:80486960 | T | A | 1 | a0001c0001t0003g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.303+1575A>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80486960 | |||||||
| chr7:80486971 | G | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0230 a0001c0001t0001g0231 others(7): Show |
12 | HG00673.hp1 HG02683.hp1 HG03834.hp1 others(9): Show |
intron_variant | MODIFIER | c.303+1564C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80486971 | |||||||
| chr7:80486980 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.303+1555A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80486980 | |||||||
| chr7:80486988 | T | C | 1 | a0001c0002t0002g0228 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.303+1547A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80486988 | |||||||
| chr7:80487119 | T | C | 52 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0042 others(49): Show |
63 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.303+1416A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80487119 | |||||||
| chr7:80487145 | GTGGGTAT others(4): Show |
G | 3 | a0001c0001t0001g0288 a0001c0001t0003g0007 a0001c0001t0003g0032 |
4 | HG02109.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.303+1379_303+1389d others(13): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80487145 | |||||||
| chr7:80487237 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.303+1298T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80487237 | |||||||
| chr7:80487274 | A | G | 1 | a0001c0002t0002g0272 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.303+1261T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80487274 | |||||||
| chr7:80487502 | A | C | 9 | a0001c0001t0001g0004 a0001c0001t0001g0230 a0001c0001t0001g0231 others(6): Show |
11 | HG00673.hp1 HG03834.hp2 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.303+1033T>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80487502 | |||||||
| chr7:80487613 | G | T | 83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(80): Show |
99 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.303+922C>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80487613 | |||||||
| chr7:80487726 | A | G | 1 | a0001c0002t0002g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.303+809T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80487726 | |||||||
| chr7:80488026 | G | T | 1 | a0001c0001t0001g0291 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.303+509C>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80488026 | |||||||
| chr7:80488069 | T | A | 1 | a0001c0001t0001g0066 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.303+466A>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80488069 | |||||||
| chr7:80488070 | A | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0056 others(42): Show |
56 | HG00099.hp2 HG00642.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.303+465T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80488070 | |||||||
| chr7:80488071 | A | T | 1 | a0001c0001t0001g0191 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.303+464T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80488071 | |||||||
| chr7:80488101 | G | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0230 a0001c0001t0001g0231 others(6): Show |
11 | HG00673.hp1 HG03834.hp2 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.303+434C>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80488101 | |||||||
| chr7:80488252 | G | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0081 |
3 | NA18945.hp1 NA19064.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.303+283C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80488252 | |||||||
| chr7:80488350 | A | T | 1 | a0001c0001t0001g0133 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.303+185T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 3/7 | chr7 | 80488350 | |||||||
| chr7:80488688 | A | G | 39 | a0001c0001t0001g0001 a0001c0001t0001g0042 a0001c0001t0001g0056 others(36): Show |
47 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.162-12T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80488688 | |||||||
| chr7:80488801 | A | T | 5 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0220 others(2): Show |
5 | HG02630.hp1 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.162-125T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80488801 | |||||||
| chr7:80488938 | T | C | 28 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(25): Show |
33 | HG01261.hp1 HG01891.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.162-262A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80488938 | |||||||
| chr7:80489096 | T | C | 2 | a0001c0001t0001g0218 a0001c0001t0001g0219 |
2 | HG01433.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.162-420A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80489096 | |||||||
| chr7:80489193 | T | A | 3 | a0001c0002t0002g0206 a0001c0002t0002g0211 a0001c0002t0002g0287 |
3 | HG02922.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.162-517A>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80489193 | |||||||
| chr7:80489442 | A | C | 42 | a0001c0001t0001g0001 a0001c0001t0001g0042 a0001c0001t0001g0056 others(39): Show |
50 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(47): Show |
intron_variant | MODIFIER | c.162-766T>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80489442 | |||||||
| chr7:80489505 | A | G | 7 | a0001c0001t0001g0042 a0001c0001t0001g0218 a0001c0001t0001g0219 others(4): Show |
7 | HG00639.hp2 HG01243.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.162-829T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80489505 | |||||||
| chr7:80489596 | T | G | 1 | a0001c0002t0002g0019 | 2 | HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.162-920A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80489596 | |||||||
| chr7:80489597 | G | C | 1 | a0001c0001t0001g0187 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.162-921C>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80489597 | |||||||
| chr7:80489731 | A | G | 5 | a0001c0001t0001g0214 a0001c0002t0002g0212 a0001c0002t0002g0213 others(2): Show |
5 | HG00597.hp2 HG02155.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.162-1055T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80489731 | |||||||
| chr7:80489743 | A | G | 1 | a0001c0001t0003g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.162-1067T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80489743 | |||||||
| chr7:80489754 | G | C | 9 | a0001c0001t0001g0004 a0001c0001t0001g0230 a0001c0001t0001g0231 others(6): Show |
11 | HG00673.hp1 HG03834.hp2 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.162-1078C>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80489754 | |||||||
| chr7:80489856 | T | C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0067 a0001c0001t0001g0145 others(6): Show |
10 | HG00280.hp2 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.162-1180A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80489856 | |||||||
| chr7:80490136 | G | A | 1 | a0001c0002t0002g0280 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.162-1460C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80490136 | |||||||
| chr7:80490145 | A | G | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 |
3 | NA18975.hp2 NA18995.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.162-1469T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80490145 | |||||||
| chr7:80490215 | T | C | 10 | a0001c0001t0001g0042 a0001c0001t0001g0218 a0001c0001t0001g0219 others(7): Show |
10 | HG00639.hp2 HG01243.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.162-1539A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80490215 | |||||||
| chr7:80490269 | A | G | 1 | a0001c0001t0001g0231 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.162-1593T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80490269 | |||||||
| chr7:80490374 | G | T | 28 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(25): Show |
33 | HG01261.hp1 HG01891.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.162-1698C>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80490374 | |||||||
| chr7:80490414 | A | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(82): Show |
101 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.162-1738T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80490414 | |||||||
| chr7:80490519 | C | T | 1 | a0001c0002t0002g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.162-1843G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80490519 | |||||||
| chr7:80490611 | G | A | 1 | a0001c0002t0002g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.162-1935C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80490611 | |||||||
| chr7:80490778 | A | G | 1 | a0001c0002t0002g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.162-2102T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80490778 | |||||||
| chr7:80490784 | T | C | 1 | a0001c0002t0002g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.162-2108A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80490784 | |||||||
| chr7:80490796 | G | A | 4 | a0001c0001t0001g0288 a0001c0001t0003g0007 a0001c0001t0003g0032 others(1): Show |
5 | HG02109.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.162-2120C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80490796 | |||||||
| chr7:80490958 | C | T | 1 | a0001c0002t0001g0036 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.162-2282G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80490958 | |||||||
| chr7:80490986 | C | T | 1 | a0001c0002t0002g0197 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.162-2310G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80490986 | |||||||
| chr7:80491220 | G | C | 1 | a0001c0001t0001g0194 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.162-2544C>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80491220 | |||||||
| chr7:80491292 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.162-2616G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80491292 | |||||||
| chr7:80491413 | A | G | 7 | a0001c0001t0001g0042 a0001c0001t0001g0218 a0001c0001t0001g0219 others(4): Show |
7 | HG00639.hp2 HG01243.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.162-2737T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80491413 | |||||||
| chr7:80491562 | T | A | 14 | a0001c0001t0001g0004 a0001c0001t0001g0048 a0001c0001t0001g0230 others(11): Show |
17 | HG00673.hp1 HG02109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.162-2886A>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80491562 | |||||||
| chr7:80491738 | C | T | 17 | a0001c0001t0001g0056 a0001c0001t0001g0198 a0001c0002t0001g0199 others(14): Show |
20 | HG00099.hp2 HG00642.hp2 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.161+2867G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80491738 | |||||||
| chr7:80491848 | A | C | 7 | a0001c0001t0001g0042 a0001c0001t0001g0218 a0001c0001t0001g0219 others(4): Show |
7 | HG00639.hp2 HG01243.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.161+2757T>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80491848 | |||||||
| chr7:80491912 | C | T | 3 | a0001c0002t0002g0207 a0001c0002t0002g0208 a0001c0002t0002g0209 |
3 | HG01255.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.161+2693G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80491912 | |||||||
| chr7:80491975 | T | C | 1 | a0001c0002t0002g0203 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.161+2630A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80491975 | |||||||
| chr7:80492031 | A | C | 28 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(25): Show |
33 | HG01261.hp1 HG01891.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+2574T>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80492031 | |||||||
| chr7:80492051 | C | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0230 a0001c0001t0001g0231 others(6): Show |
11 | HG00673.hp1 HG03834.hp2 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.161+2554G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80492051 | |||||||
| chr7:80492146 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.161+2459C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80492146 | |||||||
| chr7:80492176 | C | CA | 96 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0029 others(93): Show |
108 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.161+2428dupT | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80492176 | |||||||
| chr7:80492176 | C | CAA | 18 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0143 others(15): Show |
19 | HG01123.hp1 HG01361.hp1 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.161+2427_161+2428d others(4): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80492176 | |||||||
| chr7:80492176 | CA | C | 13 | a0001c0001t0001g0011 a0001c0001t0001g0081 a0001c0001t0001g0084 others(10): Show |
14 | HG00597.hp1 HG00639.hp1 NA18612.hp1 others(11): Show |
intron_variant | MODIFIER | c.161+2428delT | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80492176 | |||||||
| chr7:80492176 | CAAA | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0042 others(47): Show |
61 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(58): Show |
intron_variant | MODIFIER | c.161+2426_161+2428d others(5): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80492176 | |||||||
| chr7:80492176 | CAAAAAA | C | 28 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(25): Show |
33 | HG01261.hp1 HG01891.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+2423_161+2428d others(8): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80492176 | |||||||
| chr7:80492355 | T | TTAAA | 29 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(26): Show |
34 | HG01261.hp1 HG01891.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.161+2246_161+2249d others(6): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80492355 | |||||||
| chr7:80492469 | T | G | 1 | a0001c0002t0002g0210 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.161+2136A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80492469 | |||||||
| chr7:80492613 | G | A | 2 | a0001c0001t0001g0248 a0001c0002t0002g0210 |
2 | HG02683.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.161+1992C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80492613 | |||||||
| chr7:80492760 | C | A | 1 | a0001c0002t0002g0239 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.161+1845G>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80492760 | |||||||
| chr7:80492928 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.161+1677T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80492928 | |||||||
| chr7:80492940 | A | G | 1 | a0001c0001t0001g0245 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.161+1665T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80492940 | |||||||
| chr7:80493037 | C | CT | 6 | a0001c0001t0001g0223 a0001c0002t0002g0050 a0001c0002t0002g0217 others(3): Show |
6 | HG01261.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.161+1567dupA | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493037 | |||||||
| chr7:80493040 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0001g0227 |
3 | HG02818.hp2 HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.161+1565C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493040 | |||||||
| chr7:80493047 | G | A | 28 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(25): Show |
33 | HG01261.hp1 HG01891.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+1558C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493047 | |||||||
| chr7:80493055 | T | C | 14 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(11): Show |
19 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(16): Show |
intron_variant | MODIFIER | c.161+1550A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493055 | |||||||
| chr7:80493066 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.161+1539T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493066 | |||||||
| chr7:80493109 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.161+1496G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493109 | |||||||
| chr7:80493220 | A | G | 38 | a0001c0001t0001g0001 a0001c0001t0001g0042 a0001c0001t0001g0056 others(35): Show |
46 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.161+1385T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493220 | |||||||
| chr7:80493325 | G | A | 28 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(25): Show |
33 | HG01261.hp1 HG01891.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+1280C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493325 | |||||||
| chr7:80493392 | T | C | 7 | a0001c0001t0001g0042 a0001c0001t0001g0218 a0001c0001t0001g0219 others(4): Show |
7 | HG00639.hp2 HG01243.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.161+1213A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493392 | |||||||
| chr7:80493436 | A | G | 5 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0220 others(2): Show |
5 | HG02630.hp1 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+1169T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493436 | |||||||
| chr7:80493440 | G | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0021 others(187): Show |
219 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.161+1165C>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493440 | |||||||
| chr7:80493548 | C | T | 7 | a0001c0001t0001g0223 a0001c0002t0002g0050 a0001c0002t0002g0217 others(4): Show |
7 | HG01261.hp1 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.161+1057G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493548 | |||||||
| chr7:80493565 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(83): Show |
102 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.161+1040A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493565 | |||||||
| chr7:80493592 | ATCCTCCT others(47): Show |
A | 32 | a0001c0001t0001g0001 a0001c0001t0001g0056 a0001c0001t0001g0191 others(29): Show |
40 | HG00099.hp2 HG00642.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.161+959_161+1012de others(55): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493592 | |||||||
| chr7:80493604 | CCTCCTCC others(44): Show |
C | 2 | a0001c0001t0001g0046 a0005c0007t0001g0294 |
2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.161+950_161+1000de others(52): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493604 | |||||||
| chr7:80493605 | CTCCTCCT others(44): Show |
C | 12 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(9): Show |
17 | HG01891.hp1 HG02055.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.161+949_161+999del others(51): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493605 | |||||||
| chr7:80493606 | TC | T | 7 | a0001c0001t0001g0042 a0001c0001t0001g0218 a0001c0001t0001g0219 others(4): Show |
7 | HG00639.hp2 HG01243.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.161+998delG | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493606 | |||||||
| chr7:80493624 | TTCCTCCT others(28): Show |
T | 9 | a0001c0001t0001g0187 a0001c0001t0001g0223 a0001c0001t0003g0031 others(6): Show |
9 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.161+946_161+980del others(35): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493624 | |||||||
| chr7:80493637 | TTCC | T | 8 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0220 others(5): Show |
8 | HG02630.hp1 HG02965.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.161+965_161+967del others(3): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493637 | |||||||
| chr7:80493637 | TTCCTCCT others(12): Show |
T | 3 | a0001c0001t0001g0012 a0001c0002t0002g0063 a0001c0002t0002g0210 |
3 | HG01496.hp1 HG02683.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.161+949_161+967del others(19): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493637 | |||||||
| chr7:80493640 | C | CTCCTCCT others(9): Show |
1 | a0001c0001t0001g0049 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.161+949_161+964dup others(16): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493640 | |||||||
| chr7:80493640 | C | CTCCTCCT others(41): Show |
1 | a0001c0002t0002g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.161+917_161+964dup others(48): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493640 | |||||||
| chr7:80493640 | C | CTCCTCCT others(6): Show |
7 | a0001c0001t0001g0042 a0001c0001t0001g0218 a0001c0001t0001g0219 others(4): Show |
7 | HG00639.hp2 HG01243.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.161+964_161+965ins others(13): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493640 | |||||||
| chr7:80493640 | CTCCTCCT others(9): Show |
C | 1 | a0001c0001t0001g0072 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.161+949_161+964del others(16): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493640 | |||||||
| chr7:80493640 | CTCCTCCT others(25): Show |
C | 1 | a0001c0002t0002g0167 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.161+933_161+964del others(32): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493640 | |||||||
| chr7:80493656 | T | G | 2 | a0001c0001t0001g0046 a0005c0007t0001g0294 |
2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.161+949A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493656 | |||||||
| chr7:80493670 | CTTTCCTC others(41): Show |
C | 1 | a0001c0002t0002g0287 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.161+887_161+934del others(48): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493670 | |||||||
| chr7:80493671 | T | C | 1 | a0001c0002t0002g0206 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.161+934A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493671 | |||||||
| chr7:80493673 | T | C | 1 | a0001c0002t0002g0206 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.161+932A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493673 | |||||||
| chr7:80493673 | TCCTCCTC others(6): Show |
T | 5 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0220 others(2): Show |
5 | HG02630.hp1 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+919_161+931del others(13): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493673 | |||||||
| chr7:80493674 | C | T | 1 | a0001c0002t0002g0206 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.161+931G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493674 | |||||||
| chr7:80493675 | C | T | 1 | a0001c0002t0002g0206 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.161+930G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493675 | |||||||
| chr7:80493683 | CCTCTTTC others(28): Show |
C | 8 | a0001c0001t0001g0017 a0001c0001t0001g0067 a0001c0001t0001g0145 others(5): Show |
9 | HG00280.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.161+887_161+921del others(35): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493683 | |||||||
| chr7:80493687 | T | G | 5 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0220 others(2): Show |
5 | HG02630.hp1 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+918A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493687 | |||||||
| chr7:80493699 | C | T | 6 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0220 others(3): Show |
6 | HG02630.hp1 HG02965.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.161+906G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493699 | |||||||
| chr7:80493701 | TCTTTGTT others(44): Show |
T | 1 | a0001c0002t0002g0149 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.161+853_161+903del others(51): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493701 | |||||||
| chr7:80493706 | G | C | 7 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0220 others(4): Show |
7 | HG02630.hp1 HG02965.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.161+899C>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493706 | |||||||
| chr7:80493707 | T | C | 7 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0220 others(4): Show |
7 | HG02630.hp1 HG02965.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.161+898A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493707 | |||||||
| chr7:80493718 | T | C | 7 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0220 others(4): Show |
7 | HG02630.hp1 HG02965.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.161+887A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493718 | |||||||
| chr7:80493718 | TCTCTTTC others(12): Show |
T | 7 | a0001c0001t0001g0042 a0001c0001t0001g0218 a0001c0001t0001g0219 others(4): Show |
7 | HG00639.hp2 HG01243.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.161+868_161+886del others(19): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493718 | |||||||
| chr7:80493723 | TTCC | T | 8 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0220 others(5): Show |
8 | HG02630.hp1 HG02965.hp2 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.161+879_161+881del others(3): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493723 | |||||||
| chr7:80493736 | T | A | 3 | a0001c0001t0001g0248 a0001c0002t0002g0206 a0001c0002t0002g0287 |
3 | HG03195.hp2 HG03834.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.161+869A>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493736 | |||||||
| chr7:80493736 | T | TCCTCTTT others(9): Show |
1 | a0001c0002t0002g0185 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.161+853_161+868dup others(16): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493736 | |||||||
| chr7:80493736 | TCCTCTTT others(9): Show |
T | 13 | a0001c0001t0001g0056 a0001c0001t0001g0125 a0001c0001t0001g0133 others(10): Show |
15 | HG00099.hp2 HG00609.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.161+853_161+868del others(16): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493736 | |||||||
| chr7:80493752 | A | T | 28 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(25): Show |
33 | HG01261.hp1 HG01891.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+853T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493752 | |||||||
| chr7:80493768 | A | ACCTCTTT others(9): Show |
11 | a0001c0001t0001g0001 a0001c0001t0001g0191 a0001c0001t0001g0192 others(8): Show |
16 | HG01123.hp1 HG02027.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.161+836_161+837ins others(16): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493768 | |||||||
| chr7:80493768 | A | T | 2 | a0001c0001t0001g0196 a0001c0002t0002g0225 |
2 | NA18946.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.161+837T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493768 | |||||||
| chr7:80493768 | ACCTCTTT others(25): Show |
A | 99 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0029 others(96): Show |
112 | HG00099.hp1 HG00280.hp1 HG00597.hp2 others(109): Show |
intron_variant | MODIFIER | c.161+805_161+836del others(32): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493768 | |||||||
| chr7:80493768 | ACCTCTTT others(41): Show |
A | 2 | a0001c0002t0002g0249 a0001c0002t0002g0250 |
2 | HG02257.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.161+789_161+836del others(48): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493768 | |||||||
| chr7:80493784 | A | ACCTCTTT others(9): Show |
9 | a0001c0001t0001g0014 a0001c0001t0001g0048 a0001c0001t0001g0114 others(6): Show |
9 | HG00438.hp1 HG02109.hp2 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.161+805_161+820dup others(16): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493784 | |||||||
| chr7:80493784 | A | ACCTCTTT others(25): Show |
3 | a0001c0001t0003g0007 a0001c0001t0003g0032 a0001c0002t0002g0228 |
4 | HG02895.hp2 HG02897.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.161+789_161+820dup others(32): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493784 | |||||||
| chr7:80493784 | A | ACCTCTTT others(41): Show |
1 | a0001c0001t0001g0288 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.161+773_161+820dup others(48): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493784 | |||||||
| chr7:80493784 | A | T | 26 | a0001c0001t0001g0001 a0001c0001t0001g0085 a0001c0001t0001g0110 others(23): Show |
32 | HG01123.hp1 HG01243.hp2 HG01934.hp1 others(29): Show |
intron_variant | MODIFIER | c.161+821T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493784 | |||||||
| chr7:80493784 | ACCTCTTT others(9): Show |
A | 31 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0012 others(28): Show |
34 | HG00673.hp1 HG01261.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.161+805_161+820del others(16): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493784 | |||||||
| chr7:80493800 | T | A | 20 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(17): Show |
24 | HG00738.hp2 HG01891.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.161+805A>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493800 | |||||||
| chr7:80493816 | T | A | 28 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(25): Show |
33 | HG01261.hp1 HG01891.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.161+789A>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493816 | |||||||
| chr7:80493832 | T | A | 12 | a0001c0001t0001g0027 a0001c0001t0001g0066 a0001c0001t0001g0187 others(9): Show |
13 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.161+773A>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493832 | |||||||
| chr7:80493848 | T | A | 6 | a0001c0001t0001g0223 a0001c0002t0002g0050 a0001c0002t0002g0217 others(3): Show |
6 | HG01261.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.161+757A>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493848 | |||||||
| chr7:80493857 | C | CTCCTCCT others(6): Show |
1 | a0001c0002t0002g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.161+735_161+747dup others(13): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493857 | |||||||
| chr7:80493875 | C | T | 5 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0220 others(2): Show |
5 | HG02630.hp1 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.161+730G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493875 | |||||||
| chr7:80493913 | C | T | 29 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(26): Show |
34 | HG01261.hp1 HG01891.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.161+692G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493913 | |||||||
| chr7:80493943 | T | C | 29 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(26): Show |
34 | HG01261.hp1 HG01891.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.161+662A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80493943 | |||||||
| chr7:80494038 | G | C | 1 | a0001c0002t0002g0259 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.161+567C>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80494038 | |||||||
| chr7:80494045 | C | T | 1 | a0001c0002t0002g0267 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.161+560G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80494045 | |||||||
| chr7:80494121 | G | A | 29 | a0001c0001t0001g0027 a0001c0001t0001g0043 a0001c0001t0001g0044 others(26): Show |
34 | HG01261.hp1 HG01891.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.161+484C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80494121 | |||||||
| chr7:80494187 | C | A | 1 | a0001c0002t0002g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.161+418G>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80494187 | |||||||
| chr7:80494217 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.161+388G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80494217 | |||||||
| chr7:80494310 | A | G | 39 | a0001c0001t0001g0001 a0001c0001t0001g0042 a0001c0001t0001g0056 others(36): Show |
47 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.161+295T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80494310 | |||||||
| chr7:80494386 | G | T | 1 | a0001c0002t0002g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.161+219C>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80494386 | |||||||
| chr7:80494534 | T | A | 1 | a0001c0002t0002g0151 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.161+71A>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80494534 | |||||||
| chr7:80494551 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.161+54G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 2/7 | chr7 | 80494551 | |||||||
| chr7:80494654 | C | T | 1 | a0001c0004t0001g0033 | 1 | HG02015.hp1 | splice_region_variant&intron_variant | LOW | c.119-7G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80494654 | |||||||
| chr7:80494683 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(83): Show |
102 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.119-36A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80494683 | |||||||
| chr7:80494701 | A | G | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0238 |
3 | HG02630.hp1 HG02965.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.119-54T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80494701 | |||||||
| chr7:80494735 | A | AT | 85 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(82): Show |
101 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.119-89dupA | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80494735 | |||||||
| chr7:80495070 | A | AT | 5 | a0001c0001t0001g0048 a0001c0001t0001g0288 a0001c0001t0003g0007 others(2): Show |
6 | HG02109.hp1 HG02109.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-424dupA | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80495070 | |||||||
| chr7:80495128 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.119-481T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80495128 | |||||||
| chr7:80495247 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(83): Show |
102 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.119-600A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80495247 | |||||||
| chr7:80495411 | T | C | 1 | a0001c0002t0002g0228 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.119-764A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80495411 | |||||||
| chr7:80495425 | A | T | 1 | a0001c0002t0002g0201 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.119-778T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80495425 | |||||||
| chr7:80495465 | GGTTT | G | 10 | a0001c0001t0001g0004 a0001c0001t0001g0230 a0001c0001t0001g0231 others(7): Show |
12 | HG00673.hp1 HG03041.hp1 HG03834.hp2 others(9): Show |
intron_variant | MODIFIER | c.119-822_119-819del others(4): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80495465 | |||||||
| chr7:80495469 | T | G | 4 | a0001c0001t0001g0048 a0001c0001t0001g0288 a0001c0001t0003g0007 others(1): Show |
5 | HG02109.hp1 HG02109.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.119-822A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80495469 | |||||||
| chr7:80495572 | T | C | 56 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0042 others(53): Show |
67 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.119-925A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80495572 | |||||||
| chr7:80495632 | G | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0042 a0001c0001t0001g0056 others(36): Show |
47 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.119-985C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80495632 | |||||||
| chr7:80495718 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0027 others(83): Show |
102 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.119-1071A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80495718 | |||||||
| chr7:80495811 | G | C | 5 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0220 others(2): Show |
5 | HG02630.hp1 HG02965.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.119-1164C>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80495811 | |||||||
| chr7:80495844 | A | G | 3 | a0001c0002t0002g0201 a0001c0002t0002g0202 a0001c0002t0002g0203 |
3 | HG01243.hp2 HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.119-1197T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80495844 | |||||||
| chr7:80495957 | T | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0042 others(50): Show |
64 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.119-1310A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80495957 | |||||||
| chr7:80496226 | G | A | 1 | a0001c0002t0002g0228 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.119-1579C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80496226 | |||||||
| chr7:80496283 | A | G | 7 | a0001c0001t0001g0042 a0001c0001t0001g0218 a0001c0001t0001g0219 others(4): Show |
7 | HG00639.hp2 HG01243.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.119-1636T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80496283 | |||||||
| chr7:80496499 | CTTTCCTA others(7): Show |
C | 1 | a0001c0002t0002g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.119-1866_119-1853d others(16): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80496499 | |||||||
| chr7:80496567 | A | T | 2 | a0001c0001t0001g0034 a0001c0002t0002g0070 |
2 | HG01123.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.119-1920T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80496567 | |||||||
| chr7:80496612 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.119-1965C>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80496612 | |||||||
| chr7:80496714 | C | G | 1 | a0001c0002t0002g0167 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.119-2067G>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80496714 | |||||||
| chr7:80496754 | T | G | 2 | a0001c0002t0002g0208 a0001c0002t0002g0209 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.119-2107A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80496754 | |||||||
| chr7:80496775 | A | G | 7 | a0001c0001t0001g0042 a0001c0001t0001g0218 a0001c0001t0001g0219 others(4): Show |
7 | HG00639.hp2 HG01243.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.119-2128T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80496775 | |||||||
| chr7:80496802 | G | A | 1 | a0001c0001t0001g0237 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.119-2155C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80496802 | |||||||
| chr7:80496822 | C | T | 2 | a0001c0001t0001g0098 a0001c0001t0001g0103 |
2 | NA18979.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.119-2175G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80496822 | |||||||
| chr7:80497192 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.119-2545G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497192 | |||||||
| chr7:80497238 | C | G | 32 | a0001c0001t0001g0001 a0001c0001t0001g0056 a0001c0001t0001g0191 others(29): Show |
40 | HG00099.hp2 HG00642.hp2 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.119-2591G>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497238 | |||||||
| chr7:80497254 | A | G | 8 | a0001c0001t0001g0091 a0001c0001t0001g0111 a0001c0001t0001g0112 others(5): Show |
8 | HG00423.hp2 HG00438.hp2 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.119-2607T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497254 | |||||||
| chr7:80497334 | T | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0191 a0001c0001t0001g0192 others(9): Show |
17 | HG01123.hp1 HG02027.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.119-2687A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497334 | |||||||
| chr7:80497407 | A | G | 1 | a0001c0001t0001g0111 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.119-2760T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497407 | |||||||
| chr7:80497522 | G | A | 56 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0042 others(53): Show |
67 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.119-2875C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497522 | |||||||
| chr7:80497534 | A | C | 5 | a0001c0001t0001g0157 a0001c0002t0002g0026 a0001c0002t0002g0188 others(2): Show |
6 | HG01257.hp1 HG02818.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.119-2887T>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497534 | |||||||
| chr7:80497537 | T | C | 1 | a0001c0001t0001g0088 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.119-2890A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497537 | |||||||
| chr7:80497543 | C | CACATATA others(21): Show |
1 | a0001c0001t0001g0121 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.119-2897_119-2896i others(30): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497543 | |||||||
| chr7:80497543 | C | CACATATA others(7): Show |
39 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0025 others(36): Show |
44 | HG00423.hp2 HG00438.hp1 HG00621.hp2 others(41): Show |
intron_variant | MODIFIER | c.119-2910_119-2897d others(16): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497543 | |||||||
| chr7:80497543 | C | CACATATA others(21): Show |
18 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0068 others(15): Show |
20 | HG00438.hp2 HG01081.hp1 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.119-2924_119-2897d others(30): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497543 | |||||||
| chr7:80497543 | C | CACATATA others(51): Show |
1 | a0001c0001t0001g0110 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.119-2897_119-2896i others(60): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497543 | |||||||
| chr7:80497543 | C | CACATATA others(79): Show |
1 | a0001c0001t0001g0120 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.119-2897_119-2896i others(88): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497543 | |||||||
| chr7:80497543 | C | CACATATA others(111): Show |
1 | a0001c0001t0001g0085 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.119-2897_119-2896i others(120): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497543 | |||||||
| chr7:80497543 | C | CACATATA others(35): Show |
17 | a0001c0001t0001g0011 a0001c0001t0001g0071 a0001c0001t0001g0103 others(14): Show |
18 | HG00642.hp1 HG01099.hp2 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.119-2938_119-2897d others(44): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497543 | |||||||
| chr7:80497543 | C | CACATATA others(49): Show |
12 | a0001c0001t0001g0037 a0001c0001t0001g0098 a0001c0001t0001g0099 others(9): Show |
12 | HG00639.hp1 HG02083.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.119-2952_119-2897d others(58): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497543 | |||||||
| chr7:80497543 | C | CACATATA others(63): Show |
9 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0065 others(6): Show |
11 | HG00597.hp1 HG01943.hp2 HG02273.hp2 others(8): Show |
intron_variant | MODIFIER | c.119-2966_119-2897d others(72): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497543 | |||||||
| chr7:80497543 | C | CACATATA others(77): Show |
2 | a0001c0001t0001g0153 a0001c0002t0002g0047 |
2 | NA18612.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.119-2980_119-2897d others(86): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497543 | |||||||
| chr7:80497543 | C | CACATATA others(91): Show |
2 | a0001c0001t0001g0091 a0001c0001t0001g0186 |
2 | HG02293.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.119-2994_119-2897d others(100): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497543 | |||||||
| chr7:80497543 | C | CACATATA others(105): Show |
5 | a0001c0001t0001g0216 a0001c0001t0001g0221 a0001c0001t0001g0227 others(2): Show |
5 | HG00642.hp2 HG02886.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.119-3008_119-2897d others(114): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497543 | |||||||
| chr7:80497543 | C | CACATATA others(119): Show |
1 | a0001c0002t0002g0090 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.119-3022_119-2897d others(128): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497543 | |||||||
| chr7:80497543 | C | CACATATA others(133): Show |
2 | a0001c0001t0001g0238 a0001c0002t0002g0249 |
2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.119-2897_119-2896i others(142): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497543 | |||||||
| chr7:80497543 | C | CACATATA others(169): Show |
1 | a0001c0001t0001g0220 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.119-2897_119-2896i others(178): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497543 | |||||||
| chr7:80497543 | C | CACATATA others(105): Show |
1 | a0001c0001t0001g0087 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.119-2897_119-2896i others(114): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497543 | |||||||
| chr7:80497543 | C | CACATATA others(147): Show |
1 | a0001c0001t0001g0089 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.119-2897_119-2896i others(156): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497543 | |||||||
| chr7:80497543 | C | CGTATATA others(55): Show |
1 | a0001c0001t0001g0088 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.119-2897_119-2896i others(64): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497543 | |||||||
| chr7:80497543 | CACATATA others(7): Show |
C | 40 | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0141 others(37): Show |
45 | HG00280.hp1 HG00597.hp2 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.119-2910_119-2897d others(16): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497543 | |||||||
| chr7:80497543 | CACATATA others(21): Show |
C | 9 | a0001c0001t0001g0162 a0001c0001t0001g0187 a0001c0002t0002g0015 others(6): Show |
12 | HG00621.hp1 HG01081.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.119-2924_119-2897d others(30): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497543 | |||||||
| chr7:80497543 | CACATATA others(35): Show |
C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0067 a0001c0001t0001g0145 others(6): Show |
10 | HG00280.hp2 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.119-2938_119-2897d others(44): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497543 | |||||||
| chr7:80497547 | T | TATACGTA others(51): Show |
1 | a0001c0002t0002g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.119-2901_119-2900i others(60): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497547 | |||||||
| chr7:80497558 | A | G | 7 | a0001c0001t0001g0042 a0001c0001t0001g0218 a0001c0001t0001g0219 others(4): Show |
7 | HG00639.hp2 HG01243.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.119-2911T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497558 | |||||||
| chr7:80497559 | C | T | 7 | a0001c0001t0001g0042 a0001c0001t0001g0218 a0001c0001t0001g0219 others(4): Show |
7 | HG00639.hp2 HG01243.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.119-2912G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497559 | |||||||
| chr7:80497560 | A | G | 24 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0044 others(21): Show |
33 | HG01123.hp1 HG01891.hp1 HG02027.hp1 others(30): Show |
intron_variant | MODIFIER | c.119-2913T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497560 | |||||||
| chr7:80497561 | T | C | 1 | a0001c0002t0002g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.119-2914A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497561 | |||||||
| chr7:80497566 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0230 a0001c0001t0001g0231 others(5): Show |
10 | HG00673.hp1 HG03834.hp2 NA18747.hp2 others(7): Show |
intron_variant | MODIFIER | c.119-2919C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497566 | |||||||
| chr7:80497566 | G | T | 1 | a0001c0001t0001g0236 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.119-2919C>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497566 | |||||||
| chr7:80497572 | A | G | 8 | a0001c0001t0001g0042 a0001c0001t0001g0166 a0001c0001t0001g0218 others(5): Show |
8 | HG00639.hp2 HG01243.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.119-2925T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497572 | |||||||
| chr7:80497573 | C | T | 7 | a0001c0001t0001g0042 a0001c0001t0001g0218 a0001c0001t0001g0219 others(4): Show |
7 | HG00639.hp2 HG01243.hp1 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.119-2926G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497573 | |||||||
| chr7:80497574 | A | ATATACGT others(63): Show |
1 | a0001c0001t0001g0086 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.119-2928_119-2927i others(72): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497574 | |||||||
| chr7:80497574 | A | G | 27 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0044 others(24): Show |
36 | HG01123.hp1 HG01891.hp1 HG02027.hp1 others(33): Show |
intron_variant | MODIFIER | c.119-2927T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497574 | |||||||
| chr7:80497575 | T | C | 1 | a0001c0002t0002g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.119-2928A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497575 | |||||||
| chr7:80497580 | GTATATAC others(89): Show |
G | 17 | a0001c0001t0001g0001 a0001c0001t0001g0042 a0001c0001t0001g0191 others(14): Show |
22 | HG00639.hp2 HG01243.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.119-3029_119-2934d others(98): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497580 | |||||||
| chr7:80497586 | A | ACATATAC others(7): Show |
18 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0166 others(15): Show |
21 | HG00735.hp1 HG01071.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.119-2940_119-2939i others(16): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497586 | |||||||
| chr7:80497586 | A | ACATATAC others(35): Show |
1 | a0001c0002t0002g0074 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.119-2940_119-2939i others(44): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497586 | |||||||
| chr7:80497586 | A | ACATATAC others(63): Show |
1 | a0001c0002t0002g0064 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.119-2940_119-2939i others(72): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497586 | |||||||
| chr7:80497588 | A | G | 18 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(15): Show |
22 | HG01123.hp1 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.119-2941T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497588 | |||||||
| chr7:80497589 | T | C | 1 | a0001c0002t0002g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.119-2942A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497589 | |||||||
| chr7:80497594 | GTATATAC others(75): Show |
G | 1 | a0001c0001t0001g0196 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.119-3029_119-2948d others(84): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497594 | |||||||
| chr7:80497595 | TATATACA others(73): Show |
T | 12 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(9): Show |
16 | HG01891.hp1 HG02055.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.119-3028_119-2949d others(82): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497595 | |||||||
| chr7:80497602 | A | G | 5 | a0001c0001t0001g0049 a0001c0002t0002g0151 a0001c0002t0002g0286 others(2): Show |
5 | HG01123.hp1 HG02615.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.119-2955T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497602 | |||||||
| chr7:80497603 | T | C | 1 | a0001c0002t0002g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.119-2956A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497603 | |||||||
| chr7:80497608 | G | GTATATAC others(7): Show |
1 | a0001c0002t0002g0266 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.119-2962_119-2961i others(16): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497608 | |||||||
| chr7:80497608 | GTATATAC others(61): Show |
G | 2 | a0001c0001t0001g0248 a0001c0002t0002g0151 |
2 | HG01123.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.119-3029_119-2962d others(70): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497608 | |||||||
| chr7:80497614 | A | G | 22 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0166 others(19): Show |
25 | HG00280.hp1 HG00741.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.119-2967T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497614 | |||||||
| chr7:80497616 | A | ATACACGT others(105): Show |
1 | a0001c0002t0002g0222 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.119-2970_119-2969i others(114): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497616 | |||||||
| chr7:80497616 | A | G | 5 | a0001c0001t0001g0049 a0001c0002t0002g0228 a0001c0002t0002g0286 others(2): Show |
5 | HG02615.hp2 HG02723.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.119-2969T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497616 | |||||||
| chr7:80497617 | T | C | 1 | a0001c0002t0002g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.119-2970A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497617 | |||||||
| chr7:80497619 | T | C | 1 | a0001c0002t0002g0222 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.119-2972A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497619 | |||||||
| chr7:80497622 | GTATATAC others(47): Show |
G | 3 | a0001c0002t0002g0286 a0002c0003t0001g0284 a0002c0003t0001g0285 |
3 | HG02615.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.119-3029_119-2976d others(56): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497622 | |||||||
| chr7:80497629 | C | CATATACG others(21): Show |
1 | a0001c0001t0003g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.119-2983_119-2982i others(30): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497629 | |||||||
| chr7:80497630 | A | G | 2 | a0001c0001t0001g0049 a0001c0002t0002g0228 |
2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.119-2983T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497630 | |||||||
| chr7:80497631 | T | C | 1 | a0001c0002t0002g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.119-2984A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497631 | |||||||
| chr7:80497636 | GTATATAC others(33): Show |
G | 4 | a0001c0002t0002g0026 a0001c0002t0002g0188 a0001c0002t0002g0189 others(1): Show |
5 | HG02818.hp1 HG03098.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.119-3029_119-2990d others(42): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497636 | |||||||
| chr7:80497642 | A | G | 20 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0166 others(17): Show |
22 | HG00280.hp1 HG00741.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.119-2995T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497642 | |||||||
| chr7:80497644 | A | G | 2 | a0001c0001t0001g0049 a0001c0002t0002g0228 |
2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.119-2997T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497644 | |||||||
| chr7:80497650 | GTATATAC others(19): Show |
G | 4 | a0001c0001t0001g0004 a0001c0001t0001g0234 a0001c0002t0002g0206 others(1): Show |
4 | HG02683.hp1 HG03195.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-3029_119-3004d others(28): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497650 | |||||||
| chr7:80497658 | A | G | 2 | a0001c0001t0001g0049 a0001c0002t0002g0228 |
2 | HG02723.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.119-3011T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497658 | |||||||
| chr7:80497664 | GTATATAC others(5): Show |
G | 10 | a0001c0001t0001g0004 a0001c0001t0001g0230 a0001c0001t0001g0231 others(7): Show |
11 | HG00673.hp1 HG01099.hp1 HG03834.hp2 others(8): Show |
intron_variant | MODIFIER | c.119-3029_119-3018d others(14): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497664 | |||||||
| chr7:80497671 | C | CAT | 7 | a0001c0001t0001g0056 a0001c0001t0001g0227 a0001c0002t0002g0053 others(4): Show |
7 | HG00642.hp2 HG01243.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.119-3026_119-3025d others(4): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497671 | |||||||
| chr7:80497671 | C | CATATACG others(9): Show |
2 | a0001c0002t0002g0003 a0001c0002t0002g0197 |
3 | HG02970.hp2 HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.119-3025_119-3024i others(18): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497671 | |||||||
| chr7:80497671 | C | CATATACG others(23): Show |
1 | a0001c0001t0001g0198 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.119-3025_119-3024i others(32): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497671 | |||||||
| chr7:80497671 | C | CATATACG others(37): Show |
2 | a0001c0001t0001g0038 a0001c0002t0002g0052 |
2 | HG02886.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.119-3025_119-3024i others(46): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497671 | |||||||
| chr7:80497671 | C | CATATACG others(51): Show |
2 | a0001c0001t0001g0027 a0001c0002t0002g0057 |
2 | HG02818.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.119-3025_119-3024i others(60): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497671 | |||||||
| chr7:80497671 | C | CATATACG others(65): Show |
2 | a0001c0001t0001g0027 a0001c0002t0002g0055 |
2 | HG01256.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.119-3025_119-3024i others(74): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497671 | |||||||
| chr7:80497671 | C | CATATACG others(157): Show |
2 | a0001c0001t0003g0007 a0001c0001t0003g0032 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.119-3025_119-3024i others(166): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497671 | |||||||
| chr7:80497671 | C | CATATACG others(125): Show |
1 | a0001c0001t0001g0288 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.119-3025_119-3024i others(134): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497671 | |||||||
| chr7:80497671 | C | CATATACG others(79): Show |
1 | a0001c0002t0002g0054 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.119-3025_119-3024i others(88): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497671 | |||||||
| chr7:80497671 | C | CATATACG others(169): Show |
1 | a0001c0001t0003g0007 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.119-3025_119-3024i others(178): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497671 | |||||||
| chr7:80497671 | C | CATATACG others(93): Show |
1 | a0001c0001t0001g0134 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.119-3025_119-3024i others(102): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497671 | |||||||
| chr7:80497671 | C | CATATACG others(197): Show |
1 | a0001c0001t0001g0048 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.119-3025_119-3024i others(206): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497671 | |||||||
| chr7:80497672 | A | ATATACGT others(7): Show |
4 | a0001c0002t0002g0050 a0001c0002t0002g0217 a0001c0002t0002g0225 others(1): Show |
4 | HG01261.hp1 HG02622.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.119-3026_119-3025i others(16): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497672 | |||||||
| chr7:80497672 | A | C | 3 | a0001c0001t0001g0223 a0001c0002t0002g0222 a0001c0002t0002g0224 |
3 | HG02145.hp2 HG02717.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.119-3025T>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497672 | |||||||
| chr7:80497675 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.119-3028G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497675 | |||||||
| chr7:80497676 | A | ACGTATAT others(77): Show |
1 | a0001c0001t0001g0215 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.119-3030_119-3029i others(86): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497676 | |||||||
| chr7:80497676 | A | G | 26 | a0001c0001t0001g0027 a0001c0001t0001g0038 a0001c0001t0001g0048 others(23): Show |
29 | HG00099.hp2 HG00642.hp2 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.119-3029T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497676 | |||||||
| chr7:80497786 | T | C | 1 | a0001c0002t0002g0228 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.119-3139A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497786 | |||||||
| chr7:80497852 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.119-3205T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497852 | |||||||
| chr7:80497875 | T | A | 1 | a0001c0001t0001g0150 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.119-3228A>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80497875 | |||||||
| chr7:80498237 | T | G | 2 | a0001c0001t0001g0248 a0001c0002t0002g0210 |
2 | HG02683.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.119-3590A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80498237 | |||||||
| chr7:80498352 | T | C | 3 | a0001c0002t0002g0201 a0001c0002t0002g0202 a0001c0002t0002g0203 |
3 | HG01243.hp2 HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.119-3705A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80498352 | |||||||
| chr7:80498456 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.119-3809C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80498456 | |||||||
| chr7:80498509 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.119-3862T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80498509 | |||||||
| chr7:80498573 | T | G | 7 | a0001c0001t0001g0223 a0001c0002t0002g0050 a0001c0002t0002g0217 others(4): Show |
7 | HG01261.hp1 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.119-3926A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80498573 | |||||||
| chr7:80498787 | T | C | 2 | a0001c0002t0002g0206 a0001c0002t0002g0287 |
2 | HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.119-4140A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80498787 | |||||||
| chr7:80498832 | T | C | 15 | a0001c0001t0001g0027 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
20 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.119-4185A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80498832 | |||||||
| chr7:80498859 | G | C | 2 | a0001c0001t0001g0046 a0005c0007t0001g0294 |
2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.119-4212C>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80498859 | |||||||
| chr7:80498919 | T | A | 1 | a0001c0001t0001g0216 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.119-4272A>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80498919 | |||||||
| chr7:80498979 | C | T | 1 | a0001c0002t0002g0165 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.119-4332G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80498979 | |||||||
| chr7:80499293 | T | G | 6 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0290 others(3): Show |
6 | HG00639.hp2 HG01243.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-4646A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80499293 | |||||||
| chr7:80499425 | G | T | 9 | a0001c0001t0001g0187 a0001c0001t0001g0223 a0001c0001t0003g0031 others(6): Show |
9 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.119-4778C>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80499425 | |||||||
| chr7:80499678 | T | G | 6 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0290 others(3): Show |
6 | HG00639.hp2 HG01243.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-5031A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80499678 | |||||||
| chr7:80499761 | G | T | 2 | a0001c0001t0001g0248 a0001c0002t0002g0210 |
2 | HG02683.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.119-5114C>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80499761 | |||||||
| chr7:80499789 | ATC | A | 15 | a0001c0001t0001g0027 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
20 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.119-5144_119-5143d others(4): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80499789 | |||||||
| chr7:80500172 | G | C | 34 | a0001c0001t0001g0027 a0001c0001t0001g0042 a0001c0001t0001g0043 others(31): Show |
39 | HG01261.hp1 HG01891.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.119-5525C>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80500172 | |||||||
| chr7:80500211 | A | G | 2 | a0001c0001t0001g0025 a0001c0002t0002g0047 |
3 | HG02896.hp1 HG02897.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.119-5564T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80500211 | |||||||
| chr7:80500213 | C | T | 2 | a0001c0002t0002g0249 a0001c0002t0002g0250 |
2 | HG02257.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.119-5566G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80500213 | |||||||
| chr7:80500230 | C | CT | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0048 others(58): Show |
72 | HG00099.hp2 HG00642.hp2 HG00673.hp1 others(69): Show |
intron_variant | MODIFIER | c.119-5584dupA | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80500230 | |||||||
| chr7:80500230 | C | CTT | 17 | a0001c0001t0001g0027 a0001c0001t0001g0042 a0001c0001t0001g0043 others(14): Show |
22 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.119-5585_119-5584d others(4): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80500230 | |||||||
| chr7:80500268 | A | G | 1 | a0001c0001t0003g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.119-5621T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80500268 | |||||||
| chr7:80500557 | G | T | 1 | a0001c0001t0001g0084 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.119-5910C>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80500557 | |||||||
| chr7:80500590 | A | G | 2 | a0001c0002t0002g0163 a0001c0002t0002g0164 |
2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.119-5943T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80500590 | |||||||
| chr7:80500756 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.119-6109A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80500756 | |||||||
| chr7:80500830 | A | AT | 35 | a0001c0001t0001g0027 a0001c0001t0001g0042 a0001c0001t0001g0043 others(32): Show |
41 | HG01261.hp1 HG01891.hp1 HG01891.hp2 others(38): Show |
intron_variant | MODIFIER | c.119-6184dupA | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80500830 | |||||||
| chr7:80500883 | C | T | 3 | a0001c0001t0001g0048 a0001c0001t0003g0007 a0001c0001t0003g0032 |
4 | HG02109.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.119-6236G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80500883 | |||||||
| chr7:80500914 | C | A | 1 | a0001c0001t0001g0154 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.119-6267G>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80500914 | |||||||
| chr7:80501159 | T | C | 2 | a0001c0001t0001g0025 a0001c0002t0002g0047 |
3 | HG02896.hp1 HG02897.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.119-6512A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80501159 | |||||||
| chr7:80501215 | T | C | 29 | a0001c0001t0001g0001 a0001c0001t0001g0056 a0001c0001t0001g0191 others(26): Show |
37 | HG00099.hp2 HG00642.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.119-6568A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80501215 | |||||||
| chr7:80501454 | T | G | 1 | a0001c0002t0002g0152 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.119-6807A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80501454 | |||||||
| chr7:80501630 | T | G | 5 | a0001c0001t0001g0048 a0001c0001t0001g0288 a0001c0001t0003g0007 others(2): Show |
6 | HG02109.hp1 HG02109.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.119-6983A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80501630 | |||||||
| chr7:80501824 | A | G | 5 | a0001c0002t0002g0206 a0001c0002t0002g0286 a0001c0002t0002g0287 others(2): Show |
5 | HG02615.hp2 HG03130.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.119-7177T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80501824 | |||||||
| chr7:80502057 | G | C | 5 | a0001c0002t0002g0206 a0001c0002t0002g0286 a0001c0002t0002g0287 others(2): Show |
5 | HG02615.hp2 HG03130.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.119-7410C>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80502057 | |||||||
| chr7:80502259 | T | C | 5 | a0001c0002t0002g0206 a0001c0002t0002g0286 a0001c0002t0002g0287 others(2): Show |
5 | HG02615.hp2 HG03130.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.119-7612A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80502259 | |||||||
| chr7:80502458 | CTAAGTGT others(4): Show |
C | 1 | a0001c0001t0001g0187 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.119-7822_119-7812d others(13): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80502458 | |||||||
| chr7:80502526 | C | T | 34 | a0001c0001t0001g0027 a0001c0001t0001g0042 a0001c0001t0001g0043 others(31): Show |
40 | HG01261.hp1 HG01891.hp1 HG01891.hp2 others(37): Show |
intron_variant | MODIFIER | c.119-7879G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80502526 | |||||||
| chr7:80502542 | C | T | 15 | a0001c0001t0001g0027 a0001c0001t0001g0042 a0001c0001t0001g0043 others(12): Show |
20 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.119-7895G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80502542 | |||||||
| chr7:80502736 | T | C | 1 | a0001c0001t0003g0031 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.119-8089A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80502736 | |||||||
| chr7:80502820 | C | A | 1 | a0001c0001t0001g0018 | 2 | HG02074.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.119-8173G>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80502820 | |||||||
| chr7:80502840 | C | T | 1 | a0001c0002t0002g0210 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.119-8193G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80502840 | |||||||
| chr7:80503058 | T | A | 5 | a0001c0001t0001g0066 a0001c0002t0002g0024 a0001c0002t0002g0069 others(2): Show |
6 | HG02559.hp2 HG02572.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.119-8411A>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80503058 | |||||||
| chr7:80503202 | A | G | 1 | a0001c0002t0002g0247 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.119-8555T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80503202 | |||||||
| chr7:80503203 | C | A | 1 | a0001c0001t0001g0153 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.119-8556G>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80503203 | |||||||
| chr7:80503213 | A | G | 1 | a0001c0002t0002g0222 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.119-8566T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80503213 | |||||||
| chr7:80503312 | A | G | 14 | a0001c0001t0001g0187 a0001c0001t0001g0215 a0001c0001t0001g0216 others(11): Show |
14 | HG01261.hp1 HG01891.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.118+8497T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80503312 | |||||||
| chr7:80503409 | A | G | 4 | a0001c0002t0002g0026 a0001c0002t0002g0188 a0001c0002t0002g0189 others(1): Show |
5 | HG02818.hp1 HG03098.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.118+8400T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80503409 | |||||||
| chr7:80503618 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.118+8191C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80503618 | |||||||
| chr7:80503713 | G | A | 1 | a0001c0002t0002g0210 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.118+8096C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80503713 | |||||||
| chr7:80503728 | G | C | 5 | a0001c0001t0001g0048 a0001c0001t0001g0288 a0001c0001t0003g0007 others(2): Show |
6 | HG02109.hp1 HG02109.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.118+8081C>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80503728 | |||||||
| chr7:80503732 | G | A | 3 | a0001c0002t0002g0201 a0001c0002t0002g0202 a0001c0002t0002g0203 |
3 | HG01243.hp2 HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.118+8077C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80503732 | |||||||
| chr7:80503794 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.118+8015T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80503794 | |||||||
| chr7:80503858 | G | A | 1 | a0001c0002t0002g0283 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.118+7951C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80503858 | |||||||
| chr7:80504029 | G | C | 5 | a0001c0001t0001g0048 a0001c0001t0001g0288 a0001c0001t0003g0007 others(2): Show |
6 | HG02109.hp1 HG02109.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.118+7780C>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80504029 | |||||||
| chr7:80504069 | A | G | 1 | a0001c0001t0001g0035 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.118+7740T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80504069 | |||||||
| chr7:80504095 | C | T | 2 | a0001c0002t0002g0082 a0001c0002t0002g0083 |
2 | NA18953.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.118+7714G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80504095 | |||||||
| chr7:80504178 | T | C | 1 | a0001c0002t0002g0283 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.118+7631A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80504178 | |||||||
| chr7:80504208 | G | C | 2 | a0001c0001t0001g0155 a0001c0001t0001g0156 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.118+7601C>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80504208 | |||||||
| chr7:80504426 | A | G | 1 | a0001c0002t0002g0228 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.118+7383T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80504426 | |||||||
| chr7:80504433 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.118+7376C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80504433 | |||||||
| chr7:80504474 | T | C | 1 | a0001c0002t0002g0210 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.118+7335A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80504474 | |||||||
| chr7:80504517 | G | T | 9 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0157 others(6): Show |
9 | HG01071.hp2 HG01081.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.118+7292C>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80504517 | |||||||
| chr7:80504675 | A | G | 1 | a0001c0002t0002g0210 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.118+7134T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80504675 | |||||||
| chr7:80504716 | T | G | 68 | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0027 others(65): Show |
77 | HG00280.hp1 HG00735.hp1 HG00741.hp1 others(74): Show |
intron_variant | MODIFIER | c.118+7093A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80504716 | |||||||
| chr7:80504847 | T | TG | 7 | a0001c0001t0001g0223 a0001c0002t0002g0050 a0001c0002t0002g0217 others(4): Show |
7 | HG01261.hp1 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.118+6961dupC | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80504847 | |||||||
| chr7:80504978 | G | T | 1 | a0001c0001t0001g0081 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.118+6831C>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80504978 | |||||||
| chr7:80505032 | G | T | 38 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0056 others(35): Show |
48 | HG00099.hp2 HG00642.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.118+6777C>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80505032 | |||||||
| chr7:80505039 | T | G | 38 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0056 others(35): Show |
48 | HG00099.hp2 HG00642.hp2 HG00673.hp1 others(45): Show |
intron_variant | MODIFIER | c.118+6770A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80505039 | |||||||
| chr7:80505116 | T | A | 1 | a0001c0001t0001g0181 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.118+6693A>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80505116 | |||||||
| chr7:80505129 | A | G | 1 | a0001c0002t0002g0207 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.118+6680T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80505129 | |||||||
| chr7:80505165 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.118+6644T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80505165 | |||||||
| chr7:80505169 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.118+6640T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80505169 | |||||||
| chr7:80505280 | T | A | 1 | a0001c0002t0002g0182 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.118+6529A>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80505280 | |||||||
| chr7:80505401 | T | G | 5 | a0001c0001t0001g0048 a0001c0001t0001g0288 a0001c0001t0003g0007 others(2): Show |
6 | HG02109.hp1 HG02109.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.118+6408A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80505401 | |||||||
| chr7:80505466 | A | G | 6 | a0001c0001t0001g0218 a0001c0001t0001g0219 a0001c0001t0001g0290 others(3): Show |
6 | HG00639.hp2 HG01243.hp1 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.118+6343T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80505466 | |||||||
| chr7:80505484 | A | G | 7 | a0001c0002t0002g0074 a0001c0002t0002g0075 a0001c0002t0002g0076 others(4): Show |
7 | HG00280.hp1 HG00741.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.118+6325T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80505484 | |||||||
| chr7:80505520 | A | C | 1 | a0001c0002t0002g0069 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.118+6289T>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80505520 | |||||||
| chr7:80505573 | A | G | 3 | a0001c0002t0002g0286 a0002c0003t0001g0284 a0002c0003t0001g0285 |
3 | HG02615.hp2 HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.118+6236T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80505573 | |||||||
| chr7:80505583 | G | A | 22 | a0001c0001t0001g0027 a0001c0001t0001g0215 a0001c0001t0001g0216 others(19): Show |
23 | HG01261.hp1 HG01433.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.118+6226C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80505583 | |||||||
| chr7:80505632 | C | T | 1 | a0001c0002t0002g0217 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.118+6177G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80505632 | |||||||
| chr7:80505660 | C | G | 1 | a0001c0002t0002g0246 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.118+6149G>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80505660 | |||||||
| chr7:80505734 | T | C | 40 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0056 others(37): Show |
50 | HG00099.hp2 HG00642.hp2 HG00673.hp1 others(47): Show |
intron_variant | MODIFIER | c.118+6075A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80505734 | |||||||
| chr7:80505763 | C | T | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0002t0002g0070 |
3 | HG01081.hp1 HG01099.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.118+6046G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80505763 | |||||||
| chr7:80505772 | T | G | 14 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0218 others(11): Show |
14 | HG01261.hp1 HG01433.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.118+6037A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80505772 | |||||||
| chr7:80505822 | G | T | 1 | a0001c0002t0002g0069 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.118+5987C>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80505822 | |||||||
| chr7:80505893 | G | C | 2 | a0001c0001t0001g0027 a0001c0001t0001g0227 |
3 | HG02818.hp2 HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.118+5916C>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80505893 | |||||||
| chr7:80505959 | G | A | 39 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0056 others(36): Show |
49 | HG00099.hp2 HG00642.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.118+5850C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80505959 | |||||||
| chr7:80505964 | G | T | 1 | a0001c0001t0001g0068 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.118+5845C>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80505964 | |||||||
| chr7:80505998 | C | T | 4 | a0001c0001t0001g0048 a0001c0001t0001g0288 a0001c0001t0003g0007 others(1): Show |
5 | HG02109.hp1 HG02109.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.118+5811G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80505998 | |||||||
| chr7:80506339 | T | G | 17 | a0001c0001t0001g0027 a0001c0001t0001g0215 a0001c0001t0001g0216 others(14): Show |
18 | HG01261.hp1 HG01433.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.118+5470A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80506339 | |||||||
| chr7:80506529 | A | C | 2 | a0001c0001t0003g0007 a0001c0001t0003g0032 |
3 | HG02895.hp2 HG02897.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.118+5280T>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80506529 | |||||||
| chr7:80506656 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.118+5153G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80506656 | |||||||
| chr7:80506715 | C | A | 1 | a0001c0002t0002g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.118+5094G>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80506715 | |||||||
| chr7:80506870 | G | C | 22 | a0001c0001t0001g0027 a0001c0001t0001g0048 a0001c0001t0001g0215 others(19): Show |
24 | HG01261.hp1 HG01433.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.118+4939C>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80506870 | |||||||
| chr7:80506899 | G | T | 21 | a0001c0001t0001g0027 a0001c0001t0001g0215 a0001c0001t0001g0216 others(18): Show |
23 | HG01261.hp1 HG01433.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.118+4910C>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80506899 | |||||||
| chr7:80506910 | T | G | 1 | a0001c0002t0002g0183 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.118+4899A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80506910 | |||||||
| chr7:80506948 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.118+4861A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80506948 | |||||||
| chr7:80506999 | A | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0025 others(68): Show |
84 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.118+4810T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80506999 | |||||||
| chr7:80507035 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.118+4774T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80507035 | |||||||
| chr7:80507170 | G | GTT | 9 | a0001c0001t0001g0004 a0001c0001t0001g0230 a0001c0001t0001g0231 others(6): Show |
11 | HG00673.hp1 HG03834.hp2 NA18747.hp2 others(8): Show |
intron_variant | MODIFIER | c.118+4637_118+4638d others(4): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80507170 | |||||||
| chr7:80507254 | T | C | 10 | a0001c0001t0001g0004 a0001c0001t0001g0230 a0001c0001t0001g0231 others(7): Show |
12 | HG00673.hp1 HG03041.hp1 HG03834.hp2 others(9): Show |
intron_variant | MODIFIER | c.118+4555A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80507254 | |||||||
| chr7:80507311 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.118+4498T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80507311 | |||||||
| chr7:80507327 | A | T | 30 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0056 others(27): Show |
39 | HG00099.hp2 HG00642.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.118+4482T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80507327 | |||||||
| chr7:80507413 | A | T | 10 | a0001c0001t0001g0004 a0001c0001t0001g0230 a0001c0001t0001g0231 others(7): Show |
12 | HG00673.hp1 HG02683.hp1 HG03834.hp2 others(9): Show |
intron_variant | MODIFIER | c.118+4396T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80507413 | |||||||
| chr7:80507483 | T | C | 1 | a0001c0001t0001g0205 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.118+4326A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80507483 | |||||||
| chr7:80507493 | C | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0230 a0001c0001t0001g0231 others(7): Show |
12 | HG00673.hp1 HG03041.hp1 HG03834.hp2 others(9): Show |
intron_variant | MODIFIER | c.118+4316G>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80507493 | |||||||
| chr7:80507785 | G | T | 1 | a0001c0002t0002g0185 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.118+4024C>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80507785 | |||||||
| chr7:80507917 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.118+3892G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80507917 | |||||||
| chr7:80508087 | A | C | 30 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0056 others(27): Show |
39 | HG00099.hp2 HG00642.hp2 HG01099.hp1 others(36): Show |
intron_variant | MODIFIER | c.118+3722T>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80508087 | |||||||
| chr7:80508166 | A | G | 1 | a0001c0002t0002g0244 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.118+3643T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80508166 | |||||||
| chr7:80508189 | A | C | 13 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0218 others(10): Show |
13 | HG01261.hp1 HG01433.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.118+3620T>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80508189 | |||||||
| chr7:80508232 | T | C | 29 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0056 others(26): Show |
38 | HG00099.hp2 HG00642.hp2 HG01099.hp1 others(35): Show |
intron_variant | MODIFIER | c.118+3577A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80508232 | |||||||
| chr7:80508272 | CA | C | 28 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0215 others(25): Show |
31 | HG00673.hp1 HG01261.hp1 HG01433.hp2 others(28): Show |
intron_variant | MODIFIER | c.118+3536delT | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80508272 | |||||||
| chr7:80508347 | G | T | 1 | a0001c0001t0001g0065 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.118+3462C>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80508347 | |||||||
| chr7:80508636 | T | C | 34 | a0001c0001t0001g0001 a0001c0001t0001g0025 a0001c0001t0001g0048 others(31): Show |
44 | HG00099.hp2 HG00642.hp2 HG01099.hp1 others(41): Show |
intron_variant | MODIFIER | c.118+3173A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80508636 | |||||||
| chr7:80508748 | G | A | 10 | a0001c0001t0001g0004 a0001c0001t0001g0230 a0001c0001t0001g0231 others(7): Show |
12 | HG00673.hp1 HG02683.hp1 HG03834.hp2 others(9): Show |
intron_variant | MODIFIER | c.118+3061C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80508748 | |||||||
| chr7:80508758 | C | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0025 others(59): Show |
75 | HG00099.hp2 HG00642.hp2 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.118+3051G>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80508758 | |||||||
| chr7:80508862 | T | C | 62 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0025 others(59): Show |
75 | HG00099.hp2 HG00642.hp2 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.118+2947A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80508862 | |||||||
| chr7:80508981 | A | G | 5 | a0001c0001t0001g0243 a0001c0002t0002g0239 a0001c0002t0002g0240 others(2): Show |
5 | HG02129.hp1 NA18947.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.118+2828T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80508981 | |||||||
| chr7:80508987 | G | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0025 others(68): Show |
84 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.118+2822C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80508987 | |||||||
| chr7:80509158 | A | G | 5 | a0001c0002t0002g0008 a0001c0002t0002g0061 a0001c0002t0002g0062 others(2): Show |
6 | HG01168.hp1 HG01358.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+2651T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80509158 | |||||||
| chr7:80509246 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.118+2563A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80509246 | |||||||
| chr7:80509298 | T | C | 1 | a0001c0002t0002g0289 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.118+2511A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80509298 | |||||||
| chr7:80509384 | A | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0025 others(55): Show |
70 | HG00099.hp2 HG00642.hp2 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.118+2425T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80509384 | |||||||
| chr7:80509425 | C | T | 2 | a0001c0001t0001g0215 a0001c0001t0001g0216 |
2 | HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.118+2384G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80509425 | |||||||
| chr7:80509655 | G | A | 1 | a0001c0002t0002g0185 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.118+2154C>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80509655 | |||||||
| chr7:80509733 | A | T | 1 | a0001c0002t0002g0052 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.118+2076T>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80509733 | |||||||
| chr7:80509828 | C | A | 2 | a0001c0001t0001g0049 a0001c0002t0002g0050 |
2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.118+1981G>T | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80509828 | |||||||
| chr7:80509840 | AT | A | 4 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 others(1): Show |
4 | HG00639.hp2 HG01243.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.118+1968delA | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80509840 | |||||||
| chr7:80509862 | C | T | 3 | a0001c0001t0001g0214 a0001c0002t0002g0212 a0001c0002t0002g0213 |
3 | HG02155.hp1 NA19012.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.118+1947G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80509862 | |||||||
| chr7:80510079 | T | G | 1 | a0001c0001t0001g0186 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.118+1730A>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80510079 | |||||||
| chr7:80510096 | T | C | 1 | a0001c0002t0002g0210 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.118+1713A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80510096 | |||||||
| chr7:80510334 | A | G | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 |
3 | NA18975.hp2 NA18995.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.118+1475T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80510334 | |||||||
| chr7:80510513 | A | C | 1 | a0001c0001t0001g0187 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.118+1296T>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80510513 | |||||||
| chr7:80510661 | G | T | 1 | a0001c0002t0002g0211 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.118+1148C>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80510661 | |||||||
| chr7:80510901 | A | G | 168 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(165): Show |
187 | HG00280.hp1 HG00280.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.118+908T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80510901 | |||||||
| chr7:80511035 | T | C | 1 | a0001c0002t0002g0051 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.118+774A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80511035 | |||||||
| chr7:80511086 | A | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(195): Show |
226 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.118+723T>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80511086 | |||||||
| chr7:80511364 | A | G | 3 | a0001c0002t0002g0207 a0001c0002t0002g0208 a0001c0002t0002g0209 |
3 | HG01255.hp1 HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.118+445T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80511364 | |||||||
| chr7:80511527 | T | C | 20 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0037 others(17): Show |
22 | HG00639.hp1 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.118+282A>G | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80511527 | |||||||
| chr7:80511558 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(194): Show |
225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.118+251G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80511558 | |||||||
| chr7:80511599 | C | T | 6 | a0001c0001t0001g0056 a0001c0002t0002g0052 a0001c0002t0002g0053 others(3): Show |
6 | HG00099.hp2 HG00642.hp2 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.118+210G>A | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80511599 | |||||||
| chr7:80511643 | TTAAA | T | 20 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0037 others(17): Show |
22 | HG00639.hp1 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.118+162_118+165del others(4): Show |
GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80511643 | |||||||
| chr7:80511753 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0010 others(194): Show |
225 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(222): Show |
intron_variant | MODIFIER | c.118+56T>C | GNAT3 | ENSG00000214415.4 | transcript | ENST00000398291.4 | protein_coding | 1/7 | chr7 | 80511753 |