Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79695 |
| ensemblid | ENSG00000119514.7 |
| hgncid | 19877 |
| symbol | GALNT12 |
| name | polypeptide N-acetylgalactosaminyltransferase 12 |
| refseq_nuc | NM_024642.5 |
| refseq_prot | NP_078918.3 |
| ensembl_nuc | ENST00000375011.4 |
| ensembl_prot | ENSP00000364150.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 98807670 |
| end | 98850081 |
| strand | + |
| ver | v1.2 |
| region | chr9:98807670-98850081 |
| region5000 | chr9:98802670-98855081 |
| regionname0 | GALNT12_chr9_98807670_98850081 |
| regionname5000 | GALNT12_chr9_98802670_98855081 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 581 | 325 | 94 | 59 | 119 | 13 | 38 | 89 | GALNT12_chr9_98802670_98855081 | GALNT12 | MWGRT others(576): Show |
chr9 | 98802670 | 98855081 |
| a0002 | 0/0 | 581 | 43 | 0 | 7 | 30 | 1 | 5 | 23 | GALNT12_chr9_98802670_98855081 | GALNT12 | MWGRT others(576): Show |
chr9 | 98802670 | 98855081 |
| a0003 | 0/0 | 581 | 3 | 0 | 2 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | MWGRT others(576): Show |
chr9 | 98802670 | 98855081 |
| a0004 | 0/0 | 581 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | MWGRT others(576): Show |
chr9 | 98802670 | 98855081 |
| a0005 | 0/0 | 581 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | MWGRT others(576): Show |
chr9 | 98802670 | 98855081 |
| a0006 | 0/0 | 581 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | MWGRT others(576): Show |
chr9 | 98802670 | 98855081 |
| a0007 | 0/0 | 581 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | MWGRT others(576): Show |
chr9 | 98802670 | 98855081 |
| a0008 | 0/0 | 581 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | MWGRT others(576): Show |
chr9 | 98802670 | 98855081 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1743 | 243 | 59 | 45 | 89 | 12 | 36 | GALNT12_chr9_98802670_98855081 | GALNT12 | ATGTG others(1738): Show |
chr9 | 98802670 | 98855081 | ||
| a0001c0002 | 0/0 | 1743 | 54 | 11 | 12 | 29 | 1 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | ATGTG others(1738): Show |
chr9 | 98802670 | 98855081 | ||
| a0001c0004 | 0/0 | 1743 | 11 | 10 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | ATGTG others(1738): Show |
chr9 | 98802670 | 98855081 | ||
| a0001c0006 | 0/0 | 1743 | 6 | 6 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | ATGTG others(1738): Show |
chr9 | 98802670 | 98855081 | ||
| a0001c0007 | 0/0 | 1743 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | ATGTG others(1738): Show |
chr9 | 98802670 | 98855081 | ||
| a0001c0008 | 0/0 | 1743 | 3 | 2 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | ATGTG others(1738): Show |
chr9 | 98802670 | 98855081 | ||
| a0001c0016 | 0/0 | 1743 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | ATGTG others(1738): Show |
chr9 | 98802670 | 98855081 | ||
| a0001c0017 | 0/0 | 1743 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | ATGTG others(1738): Show |
chr9 | 98802670 | 98855081 | ||
| a0001c0019 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | ATGTG others(1738): Show |
chr9 | 98802670 | 98855081 | ||
| a0001c0020 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | ATGTG others(1738): Show |
chr9 | 98802670 | 98855081 | ||
| a0001c0021 | 0/0 | 1743 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | ATGTG others(1738): Show |
chr9 | 98802670 | 98855081 | ||
| a0002c0003 | 0/0 | 1743 | 34 | 0 | 4 | 24 | 1 | 5 | GALNT12_chr9_98802670_98855081 | GALNT12 | ATGTG others(1738): Show |
chr9 | 98802670 | 98855081 | ||
| a0002c0005 | 0/0 | 1743 | 7 | 0 | 2 | 5 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | ATGTG others(1738): Show |
chr9 | 98802670 | 98855081 | ||
| a0002c0010 | 0/0 | 1743 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | ATGTG others(1738): Show |
chr9 | 98802670 | 98855081 | ||
| a0002c0011 | 0/0 | 1743 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | ATGTG others(1738): Show |
chr9 | 98802670 | 98855081 | ||
| a0003c0009 | 0/0 | 1743 | 3 | 0 | 2 | 0 | 1 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | ATGTG others(1738): Show |
chr9 | 98802670 | 98855081 | ||
| a0004c0013 | 0/0 | 1743 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | ATGTG others(1738): Show |
chr9 | 98802670 | 98855081 | ||
| a0005c0012 | 0/0 | 1743 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | ATGTG others(1738): Show |
chr9 | 98802670 | 98855081 | ||
| a0006c0018 | 0/0 | 1743 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | ATGTG others(1738): Show |
chr9 | 98802670 | 98855081 | ||
| a0007c0014 | 0/0 | 1743 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | ATGTG others(1738): Show |
chr9 | 98802670 | 98855081 | ||
| a0008c0015 | 0/0 | 1743 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | ATGTG others(1738): Show |
chr9 | 98802670 | 98855081 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2764 | 174 | 46 | 31 | 48 | 12 | 35 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0001c0001t0003 | 0/0 | 2764 | 38 | 8 | 12 | 17 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0001c0001t0004 | 0/0 | 2764 | 16 | 0 | 2 | 14 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0001c0001t0005 | 0/0 | 2764 | 8 | 0 | 0 | 8 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0001c0001t0006 | 0/0 | 2764 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0001c0001t0007 | 0/0 | 2764 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCACA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0001c0001t0009 | 0/0 | 2764 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0001c0001t0010 | 0/0 | 2764 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0001c0001t0011 | 0/0 | 2764 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0001c0002t0002 | 0/0 | 2764 | 54 | 11 | 12 | 29 | 1 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0001c0004t0001 | 0/0 | 2764 | 10 | 9 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0001c0004t0006 | 0/0 | 2764 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0001c0006t0002 | 0/0 | 2764 | 5 | 5 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0001c0006t0008 | 0/0 | 2764 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0001c0007t0002 | 0/0 | 2764 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0001c0008t0001 | 0/0 | 2764 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0001c0008t0006 | 0/0 | 2764 | 2 | 1 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0001c0016t0001 | 0/0 | 2764 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0001c0017t0003 | 0/0 | 2764 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0001c0019t0006 | 0/0 | 2764 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0001c0020t0001 | 0/0 | 2764 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0001c0021t0001 | 0/0 | 2764 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0002c0003t0001 | 0/0 | 2764 | 26 | 0 | 4 | 16 | 1 | 5 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0002c0003t0003 | 0/0 | 2764 | 3 | 0 | 0 | 3 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0002c0003t0004 | 0/0 | 2764 | 3 | 0 | 0 | 3 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0002c0003t0005 | 0/0 | 2764 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0002c0005t0002 | 0/0 | 2764 | 7 | 0 | 2 | 5 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0002c0010t0002 | 0/0 | 2764 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0002c0011t0001 | 0/0 | 2764 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0003c0009t0001 | 0/0 | 2764 | 3 | 0 | 2 | 0 | 1 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0004c0013t0001 | 0/0 | 2764 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0005c0012t0001 | 0/0 | 2764 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0006c0018t0002 | 0/0 | 2764 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0007c0014t0002 | 0/0 | 2764 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| a0008c0015t0001 | 0/0 | 2764 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | GCAGA others(2759): Show |
chr9 | 98802670 | 98855081 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 1/0 | 2 | 0 | 0 | 0 | 1 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0257 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0001 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0003g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0004g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0005g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0005g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0005g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0005g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0005g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0005g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0006g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0007g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0009g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0010g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0001t0011g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0002t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0004t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0004t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0004t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0004t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0004t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0004t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0004t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0004t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0004t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0004t0001g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0004t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0006t0002g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0006t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0006t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0006t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0006t0008g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0007t0002g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0007t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0007t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0008t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0008t0006g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0008t0006g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0016t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0017t0003g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0019t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0020t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0001c0021t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0003g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0004g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0003t0005g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0005t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0005t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0005t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0005t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0005t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0005t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0005t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0010t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0002c0011t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0003c0009t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0003c0009t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0003c0009t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0004c0013t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0005c0012t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0006c0018t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0007c0014t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| a0008c0015t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0302 | EUR | GBR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00140 | hp1 | a0003 | c0009 | t0001 | g0122 | EUR | GBR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | GBR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00280 | hp1 | a0002 | c0003 | t0001 | g0324 | EUR | FIN | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0306 | EUR | FIN | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | FIN | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | FIN | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | CHS | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00408 | hp2 | a0001 | c0002 | t0002 | g0116 | EAS | CHS | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00423 | hp2 | a0002 | c0005 | t0002 | g0286 | EAS | CHS | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00438 | hp1 | a0001 | c0002 | t0002 | g0263 | EAS | CHS | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00544 | hp1 | a0002 | c0003 | t0001 | g0250 | EAS | CHS | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | CHS | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0341 | EAS | CHS | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | CHS | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0054 | EAS | CHS | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0218 | EAS | CHS | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00621 | hp2 | a0002 | c0003 | t0004 | g0022 | EAS | CHS | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0233 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00673 | hp1 | a0001 | c0001 | t0003 | g0026 | EAS | CHS | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00673 | hp2 | a0001 | c0002 | t0002 | g0137 | EAS | CHS | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00738 | hp1 | a0003 | c0009 | t0001 | g0189 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG00741 | hp2 | a0002 | c0005 | t0002 | g0280 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0051 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0163 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01074 | hp2 | a0003 | c0009 | t0001 | g0150 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01081 | hp1 | a0001 | c0008 | t0006 | g0349 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01081 | hp2 | a0001 | c0004 | t0001 | g0344 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01106 | hp2 | a0001 | c0002 | t0002 | g0052 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01109 | hp1 | a0001 | c0002 | t0002 | g0240 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01168 | hp1 | a0001 | c0002 | t0002 | g0243 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01243 | hp1 | a0001 | c0002 | t0002 | g0339 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0201 | AMR | PUR | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0139 | AMR | CLM | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | CLM | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01258 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | CLM | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01261 | hp1 | a0001 | c0002 | t0002 | g0244 | AMR | CLM | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | CLM | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01346 | hp2 | a0001 | c0002 | t0002 | g0158 | AMR | CLM | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01433 | hp1 | a0001 | c0001 | t0003 | g0020 | AMR | CLM | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01496 | hp2 | a0002 | c0010 | t0002 | g0325 | AMR | CLM | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0264 | EUR | IBS | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01517 | hp1 | a0001 | c0002 | t0002 | g0299 | EUR | IBS | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0197 | AFR | ACB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0236 | AFR | ACB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01891 | hp1 | a0001 | c0002 | t0002 | g0204 | AFR | ACB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01891 | hp2 | a0001 | c0008 | t0006 | g0347 | AFR | ACB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01934 | hp1 | a0001 | c0002 | t0002 | g0183 | AMR | PEL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01934 | hp2 | a0002 | c0003 | t0001 | g0260 | AMR | PEL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0293 | AMR | PEL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01943 | hp2 | a0002 | c0003 | t0001 | g0283 | AMR | PEL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0291 | AMR | PEL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01981 | hp2 | a0002 | c0003 | t0001 | g0284 | AMR | PEL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | KHV | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02015 | hp2 | a0001 | c0001 | t0004 | g0219 | EAS | KHV | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02027 | hp1 | a0001 | c0001 | t0007 | g0303 | EAS | KHV | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02056 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | KHV | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02056 | hp2 | a0001 | c0002 | t0002 | g0119 | EAS | KHV | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0256 | EAS | KHV | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0221 | EAS | KHV | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02083 | hp1 | a0001 | c0002 | t0002 | g0043 | EAS | KHV | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02083 | hp2 | a0001 | c0001 | t0004 | g0153 | EAS | KHV | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02132 | hp1 | a0002 | c0003 | t0003 | g0268 | EAS | KHV | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02135 | hp1 | a0001 | c0002 | t0002 | g0066 | EAS | KHV | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02135 | hp2 | a0002 | c0003 | t0001 | g0317 | EAS | KHV | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02145 | hp1 | a0001 | c0006 | t0002 | g0210 | AFR | ACB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02145 | hp2 | a0001 | c0006 | t0002 | g0019 | AFR | ACB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0184 | AMR | PEL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02148 | hp2 | a0002 | c0003 | t0001 | g0279 | AMR | PEL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02155 | hp1 | a0002 | c0003 | t0001 | g0274 | EAS | CDX | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | CDX | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02165 | hp1 | a0001 | c0001 | t0004 | g0238 | EAS | CDX | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02165 | hp2 | a0004 | c0013 | t0001 | g0108 | EAS | CDX | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02257 | hp1 | a0001 | c0004 | t0001 | g0145 | AFR | ACB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02258 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | ACB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02273 | hp2 | a0001 | c0002 | t0002 | g0226 | AMR | PEL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02293 | hp1 | a0002 | c0005 | t0002 | g0328 | AMR | PEL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02293 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02451 | hp1 | a0001 | c0001 | t0006 | g0104 | AFR | ACB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02572 | hp2 | a0001 | c0004 | t0001 | g0192 | AFR | GWD | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0333 | SAS | PJL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02602 | hp2 | a0002 | c0003 | t0001 | g0269 | SAS | PJL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02615 | hp1 | a0001 | c0008 | t0001 | g0348 | AFR | GWD | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02615 | hp2 | a0001 | c0004 | t0006 | g0015 | AFR | GWD | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02622 | hp1 | a0001 | c0021 | t0001 | g0027 | AFR | GWD | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0309 | SAS | PJL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02698 | hp2 | a0002 | c0003 | t0001 | g0323 | SAS | PJL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02723 | hp2 | a0001 | c0004 | t0001 | g0229 | AFR | GWD | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | GWD | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02809 | hp2 | a0001 | c0001 | t0009 | g0115 | AFR | GWD | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | GWD | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02886 | hp1 | a0001 | c0001 | t0011 | g0278 | AFR | GWD | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02897 | hp2 | a0001 | c0002 | t0002 | g0081 | AFR | GWD | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02922 | hp1 | a0001 | c0020 | t0001 | g0350 | AFR | ESN | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0346 | AFR | ESN | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | ESN | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0077 | AFR | ESN | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0157 | AFR | ESN | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02976 | hp1 | a0001 | c0004 | t0001 | g0099 | AFR | ESN | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03041 | hp1 | a0001 | c0006 | t0002 | g0019 | AFR | GWD | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03098 | hp1 | a0001 | c0002 | t0002 | g0128 | AFR | MSL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | MSL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0198 | AFR | ESN | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03139 | hp1 | a0001 | c0007 | t0002 | g0111 | AFR | ESN | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0125 | AFR | ESN | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03195 | hp1 | a0001 | c0019 | t0006 | g0015 | AFR | ESN | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0343 | AFR | ESN | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0242 | AFR | MSL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | MSL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | MSL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | MSL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0200 | AFR | MSL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03516 | hp1 | a0001 | c0004 | t0001 | g0142 | AFR | ESN | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0241 | AFR | ESN | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03540 | hp1 | a0001 | c0001 | t0006 | g0083 | AFR | GWD | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0345 | AFR | MSL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03579 | hp2 | a0001 | c0002 | t0002 | g0151 | AFR | MSL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03669 | hp2 | a0001 | c0016 | t0001 | g0029 | SAS | PJL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0072 | SAS | STU | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | STU | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | BEB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03831 | hp2 | a0002 | c0003 | t0001 | g0316 | SAS | BEB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03834 | hp2 | a0002 | c0003 | t0001 | g0287 | SAS | BEB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0334 | SAS | BEB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03942 | hp1 | a0002 | c0003 | t0001 | g0277 | SAS | BEB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG04115 | hp1 | a0005 | c0012 | t0001 | g0285 | SAS | STU | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | STU | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | BEB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | BEB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | STU | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | STU | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | STU | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG04228 | hp2 | a0001 | c0002 | t0002 | g0046 | SAS | STU | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0203 | AFR | YRI | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0121 | AFR | YRI | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0028 | EAS | CHB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18747 | hp2 | a0002 | c0003 | t0001 | g0311 | EAS | CHB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | YRI | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | YRI | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18939 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18944 | hp1 | a0002 | c0005 | t0002 | g0265 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18944 | hp2 | a0001 | c0001 | t0005 | g0208 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18945 | hp1 | a0002 | c0003 | t0005 | g0237 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18945 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18947 | hp1 | a0001 | c0001 | t0005 | g0032 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18947 | hp2 | a0002 | c0011 | t0001 | g0258 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18948 | hp1 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18952 | hp1 | a0001 | c0001 | t0005 | g0127 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18952 | hp2 | a0002 | c0003 | t0001 | g0249 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18954 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18959 | hp1 | a0001 | c0002 | t0002 | g0025 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18963 | hp1 | a0002 | c0003 | t0004 | g0022 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18964 | hp2 | a0002 | c0003 | t0001 | g0326 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18966 | hp1 | a0002 | c0005 | t0002 | g0270 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18966 | hp2 | a0001 | c0002 | t0002 | g0170 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18969 | hp1 | a0001 | c0001 | t0005 | g0222 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18969 | hp2 | a0002 | c0003 | t0003 | g0327 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18970 | hp1 | a0002 | c0003 | t0003 | g0273 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18971 | hp1 | a0001 | c0002 | t0002 | g0220 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18971 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18978 | hp2 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18979 | hp1 | a0002 | c0003 | t0001 | g0322 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18979 | hp2 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18980 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18982 | hp2 | a0002 | c0003 | t0001 | g0272 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18983 | hp2 | a0001 | c0002 | t0002 | g0070 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18984 | hp1 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18984 | hp2 | a0002 | c0003 | t0005 | g0251 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18985 | hp1 | a0002 | c0003 | t0004 | g0262 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18988 | hp1 | a0006 | c0018 | t0002 | g0149 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18990 | hp1 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18990 | hp2 | a0001 | c0002 | t0002 | g0207 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18991 | hp1 | a0001 | c0002 | t0002 | g0340 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18991 | hp2 | a0001 | c0001 | t0010 | g0321 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18993 | hp2 | a0001 | c0002 | t0002 | g0301 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18998 | hp1 | a0001 | c0002 | t0002 | g0159 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19001 | hp2 | a0002 | c0005 | t0002 | g0261 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19002 | hp1 | a0002 | c0003 | t0001 | g0312 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19002 | hp2 | a0001 | c0002 | t0002 | g0131 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19003 | hp1 | a0002 | c0003 | t0001 | g0318 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19004 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19006 | hp1 | a0001 | c0002 | t0002 | g0058 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19006 | hp2 | a0002 | c0003 | t0001 | g0313 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19007 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19007 | hp2 | a0001 | c0001 | t0005 | g0294 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19009 | hp1 | a0001 | c0001 | t0004 | g0223 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19010 | hp2 | a0001 | c0001 | t0005 | g0041 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19011 | hp2 | a0001 | c0017 | t0003 | g0295 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19030 | hp1 | a0001 | c0006 | t0002 | g0147 | AFR | LWK | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | LWK | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | LWK | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19043 | hp2 | a0001 | c0004 | t0001 | g0098 | AFR | LWK | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19055 | hp1 | a0001 | c0002 | t0002 | g0307 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19059 | hp1 | a0002 | c0003 | t0001 | g0267 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19059 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19063 | hp2 | a0007 | c0014 | t0002 | g0064 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19064 | hp1 | a0001 | c0002 | t0002 | g0308 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19064 | hp2 | a0001 | c0001 | t0004 | g0161 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19067 | hp2 | a0001 | c0002 | t0002 | g0154 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19074 | hp1 | a0001 | c0001 | t0005 | g0136 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19074 | hp2 | a0002 | c0003 | t0001 | g0271 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19075 | hp2 | a0001 | c0001 | t0004 | g0067 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19079 | hp1 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19079 | hp2 | a0001 | c0002 | t0002 | g0133 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19080 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19080 | hp2 | a0002 | c0003 | t0001 | g0282 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19085 | hp1 | a0001 | c0001 | t0005 | g0300 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19085 | hp2 | a0002 | c0005 | t0002 | g0297 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19089 | hp1 | a0002 | c0003 | t0001 | g0254 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19089 | hp2 | a0001 | c0002 | t0002 | g0112 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19090 | hp2 | a0002 | c0003 | t0001 | g0281 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19091 | hp1 | a0001 | c0002 | t0002 | g0206 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19091 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19240 | hp1 | a0001 | c0006 | t0008 | g0214 | AFR | YRI | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA19240 | hp2 | a0001 | c0004 | t0001 | g0101 | AFR | YRI | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA20129 | hp1 | a0001 | c0006 | t0002 | g0215 | AFR | ASW | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ASW | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0092 | EUR | TSI | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0231 | EUR | TSI | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | TSI | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA20805 | hp2 | a0008 | c0015 | t0001 | g0259 | EUR | TSI | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | GIH | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | GIH | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0020 | AMR | CLM | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0010 | AFR | ACB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | ACB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG02486 | hp2 | a0001 | c0007 | t0002 | g0088 | AFR | ACB | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03471 | hp1 | a0001 | c0001 | t0006 | g0336 | AFR | MSL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG03471 | hp2 | a0001 | c0004 | t0001 | g0337 | AFR | MSL | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | USA | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| HG06807 | hp2 | a0001 | c0004 | t0001 | g0217 | AFR | USA | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | USA | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA20300 | hp2 | a0001 | c0007 | t0002 | g0209 | AFR | USA | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | LWK | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0257 | REF | REF | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | GALNT12_chr9_98802670_98855081 | GALNT12 | chr9 | 98802670 | 98855081 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:98807834 | G | A | 2 | a0002 a0005 |
44 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(41): Show |
missense_variant | MODERATE | c.136G>A | p.Gly46Arg | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/10 | 165/2764 | 136/1746 | 46/581 | chr9 | 98807834 | |||
| chr9:98808054 | A | T | 1 | a0003 | 3 | HG00140.hp1 HG00738.hp1 HG01074.hp2 |
missense_variant | MODERATE | c.356A>T | p.Glu119Val | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/10 | 385/2764 | 356/1746 | 119/581 | chr9 | 98808054 | |||
| chr9:98823288 | T | C | 1 | a0004 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.404T>C | p.Leu135Ser | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 2/10 | 433/2764 | 404/1746 | 135/581 | chr9 | 98823288 | |||
| chr9:98826763 | G | C | 1 | a0007 | 1 | NA19063.hp2 | missense_variant | MODERATE | c.553G>C | p.Glu185Gln | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/10 | 582/2764 | 553/1746 | 185/581 | chr9 | 98826763 | |||
| chr9:98826929 | C | T | 1 | a0006 | 1 | NA18988.hp1 | missense_variant | MODERATE | c.719C>T | p.Pro240Leu | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/10 | 748/2764 | 719/1746 | 240/581 | chr9 | 98826929 | |||
| chr9:98831821 | G | A | 1 | a0008 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.781G>A | p.Asp261Asn | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/10 | 810/2764 | 781/1746 | 261/581 | chr9 | 98831821 | |||
| chr9:98831897 | C | T | 1 | a0005 | 1 | HG04115.hp1 | missense_variant | MODERATE | c.857C>T | p.Thr286Met | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/10 | 886/2764 | 857/1746 | 286/581 | chr9 | 98831897 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:98807836 | G | A | 1 | a0002c0010 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.138G>A | p.Gly46Gly | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/10 | 167/2764 | 138/1746 | 46/581 | chr9 | 98807836 | |||
| chr9:98808010 | C | T | 1 | a0001c0021 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.312C>T | p.Asn104Asn | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/10 | 341/2764 | 312/1746 | 104/581 | chr9 | 98808010 | |||
| chr9:98808052 | C | T | 1 | a0001c0020 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.354C>T | p.Pro118Pro | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/10 | 383/2764 | 354/1746 | 118/581 | chr9 | 98808052 | |||
| chr9:98823259 | C | T | 1 | a0001c0008 | 3 | HG01081.hp1 HG01891.hp2 HG02615.hp1 |
synonymous_variant | LOW | c.375C>T | p.Cys125Cys | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 2/10 | 404/2764 | 375/1746 | 125/581 | chr9 | 98823259 | |||
| chr9:98826789 | A | G | 1 | a0001c0019 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.579A>G | p.Gly193Gly | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/10 | 608/2764 | 579/1746 | 193/581 | chr9 | 98826789 | |||
| chr9:98831871 | C | T | 1 | a0001c0017 | 1 | NA19011.hp2 | synonymous_variant | LOW | c.831C>T | p.Gly277Gly | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/10 | 860/2764 | 831/1746 | 277/581 | chr9 | 98831871 | |||
| chr9:98831937 | A | G | 2 | a0001c0004 a0001c0006 |
17 | HG01081.hp2 HG02145.hp1 HG02145.hp2 others(14): Show |
synonymous_variant | LOW | c.897A>G | p.Gln299Gln | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/10 | 926/2764 | 897/1746 | 299/581 | chr9 | 98831937 | |||
| chr9:98835267 | T | A | 1 | a0001c0016 | 1 | HG03669.hp2 | synonymous_variant | LOW | c.936T>A | p.Gly312Gly | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 5/10 | 965/2764 | 936/1746 | 312/581 | chr9 | 98835267 | |||
| chr9:98844143 | C | T | 1 | a0002c0011 | 1 | NA18947.hp2 | synonymous_variant | LOW | c.1392C>T | p.Pro464Pro | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 8/10 | 1421/2764 | 1392/1746 | 464/581 | chr9 | 98844143 | |||
| chr9:98849023 | C | T | 1 | a0001c0007 | 3 | HG02486.hp2 HG03139.hp1 NA20300.hp2 |
synonymous_variant | LOW | c.1677C>T | p.Phe559Phe | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 10/10 | 1706/2764 | 1677/1746 | 559/581 | chr9 | 98849023 | |||
| chr9:98849053 | G | C | 7 | a0001c0002 a0001c0006 a0001c0007 others(4): Show |
73 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(70): Show |
synonymous_variant | LOW | c.1707G>C | p.Ser569Ser | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 10/10 | 1736/2764 | 1707/1746 | 569/581 | chr9 | 98849053 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:98807673 | G | C | 1 | a0001c0001t0007 | 1 | HG02027.hp1 | 5_prime_UTR_variant | MODIFIER | c.-26G>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/10 | 26 | chr9 | 98807673 | ||||||
| chr9:98807688 | T | C | 1 | a0001c0006t0008 | 1 | NA19240.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-11T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/10 | chr9 | 98807688 | |||||||
| chr9:98849134 | C | G | 1 | a0001c0001t0011 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*42C>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 10/10 | 42 | chr9 | 98849134 | ||||||
| chr9:98849159 | A | T | 4 | a0001c0001t0006 a0001c0004t0006 a0001c0008t0006 others(1): Show |
7 | HG01081.hp1 HG01891.hp2 HG02451.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*67A>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 10/10 | 67 | chr9 | 98849159 | ||||||
| chr9:98849263 | A | G | 8 | a0001c0002t0002 a0001c0006t0002 a0001c0006t0008 others(5): Show |
73 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*171A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 10/10 | 171 | chr9 | 98849263 | ||||||
| chr9:98849418 | C | G | 1 | a0001c0001t0011 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*326C>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 10/10 | 326 | chr9 | 98849418 | ||||||
| chr9:98849513 | G | A | 2 | a0001c0001t0004 a0002c0003t0004 |
19 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*421G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 10/10 | 421 | chr9 | 98849513 | ||||||
| chr9:98849587 | A | T | 1 | a0001c0001t0010 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*495A>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 10/10 | 495 | chr9 | 98849587 | ||||||
| chr9:98849605 | C | G | 3 | a0001c0001t0003 a0001c0017t0003 a0002c0003t0003 |
42 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*513C>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 10/10 | 513 | chr9 | 98849605 | ||||||
| chr9:98849919 | A | G | 2 | a0001c0001t0005 a0002c0003t0005 |
10 | NA18944.hp2 NA18945.hp1 NA18947.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*827A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 10/10 | 827 | chr9 | 98849919 | ||||||
| chr9:98849971 | G | T | 1 | a0001c0001t0009 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*879G>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 10/10 | 879 | chr9 | 98849971 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:98808199 | A | T | 2 | a0001c0001t0001g0024 a0001c0020t0001g0350 |
3 | HG02922.hp1 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.371+130A>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98808199 | |||||||
| chr9:98808350 | T | C | 1 | a0001c0002t0002g0025 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.371+281T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98808350 | |||||||
| chr9:98808520 | A | G | 3 | a0001c0008t0001g0348 a0001c0008t0006g0347 a0001c0008t0006g0349 |
3 | HG01081.hp1 HG01891.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.371+451A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98808520 | |||||||
| chr9:98808568 | T | C | 1 | a0001c0001t0003g0026 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.371+499T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98808568 | |||||||
| chr9:98808570 | G | A | 1 | a0001c0001t0003g0026 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.371+501G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98808570 | |||||||
| chr9:98808592 | T | A | 1 | a0001c0021t0001g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.371+523T>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98808592 | |||||||
| chr9:98808871 | A | G | 295 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(292): Show |
310 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.371+802A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98808871 | |||||||
| chr9:98808918 | C | G | 1 | a0001c0001t0001g0073 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.371+849C>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98808918 | |||||||
| chr9:98809142 | A | T | 1 | a0001c0001t0001g0346 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.371+1073A>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98809142 | |||||||
| chr9:98809281 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.371+1212T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98809281 | |||||||
| chr9:98809373 | G | A | 179 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(176): Show |
192 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.371+1304G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98809373 | |||||||
| chr9:98809388 | C | G | 1 | a0001c0002t0002g0236 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.371+1319C>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98809388 | |||||||
| chr9:98809402 | T | C | 100 | a0001c0001t0001g0023 a0001c0001t0001g0239 a0001c0001t0001g0245 others(97): Show |
102 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.371+1333T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98809402 | |||||||
| chr9:98809715 | C | T | 4 | a0001c0001t0001g0342 a0001c0001t0001g0343 a0001c0001t0001g0345 others(1): Show |
4 | HG01081.hp2 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.371+1646C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98809715 | |||||||
| chr9:98809807 | C | G | 2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG02602.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.371+1738C>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98809807 | |||||||
| chr9:98809813 | G | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0341 a0001c0002t0002g0340 |
3 | HG00597.hp1 HG02055.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.371+1744G>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98809813 | |||||||
| chr9:98809822 | T | C | 1 | a0002c0003t0005g0237 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.371+1753T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98809822 | |||||||
| chr9:98809864 | C | T | 6 | a0001c0001t0001g0021 a0001c0001t0001g0231 a0001c0001t0001g0232 others(3): Show |
7 | HG00140.hp2 HG00639.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.371+1795C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98809864 | |||||||
| chr9:98809968 | T | C | 2 | a0001c0001t0001g0024 a0001c0020t0001g0350 |
3 | HG02922.hp1 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.371+1899T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98809968 | |||||||
| chr9:98810362 | A | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0235 |
3 | HG00140.hp2 HG03490.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.371+2293A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98810362 | |||||||
| chr9:98810460 | A | G | 2 | a0001c0001t0001g0333 a0001c0001t0001g0334 |
2 | HG02602.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.371+2391A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98810460 | |||||||
| chr9:98810568 | T | C | 4 | a0001c0001t0001g0074 a0001c0001t0001g0341 a0001c0001t0004g0238 others(1): Show |
4 | HG00597.hp1 HG02055.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.371+2499T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98810568 | |||||||
| chr9:98810662 | C | T | 1 | a0001c0001t0001g0332 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.371+2593C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98810662 | |||||||
| chr9:98810761 | A | G | 4 | a0001c0001t0001g0074 a0001c0001t0001g0341 a0001c0001t0004g0238 others(1): Show |
4 | HG00597.hp1 HG02055.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.371+2692A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98810761 | |||||||
| chr9:98811131 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.371+3062G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98811131 | |||||||
| chr9:98811139 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.371+3070G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98811139 | |||||||
| chr9:98811185 | T | G | 4 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(1): Show |
4 | HG02257.hp2 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.371+3116T>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98811185 | |||||||
| chr9:98811192 | T | A | 1 | a0001c0001t0001g0239 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.371+3123T>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98811192 | |||||||
| chr9:98811418 | T | G | 4 | a0001c0001t0001g0346 a0001c0002t0002g0240 a0001c0002t0002g0241 others(1): Show |
4 | HG01109.hp1 HG02922.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.371+3349T>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98811418 | |||||||
| chr9:98811537 | G | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0341 a0001c0002t0002g0340 |
3 | HG00597.hp1 HG02055.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.371+3468G>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98811537 | |||||||
| chr9:98811683 | C | CT | 147 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(144): Show |
157 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.371+3631dupT | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 98811683 | ||||||
| chr9:98811807 | C | T | 4 | a0001c0001t0001g0338 a0001c0002t0002g0339 a0001c0004t0001g0337 others(1): Show |
4 | HG01243.hp1 HG02622.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.371+3738C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98811807 | |||||||
| chr9:98811870 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.371+3801A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98811870 | |||||||
| chr9:98811962 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0331 |
3 | HG00738.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.371+3893C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98811962 | |||||||
| chr9:98812013 | A | G | 2 | a0001c0001t0001g0345 a0001c0004t0001g0344 |
2 | HG01081.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.371+3944A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98812013 | |||||||
| chr9:98812035 | C | T | 1 | a0001c0004t0001g0229 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.371+3966C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98812035 | |||||||
| chr9:98812081 | C | T | 3 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0006g0104 |
3 | HG02451.hp1 HG03041.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.371+4012C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98812081 | |||||||
| chr9:98812329 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.371+4260G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98812329 | |||||||
| chr9:98812451 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.371+4382C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98812451 | |||||||
| chr9:98812455 | G | T | 3 | a0001c0008t0001g0348 a0001c0008t0006g0347 a0001c0008t0006g0349 |
3 | HG01081.hp1 HG01891.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.371+4386G>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98812455 | |||||||
| chr9:98812473 | C | G | 184 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(181): Show |
197 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.371+4404C>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98812473 | |||||||
| chr9:98812517 | G | A | 4 | a0001c0001t0001g0074 a0001c0001t0001g0341 a0001c0002t0002g0340 others(1): Show |
4 | HG00597.hp1 HG02055.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.371+4448G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98812517 | |||||||
| chr9:98812525 | G | C | 1 | a0001c0001t0004g0028 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.371+4456G>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98812525 | |||||||
| chr9:98812570 | C | T | 2 | a0001c0001t0001g0345 a0001c0004t0001g0344 |
2 | HG01081.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.371+4501C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98812570 | |||||||
| chr9:98812792 | T | C | 1 | a0001c0001t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.371+4723T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98812792 | |||||||
| chr9:98812814 | T | C | 1 | a0001c0002t0002g0081 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.371+4745T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98812814 | |||||||
| chr9:98812878 | T | G | 1 | a0001c0002t0002g0243 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.371+4809T>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98812878 | |||||||
| chr9:98813103 | TCTC | T | 4 | a0001c0001t0001g0074 a0001c0001t0001g0341 a0001c0002t0002g0340 others(1): Show |
4 | HG00597.hp1 HG02055.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.371+5037_371+5039d others(5): Show |
GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 98813103 | ||||||
| chr9:98813121 | A | G | 2 | a0001c0001t0001g0345 a0001c0004t0001g0344 |
2 | HG01081.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.371+5052A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98813121 | |||||||
| chr9:98813266 | C | G | 1 | a0001c0001t0003g0072 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.371+5197C>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98813266 | |||||||
| chr9:98813311 | A | G | 1 | a0002c0003t0005g0237 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.371+5242A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98813311 | |||||||
| chr9:98813316 | G | T | 1 | a0001c0001t0001g0071 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.371+5247G>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98813316 | |||||||
| chr9:98813450 | A | G | 4 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(1): Show |
4 | HG02257.hp2 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.371+5381A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98813450 | |||||||
| chr9:98813499 | A | AG | 100 | a0001c0001t0001g0023 a0001c0001t0001g0074 a0001c0001t0001g0227 others(97): Show |
102 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.371+5430_371+5431i others(3): Show |
GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98813499 | |||||||
| chr9:98813500 | A | G | 195 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(192): Show |
208 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.371+5431A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98813500 | |||||||
| chr9:98813501 | A | T | 100 | a0001c0001t0001g0023 a0001c0001t0001g0074 a0001c0001t0001g0227 others(97): Show |
102 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.371+5432A>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98813501 | |||||||
| chr9:98813540 | C | T | 1 | a0001c0002t0002g0010 | 2 | HG02109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.371+5471C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98813540 | |||||||
| chr9:98813579 | C | G | 4 | a0001c0001t0001g0074 a0001c0001t0001g0341 a0001c0002t0002g0340 others(1): Show |
4 | HG00597.hp1 HG02055.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.371+5510C>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98813579 | |||||||
| chr9:98813722 | A | T | 10 | a0001c0001t0001g0224 a0001c0001t0003g0020 a0001c0001t0004g0218 others(7): Show |
11 | HG00621.hp1 HG01123.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.371+5653A>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98813722 | |||||||
| chr9:98813791 | C | T | 1 | a0001c0002t0002g0070 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.371+5722C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98813791 | |||||||
| chr9:98813808 | TA | T | 289 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(286): Show |
304 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.371+5751delA | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 98813808 | ||||||
| chr9:98813810 | A | T | 9 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(6): Show |
10 | HG02145.hp2 HG02723.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.371+5741A>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98813810 | |||||||
| chr9:98813918 | T | G | 152 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(149): Show |
161 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.371+5849T>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98813918 | |||||||
| chr9:98813920 | A | T | 4 | a0001c0001t0001g0342 a0001c0001t0001g0343 a0001c0001t0001g0345 others(1): Show |
4 | HG01081.hp2 HG02965.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.371+5851A>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98813920 | |||||||
| chr9:98813974 | A | G | 1 | a0002c0010t0002g0325 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.371+5905A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98813974 | |||||||
| chr9:98814016 | G | A | 2 | a0001c0001t0001g0024 a0001c0020t0001g0350 |
3 | HG02922.hp1 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.371+5947G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98814016 | |||||||
| chr9:98814100 | C | T | 1 | a0001c0007t0002g0209 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.371+6031C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98814100 | |||||||
| chr9:98814197 | T | C | 1 | a0001c0001t0001g0342 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.371+6128T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98814197 | |||||||
| chr9:98814265 | A | T | 3 | a0001c0001t0001g0343 a0001c0001t0001g0345 a0001c0004t0001g0344 |
3 | HG01081.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.371+6196A>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98814265 | |||||||
| chr9:98814327 | C | G | 4 | a0001c0001t0001g0074 a0001c0001t0001g0341 a0001c0002t0002g0340 others(1): Show |
4 | HG00597.hp1 HG02055.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.371+6258C>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98814327 | |||||||
| chr9:98814428 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.371+6359G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98814428 | |||||||
| chr9:98814539 | G | A | 2 | a0001c0001t0001g0335 a0001c0001t0006g0336 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.371+6470G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98814539 | |||||||
| chr9:98814579 | G | A | 6 | a0001c0001t0001g0335 a0001c0001t0001g0338 a0001c0001t0006g0336 others(3): Show |
6 | HG01243.hp1 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.371+6510G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98814579 | |||||||
| chr9:98814792 | C | T | 4 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(1): Show |
4 | HG02257.hp2 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.371+6723C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98814792 | |||||||
| chr9:98814798 | A | G | 2 | a0001c0001t0001g0335 a0001c0001t0006g0336 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.371+6729A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98814798 | |||||||
| chr9:98814854 | C | T | 1 | a0001c0001t0005g0208 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.371+6785C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98814854 | |||||||
| chr9:98814937 | C | G | 2 | a0001c0001t0001g0335 a0001c0001t0006g0336 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.371+6868C>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98814937 | |||||||
| chr9:98815104 | C | T | 3 | a0001c0001t0001g0094 a0001c0001t0001g0103 a0001c0002t0002g0236 |
3 | HG01884.hp2 HG02451.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.371+7035C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98815104 | |||||||
| chr9:98815171 | A | G | 3 | a0001c0008t0001g0348 a0001c0008t0006g0347 a0001c0008t0006g0349 |
3 | HG01081.hp1 HG01891.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.371+7102A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98815171 | |||||||
| chr9:98815204 | C | T | 2 | a0001c0001t0001g0335 a0001c0001t0006g0336 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.371+7135C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98815204 | |||||||
| chr9:98815401 | G | T | 1 | a0001c0002t0002g0207 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.371+7332G>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98815401 | |||||||
| chr9:98815408 | A | C | 184 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(181): Show |
197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.371+7339A>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98815408 | |||||||
| chr9:98815413 | G | T | 1 | a0001c0001t0001g0102 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.371+7344G>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98815413 | |||||||
| chr9:98815784 | T | G | 6 | a0001c0001t0001g0335 a0001c0001t0001g0338 a0001c0001t0006g0336 others(3): Show |
6 | HG01243.hp1 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.372-7472T>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98815784 | |||||||
| chr9:98815835 | G | A | 4 | a0001c0001t0001g0343 a0001c0008t0001g0348 a0001c0008t0006g0347 others(1): Show |
4 | HG01081.hp1 HG01891.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.372-7421G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98815835 | |||||||
| chr9:98815871 | A | G | 2 | a0001c0001t0001g0093 a0001c0002t0002g0206 |
2 | NA18957.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.372-7385A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98815871 | |||||||
| chr9:98816118 | G | A | 5 | a0001c0001t0001g0074 a0001c0001t0001g0341 a0001c0001t0004g0238 others(2): Show |
5 | HG00597.hp1 HG02055.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.372-7138G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98816118 | |||||||
| chr9:98816121 | G | A | 96 | a0001c0001t0001g0023 a0001c0001t0001g0239 a0001c0001t0001g0245 others(93): Show |
98 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.372-7135G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98816121 | |||||||
| chr9:98816389 | G | GA | 179 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(176): Show |
192 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.372-6852dupA | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 98816389 | ||||||
| chr9:98816494 | C | T | 1 | a0001c0001t0003g0203 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.372-6762C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98816494 | |||||||
| chr9:98816557 | G | C | 1 | a0001c0001t0001g0093 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.372-6699G>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98816557 | |||||||
| chr9:98816585 | A | G | 1 | a0002c0003t0001g0323 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.372-6671A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98816585 | |||||||
| chr9:98816651 | C | CT | 11 | a0001c0001t0001g0094 a0001c0001t0001g0103 a0001c0001t0001g0199 others(8): Show |
11 | HG01243.hp2 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.372-6588dupT | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 98816651 | ||||||
| chr9:98816651 | CT | C | 11 | a0001c0001t0001g0095 a0001c0001t0001g0102 a0001c0001t0001g0342 others(8): Show |
12 | HG01081.hp1 HG01081.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.372-6588delT | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 98816651 | ||||||
| chr9:98816736 | C | T | 1 | a0001c0002t0002g0010 | 2 | HG02109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.372-6520C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98816736 | |||||||
| chr9:98816749 | C | G | 4 | a0001c0001t0001g0074 a0001c0001t0001g0341 a0001c0002t0002g0340 others(1): Show |
4 | HG00597.hp1 HG02055.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.372-6507C>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98816749 | |||||||
| chr9:98816817 | A | AT | 12 | a0001c0001t0001g0341 a0001c0001t0004g0067 a0001c0001t0004g0238 others(9): Show |
12 | HG00597.hp1 HG01081.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.372-6416dupT | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 98816817 | ||||||
| chr9:98816817 | AT | A | 236 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(233): Show |
250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.372-6416delT | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 98816817 | ||||||
| chr9:98817033 | A | G | 1 | a0001c0021t0001g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.372-6223A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98817033 | |||||||
| chr9:98817090 | T | C | 1 | a0002c0003t0001g0249 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.372-6166T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98817090 | |||||||
| chr9:98817109 | G | A | 148 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(145): Show |
157 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.372-6147G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98817109 | |||||||
| chr9:98817149 | AG | A | 4 | a0001c0001t0001g0074 a0001c0001t0001g0341 a0001c0002t0002g0340 others(1): Show |
4 | HG00597.hp1 HG02055.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.372-6106delG | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98817149 | |||||||
| chr9:98817397 | CAT | C | 4 | a0001c0001t0001g0074 a0001c0001t0001g0341 a0001c0002t0002g0340 others(1): Show |
4 | HG00597.hp1 HG02055.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.372-5856_372-5855d others(4): Show |
GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 98817397 | ||||||
| chr9:98817398 | A | C | 1 | a0001c0006t0008g0214 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.372-5858A>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98817398 | |||||||
| chr9:98817408 | C | T | 1 | a0001c0016t0001g0029 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.372-5848C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98817408 | |||||||
| chr9:98817488 | A | T | 1 | a0001c0001t0001g0185 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.372-5768A>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98817488 | |||||||
| chr9:98817653 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.372-5603G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98817653 | |||||||
| chr9:98817788 | G | A | 7 | a0001c0001t0001g0199 a0001c0001t0001g0202 a0001c0001t0003g0197 others(4): Show |
7 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.372-5468G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98817788 | |||||||
| chr9:98818200 | C | T | 2 | a0001c0001t0001g0335 a0001c0001t0006g0336 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.372-5056C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98818200 | |||||||
| chr9:98818231 | T | A | 7 | a0001c0001t0001g0074 a0001c0001t0001g0341 a0001c0002t0002g0340 others(4): Show |
7 | HG00597.hp1 HG01081.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.372-5025T>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98818231 | |||||||
| chr9:98818245 | C | T | 4 | a0001c0001t0001g0074 a0001c0001t0001g0341 a0001c0002t0002g0340 others(1): Show |
4 | HG00597.hp1 HG02055.hp1 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.372-5011C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98818245 | |||||||
| chr9:98818253 | C | T | 5 | a0001c0001t0001g0180 a0001c0001t0001g0181 a0001c0001t0001g0182 others(2): Show |
5 | HG01261.hp2 HG01934.hp1 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.372-5003C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98818253 | |||||||
| chr9:98818309 | G | A | 1 | a0001c0001t0001g0335 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.372-4947G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98818309 | |||||||
| chr9:98818444 | C | T | 1 | a0001c0001t0001g0247 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.372-4812C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98818444 | |||||||
| chr9:98818516 | C | T | 5 | a0001c0001t0001g0063 a0001c0001t0003g0065 a0001c0001t0004g0028 others(2): Show |
5 | NA18747.hp1 NA18954.hp2 NA18963.hp2 others(2): Show |
intron_variant | MODIFIER | c.372-4740C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98818516 | |||||||
| chr9:98818719 | C | T | 131 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(128): Show |
136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.372-4537C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98818719 | |||||||
| chr9:98819082 | G | A | 1 | a0001c0001t0003g0001 | 4 | HG01070.hp1 HG01167.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.372-4174G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98819082 | |||||||
| chr9:98819181 | A | T | 5 | a0001c0001t0001g0074 a0001c0001t0001g0341 a0001c0001t0004g0238 others(2): Show |
5 | HG00597.hp1 HG02055.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.372-4075A>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98819181 | |||||||
| chr9:98819250 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.372-4006G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98819250 | |||||||
| chr9:98819296 | A | G | 1 | a0001c0001t0001g0074 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.372-3960A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98819296 | |||||||
| chr9:98819321 | T | A | 1 | a0001c0002t0002g0030 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.372-3935T>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98819321 | |||||||
| chr9:98819368 | C | T | 18 | a0001c0001t0001g0024 a0001c0001t0001g0094 a0001c0001t0001g0095 others(15): Show |
21 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.372-3888C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98819368 | |||||||
| chr9:98819384 | A | G | 9 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(6): Show |
10 | HG02145.hp2 HG02723.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.372-3872A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98819384 | |||||||
| chr9:98819693 | C | T | 2 | a0001c0001t0001g0024 a0001c0020t0001g0350 |
3 | HG02922.hp1 HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.372-3563C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98819693 | |||||||
| chr9:98819857 | C | A | 1 | a0002c0003t0005g0237 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.372-3399C>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98819857 | |||||||
| chr9:98819875 | G | A | 1 | a0001c0001t0003g0152 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.372-3381G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98819875 | |||||||
| chr9:98820007 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.372-3249T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98820007 | |||||||
| chr9:98820155 | ACGTGTGC others(5): Show |
A | 1 | a0001c0001t0003g0089 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.372-3100_372-3089d others(14): Show |
GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98820155 | |||||||
| chr9:98820171 | T | G | 1 | a0001c0001t0001g0343 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.372-3085T>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98820171 | |||||||
| chr9:98820269 | C | T | 1 | a0001c0002t0002g0151 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.372-2987C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98820269 | |||||||
| chr9:98820403 | A | ATG | 15 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0053 others(12): Show |
15 | HG00438.hp2 HG00609.hp2 HG01069.hp1 others(12): Show |
intron_variant | MODIFIER | c.372-2851_372-2850d others(4): Show |
GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 98820403 | ||||||
| chr9:98820403 | A | G | 112 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(109): Show |
118 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.372-2853A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98820403 | |||||||
| chr9:98820486 | T | C | 1 | a0001c0001t0001g0049 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.372-2770T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98820486 | |||||||
| chr9:98820560 | C | T | 149 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(146): Show |
159 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.372-2696C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98820560 | |||||||
| chr9:98820635 | A | G | 1 | a0001c0001t0001g0342 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.372-2621A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98820635 | |||||||
| chr9:98820668 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.372-2588C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98820668 | |||||||
| chr9:98820690 | A | G | 151 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(148): Show |
161 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.372-2566A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98820690 | |||||||
| chr9:98820767 | C | T | 348 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(345): Show |
372 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(369): Show |
intron_variant | MODIFIER | c.372-2489C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98820767 | |||||||
| chr9:98820824 | G | A | 151 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(148): Show |
161 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.372-2432G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98820824 | |||||||
| chr9:98820842 | T | G | 2 | a0001c0001t0001g0335 a0001c0001t0006g0336 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.372-2414T>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98820842 | |||||||
| chr9:98820971 | C | T | 3 | a0001c0001t0001g0343 a0001c0001t0001g0345 a0001c0004t0001g0344 |
3 | HG01081.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.372-2285C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98820971 | |||||||
| chr9:98821057 | A | G | 2 | a0001c0001t0001g0091 a0001c0001t0001g0179 |
2 | HG02735.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.372-2199A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98821057 | |||||||
| chr9:98821071 | C | T | 2 | a0001c0001t0001g0335 a0001c0001t0006g0336 |
2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.372-2185C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98821071 | |||||||
| chr9:98821255 | C | T | 276 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(273): Show |
291 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(288): Show |
intron_variant | MODIFIER | c.372-2001C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98821255 | |||||||
| chr9:98821273 | G | A | 133 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(130): Show |
138 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.372-1983G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98821273 | |||||||
| chr9:98821387 | C | T | 286 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(283): Show |
301 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.372-1869C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98821387 | |||||||
| chr9:98821396 | C | T | 2 | a0001c0001t0003g0047 a0001c0001t0003g0048 |
2 | HG00544.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.372-1860C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98821396 | |||||||
| chr9:98821407 | G | T | 1 | a0001c0001t0004g0184 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.372-1849G>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98821407 | |||||||
| chr9:98821482 | G | A | 2 | a0001c0001t0001g0063 a0001c0002t0002g0062 |
2 | NA18954.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.372-1774G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98821482 | |||||||
| chr9:98821620 | A | G | 134 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(131): Show |
139 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.372-1636A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98821620 | |||||||
| chr9:98821624 | C | CA | 145 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(142): Show |
155 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.372-1619dupA | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 98821624 | ||||||
| chr9:98821624 | C | CAAAAAAA others(6): Show |
1 | a0002c0003t0001g0311 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.372-1631_372-1619d others(15): Show |
GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 98821624 | ||||||
| chr9:98821624 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0001g0310 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.372-1619_372-1618i others(17): Show |
GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 98821624 | ||||||
| chr9:98821624 | C | CAAAAAAA others(9): Show |
29 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0246 others(26): Show |
29 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.372-1619_372-1618i others(18): Show |
GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 98821624 | ||||||
| chr9:98821624 | C | CAAAAAAA others(10): Show |
71 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(68): Show |
75 | HG00280.hp1 HG00423.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.372-1619_372-1618i others(19): Show |
GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 98821624 | ||||||
| chr9:98821624 | C | CAAAAAAA others(11): Show |
28 | a0001c0001t0001g0023 a0001c0001t0001g0075 a0001c0001t0001g0155 others(25): Show |
29 | HG00609.hp1 HG00738.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.372-1619_372-1618i others(20): Show |
GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 98821624 | ||||||
| chr9:98821624 | C | CAAAAAAA others(12): Show |
2 | a0001c0002t0002g0154 a0002c0003t0001g0250 |
2 | HG00544.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.372-1619_372-1618i others(21): Show |
GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr9 | 98821624 | ||||||
| chr9:98821659 | A | C | 1 | a0001c0001t0001g0228 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.372-1597A>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98821659 | |||||||
| chr9:98821873 | T | C | 7 | a0001c0001t0001g0199 a0001c0001t0001g0202 a0001c0001t0003g0197 others(4): Show |
7 | HG01243.hp2 HG01884.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.372-1383T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98821873 | |||||||
| chr9:98821934 | C | G | 5 | a0001c0001t0001g0074 a0001c0001t0001g0341 a0001c0001t0004g0238 others(2): Show |
5 | HG00597.hp1 HG02055.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.372-1322C>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98821934 | |||||||
| chr9:98821993 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.372-1263C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98821993 | |||||||
| chr9:98822046 | A | G | 286 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(283): Show |
301 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.372-1210A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98822046 | |||||||
| chr9:98822400 | G | A | 5 | a0001c0001t0001g0097 a0001c0001t0001g0338 a0001c0002t0002g0339 others(2): Show |
5 | HG01243.hp1 HG02622.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.372-856G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98822400 | |||||||
| chr9:98822448 | C | T | 1 | a0001c0001t0001g0288 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.372-808C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98822448 | |||||||
| chr9:98822504 | C | T | 143 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(140): Show |
148 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.372-752C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98822504 | |||||||
| chr9:98822758 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.372-498C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98822758 | |||||||
| chr9:98822764 | C | T | 286 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(283): Show |
301 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.372-492C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98822764 | |||||||
| chr9:98822855 | A | C | 1 | a0002c0003t0001g0326 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.372-401A>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98822855 | |||||||
| chr9:98822924 | G | T | 1 | a0001c0001t0001g0216 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.372-332G>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98822924 | |||||||
| chr9:98823135 | A | T | 1 | a0002c0003t0001g0287 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.372-121A>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98823135 | |||||||
| chr9:98823162 | G | C | 286 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(283): Show |
301 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.372-94G>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98823162 | |||||||
| chr9:98823249 | T | A | 12 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0292 others(9): Show |
12 | HG00438.hp1 HG00558.hp2 HG01943.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.372-7T>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 1/9 | chr9 | 98823249 | |||||||
| chr9:98823499 | G | T | 8 | a0001c0001t0001g0100 a0001c0001t0001g0105 a0001c0001t0001g0106 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.541+74G>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 2/9 | chr9 | 98823499 | |||||||
| chr9:98823504 | G | A | 1 | a0001c0001t0001g0343 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.541+79G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 2/9 | chr9 | 98823504 | |||||||
| chr9:98823549 | C | T | 143 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(140): Show |
153 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.541+124C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 2/9 | chr9 | 98823549 | |||||||
| chr9:98823671 | G | C | 1 | a0001c0002t0002g0243 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.541+246G>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 2/9 | chr9 | 98823671 | |||||||
| chr9:98823710 | G | A | 143 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(140): Show |
148 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.541+285G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 2/9 | chr9 | 98823710 | |||||||
| chr9:98823907 | C | T | 3 | a0001c0008t0001g0348 a0001c0008t0006g0347 a0001c0008t0006g0349 |
3 | HG01081.hp1 HG01891.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.541+482C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 2/9 | chr9 | 98823907 | |||||||
| chr9:98824574 | C | T | 3 | a0001c0001t0001g0095 a0001c0001t0001g0102 a0001c0001t0003g0009 |
4 | HG02622.hp2 HG03225.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.541+1149C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 2/9 | chr9 | 98824574 | |||||||
| chr9:98824856 | G | T | 1 | a0001c0001t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.541+1431G>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 2/9 | chr9 | 98824856 | |||||||
| chr9:98824880 | C | T | 142 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(139): Show |
152 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.541+1455C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 2/9 | chr9 | 98824880 | |||||||
| chr9:98824961 | C | A | 3 | a0001c0001t0001g0050 a0001c0001t0003g0051 a0001c0002t0002g0052 |
3 | HG01069.hp1 HG01106.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.541+1536C>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 2/9 | chr9 | 98824961 | |||||||
| chr9:98825045 | T | C | 3 | a0001c0001t0001g0094 a0001c0001t0001g0103 a0001c0002t0002g0236 |
3 | HG01884.hp2 HG02451.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.541+1620T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 2/9 | chr9 | 98825045 | |||||||
| chr9:98825101 | T | G | 1 | a0001c0001t0001g0090 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.542-1651T>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 2/9 | chr9 | 98825101 | |||||||
| chr9:98825199 | A | G | 4 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(1): Show |
4 | HG02257.hp2 HG02818.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.542-1553A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 2/9 | chr9 | 98825199 | |||||||
| chr9:98825229 | T | G | 6 | a0001c0001t0001g0074 a0001c0001t0001g0335 a0001c0001t0001g0341 others(3): Show |
6 | HG00597.hp1 HG02055.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.542-1523T>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 2/9 | chr9 | 98825229 | |||||||
| chr9:98825765 | G | A | 6 | a0001c0001t0001g0074 a0001c0001t0001g0335 a0001c0001t0001g0341 others(3): Show |
6 | HG00597.hp1 HG02055.hp1 HG02165.hp2 others(3): Show |
intron_variant | MODIFIER | c.542-987G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 2/9 | chr9 | 98825765 | |||||||
| chr9:98825930 | A | G | 8 | a0001c0001t0001g0074 a0001c0001t0001g0335 a0001c0001t0001g0341 others(5): Show |
8 | HG00597.hp1 HG02055.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.542-822A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 2/9 | chr9 | 98825930 | |||||||
| chr9:98825958 | G | C | 2 | a0002c0003t0005g0251 a0002c0005t0002g0297 |
2 | NA18984.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.542-794G>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 2/9 | chr9 | 98825958 | |||||||
| chr9:98825974 | C | CA | 27 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0053 others(24): Show |
29 | HG00323.hp2 HG00639.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.542-765dupA | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr9 | 98825974 | ||||||
| chr9:98826115 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.542-637T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 2/9 | chr9 | 98826115 | |||||||
| chr9:98826191 | T | G | 1 | a0001c0001t0006g0336 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.542-561T>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 2/9 | chr9 | 98826191 | |||||||
| chr9:98826251 | G | C | 1 | a0001c0001t0006g0336 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.542-501G>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 2/9 | chr9 | 98826251 | |||||||
| chr9:98826373 | G | A | 3 | a0001c0001t0001g0095 a0001c0001t0001g0102 a0001c0001t0003g0009 |
4 | HG02622.hp2 HG03225.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.542-379G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 2/9 | chr9 | 98826373 | |||||||
| chr9:98826448 | T | G | 10 | a0001c0001t0001g0097 a0001c0001t0001g0245 a0001c0001t0001g0246 others(7): Show |
10 | HG01168.hp1 HG01243.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.542-304T>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 2/9 | chr9 | 98826448 | |||||||
| chr9:98826634 | G | A | 1 | a0001c0001t0006g0336 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.542-118G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 2/9 | chr9 | 98826634 | |||||||
| chr9:98826719 | C | T | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG03239.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.542-33C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 2/9 | chr9 | 98826719 | |||||||
| chr9:98826953 | G | A | 1 | a0001c0002t0002g0170 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.731+12G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98826953 | |||||||
| chr9:98827031 | C | T | 1 | a0001c0001t0006g0336 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.731+90C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98827031 | |||||||
| chr9:98827068 | C | A | 1 | a0001c0001t0001g0332 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.731+127C>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98827068 | |||||||
| chr9:98827248 | A | G | 4 | a0001c0001t0001g0343 a0001c0001t0001g0345 a0001c0001t0006g0336 others(1): Show |
4 | HG01081.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.731+307A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98827248 | |||||||
| chr9:98827268 | C | T | 1 | a0001c0001t0001g0343 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.731+327C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98827268 | |||||||
| chr9:98827272 | C | A | 4 | a0001c0001t0001g0343 a0001c0001t0001g0345 a0001c0001t0006g0336 others(1): Show |
4 | HG01081.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.731+331C>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98827272 | |||||||
| chr9:98827298 | TCTCCTCC others(3): Show |
T | 4 | a0001c0001t0001g0343 a0001c0001t0001g0345 a0001c0001t0006g0336 others(1): Show |
4 | HG01081.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.731+368_731+377del others(10): Show |
GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 98827298 | ||||||
| chr9:98827358 | A | C | 4 | a0001c0001t0001g0343 a0001c0001t0001g0345 a0001c0001t0006g0336 others(1): Show |
4 | HG01081.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.731+417A>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98827358 | |||||||
| chr9:98827361 | T | C | 137 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(134): Show |
142 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.731+420T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98827361 | |||||||
| chr9:98827430 | A | G | 3 | a0001c0008t0001g0348 a0001c0008t0006g0347 a0001c0008t0006g0349 |
3 | HG01081.hp1 HG01891.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.731+489A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98827430 | |||||||
| chr9:98827460 | A | G | 1 | a0001c0001t0006g0336 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.731+519A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98827460 | |||||||
| chr9:98827485 | T | C | 1 | a0001c0001t0001g0097 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.731+544T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98827485 | |||||||
| chr9:98827490 | C | T | 1 | a0001c0001t0006g0336 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.731+549C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98827490 | |||||||
| chr9:98827520 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.731+579C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98827520 | |||||||
| chr9:98827551 | G | A | 4 | a0001c0001t0001g0343 a0001c0001t0001g0345 a0001c0001t0006g0336 others(1): Show |
4 | HG01081.hp2 HG03195.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.731+610G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98827551 | |||||||
| chr9:98827618 | A | T | 3 | a0001c0001t0001g0343 a0001c0001t0001g0345 a0001c0004t0001g0344 |
3 | HG01081.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.731+677A>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98827618 | |||||||
| chr9:98827658 | A | T | 3 | a0001c0001t0001g0343 a0001c0001t0001g0345 a0001c0004t0001g0344 |
3 | HG01081.hp2 HG03195.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.731+717A>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98827658 | |||||||
| chr9:98827818 | A | G | 7 | a0001c0001t0004g0218 a0002c0003t0001g0311 a0002c0003t0001g0313 others(4): Show |
8 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(5): Show |
intron_variant | MODIFIER | c.731+877A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98827818 | |||||||
| chr9:98827905 | C | T | 1 | a0001c0002t0002g0206 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.731+964C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98827905 | |||||||
| chr9:98827916 | C | T | 2 | a0002c0003t0001g0323 a0005c0012t0001g0285 |
2 | HG02698.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.731+975C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98827916 | |||||||
| chr9:98827930 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.731+989C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98827930 | |||||||
| chr9:98828036 | G | A | 113 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(110): Show |
119 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.731+1095G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98828036 | |||||||
| chr9:98828097 | C | T | 1 | a0001c0002t0002g0046 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.731+1156C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98828097 | |||||||
| chr9:98828602 | G | A | 293 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(290): Show |
308 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.731+1661G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98828602 | |||||||
| chr9:98828626 | T | G | 4 | a0001c0001t0003g0152 a0001c0001t0003g0171 a0001c0002t0002g0159 others(1): Show |
4 | NA18942.hp1 NA18950.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.731+1685T>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98828626 | |||||||
| chr9:98828639 | A | T | 1 | a0001c0002t0002g0070 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.731+1698A>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98828639 | |||||||
| chr9:98828891 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.731+1950G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98828891 | |||||||
| chr9:98829153 | T | TTATC | 76 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0023 others(73): Show |
79 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(76): Show |
intron_variant | MODIFIER | c.731+2262_731+2265d others(6): Show |
GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 98829153 | ||||||
| chr9:98829153 | T | TTATCTAT others(1): Show |
14 | a0001c0001t0001g0016 a0001c0001t0001g0094 a0001c0001t0001g0180 others(11): Show |
15 | HG01069.hp2 HG01071.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.731+2258_731+2265d others(10): Show |
GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 98829153 | ||||||
| chr9:98829153 | T | TTATCTAT others(5): Show |
3 | a0001c0001t0001g0114 a0001c0001t0001g0298 a0002c0003t0001g0316 |
3 | HG00408.hp1 HG03130.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.731+2254_731+2265d others(14): Show |
GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 98829153 | ||||||
| chr9:98829153 | TTATC | T | 57 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0036 others(54): Show |
63 | HG00639.hp2 HG00673.hp1 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.731+2262_731+2265d others(6): Show |
GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 98829153 | ||||||
| chr9:98829153 | TTATCTAT others(1): Show |
T | 26 | a0001c0001t0001g0008 a0001c0001t0001g0038 a0001c0001t0001g0039 others(23): Show |
29 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.731+2258_731+2265d others(10): Show |
GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 98829153 | ||||||
| chr9:98829153 | TTATCTAT others(5): Show |
T | 16 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0053 others(13): Show |
19 | HG00438.hp2 HG00741.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.731+2254_731+2265d others(14): Show |
GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 98829153 | ||||||
| chr9:98829153 | TTATCTAT others(9): Show |
T | 11 | a0001c0001t0001g0185 a0001c0004t0001g0145 a0001c0004t0001g0192 others(8): Show |
11 | HG00544.hp1 HG01934.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.731+2250_731+2265d others(18): Show |
GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 98829153 | ||||||
| chr9:98829250 | G | A | 3 | a0001c0001t0001g0338 a0001c0002t0002g0339 a0001c0004t0001g0337 |
3 | HG01243.hp1 HG02818.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.731+2309G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98829250 | |||||||
| chr9:98829448 | C | G | 1 | a0001c0001t0006g0083 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.732-2324C>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98829448 | |||||||
| chr9:98829449 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.732-2323A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98829449 | |||||||
| chr9:98829516 | A | T | 1 | a0001c0001t0001g0320 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.732-2256A>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98829516 | |||||||
| chr9:98829516 | AT | A | 14 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0100 others(11): Show |
15 | HG02145.hp1 HG02258.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.732-2244delT | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 98829516 | ||||||
| chr9:98829516 | ATT | A | 9 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0213 others(6): Show |
10 | HG02145.hp2 HG02723.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.732-2245_732-2244d others(4): Show |
GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr9 | 98829516 | ||||||
| chr9:98829519 | T | A | 53 | a0001c0001t0001g0023 a0001c0001t0001g0186 a0001c0001t0001g0239 others(50): Show |
55 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.732-2253T>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98829519 | |||||||
| chr9:98829581 | A | C | 1 | a0001c0001t0001g0087 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.732-2191A>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98829581 | |||||||
| chr9:98829884 | C | T | 1 | a0001c0001t0001g0342 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.732-1888C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98829884 | |||||||
| chr9:98829955 | G | A | 1 | a0001c0001t0001g0342 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.732-1817G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98829955 | |||||||
| chr9:98830066 | G | C | 1 | a0001c0001t0001g0097 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.732-1706G>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98830066 | |||||||
| chr9:98830367 | T | C | 1 | a0001c0001t0001g0290 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.732-1405T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98830367 | |||||||
| chr9:98830577 | A | G | 1 | a0001c0001t0001g0138 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.732-1195A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98830577 | |||||||
| chr9:98830987 | C | T | 1 | a0001c0001t0001g0345 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732-785C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98830987 | |||||||
| chr9:98831082 | T | C | 1 | a0001c0001t0006g0083 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.732-690T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98831082 | |||||||
| chr9:98831106 | C | T | 1 | a0001c0004t0001g0344 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.732-666C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98831106 | |||||||
| chr9:98831120 | C | A | 1 | a0001c0001t0001g0034 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.732-652C>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98831120 | |||||||
| chr9:98831543 | T | C | 114 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0024 others(111): Show |
119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.732-229T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98831543 | |||||||
| chr9:98831569 | G | A | 2 | a0001c0001t0001g0050 a0001c0001t0003g0004 |
3 | HG01099.hp2 HG01192.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.732-203G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98831569 | |||||||
| chr9:98831601 | T | G | 236 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(233): Show |
250 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(247): Show |
intron_variant | MODIFIER | c.732-171T>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98831601 | |||||||
| chr9:98831712 | A | G | 8 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(5): Show |
9 | HG02109.hp2 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.732-60A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 3/9 | chr9 | 98831712 | |||||||
| chr9:98831981 | C | T | 19 | a0001c0001t0001g0143 a0001c0001t0001g0224 a0001c0001t0003g0171 others(16): Show |
20 | HG00408.hp2 HG00621.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.917+24C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98831981 | |||||||
| chr9:98831994 | C | A | 1 | a0001c0001t0001g0343 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.917+37C>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98831994 | |||||||
| chr9:98832118 | G | A | 4 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0106 others(1): Show |
4 | HG02280.hp1 HG02886.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.917+161G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98832118 | |||||||
| chr9:98832130 | CAT | C | 3 | a0001c0001t0001g0094 a0001c0001t0001g0164 a0001c0021t0001g0027 |
3 | HG02572.hp1 HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.917+174_917+175del others(2): Show |
GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98832130 | |||||||
| chr9:98832232 | A | G | 17 | a0001c0001t0001g0224 a0001c0001t0003g0171 a0001c0001t0004g0028 others(14): Show |
18 | HG00438.hp1 HG00544.hp1 HG00621.hp2 others(15): Show |
intron_variant | MODIFIER | c.917+275A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98832232 | |||||||
| chr9:98832267 | C | T | 99 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0014 others(96): Show |
105 | HG00423.hp1 HG00423.hp2 HG00544.hp2 others(102): Show |
intron_variant | MODIFIER | c.917+310C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98832267 | |||||||
| chr9:98832383 | C | G | 309 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(306): Show |
330 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(327): Show |
intron_variant | MODIFIER | c.917+426C>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98832383 | |||||||
| chr9:98832434 | G | A | 1 | a0002c0003t0001g0277 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.917+477G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98832434 | |||||||
| chr9:98832476 | G | A | 1 | a0001c0001t0011g0278 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.917+519G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98832476 | |||||||
| chr9:98832493 | G | A | 1 | a0001c0001t0004g0028 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.917+536G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98832493 | |||||||
| chr9:98832496 | C | G | 18 | a0001c0001t0001g0224 a0001c0001t0003g0171 a0001c0001t0004g0028 others(15): Show |
19 | HG00544.hp1 HG00621.hp1 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.917+539C>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98832496 | |||||||
| chr9:98832501 | G | C | 63 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0013 others(60): Show |
67 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.917+544G>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98832501 | |||||||
| chr9:98832578 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.917+621G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98832578 | |||||||
| chr9:98832584 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.917+627G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98832584 | |||||||
| chr9:98832682 | C | A | 3 | a0001c0001t0001g0094 a0001c0001t0001g0164 a0001c0021t0001g0027 |
3 | HG02572.hp1 HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.917+725C>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98832682 | |||||||
| chr9:98832708 | G | A | 1 | a0001c0001t0003g0072 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.917+751G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98832708 | |||||||
| chr9:98832790 | G | A | 15 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0135 others(12): Show |
17 | HG00597.hp2 HG02056.hp1 HG02132.hp1 others(14): Show |
intron_variant | MODIFIER | c.917+833G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98832790 | |||||||
| chr9:98832923 | C | T | 10 | a0001c0001t0001g0345 a0001c0004t0001g0098 a0001c0004t0001g0099 others(7): Show |
10 | HG01081.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.917+966C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98832923 | |||||||
| chr9:98832998 | T | C | 5 | a0001c0002t0002g0236 a0001c0006t0002g0019 a0001c0006t0002g0147 others(2): Show |
6 | HG01884.hp2 HG02145.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.917+1041T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98832998 | |||||||
| chr9:98833151 | T | G | 1 | a0002c0005t0002g0328 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.917+1194T>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98833151 | |||||||
| chr9:98833161 | T | G | 114 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(111): Show |
121 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.917+1204T>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98833161 | |||||||
| chr9:98833268 | C | T | 3 | a0001c0001t0006g0083 a0001c0004t0006g0015 a0001c0019t0006g0015 |
3 | HG02615.hp2 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.917+1311C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98833268 | |||||||
| chr9:98833304 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.917+1347C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98833304 | |||||||
| chr9:98833453 | G | A | 8 | a0001c0001t0001g0106 a0001c0001t0001g0117 a0001c0001t0001g0143 others(5): Show |
8 | HG00280.hp2 HG02055.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.917+1496G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98833453 | |||||||
| chr9:98833526 | G | C | 4 | a0001c0001t0003g0009 a0001c0001t0003g0077 a0001c0001t0003g0200 others(1): Show |
5 | HG01243.hp2 HG02970.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.917+1569G>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98833526 | |||||||
| chr9:98833797 | G | A | 1 | a0001c0002t0002g0066 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.918-1452G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98833797 | |||||||
| chr9:98833826 | T | A | 1 | a0001c0001t0001g0110 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.918-1423T>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98833826 | |||||||
| chr9:98834102 | C | T | 15 | a0001c0001t0001g0224 a0001c0001t0004g0028 a0001c0001t0004g0061 others(12): Show |
16 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.918-1147C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98834102 | |||||||
| chr9:98834150 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.918-1099G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98834150 | |||||||
| chr9:98834160 | C | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0036 |
3 | NA18946.hp1 NA18993.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.918-1089C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98834160 | |||||||
| chr9:98834187 | C | G | 15 | a0001c0001t0001g0224 a0001c0001t0004g0028 a0001c0001t0004g0061 others(12): Show |
16 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(13): Show |
intron_variant | MODIFIER | c.918-1062C>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98834187 | |||||||
| chr9:98834317 | C | T | 123 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0018 others(120): Show |
129 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.918-932C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98834317 | |||||||
| chr9:98834355 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.918-894A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98834355 | |||||||
| chr9:98834361 | T | C | 1 | a0001c0001t0004g0184 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.918-888T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98834361 | |||||||
| chr9:98834442 | T | C | 1 | a0001c0004t0001g0145 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.918-807T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98834442 | |||||||
| chr9:98834561 | G | A | 1 | a0001c0001t0005g0136 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.918-688G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98834561 | |||||||
| chr9:98834579 | A | C | 123 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(120): Show |
131 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.918-670A>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98834579 | |||||||
| chr9:98834666 | A | G | 3 | a0001c0001t0001g0094 a0001c0001t0001g0164 a0001c0021t0001g0027 |
3 | HG02572.hp1 HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.918-583A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98834666 | |||||||
| chr9:98834706 | C | T | 1 | a0001c0002t0002g0131 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.918-543C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98834706 | |||||||
| chr9:98834753 | T | C | 126 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0018 others(123): Show |
132 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.918-496T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98834753 | |||||||
| chr9:98834785 | G | T | 1 | a0003c0009t0001g0150 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.918-464G>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98834785 | |||||||
| chr9:98834866 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.918-383C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98834866 | |||||||
| chr9:98834986 | A | C | 76 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0034 others(73): Show |
79 | HG00423.hp1 HG00423.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.918-263A>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98834986 | |||||||
| chr9:98835072 | A | T | 2 | a0001c0001t0003g0069 a0001c0001t0003g0291 |
2 | HG01975.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.918-177A>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98835072 | |||||||
| chr9:98835118 | C | A | 4 | a0001c0001t0001g0228 a0001c0001t0006g0104 a0001c0008t0006g0347 others(1): Show |
4 | HG01081.hp1 HG01255.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.918-131C>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98835118 | |||||||
| chr9:98835130 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.918-119C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 4/9 | chr9 | 98835130 | |||||||
| chr9:98835530 | C | A | 3 | a0001c0001t0006g0083 a0001c0004t0006g0015 a0001c0019t0006g0015 |
3 | HG02615.hp2 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1035+164C>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 5/9 | chr9 | 98835530 | |||||||
| chr9:98835739 | C | CT | 12 | a0001c0001t0001g0033 a0001c0001t0001g0216 a0001c0001t0001g0342 others(9): Show |
13 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.1035+387dupT | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 98835739 | ||||||
| chr9:98835739 | CT | C | 10 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0091 others(7): Show |
10 | HG00639.hp1 HG01109.hp2 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.1035+387delT | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr9 | 98835739 | ||||||
| chr9:98835777 | C | G | 7 | a0001c0001t0001g0266 a0001c0001t0001g0304 a0001c0002t0002g0081 others(4): Show |
7 | HG01891.hp1 HG02897.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1035+411C>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 5/9 | chr9 | 98835777 | |||||||
| chr9:98835789 | G | A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(136): Show |
147 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(144): Show |
intron_variant | MODIFIER | c.1035+423G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 5/9 | chr9 | 98835789 | |||||||
| chr9:98835791 | A | G | 3 | a0001c0001t0001g0094 a0001c0001t0001g0164 a0001c0021t0001g0027 |
3 | HG02572.hp1 HG02622.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1035+425A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 5/9 | chr9 | 98835791 | |||||||
| chr9:98835802 | C | G | 154 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(151): Show |
166 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1035+436C>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 5/9 | chr9 | 98835802 | |||||||
| chr9:98835896 | C | T | 4 | a0001c0001t0001g0021 a0001c0001t0001g0109 a0001c0001t0001g0138 others(1): Show |
5 | HG00140.hp2 HG01255.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1035+530C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 5/9 | chr9 | 98835896 | |||||||
| chr9:98835924 | C | T | 11 | a0001c0001t0001g0216 a0001c0001t0001g0342 a0001c0001t0003g0009 others(8): Show |
12 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1035+558C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 5/9 | chr9 | 98835924 | |||||||
| chr9:98836136 | A | T | 1 | a0001c0001t0003g0248 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1035+770A>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 5/9 | chr9 | 98836136 | |||||||
| chr9:98836159 | T | A | 154 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0016 others(151): Show |
166 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.1035+793T>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 5/9 | chr9 | 98836159 | |||||||
| chr9:98836184 | C | T | 1 | a0002c0010t0002g0325 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1036-788C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 5/9 | chr9 | 98836184 | |||||||
| chr9:98836195 | G | A | 3 | a0001c0001t0001g0095 a0001c0001t0001g0102 a0001c0008t0001g0348 |
3 | HG02615.hp1 HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1036-777G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 5/9 | chr9 | 98836195 | |||||||
| chr9:98836322 | A | T | 30 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0135 others(27): Show |
36 | HG00408.hp2 HG00597.hp2 HG00673.hp1 others(33): Show |
intron_variant | MODIFIER | c.1036-650A>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 5/9 | chr9 | 98836322 | |||||||
| chr9:98836327 | G | A | 124 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0018 others(121): Show |
130 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.1036-645G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 5/9 | chr9 | 98836327 | |||||||
| chr9:98836457 | A | C | 3 | a0001c0001t0006g0083 a0001c0004t0006g0015 a0001c0019t0006g0015 |
3 | HG02615.hp2 HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1036-515A>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 5/9 | chr9 | 98836457 | |||||||
| chr9:98836528 | G | T | 10 | a0001c0001t0001g0345 a0001c0004t0001g0098 a0001c0004t0001g0099 others(7): Show |
10 | HG01081.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.1036-444G>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 5/9 | chr9 | 98836528 | |||||||
| chr9:98836686 | C | T | 1 | a0001c0002t0002g0207 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1036-286C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 5/9 | chr9 | 98836686 | |||||||
| chr9:98836768 | A | G | 10 | a0001c0001t0001g0216 a0001c0001t0001g0342 a0001c0001t0003g0009 others(7): Show |
11 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1036-204A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 5/9 | chr9 | 98836768 | |||||||
| chr9:98836824 | G | C | 2 | a0001c0001t0001g0087 a0001c0001t0001g0156 |
2 | HG01167.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.1036-148G>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 5/9 | chr9 | 98836824 | |||||||
| chr9:98836913 | T | C | 9 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(6): Show |
9 | HG02257.hp2 HG02451.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1036-59T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 5/9 | chr9 | 98836913 | |||||||
| chr9:98836929 | AT | A | 36 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0044 others(33): Show |
39 | HG00544.hp2 HG00609.hp1 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1036-42delT | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 5/9 | chr9 | 98836929 | |||||||
| chr9:98837276 | A | T | 141 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0034 others(138): Show |
151 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.1212+128A>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98837276 | |||||||
| chr9:98837326 | C | G | 142 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0034 others(139): Show |
152 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.1212+178C>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98837326 | |||||||
| chr9:98837444 | T | C | 2 | a0001c0001t0001g0059 a0001c0001t0001g0118 |
2 | NA18959.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1212+296T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98837444 | |||||||
| chr9:98837476 | A | G | 122 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0075 others(119): Show |
131 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.1212+328A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98837476 | |||||||
| chr9:98837497 | C | T | 7 | a0001c0001t0001g0117 a0001c0001t0001g0143 a0001c0001t0001g0227 others(4): Show |
7 | HG00280.hp2 HG02055.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.1212+349C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98837497 | |||||||
| chr9:98837645 | A | G | 95 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0075 others(92): Show |
99 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1212+497A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98837645 | |||||||
| chr9:98837649 | C | T | 33 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0009 others(30): Show |
39 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1212+501C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98837649 | |||||||
| chr9:98837652 | C | T | 130 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0075 others(127): Show |
140 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.1212+504C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98837652 | |||||||
| chr9:98837786 | A | C | 96 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0075 others(93): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1212+638A>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98837786 | |||||||
| chr9:98837788 | A | G | 96 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0075 others(93): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.1212+640A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98837788 | |||||||
| chr9:98837847 | G | C | 15 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(12): Show |
15 | HG01109.hp1 HG02257.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1212+699G>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98837847 | |||||||
| chr9:98837970 | T | C | 97 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0075 others(94): Show |
101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.1212+822T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98837970 | |||||||
| chr9:98838018 | G | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0343 |
2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1212+870G>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98838018 | |||||||
| chr9:98838131 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1212+983G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98838131 | |||||||
| chr9:98838168 | C | T | 4 | a0001c0001t0001g0143 a0001c0001t0001g0227 a0001c0001t0001g0288 others(1): Show |
4 | HG00280.hp2 HG02055.hp2 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.1212+1020C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98838168 | |||||||
| chr9:98838216 | C | T | 97 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0075 others(94): Show |
101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.1212+1068C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98838216 | |||||||
| chr9:98838418 | C | G | 2 | a0001c0001t0001g0090 a0001c0001t0001g0343 |
2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1212+1270C>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98838418 | |||||||
| chr9:98838619 | G | C | 1 | a0001c0001t0011g0278 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1213-1383G>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98838619 | |||||||
| chr9:98838793 | G | T | 1 | a0001c0001t0001g0060 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1213-1209G>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98838793 | |||||||
| chr9:98838897 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1213-1105G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98838897 | |||||||
| chr9:98839030 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1213-972T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98839030 | |||||||
| chr9:98839149 | G | C | 1 | a0005c0012t0001g0285 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1213-853G>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98839149 | |||||||
| chr9:98839150 | G | A | 17 | a0001c0001t0001g0106 a0001c0001t0001g0117 a0001c0001t0001g0143 others(14): Show |
17 | HG00280.hp2 HG01081.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1213-852G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98839150 | |||||||
| chr9:98839186 | C | T | 6 | a0001c0001t0006g0083 a0001c0001t0006g0104 a0001c0004t0006g0015 others(3): Show |
6 | HG01081.hp1 HG01891.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1213-816C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98839186 | |||||||
| chr9:98839288 | G | A | 1 | a0002c0003t0003g0273 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1213-714G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98839288 | |||||||
| chr9:98839363 | T | C | 81 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0075 others(78): Show |
85 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.1213-639T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98839363 | |||||||
| chr9:98839485 | A | G | 2 | a0001c0001t0001g0275 a0008c0015t0001g0259 |
2 | NA19084.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1213-517A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98839485 | |||||||
| chr9:98839556 | G | A | 17 | a0001c0001t0001g0106 a0001c0001t0001g0117 a0001c0001t0001g0143 others(14): Show |
17 | HG00280.hp2 HG01081.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.1213-446G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98839556 | |||||||
| chr9:98839606 | G | A | 29 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0135 others(26): Show |
35 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1213-396G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98839606 | |||||||
| chr9:98839700 | C | CA | 17 | a0001c0001t0004g0028 a0001c0001t0004g0061 a0001c0001t0004g0153 others(14): Show |
18 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.1213-301dupA | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr9 | 98839700 | ||||||
| chr9:98839889 | C | G | 145 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(142): Show |
156 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.1213-113C>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98839889 | |||||||
| chr9:98839975 | G | A | 1 | a0001c0004t0001g0344 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1213-27G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 6/9 | chr9 | 98839975 | |||||||
| chr9:98840194 | G | T | 17 | a0001c0001t0004g0028 a0001c0001t0004g0061 a0001c0001t0004g0153 others(14): Show |
18 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.1344+61G>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98840194 | |||||||
| chr9:98840262 | A | AC | 19 | a0001c0001t0001g0110 a0001c0001t0001g0288 a0001c0001t0004g0028 others(16): Show |
20 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.1344+135dupC | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr9 | 98840262 | ||||||
| chr9:98840424 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1344+291C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98840424 | |||||||
| chr9:98840615 | G | C | 8 | a0001c0001t0003g0009 a0001c0001t0003g0077 a0001c0001t0003g0121 others(5): Show |
9 | HG01243.hp2 HG01884.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1344+482G>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98840615 | |||||||
| chr9:98840661 | C | T | 2 | a0001c0004t0006g0015 a0001c0019t0006g0015 |
2 | HG02615.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1344+528C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98840661 | |||||||
| chr9:98840662 | C | T | 37 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0135 others(34): Show |
44 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.1344+529C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98840662 | |||||||
| chr9:98840683 | A | G | 1 | a0001c0001t0001g0044 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1344+550A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98840683 | |||||||
| chr9:98840743 | G | C | 143 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(140): Show |
153 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.1344+610G>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98840743 | |||||||
| chr9:98840910 | A | C | 1 | a0001c0001t0001g0343 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1344+777A>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98840910 | |||||||
| chr9:98841052 | G | A | 37 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0135 others(34): Show |
44 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.1344+919G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98841052 | |||||||
| chr9:98841240 | A | T | 1 | a0001c0002t0002g0046 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1344+1107A>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98841240 | |||||||
| chr9:98841284 | T | A | 3 | a0001c0002t0002g0240 a0001c0002t0002g0242 a0001c0004t0001g0229 |
3 | HG01109.hp1 HG02723.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1344+1151T>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98841284 | |||||||
| chr9:98841430 | C | T | 142 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(139): Show |
152 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.1344+1297C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98841430 | |||||||
| chr9:98841501 | C | A | 10 | a0001c0001t0001g0106 a0001c0001t0001g0117 a0001c0001t0001g0143 others(7): Show |
10 | HG00280.hp2 HG02055.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.1344+1368C>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98841501 | |||||||
| chr9:98841663 | C | T | 1 | a0001c0002t0002g0054 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1344+1530C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98841663 | |||||||
| chr9:98841672 | C | CT | 7 | a0001c0001t0001g0034 a0001c0001t0001g0216 a0001c0001t0001g0342 others(4): Show |
7 | HG00423.hp1 HG01109.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1344+1553dupT | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr9 | 98841672 | ||||||
| chr9:98841732 | G | A | 8 | a0001c0004t0001g0098 a0001c0004t0001g0099 a0001c0004t0001g0101 others(5): Show |
8 | HG01081.hp2 HG02257.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.1344+1599G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98841732 | |||||||
| chr9:98841765 | G | A | 1 | a0001c0002t0002g0139 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1344+1632G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98841765 | |||||||
| chr9:98841974 | G | A | 1 | a0001c0001t0003g0004 | 2 | HG01099.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1344+1841G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98841974 | |||||||
| chr9:98842071 | GT | G | 299 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(296): Show |
321 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.1344+1949delT | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr9 | 98842071 | ||||||
| chr9:98842249 | T | C | 98 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0075 others(95): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1345-1847T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98842249 | |||||||
| chr9:98842363 | T | C | 100 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0075 others(97): Show |
104 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1345-1733T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98842363 | |||||||
| chr9:98842386 | G | A | 1 | a0001c0001t0003g0086 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1345-1710G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98842386 | |||||||
| chr9:98842466 | G | A | 25 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0020 others(22): Show |
30 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.1345-1630G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98842466 | |||||||
| chr9:98842579 | T | A | 1 | a0001c0001t0001g0087 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1345-1517T>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98842579 | |||||||
| chr9:98842670 | T | C | 1 | a0001c0001t0001g0023 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1345-1426T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98842670 | |||||||
| chr9:98842763 | T | C | 1 | a0001c0001t0001g0343 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1345-1333T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98842763 | |||||||
| chr9:98842808 | T | TA | 87 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0107 others(84): Show |
90 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.1345-1279dupA | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr9 | 98842808 | ||||||
| chr9:98842808 | T | TAA | 8 | a0001c0001t0001g0117 a0001c0001t0001g0143 a0001c0001t0001g0227 others(5): Show |
8 | HG00280.hp2 HG02055.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.1345-1280_1345-127 others(6): Show |
GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr9 | 98842808 | ||||||
| chr9:98842914 | C | CT | 4 | a0001c0002t0002g0081 a0001c0002t0002g0151 a0001c0002t0002g0198 others(1): Show |
4 | HG01891.hp1 HG02897.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1345-1176dupT | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr9 | 98842914 | ||||||
| chr9:98842959 | A | G | 1 | a0001c0002t0002g0299 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1345-1137A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98842959 | |||||||
| chr9:98842967 | T | C | 95 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0107 others(92): Show |
98 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1345-1129T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98842967 | |||||||
| chr9:98843494 | T | C | 1 | a0001c0001t0001g0343 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1345-602T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98843494 | |||||||
| chr9:98843524 | A | G | 2 | a0001c0001t0003g0172 a0001c0001t0003g0173 |
2 | NA18971.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.1345-572A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98843524 | |||||||
| chr9:98843531 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1345-565C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98843531 | |||||||
| chr9:98843607 | G | A | 147 | a0001c0001t0001g0037 a0001c0001t0001g0090 a0001c0001t0001g0106 others(144): Show |
157 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(154): Show |
intron_variant | MODIFIER | c.1345-489G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98843607 | |||||||
| chr9:98843661 | T | C | 321 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(318): Show |
343 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(340): Show |
intron_variant | MODIFIER | c.1345-435T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98843661 | |||||||
| chr9:98843762 | T | G | 1 | a0001c0001t0001g0187 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1345-334T>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98843762 | |||||||
| chr9:98843981 | G | A | 1 | a0001c0001t0001g0343 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1345-115G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 7/9 | chr9 | 98843981 | |||||||
| chr9:98844267 | G | T | 294 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(291): Show |
315 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.1458+58G>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 8/9 | chr9 | 98844267 | |||||||
| chr9:98844337 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1458+128A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 8/9 | chr9 | 98844337 | |||||||
| chr9:98844375 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1458+166C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 8/9 | chr9 | 98844375 | |||||||
| chr9:98844376 | A | G | 1 | a0001c0002t0002g0301 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1458+167A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 8/9 | chr9 | 98844376 | |||||||
| chr9:98844398 | C | T | 96 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0107 others(93): Show |
99 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(96): Show |
intron_variant | MODIFIER | c.1458+189C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 8/9 | chr9 | 98844398 | |||||||
| chr9:98844671 | C | T | 82 | a0001c0001t0001g0037 a0001c0001t0001g0107 a0001c0001t0001g0176 others(79): Show |
85 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1458+462C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 8/9 | chr9 | 98844671 | |||||||
| chr9:98844682 | A | G | 1 | a0001c0001t0011g0278 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1458+473A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 8/9 | chr9 | 98844682 | |||||||
| chr9:98844685 | G | C | 17 | a0001c0001t0004g0028 a0001c0001t0004g0061 a0001c0001t0004g0153 others(14): Show |
18 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.1458+476G>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 8/9 | chr9 | 98844685 | |||||||
| chr9:98844848 | C | T | 33 | a0001c0001t0003g0001 a0001c0001t0003g0007 a0001c0001t0003g0009 others(30): Show |
39 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.1458+639C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 8/9 | chr9 | 98844848 | |||||||
| chr9:98844965 | A | G | 95 | a0001c0001t0001g0037 a0001c0001t0001g0106 a0001c0001t0001g0107 others(92): Show |
98 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.1458+756A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 8/9 | chr9 | 98844965 | |||||||
| chr9:98845139 | C | A | 1 | a0001c0001t0001g0343 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1459-838C>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 8/9 | chr9 | 98845139 | |||||||
| chr9:98845259 | A | G | 39 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0135 others(36): Show |
46 | HG00544.hp1 HG00544.hp2 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.1459-718A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 8/9 | chr9 | 98845259 | |||||||
| chr9:98845334 | T | A | 10 | a0001c0001t0001g0106 a0001c0001t0001g0117 a0001c0001t0001g0143 others(7): Show |
10 | HG00280.hp2 HG02055.hp2 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.1459-643T>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 8/9 | chr9 | 98845334 | |||||||
| chr9:98845343 | A | C | 1 | a0001c0001t0001g0100 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1459-634A>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 8/9 | chr9 | 98845343 | |||||||
| chr9:98845439 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1459-538C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 8/9 | chr9 | 98845439 | |||||||
| chr9:98845650 | T | A | 19 | a0001c0001t0001g0109 a0001c0001t0004g0028 a0001c0001t0004g0061 others(16): Show |
20 | HG00621.hp1 HG00621.hp2 HG00639.hp2 others(17): Show |
intron_variant | MODIFIER | c.1459-327T>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 8/9 | chr9 | 98845650 | |||||||
| chr9:98845743 | C | A | 75 | a0001c0001t0001g0037 a0001c0001t0001g0107 a0001c0001t0001g0176 others(72): Show |
78 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.1459-234C>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 8/9 | chr9 | 98845743 | |||||||
| chr9:98845761 | G | A | 14 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(11): Show |
14 | HG02257.hp2 HG02451.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1459-216G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 8/9 | chr9 | 98845761 | |||||||
| chr9:98845872 | T | A | 9 | a0001c0004t0001g0098 a0001c0004t0001g0099 a0001c0004t0001g0101 others(6): Show |
9 | HG01081.hp2 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.1459-105T>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 8/9 | chr9 | 98845872 | |||||||
| chr9:98846127 | G | A | 3 | a0001c0001t0006g0083 a0001c0004t0006g0015 a0001c0019t0006g0015 |
3 | HG02615.hp2 HG03195.hp1 HG03540.hp1 |
splice_region_variant&intron_variant | LOW | c.1605+4G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98846127 | |||||||
| chr9:98846192 | C | T | 1 | a0002c0005t0002g0286 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1605+69C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98846192 | |||||||
| chr9:98846315 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1605+192C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98846315 | |||||||
| chr9:98846361 | C | A | 1 | a0001c0001t0001g0129 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1605+238C>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98846361 | |||||||
| chr9:98846361 | C | T | 14 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(11): Show |
14 | HG02257.hp2 HG02451.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1605+238C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98846361 | |||||||
| chr9:98846453 | A | G | 39 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0135 others(36): Show |
47 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.1605+330A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98846453 | |||||||
| chr9:98846480 | G | C | 1 | a0001c0001t0001g0129 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1605+357G>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98846480 | |||||||
| chr9:98846481 | C | G | 1 | a0001c0001t0001g0129 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1605+358C>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98846481 | |||||||
| chr9:98846568 | A | T | 1 | a0001c0001t0001g0082 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1605+445A>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98846568 | |||||||
| chr9:98846643 | C | T | 4 | a0001c0001t0001g0168 a0001c0001t0001g0175 a0001c0001t0001g0187 others(1): Show |
4 | HG03704.hp2 HG04115.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1605+520C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98846643 | |||||||
| chr9:98846698 | T | TA | 307 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(304): Show |
329 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.1605+586dupA | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 98846698 | ||||||
| chr9:98846724 | G | A | 1 | a0001c0002t0002g0299 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1605+601G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98846724 | |||||||
| chr9:98846822 | A | C | 1 | a0001c0001t0001g0182 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1605+699A>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98846822 | |||||||
| chr9:98846856 | C | CA | 201 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(198): Show |
220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1605+752dupA | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 98846856 | ||||||
| chr9:98846856 | C | CAA | 80 | a0001c0001t0001g0033 a0001c0001t0001g0076 a0001c0001t0001g0092 others(77): Show |
83 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1605+751_1605+752d others(4): Show |
GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 98846856 | ||||||
| chr9:98846856 | CA | C | 11 | a0001c0001t0001g0106 a0001c0001t0001g0117 a0001c0001t0001g0143 others(8): Show |
11 | HG00280.hp2 HG02055.hp2 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1605+752delA | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 98846856 | ||||||
| chr9:98846917 | A | G | 39 | a0001c0001t0001g0012 a0001c0001t0001g0040 a0001c0001t0001g0135 others(36): Show |
47 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(44): Show |
intron_variant | MODIFIER | c.1605+794A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98846917 | |||||||
| chr9:98846986 | C | G | 6 | a0001c0001t0006g0083 a0001c0001t0006g0104 a0001c0004t0006g0015 others(3): Show |
6 | HG01081.hp1 HG01891.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.1605+863C>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98846986 | |||||||
| chr9:98847017 | T | C | 312 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(309): Show |
334 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(331): Show |
intron_variant | MODIFIER | c.1605+894T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98847017 | |||||||
| chr9:98847053 | T | A | 1 | a0001c0001t0001g0090 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1605+930T>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98847053 | |||||||
| chr9:98847090 | C | T | 1 | a0001c0006t0008g0214 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1605+967C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98847090 | |||||||
| chr9:98847109 | T | G | 8 | a0001c0001t0001g0343 a0001c0001t0006g0083 a0001c0001t0006g0104 others(5): Show |
8 | HG01081.hp1 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1605+986T>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98847109 | |||||||
| chr9:98847165 | A | G | 1 | a0001c0002t0002g0042 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1605+1042A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98847165 | |||||||
| chr9:98847347 | G | A | 123 | a0001c0001t0001g0106 a0001c0001t0001g0117 a0001c0001t0001g0143 others(120): Show |
133 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(130): Show |
intron_variant | MODIFIER | c.1605+1224G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98847347 | |||||||
| chr9:98847405 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1605+1282C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98847405 | |||||||
| chr9:98847424 | T | C | 70 | a0001c0002t0002g0006 a0001c0002t0002g0010 a0001c0002t0002g0025 others(67): Show |
73 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.1605+1301T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98847424 | |||||||
| chr9:98847486 | T | G | 81 | a0001c0001t0001g0106 a0001c0001t0001g0117 a0001c0001t0001g0143 others(78): Show |
84 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.1605+1363T>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98847486 | |||||||
| chr9:98847548 | C | A | 63 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0012 others(60): Show |
68 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.1606-1404C>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98847548 | |||||||
| chr9:98847613 | C | T | 2 | a0001c0002t0002g0131 a0001c0002t0002g0137 |
2 | HG00673.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1606-1339C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98847613 | |||||||
| chr9:98847709 | A | T | 1 | a0001c0001t0001g0343 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1606-1243A>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98847709 | |||||||
| chr9:98847780 | A | G | 1 | a0001c0001t0003g0197 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1606-1172A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98847780 | |||||||
| chr9:98847811 | C | CT | 36 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0039 others(33): Show |
37 | HG00558.hp2 HG00621.hp1 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.1606-1119dupT | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 98847811 | ||||||
| chr9:98847811 | CT | C | 38 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(35): Show |
38 | HG00423.hp2 HG01081.hp2 HG02135.hp1 others(35): Show |
intron_variant | MODIFIER | c.1606-1119delT | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 98847811 | ||||||
| chr9:98847811 | CTT | C | 109 | a0001c0001t0001g0106 a0001c0001t0001g0117 a0001c0001t0001g0143 others(106): Show |
119 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.1606-1120_1606-111 others(6): Show |
GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 98847811 | ||||||
| chr9:98847817 | T | C | 7 | a0001c0002t0002g0066 a0001c0002t0002g0112 a0001c0002t0002g0154 others(4): Show |
7 | HG00423.hp2 HG02135.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.1606-1135T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98847817 | |||||||
| chr9:98847818 | T | C | 73 | a0001c0001t0001g0106 a0001c0001t0001g0117 a0001c0001t0001g0143 others(70): Show |
76 | HG00280.hp2 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.1606-1134T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98847818 | |||||||
| chr9:98847819 | T | C | 1 | a0001c0002t0002g0198 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1606-1133T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98847819 | |||||||
| chr9:98847922 | C | A | 1 | a0001c0001t0003g0004 | 2 | HG01099.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.1606-1030C>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98847922 | |||||||
| chr9:98847969 | C | T | 8 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(5): Show |
8 | HG02257.hp2 HG02451.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1606-983C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98847969 | |||||||
| chr9:98848061 | T | C | 2 | a0002c0003t0001g0287 a0005c0012t0001g0285 |
2 | HG03834.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1606-891T>C | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98848061 | |||||||
| chr9:98848100 | C | A | 1 | a0001c0001t0001g0289 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1606-852C>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98848100 | |||||||
| chr9:98848150 | A | G | 1 | a0002c0003t0001g0274 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1606-802A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98848150 | |||||||
| chr9:98848230 | C | T | 81 | a0001c0001t0001g0106 a0001c0001t0001g0117 a0001c0001t0001g0143 others(78): Show |
84 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.1606-722C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98848230 | |||||||
| chr9:98848241 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1606-711C>T | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98848241 | |||||||
| chr9:98848246 | ATGT | A | 4 | a0001c0001t0001g0113 a0001c0001t0001g0346 a0001c0004t0001g0142 others(1): Show |
4 | HG02630.hp1 HG02922.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1606-701_1606-699d others(5): Show |
GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr9 | 98848246 | ||||||
| chr9:98848265 | C | G | 3 | a0001c0001t0003g0007 a0001c0001t0003g0089 a0002c0003t0003g0273 |
4 | NA18945.hp2 NA18970.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.1606-687C>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98848265 | |||||||
| chr9:98848277 | C | G | 35 | a0001c0001t0003g0001 a0001c0001t0003g0004 a0001c0001t0003g0007 others(32): Show |
42 | HG00544.hp2 HG00597.hp2 HG00673.hp1 others(39): Show |
intron_variant | MODIFIER | c.1606-675C>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98848277 | |||||||
| chr9:98848313 | A | G | 4 | a0001c0001t0001g0113 a0001c0001t0001g0346 a0001c0004t0001g0142 others(1): Show |
4 | HG02630.hp1 HG02922.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1606-639A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98848313 | |||||||
| chr9:98848604 | A | G | 4 | a0001c0001t0003g0048 a0001c0001t0003g0172 a0001c0001t0003g0173 others(1): Show |
4 | HG00544.hp2 HG02155.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.1606-348A>G | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98848604 | |||||||
| chr9:98848660 | G | A | 6 | a0001c0001t0003g0007 a0001c0001t0003g0047 a0001c0001t0003g0089 others(3): Show |
7 | HG02132.hp1 NA18945.hp2 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1606-292G>A | GALNT12 | ENSG00000119514.7 | transcript | ENST00000375011.4 | protein_coding | 9/9 | chr9 | 98848660 |