Item | Value |
---|---|
geneid | 91039 |
ensemblid | ENSG00000142002.19 |
hgncid | 18648 |
symbol | DPP9 |
name | dipeptidyl peptidase 9 |
refseq_nuc | NM_139159.5 |
refseq_prot | NP_631898.3 |
ensembl_nuc | ENST00000262960.14 |
ensembl_prot | ENSP00000262960.8 |
mane_status | MANE Select |
chr | chr19 |
start | 4675227 |
end | 4723842 |
strand | - |
ver | v1.2 |
region | chr19:4675227-4723842 |
region5000 | chr19:4670227-4728842 |
regionname0 | DPP9_chr19_4675227_4723842 |
regionname5000 | DPP9_chr19_4670227_4728842 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 892 | 302 | 87 | 72 | 87 | 13 | 41 | 64 | DPP9_chr19_4670227_4728842 | DPP9 | MRKVK others(887): Show |
chr19 | 4670227 | 4728842 |
a0002 | 0/0 | 892 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | MRKVK others(887): Show |
chr19 | 4670227 | 4728842 |
a0003 | 0/0 | 892 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | MRKVK others(887): Show |
chr19 | 4670227 | 4728842 |
a0004 | 0/0 | 892 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | MRKVK others(887): Show |
chr19 | 4670227 | 4728842 |
a0005 | 0/0 | 892 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | MRKVK others(887): Show |
chr19 | 4670227 | 4728842 |
a0006 | 0/0 | 892 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | MRKVK others(887): Show |
chr19 | 4670227 | 4728842 |
a0007 | 0/0 | 892 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | MRKVK others(887): Show |
chr19 | 4670227 | 4728842 |
a0008 | 0/0 | 892 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | MRKVK others(887): Show |
chr19 | 4670227 | 4728842 |
a0009 | 0/0 | 892 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | MRKVK others(887): Show |
chr19 | 4670227 | 4728842 |
a0010 | 0/0 | 892 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | MRKVK others(887): Show |
chr19 | 4670227 | 4728842 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2676 | 261 | 60 | 68 | 77 | 13 | 41 | DPP9_chr19_4670227_4728842 | DPP9 | ATGCG others(2671): Show |
chr19 | 4670227 | 4728842 | ||
a0001c0002 | 0/0 | 2676 | 19 | 18 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | ATGCG others(2671): Show |
chr19 | 4670227 | 4728842 | ||
a0001c0003 | 0/0 | 2676 | 7 | 6 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | ATGCG others(2671): Show |
chr19 | 4670227 | 4728842 | ||
a0001c0004 | 0/0 | 2676 | 6 | 0 | 0 | 6 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | ATGCG others(2671): Show |
chr19 | 4670227 | 4728842 | ||
a0001c0007 | 0/0 | 2676 | 2 | 0 | 0 | 2 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | ATGCG others(2671): Show |
chr19 | 4670227 | 4728842 | ||
a0001c0009 | 0/0 | 2676 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | ATGCG others(2671): Show |
chr19 | 4670227 | 4728842 | ||
a0001c0010 | 0/0 | 2676 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | ATGCG others(2671): Show |
chr19 | 4670227 | 4728842 | ||
a0001c0013 | 0/0 | 2676 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | ATGCG others(2671): Show |
chr19 | 4670227 | 4728842 | ||
a0001c0014 | 0/0 | 2676 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | ATGCG others(2671): Show |
chr19 | 4670227 | 4728842 | ||
a0001c0015 | 0/0 | 2676 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | ATGCG others(2671): Show |
chr19 | 4670227 | 4728842 | ||
a0001c0016 | 0/0 | 2676 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | ATGCG others(2671): Show |
chr19 | 4670227 | 4728842 | ||
a0001c0018 | 0/0 | 2676 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | ATGCG others(2671): Show |
chr19 | 4670227 | 4728842 | ||
a0002c0005 | 0/0 | 2676 | 3 | 3 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | ATGCG others(2671): Show |
chr19 | 4670227 | 4728842 | ||
a0003c0006 | 0/0 | 2676 | 2 | 0 | 2 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | ATGCG others(2671): Show |
chr19 | 4670227 | 4728842 | ||
a0004c0019 | 0/0 | 2676 | 1 | 0 | 0 | 0 | 1 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | ATGCG others(2671): Show |
chr19 | 4670227 | 4728842 | ||
a0005c0017 | 0/0 | 2676 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | ATGCG others(2671): Show |
chr19 | 4670227 | 4728842 | ||
a0006c0020 | 0/0 | 2676 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | ATGCG others(2671): Show |
chr19 | 4670227 | 4728842 | ||
a0007c0012 | 0/0 | 2676 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | ATGCG others(2671): Show |
chr19 | 4670227 | 4728842 | ||
a0008c0021 | 0/0 | 2676 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | ATGCG others(2671): Show |
chr19 | 4670227 | 4728842 | ||
a0009c0011 | 0/0 | 2676 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | ATGCG others(2671): Show |
chr19 | 4670227 | 4728842 | ||
a0010c0008 | 0/0 | 2676 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | ATGCG others(2671): Show |
chr19 | 4670227 | 4728842 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 4273 | 153 | 19 | 48 | 50 | 7 | 27 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0001c0001t0002 | 0/0 | 4273 | 46 | 26 | 6 | 9 | 3 | 2 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0001c0001t0003 | 0/0 | 4273 | 24 | 7 | 0 | 17 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0001c0001t0004 | 0/0 | 4274 | 24 | 2 | 11 | 0 | 3 | 8 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4269): Show |
chr19 | 4670227 | 4728842 |
a0001c0001t0005 | 0/0 | 4273 | 5 | 4 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0001c0001t0007 | 0/0 | 4273 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0001c0001t0008 | 0/0 | 4273 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0001c0001t0009 | 0/0 | 4273 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0001c0001t0012 | 0/0 | 4273 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0001c0001t0013 | 0/0 | 4273 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0001c0001t0015 | 0/0 | 4274 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4269): Show |
chr19 | 4670227 | 4728842 |
a0001c0001t0016 | 0/0 | 4274 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4269): Show |
chr19 | 4670227 | 4728842 |
a0001c0001t0017 | 0/0 | 4274 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4269): Show |
chr19 | 4670227 | 4728842 |
a0001c0001t0018 | 0/0 | 4273 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0001c0002t0002 | 0/0 | 4273 | 16 | 15 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0001c0002t0005 | 0/0 | 4273 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0001c0002t0014 | 0/0 | 4273 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0001c0002t0019 | 0/0 | 4273 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0001c0003t0001 | 0/0 | 4273 | 5 | 4 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0001c0003t0002 | 0/0 | 4273 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0001c0003t0011 | 0/0 | 4273 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0001c0004t0003 | 0/0 | 4273 | 6 | 0 | 0 | 6 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0001c0007t0003 | 0/0 | 4273 | 2 | 0 | 0 | 2 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0001c0009t0001 | 0/0 | 4273 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0001c0010t0004 | 0/0 | 4274 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4269): Show |
chr19 | 4670227 | 4728842 |
a0001c0013t0001 | 0/0 | 4273 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0001c0014t0004 | 0/0 | 4274 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4269): Show |
chr19 | 4670227 | 4728842 |
a0001c0015t0001 | 0/0 | 4273 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0001c0016t0001 | 0/0 | 4273 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0001c0018t0010 | 0/0 | 4273 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0002c0005t0006 | 0/0 | 4273 | 3 | 3 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0003c0006t0001 | 0/0 | 4273 | 2 | 0 | 2 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0004c0019t0007 | 0/0 | 4273 | 1 | 0 | 0 | 0 | 1 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0005c0017t0001 | 0/0 | 4273 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0006c0020t0001 | 0/0 | 4273 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0007c0012t0001 | 0/0 | 4273 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0008c0021t0001 | 0/0 | 4273 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0009c0011t0002 | 0/0 | 4273 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
a0010c0008t0003 | 0/0 | 4273 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | AACTT others(4268): Show |
chr19 | 4670227 | 4728842 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0200 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0001g0310 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0004g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0004g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0004g0010 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0004g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0004g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0004g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0004g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0004g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0004g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0004g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0005g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0005g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0005g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0007g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0008g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0009g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0012g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0013g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0015g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0016g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0017g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0001t0018g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0002t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0002t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0002t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0002t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0002t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0002t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0002t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0002t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0002t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0002t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0002t0014g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0002t0019g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0003t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0003t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0003t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0003t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0003t0011g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0004t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0004t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0004t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0004t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0004t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0004t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0007t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0007t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0009t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0010t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0013t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0014t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0015t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0016t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0001c0018t0010g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0002c0005t0006g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0002c0005t0006g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0002c0005t0006g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0003c0006t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0003c0006t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0004c0019t0007g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0005c0017t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0006c0020t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0007c0012t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0008c0021t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0009c0011t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
a0010c0008t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0001 | g0285 | EUR | FIN | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0269 | EUR | FIN | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG00323 | hp1 | a0004 | c0019 | t0007 | g0312 | EUR | FIN | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0211 | EUR | FIN | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG00597 | hp1 | a0001 | c0004 | t0003 | g0111 | EAS | CHS | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG00609 | hp2 | a0001 | c0007 | t0003 | g0166 | EAS | CHS | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG00621 | hp1 | a0005 | c0017 | t0001 | g0307 | EAS | CHS | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0255 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0253 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01070 | hp1 | a0001 | c0001 | t0013 | g0156 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01109 | hp1 | a0001 | c0002 | t0002 | g0245 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01167 | hp1 | a0001 | c0001 | t0009 | g0062 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0258 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01168 | hp2 | a0001 | c0001 | t0004 | g0012 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0008 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01243 | hp1 | a0001 | c0001 | t0005 | g0007 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01255 | hp2 | a0001 | c0003 | t0001 | g0143 | AMR | CLM | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | CLM | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | CLM | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0176 | AMR | CLM | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01361 | hp1 | a0003 | c0006 | t0001 | g0199 | AMR | CLM | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0281 | AMR | CLM | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0280 | AMR | CLM | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0256 | EUR | IBS | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0155 | EUR | IBS | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0267 | EUR | IBS | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01516 | hp2 | a0001 | c0001 | t0004 | g0009 | EUR | IBS | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01517 | hp1 | a0001 | c0001 | t0004 | g0010 | EUR | IBS | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0254 | EUR | IBS | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0127 | AFR | ACB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0089 | AFR | ACB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01891 | hp1 | a0001 | c0003 | t0002 | g0144 | AFR | ACB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01891 | hp2 | a0002 | c0005 | t0006 | g0022 | AFR | ACB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01928 | hp1 | a0006 | c0020 | t0001 | g0208 | AMR | PEL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01928 | hp2 | a0001 | c0001 | t0004 | g0177 | AMR | PEL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0259 | AMR | PEL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PEL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PEL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01975 | hp1 | a0003 | c0006 | t0001 | g0198 | AMR | PEL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01975 | hp2 | a0001 | c0001 | t0004 | g0190 | AMR | PEL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01978 | hp1 | a0001 | c0001 | t0004 | g0175 | AMR | PEL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01993 | hp1 | a0007 | c0012 | t0001 | g0202 | AMR | PEL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG01993 | hp2 | a0001 | c0001 | t0004 | g0178 | AMR | PEL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | KHV | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02040 | hp1 | a0001 | c0004 | t0003 | g0130 | EAS | KHV | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02055 | hp2 | a0001 | c0002 | t0002 | g0237 | AFR | ACB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | KHV | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02071 | hp1 | a0001 | c0016 | t0001 | g0179 | EAS | KHV | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | KHV | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02132 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | KHV | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0064 | AFR | ACB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0115 | AMR | PEL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02155 | hp1 | a0001 | c0004 | t0003 | g0040 | EAS | CDX | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | CDX | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CDX | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | CDX | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | ACB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | ACB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02258 | hp2 | a0001 | c0002 | t0002 | g0006 | AFR | ACB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | PEL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02273 | hp2 | a0001 | c0010 | t0004 | g0162 | AMR | PEL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ACB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02280 | hp2 | a0001 | c0001 | t0005 | g0085 | AFR | ACB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02293 | hp2 | a0001 | c0014 | t0004 | g0189 | AMR | PEL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0128 | AMR | PEL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | ACB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0063 | SAS | PJL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | PJL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0304 | AFR | GWD | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02622 | hp1 | a0001 | c0002 | t0002 | g0242 | AFR | GWD | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | GWD | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02630 | hp2 | a0001 | c0002 | t0002 | g0129 | AFR | GWD | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02647 | hp2 | a0001 | c0002 | t0019 | g0024 | AFR | GWD | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0138 | SAS | PJL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02717 | hp2 | a0001 | c0003 | t0001 | g0053 | AFR | GWD | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | GWD | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02735 | hp1 | a0008 | c0021 | t0001 | g0154 | SAS | PJL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02738 | hp2 | a0001 | c0001 | t0004 | g0091 | SAS | PJL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02809 | hp1 | a0001 | c0002 | t0002 | g0244 | AFR | GWD | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02818 | hp1 | a0001 | c0002 | t0002 | g0047 | AFR | GWD | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0260 | AFR | GWD | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0092 | AFR | GWD | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02895 | hp1 | a0001 | c0002 | t0002 | g0033 | AFR | GWD | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02895 | hp2 | a0001 | c0002 | t0002 | g0243 | AFR | GWD | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02922 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | ESN | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ESN | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02965 | hp1 | a0001 | c0001 | t0008 | g0305 | AFR | ESN | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0232 | AFR | ESN | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02970 | hp1 | a0002 | c0005 | t0006 | g0021 | AFR | ESN | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ESN | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0240 | AFR | ESN | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02976 | hp2 | a0001 | c0002 | t0014 | g0157 | AFR | ESN | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | PJL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0026 | AFR | GWD | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0045 | AFR | MSL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0249 | AFR | MSL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | ESN | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03139 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | ESN | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | ESN | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | MSL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03209 | hp2 | a0001 | c0002 | t0002 | g0238 | AFR | MSL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | MSL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03225 | hp2 | a0002 | c0005 | t0006 | g0023 | AFR | MSL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03239 | hp1 | a0001 | c0001 | t0004 | g0140 | SAS | PJL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | PJL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0126 | AFR | MSL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03486 | hp2 | a0001 | c0018 | t0010 | g0233 | AFR | MSL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03491 | hp1 | a0001 | c0001 | t0007 | g0311 | SAS | PJL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03516 | hp1 | a0001 | c0003 | t0011 | g0299 | AFR | ESN | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03516 | hp2 | a0001 | c0003 | t0001 | g0146 | AFR | ESN | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | GWD | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03579 | hp1 | a0001 | c0002 | t0005 | g0049 | AFR | MSL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | MSL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03669 | hp2 | a0001 | c0001 | t0015 | g0139 | SAS | PJL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03688 | hp1 | a0001 | c0001 | t0016 | g0296 | SAS | STU | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03688 | hp2 | a0001 | c0001 | t0004 | g0137 | SAS | STU | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | BEB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03834 | hp2 | a0001 | c0001 | t0018 | g0112 | SAS | BEB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03927 | hp1 | a0001 | c0001 | t0004 | g0114 | SAS | BEB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | BEB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | BEB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG04115 | hp1 | a0001 | c0001 | t0004 | g0206 | SAS | STU | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0288 | SAS | STU | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0212 | SAS | BEB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | STU | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | STU | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | YRI | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18522 | hp2 | a0001 | c0013 | t0001 | g0230 | AFR | YRI | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18906 | hp1 | a0001 | c0002 | t0002 | g0048 | AFR | YRI | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0235 | AFR | YRI | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0101 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0106 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18967 | hp1 | a0009 | c0011 | t0002 | g0195 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18967 | hp2 | a0010 | c0008 | t0003 | g0070 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18970 | hp2 | a0001 | c0007 | t0003 | g0213 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18973 | hp2 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18974 | hp2 | a0001 | c0004 | t0003 | g0080 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18979 | hp2 | a0001 | c0009 | t0001 | g0271 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18998 | hp2 | a0001 | c0004 | t0003 | g0107 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | LWK | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | LWK | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19043 | hp1 | a0001 | c0015 | t0001 | g0309 | AFR | LWK | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19043 | hp2 | a0001 | c0001 | t0005 | g0025 | AFR | LWK | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19086 | hp2 | a0001 | c0001 | t0012 | g0060 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19090 | hp1 | a0001 | c0004 | t0003 | g0108 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0065 | AFR | YRI | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA19240 | hp2 | a0001 | c0001 | t0017 | g0234 | AFR | YRI | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA20129 | hp1 | a0001 | c0003 | t0001 | g0145 | AFR | ASW | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0262 | AFR | ASW | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0041 | EUR | TSI | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0229 | EUR | TSI | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | TSI | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA20805 | hp2 | a0001 | c0001 | t0004 | g0252 | EUR | TSI | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA20905 | hp1 | a0001 | c0001 | t0004 | g0011 | SAS | GIH | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | GIH | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0056 | AFR | ACB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | ACB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02486 | hp1 | a0001 | c0002 | t0002 | g0046 | AFR | ACB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG06807 | hp1 | a0001 | c0002 | t0002 | g0054 | AFR | USA | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | USA | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA20300 | hp1 | a0001 | c0002 | t0002 | g0055 | AFR | USA | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0093 | AFR | USA | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0310 | REF | REF | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0200 | REF | REF | DPP9_chr19_4670227_4728842 | DPP9 | chr19 | 4670227 | 4728842 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4682832 | T | C | 1 | a0002 | 3 | HG01891.hp2 HG02970.hp1 HG03225.hp2 |
missense_variant | MODERATE | c.2338A>G | p.Ile780Val | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/22 | 2595/4273 | 2338/2679 | 780/892 | chr19 | 4682832 | |||
chr19:4689617 | C | T | 1 | a0006 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.1702G>A | p.Val568Ile | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 15/22 | 1959/4273 | 1702/2679 | 568/892 | chr19 | 4689617 | |||
chr19:4689707 | C | T | 1 | a0007 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.1612G>A | p.Glu538Lys | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 15/22 | 1869/4273 | 1612/2679 | 538/892 | chr19 | 4689707 | |||
chr19:4695473 | C | G | 1 | a0009 | 1 | NA18967.hp1 | missense_variant | MODERATE | c.1258G>C | p.Glu420Gln | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 12/22 | 1515/4273 | 1258/2679 | 420/892 | chr19 | 4695473 | |||
chr19:4697618 | G | C | 1 | a0005 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.1108C>G | p.Pro370Ala | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 11/22 | 1365/4273 | 1108/2679 | 370/892 | chr19 | 4697618 | |||
chr19:4702053 | G | A | 1 | a0003 | 2 | HG01361.hp1 HG01975.hp1 |
missense_variant | MODERATE | c.986C>T | p.Thr329Met | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 9/22 | 1243/4273 | 986/2679 | 329/892 | chr19 | 4702053 | |||
chr19:4704180 | G | C | 1 | a0004 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.551C>G | p.Ala184Gly | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 6/22 | 808/4273 | 551/2679 | 184/892 | chr19 | 4704180 | |||
chr19:4714263 | G | A | 1 | a0008 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.131C>T | p.Ala44Val | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/22 | 388/4273 | 131/2679 | 44/892 | chr19 | 4714263 | |||
chr19:4714273 | C | T | 1 | a0010 | 1 | NA18967.hp2 | missense_variant | MODERATE | c.121G>A | p.Gly41Ser | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/22 | 378/4273 | 121/2679 | 41/892 | chr19 | 4714273 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4679901 | C | T | 1 | a0001c0014 | 1 | HG02293.hp2 | synonymous_variant | LOW | c.2520G>A | p.Val840Val | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/22 | 2777/4273 | 2520/2679 | 840/892 | chr19 | 4679901 | |||
chr19:4682812 | G | A | 1 | a0001c0015 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.2358C>T | p.Thr786Thr | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/22 | 2615/4273 | 2358/2679 | 786/892 | chr19 | 4682812 | |||
chr19:4685719 | C | T | 1 | a0001c0013 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.1938G>A | p.Ser646Ser | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 17/22 | 2195/4273 | 1938/2679 | 646/892 | chr19 | 4685719 | |||
chr19:4688818 | G | T | 1 | a0001c0004 | 6 | HG00597.hp1 HG02040.hp1 HG02155.hp1 others(3): Show |
synonymous_variant | LOW | c.1824C>A | p.Gly608Gly | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/22 | 2081/4273 | 1824/2679 | 608/892 | chr19 | 4688818 | |||
chr19:4689648 | G | A | 2 | a0001c0002 a0002c0005 |
22 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(19): Show |
synonymous_variant | LOW | c.1671C>T | p.Tyr557Tyr | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 15/22 | 1928/4273 | 1671/2679 | 557/892 | chr19 | 4689648 | |||
chr19:4695510 | G | A | 1 | a0001c0016 | 1 | HG02071.hp1 | synonymous_variant | LOW | c.1221C>T | p.Leu407Leu | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 12/22 | 1478/4273 | 1221/2679 | 407/892 | chr19 | 4695510 | |||
chr19:4697625 | C | G | 1 | a0001c0010 | 1 | HG02273.hp2 | synonymous_variant | LOW | c.1101G>C | p.Leu367Leu | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 11/22 | 1358/4273 | 1101/2679 | 367/892 | chr19 | 4697625 | |||
chr19:4702070 | C | T | 1 | a0001c0009 | 1 | NA18979.hp2 | synonymous_variant | LOW | c.969G>A | p.Ala323Ala | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 9/22 | 1226/4273 | 969/2679 | 323/892 | chr19 | 4702070 | |||
chr19:4702073 | A | G | 1 | a0001c0003 | 7 | HG01255.hp2 HG01891.hp1 HG02717.hp2 others(4): Show |
synonymous_variant | LOW | c.966T>C | p.Pro322Pro | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 9/22 | 1223/4273 | 966/2679 | 322/892 | chr19 | 4702073 | |||
chr19:4704152 | G | A | 1 | a0001c0018 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.579C>T | p.Asp193Asp | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 6/22 | 836/4273 | 579/2679 | 193/892 | chr19 | 4704152 | |||
chr19:4714145 | G | A | 2 | a0001c0007 a0006c0020 |
3 | HG00609.hp2 HG01928.hp1 NA18970.hp2 |
synonymous_variant | LOW | c.249C>T | p.His83His | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/22 | 506/4273 | 249/2679 | 83/892 | chr19 | 4714145 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4675339 | C | CT | 6 | a0001c0001t0004 a0001c0001t0015 a0001c0001t0016 others(3): Show |
29 | HG00733.hp2 HG01168.hp2 HG01169.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1224dupA | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 22/22 | 1224 | chr19 | 4675339 | ||||||
chr19:4675381 | G | A | 1 | a0001c0001t0009 | 1 | HG01167.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1183C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 22/22 | 1183 | chr19 | 4675381 | ||||||
chr19:4675401 | C | A | 1 | a0001c0001t0015 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1163G>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 22/22 | 1163 | chr19 | 4675401 | ||||||
chr19:4675497 | T | C | 1 | a0001c0002t0019 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1067A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 22/22 | 1067 | chr19 | 4675497 | ||||||
chr19:4675549 | C | T | 1 | a0001c0001t0008 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1015G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 22/22 | 1015 | chr19 | 4675549 | ||||||
chr19:4675559 | C | T | 1 | a0001c0018t0010 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1005G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 22/22 | 1005 | chr19 | 4675559 | ||||||
chr19:4675645 | T | C | 1 | a0001c0018t0010 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*919A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 22/22 | 919 | chr19 | 4675645 | ||||||
chr19:4675749 | G | A | 1 | a0001c0003t0011 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*815C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 22/22 | 815 | chr19 | 4675749 | ||||||
chr19:4675797 | G | A | 1 | a0001c0001t0016 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*767C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 22/22 | 767 | chr19 | 4675797 | ||||||
chr19:4675841 | G | A | 1 | a0002c0005t0006 | 3 | HG01891.hp2 HG02970.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*723C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 22/22 | 723 | chr19 | 4675841 | ||||||
chr19:4675849 | G | A | 5 | a0001c0001t0003 a0001c0001t0012 a0001c0004t0003 others(2): Show |
34 | HG00597.hp1 HG00609.hp2 HG01884.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*715C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 22/22 | 715 | chr19 | 4675849 | ||||||
chr19:4675853 | C | A | 1 | a0001c0001t0017 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*711G>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 22/22 | 711 | chr19 | 4675853 | ||||||
chr19:4675855 | T | C | 2 | a0001c0001t0005 a0001c0002t0005 |
6 | HG01243.hp1 HG02280.hp2 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*709A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 22/22 | 709 | chr19 | 4675855 | ||||||
chr19:4675967 | T | C | 1 | a0001c0001t0013 | 1 | HG01070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*597A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 22/22 | 597 | chr19 | 4675967 | ||||||
chr19:4675985 | C | T | 1 | a0001c0002t0014 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*579G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 22/22 | 579 | chr19 | 4675985 | ||||||
chr19:4676109 | C | A | 1 | a0001c0001t0018 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*455G>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 22/22 | 455 | chr19 | 4676109 | ||||||
chr19:4676128 | T | G | 20 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(17): Show |
138 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*436A>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 22/22 | 436 | chr19 | 4676128 | ||||||
chr19:4676434 | G | A | 1 | a0001c0002t0019 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*130C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 22/22 | 130 | chr19 | 4676434 | ||||||
chr19:4723795 | G | A | 2 | a0001c0001t0007 a0004c0019t0007 |
2 | HG00323.hp1 HG03491.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-210C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 1/22 | chr19 | 4723795 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:4676747 | G | T | 6 | a0001c0001t0005g0007 a0001c0001t0005g0025 a0001c0001t0005g0026 others(3): Show |
6 | HG01243.hp1 HG02280.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2587-91C>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4676747 | |||||||
chr19:4676778 | T | A | 1 | a0001c0001t0017g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2587-122A>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4676778 | |||||||
chr19:4676932 | G | C | 6 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 others(3): Show |
6 | HG01168.hp2 HG01169.hp2 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.2587-276C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4676932 | |||||||
chr19:4677059 | C | T | 1 | a0001c0018t0010g0233 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2587-403G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4677059 | |||||||
chr19:4677190 | C | T | 1 | a0001c0001t0017g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2587-534G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4677190 | |||||||
chr19:4677342 | C | A | 3 | a0001c0001t0001g0270 a0001c0001t0001g0276 a0001c0001t0001g0286 |
3 | HG02717.hp1 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2587-686G>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4677342 | |||||||
chr19:4677364 | G | A | 6 | a0001c0001t0005g0007 a0001c0001t0005g0025 a0001c0001t0005g0026 others(3): Show |
6 | HG01243.hp1 HG02280.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2587-708C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4677364 | |||||||
chr19:4677393 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.2587-737C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4677393 | |||||||
chr19:4677413 | C | T | 1 | a0001c0018t0010g0233 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2587-757G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4677413 | |||||||
chr19:4677921 | C | T | 17 | a0001c0002t0002g0004 a0001c0002t0002g0033 a0001c0002t0002g0046 others(14): Show |
17 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.2587-1265G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4677921 | |||||||
chr19:4678030 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2587-1374G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4678030 | |||||||
chr19:4678122 | T | G | 7 | a0001c0001t0003g0058 a0001c0001t0003g0069 a0001c0001t0003g0087 others(4): Show |
7 | HG00609.hp2 HG02027.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.2587-1466A>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4678122 | |||||||
chr19:4678136 | G | A | 9 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(6): Show |
9 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.2587-1480C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4678136 | |||||||
chr19:4678215 | C | T | 1 | a0001c0002t0005g0049 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2587-1559G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4678215 | |||||||
chr19:4678259 | T | C | 6 | a0001c0001t0005g0007 a0001c0001t0005g0025 a0001c0001t0005g0026 others(3): Show |
6 | HG01243.hp1 HG02280.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2586+1576A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4678259 | |||||||
chr19:4678326 | T | C | 3 | a0001c0001t0001g0270 a0001c0001t0001g0276 a0001c0001t0001g0286 |
3 | HG02717.hp1 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2586+1509A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4678326 | |||||||
chr19:4678384 | G | A | 58 | a0001c0001t0002g0005 a0001c0001t0002g0028 a0001c0001t0002g0030 others(55): Show |
58 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(55): Show |
intron_variant | MODIFIER | c.2586+1451C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4678384 | |||||||
chr19:4678393 | G | A | 6 | a0001c0001t0005g0007 a0001c0001t0005g0025 a0001c0001t0005g0026 others(3): Show |
6 | HG01243.hp1 HG02280.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2586+1442C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4678393 | |||||||
chr19:4678605 | T | C | 27 | a0001c0001t0001g0018 a0001c0001t0001g0236 a0001c0001t0001g0241 others(24): Show |
27 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.2586+1230A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4678605 | |||||||
chr19:4678887 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2586+948G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4678887 | |||||||
chr19:4678984 | A | T | 1 | a0006c0020t0001g0208 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.2586+851T>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4678984 | |||||||
chr19:4679041 | A | G | 1 | a0001c0001t0003g0150 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2586+794T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4679041 | |||||||
chr19:4679069 | G | GC | 15 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0088 others(12): Show |
15 | HG01109.hp1 HG01243.hp1 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.2586+765dupG | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4679069 | |||||||
chr19:4679521 | C | A | 1 | a0001c0001t0017g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2586+314G>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4679521 | |||||||
chr19:4679563 | GC | G | 4 | a0001c0001t0002g0045 a0001c0001t0002g0051 a0001c0001t0002g0052 others(1): Show |
4 | HG03098.hp1 HG03098.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2586+271delG | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4679563 | |||||||
chr19:4679725 | C | T | 1 | a0001c0001t0005g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2586+110G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4679725 | |||||||
chr19:4679742 | G | A | 68 | a0001c0001t0002g0005 a0001c0001t0002g0028 a0001c0001t0002g0030 others(65): Show |
68 | HG01109.hp1 HG01243.hp1 HG01255.hp2 others(65): Show |
intron_variant | MODIFIER | c.2586+93C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4679742 | |||||||
chr19:4679813 | G | A | 1 | a0001c0018t0010g0233 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2586+22C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 21/21 | chr19 | 4679813 | |||||||
chr19:4680080 | A | T | 28 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 others(25): Show |
28 | HG00733.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.2475-134T>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4680080 | |||||||
chr19:4680116 | A | T | 48 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0034 others(45): Show |
48 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(45): Show |
intron_variant | MODIFIER | c.2475-170T>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4680116 | |||||||
chr19:4680128 | T | C | 1 | a0001c0001t0017g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2475-182A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4680128 | |||||||
chr19:4680199 | T | TG | 23 | a0001c0001t0005g0007 a0001c0001t0005g0025 a0001c0001t0005g0026 others(20): Show |
23 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.2475-254_2475-253i others(3): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4680199 | |||||||
chr19:4680235 | C | CA | 7 | a0001c0001t0001g0167 a0001c0001t0001g0180 a0001c0001t0001g0246 others(4): Show |
7 | HG02055.hp1 HG02148.hp1 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.2475-290dupT | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4680235 | |||||||
chr19:4680235 | CA | C | 104 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(101): Show |
104 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(101): Show |
intron_variant | MODIFIER | c.2475-290delT | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4680235 | |||||||
chr19:4680235 | CAA | C | 10 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0001c0001t0004g0140 others(7): Show |
10 | HG01255.hp2 HG01975.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.2475-291_2475-290d others(4): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4680235 | |||||||
chr19:4680356 | G | C | 5 | a0001c0001t0002g0045 a0001c0001t0002g0051 a0001c0001t0002g0052 others(2): Show |
5 | HG03098.hp1 HG03098.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.2475-410C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4680356 | |||||||
chr19:4680412 | G | GAAAAAC | 157 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(154): Show |
157 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(154): Show |
intron_variant | MODIFIER | c.2475-472_2475-467d others(8): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4680412 | |||||||
chr19:4680542 | T | C | 1 | a0001c0001t0001g0210 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2475-596A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4680542 | |||||||
chr19:4680582 | G | A | 1 | a0001c0001t0003g0149 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2475-636C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4680582 | |||||||
chr19:4680654 | A | AT | 9 | a0001c0002t0002g0004 a0001c0002t0002g0033 a0001c0002t0002g0046 others(6): Show |
9 | HG02109.hp1 HG02486.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.2475-709dupA | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4680654 | |||||||
chr19:4680656 | T | TA | 107 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(104): Show |
107 | HG00597.hp1 HG00733.hp1 HG00733.hp2 others(104): Show |
intron_variant | MODIFIER | c.2475-711dupT | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4680656 | |||||||
chr19:4680656 | T | TAA | 24 | a0001c0001t0001g0159 a0001c0001t0002g0041 a0001c0001t0002g0081 others(21): Show |
24 | HG00609.hp2 HG01167.hp2 HG01928.hp2 others(21): Show |
intron_variant | MODIFIER | c.2475-712_2475-711d others(4): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4680656 | |||||||
chr19:4680656 | T | TTA | 7 | a0001c0001t0005g0007 a0001c0001t0005g0025 a0001c0001t0005g0026 others(4): Show |
7 | HG01243.hp1 HG02280.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.2475-711_2475-710i others(4): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4680656 | |||||||
chr19:4680657 | A | T | 5 | a0001c0002t0002g0242 a0001c0002t0002g0243 a0001c0002t0002g0244 others(2): Show |
5 | HG01109.hp1 HG02622.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2475-711T>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4680657 | |||||||
chr19:4680793 | T | C | 109 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0001c0001t0002g0003 others(106): Show |
109 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(106): Show |
intron_variant | MODIFIER | c.2475-847A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4680793 | |||||||
chr19:4680818 | G | A | 6 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0034 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.2475-872C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4680818 | |||||||
chr19:4681037 | G | A | 3 | a0001c0001t0001g0301 a0001c0004t0003g0108 a0001c0015t0001g0309 |
3 | HG02647.hp1 NA19043.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.2475-1091C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4681037 | |||||||
chr19:4681105 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.2475-1159G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4681105 | |||||||
chr19:4681140 | G | A | 11 | a0001c0001t0002g0041 a0001c0001t0002g0059 a0001c0001t0002g0061 others(8): Show |
11 | HG02056.hp1 HG02080.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.2475-1194C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4681140 | |||||||
chr19:4681162 | C | T | 1 | a0001c0001t0002g0032 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2475-1216G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4681162 | |||||||
chr19:4681347 | G | A | 1 | a0001c0001t0017g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2474+1349C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4681347 | |||||||
chr19:4681395 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2474+1301C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4681395 | |||||||
chr19:4681432 | C | G | 1 | a0001c0001t0002g0032 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2474+1264G>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4681432 | |||||||
chr19:4681457 | C | T | 1 | a0001c0001t0002g0122 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2474+1239G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4681457 | |||||||
chr19:4681516 | C | T | 1 | a0001c0001t0012g0060 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2474+1180G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4681516 | |||||||
chr19:4681553 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2474+1143G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4681553 | |||||||
chr19:4681618 | G | A | 1 | a0001c0003t0002g0144 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2474+1078C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4681618 | |||||||
chr19:4681842 | C | CT | 10 | a0001c0001t0001g0014 a0001c0001t0001g0182 a0001c0001t0001g0193 others(7): Show |
10 | HG00741.hp2 HG02056.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.2474+853dupA | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4681842 | |||||||
chr19:4681842 | CT | C | 29 | a0001c0001t0001g0194 a0001c0001t0001g0236 a0001c0001t0001g0241 others(26): Show |
29 | HG01106.hp1 HG01167.hp1 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.2474+853delA | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4681842 | |||||||
chr19:4682010 | G | C | 2 | a0001c0001t0001g0264 a0001c0001t0001g0297 |
2 | HG03239.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.2474+686C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4682010 | |||||||
chr19:4682095 | G | A | 7 | a0001c0001t0017g0234 a0001c0003t0001g0013 a0001c0003t0001g0053 others(4): Show |
7 | HG01255.hp2 HG02717.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.2474+601C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4682095 | |||||||
chr19:4682263 | C | A | 1 | a0001c0001t0017g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2474+433G>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4682263 | |||||||
chr19:4682311 | G | C | 23 | a0001c0001t0005g0007 a0001c0001t0005g0025 a0001c0001t0005g0026 others(20): Show |
23 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.2474+385C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 20/21 | chr19 | 4682311 | |||||||
chr19:4682968 | G | A | 1 | a0001c0002t0002g0245 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2332-130C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 19/21 | chr19 | 4682968 | |||||||
chr19:4683122 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2332-284C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 19/21 | chr19 | 4683122 | |||||||
chr19:4683158 | G | GC | 25 | a0001c0001t0001g0014 a0001c0001t0001g0044 a0001c0001t0001g0136 others(22): Show |
25 | HG00597.hp1 HG00597.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.2331+318dupG | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 19/21 | chr19 | 4683158 | |||||||
chr19:4683280 | G | A | 3 | a0002c0005t0006g0021 a0002c0005t0006g0022 a0002c0005t0006g0023 |
3 | HG01891.hp2 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2331+197C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 19/21 | chr19 | 4683280 | |||||||
chr19:4683454 | G | A | 1 | a0001c0001t0002g0030 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2331+23C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 19/21 | chr19 | 4683454 | |||||||
chr19:4683714 | G | A | 5 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0147 others(2): Show |
5 | HG02145.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.2179-85C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 18/21 | chr19 | 4683714 | |||||||
chr19:4683771 | T | A | 1 | a0001c0018t0010g0233 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2179-142A>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 18/21 | chr19 | 4683771 | |||||||
chr19:4683788 | A | C | 1 | a0001c0001t0017g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2179-159T>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 18/21 | chr19 | 4683788 | |||||||
chr19:4683861 | C | T | 3 | a0001c0002t0002g0242 a0001c0002t0002g0243 a0001c0002t0002g0244 |
3 | HG02622.hp1 HG02809.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2179-232G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 18/21 | chr19 | 4683861 | |||||||
chr19:4683862 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2179-233C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 18/21 | chr19 | 4683862 | |||||||
chr19:4684034 | C | T | 18 | a0001c0002t0002g0004 a0001c0002t0002g0033 a0001c0002t0002g0046 others(15): Show |
18 | HG01109.hp1 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.2179-405G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 18/21 | chr19 | 4684034 | |||||||
chr19:4684106 | C | T | 28 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 others(25): Show |
28 | HG00733.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.2179-477G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 18/21 | chr19 | 4684106 | |||||||
chr19:4684169 | G | A | 1 | a0001c0002t0002g0033 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2178+494C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 18/21 | chr19 | 4684169 | |||||||
chr19:4684360 | C | T | 6 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0002t0002g0006 others(3): Show |
6 | HG01891.hp2 HG02258.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.2178+303G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 18/21 | chr19 | 4684360 | |||||||
chr19:4684461 | C | T | 8 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0001c0003t0001g0013 others(5): Show |
8 | HG01255.hp2 HG02717.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.2178+202G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 18/21 | chr19 | 4684461 | |||||||
chr19:4684553 | G | A | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | NA18965.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.2178+110C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 18/21 | chr19 | 4684553 | |||||||
chr19:4684630 | A | G | 147 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0001c0001t0002g0003 others(144): Show |
147 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(144): Show |
intron_variant | MODIFIER | c.2178+33T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 18/21 | chr19 | 4684630 | |||||||
chr19:4684850 | G | A | 6 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(3): Show |
6 | HG02145.hp1 HG02559.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.2032-41C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 17/21 | chr19 | 4684850 | |||||||
chr19:4684879 | C | T | 1 | a0001c0002t0002g0004 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2032-70G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 17/21 | chr19 | 4684879 | |||||||
chr19:4684899 | C | A | 2 | a0001c0001t0001g0172 a0001c0001t0001g0209 |
2 | HG02056.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2032-90G>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 17/21 | chr19 | 4684899 | |||||||
chr19:4685247 | G | A | 40 | a0001c0001t0002g0254 a0001c0001t0002g0255 a0001c0001t0002g0256 others(37): Show |
40 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.2031+379C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 17/21 | chr19 | 4685247 | |||||||
chr19:4685264 | A | C | 147 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0001c0001t0002g0003 others(144): Show |
147 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(144): Show |
intron_variant | MODIFIER | c.2031+362T>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 17/21 | chr19 | 4685264 | |||||||
chr19:4685305 | T | A | 4 | a0001c0004t0003g0040 a0001c0004t0003g0080 a0001c0004t0003g0107 others(1): Show |
4 | HG02155.hp1 NA18974.hp2 NA18998.hp2 others(1): Show |
intron_variant | MODIFIER | c.2031+321A>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 17/21 | chr19 | 4685305 | |||||||
chr19:4685387 | G | A | 1 | a0001c0001t0002g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2031+239C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 17/21 | chr19 | 4685387 | |||||||
chr19:4685519 | C | T | 1 | a0001c0001t0002g0212 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2031+107G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 17/21 | chr19 | 4685519 | |||||||
chr19:4685895 | C | T | 4 | a0001c0002t0002g0242 a0001c0002t0002g0243 a0001c0002t0002g0244 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1886-124G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4685895 | |||||||
chr19:4685920 | G | GT | 12 | a0001c0001t0001g0072 a0001c0001t0001g0172 a0001c0001t0001g0209 others(9): Show |
12 | HG01496.hp2 HG01891.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.1886-150dupA | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4685920 | |||||||
chr19:4686041 | T | C | 37 | a0001c0001t0002g0032 a0001c0001t0002g0131 a0001c0001t0002g0212 others(34): Show |
37 | HG00733.hp2 HG01168.hp2 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.1886-270A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4686041 | |||||||
chr19:4686280 | G | A | 1 | a0001c0001t0001g0226 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1886-509C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4686280 | |||||||
chr19:4686311 | G | A | 1 | a0004c0019t0007g0312 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1886-540C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4686311 | |||||||
chr19:4686318 | A | AT | 57 | a0001c0001t0001g0073 a0001c0001t0001g0229 a0001c0001t0002g0003 others(54): Show |
57 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.1886-548dupA | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4686318 | |||||||
chr19:4686318 | AT | A | 44 | a0001c0001t0001g0218 a0001c0001t0001g0289 a0001c0001t0002g0005 others(41): Show |
44 | HG01109.hp1 HG01884.hp2 HG02055.hp2 others(41): Show |
intron_variant | MODIFIER | c.1886-548delA | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4686318 | |||||||
chr19:4686318 | ATT | A | 7 | a0001c0002t0002g0006 a0001c0002t0002g0242 a0001c0002t0002g0243 others(4): Show |
7 | HG01891.hp2 HG02258.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1886-549_1886-548d others(4): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4686318 | |||||||
chr19:4686338 | G | C | 1 | a0001c0016t0001g0179 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1886-567C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4686338 | |||||||
chr19:4686342 | C | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0121 a0001c0001t0001g0278 |
4 | HG01081.hp1 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1886-571G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4686342 | |||||||
chr19:4686586 | C | T | 1 | a0001c0001t0002g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1886-815G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4686586 | |||||||
chr19:4686651 | C | T | 1 | a0001c0002t0019g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1886-880G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4686651 | |||||||
chr19:4686682 | C | T | 1 | a0001c0001t0002g0082 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1886-911G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4686682 | |||||||
chr19:4686976 | G | T | 16 | a0001c0001t0001g0135 a0001c0001t0001g0142 a0001c0001t0001g0207 others(13): Show |
16 | HG00280.hp1 HG00735.hp2 HG00738.hp1 others(13): Show |
intron_variant | MODIFIER | c.1886-1205C>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4686976 | |||||||
chr19:4687034 | G | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0184 |
2 | NA19060.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1886-1263C>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4687034 | |||||||
chr19:4687063 | T | C | 32 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0001c0001t0002g0005 others(29): Show |
32 | HG01884.hp2 HG02056.hp1 HG02080.hp2 others(29): Show |
intron_variant | MODIFIER | c.1886-1292A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4687063 | |||||||
chr19:4687217 | G | A | 4 | a0001c0002t0002g0242 a0001c0002t0002g0243 a0001c0002t0002g0244 others(1): Show |
4 | HG01109.hp1 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1886-1446C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4687217 | |||||||
chr19:4687366 | G | C | 2 | a0001c0001t0001g0163 a0001c0001t0001g0298 |
2 | HG03017.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.1885+1391C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4687366 | |||||||
chr19:4687470 | G | A | 1 | a0001c0004t0003g0107 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1885+1287C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4687470 | |||||||
chr19:4687594 | C | G | 4 | a0001c0002t0002g0006 a0002c0005t0006g0021 a0002c0005t0006g0022 others(1): Show |
4 | HG01891.hp2 HG02258.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1885+1163G>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4687594 | |||||||
chr19:4687658 | GGGCCCTC others(13): Show |
G | 1 | a0001c0002t0019g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1885+1079_1885+109 others(24): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4687658 | |||||||
chr19:4687803 | G | GT | 7 | a0001c0001t0001g0118 a0001c0001t0001g0169 a0001c0001t0001g0219 others(4): Show |
7 | HG00609.hp1 HG01175.hp1 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.1885+953dupA | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4687803 | |||||||
chr19:4688018 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1885+739C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4688018 | |||||||
chr19:4688052 | T | A | 2 | a0001c0001t0004g0280 a0001c0001t0004g0281 |
2 | HG01361.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.1885+705A>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4688052 | |||||||
chr19:4688133 | GGGTCTTG others(1): Show |
G | 47 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0034 others(44): Show |
47 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.1885+616_1885+623d others(10): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4688133 | |||||||
chr19:4688134 | G | C | 1 | a0001c0004t0003g0080 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1885+623C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4688134 | |||||||
chr19:4688135 | G | C | 1 | a0001c0004t0003g0080 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1885+622C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4688135 | |||||||
chr19:4688137 | C | G | 1 | a0001c0004t0003g0080 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1885+620G>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4688137 | |||||||
chr19:4688142 | T | C | 47 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0034 others(44): Show |
47 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.1885+615A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4688142 | |||||||
chr19:4688388 | C | T | 22 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0033 others(19): Show |
22 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1885+369G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4688388 | |||||||
chr19:4688668 | C | G | 1 | a0001c0001t0002g0109 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1885+89G>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4688668 | |||||||
chr19:4688698 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1885+59C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4688698 | |||||||
chr19:4688717 | C | T | 1 | a0001c0001t0002g0160 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1885+40G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 16/21 | chr19 | 4688717 | |||||||
chr19:4688955 | G | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(5): Show |
8 | HG02145.hp1 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1750-63C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 15/21 | chr19 | 4688955 | |||||||
chr19:4689182 | C | T | 1 | a0001c0001t0016g0296 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1750-290G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 15/21 | chr19 | 4689182 | |||||||
chr19:4689319 | G | A | 5 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0147 others(2): Show |
5 | HG02145.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1749+251C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 15/21 | chr19 | 4689319 | |||||||
chr19:4689522 | A | G | 1 | a0001c0001t0004g0175 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1749+48T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 15/21 | chr19 | 4689522 | |||||||
chr19:4689562 | G | A | 1 | a0001c0001t0003g0090 | 1 | HG02027.hp1 | splice_region_variant&intron_variant | LOW | c.1749+8C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 15/21 | chr19 | 4689562 | |||||||
chr19:4689923 | G | A | 1 | a0001c0001t0003g0113 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1597-201C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 14/21 | chr19 | 4689923 | |||||||
chr19:4689989 | T | A | 1 | a0001c0001t0001g0274 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1597-267A>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 14/21 | chr19 | 4689989 | |||||||
chr19:4690052 | C | A | 2 | a0001c0001t0001g0142 a0001c0001t0001g0207 |
2 | HG00735.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.1597-330G>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 14/21 | chr19 | 4690052 | |||||||
chr19:4690247 | T | C | 149 | a0001c0001t0001g0159 a0001c0001t0001g0236 a0001c0001t0001g0241 others(146): Show |
149 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(146): Show |
intron_variant | MODIFIER | c.1597-525A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 14/21 | chr19 | 4690247 | |||||||
chr19:4690426 | T | C | 2 | a0001c0001t0001g0301 a0001c0015t0001g0309 |
2 | HG02647.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1596+452A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 14/21 | chr19 | 4690426 | |||||||
chr19:4690488 | G | A | 2 | a0001c0001t0001g0227 a0001c0001t0009g0062 |
2 | HG00621.hp2 HG01167.hp1 |
intron_variant | MODIFIER | c.1596+390C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 14/21 | chr19 | 4690488 | |||||||
chr19:4690524 | G | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(5): Show |
8 | HG02145.hp1 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596+354C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 14/21 | chr19 | 4690524 | |||||||
chr19:4690618 | A | T | 34 | a0001c0001t0003g0058 a0001c0001t0003g0064 a0001c0001t0003g0065 others(31): Show |
34 | HG00597.hp1 HG00609.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.1596+260T>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 14/21 | chr19 | 4690618 | |||||||
chr19:4690623 | C | T | 28 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 others(25): Show |
28 | HG00733.hp2 HG01168.hp2 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.1596+255G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 14/21 | chr19 | 4690623 | |||||||
chr19:4690706 | T | C | 23 | a0001c0001t0001g0246 a0001c0002t0002g0004 a0001c0002t0002g0006 others(20): Show |
23 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.1596+172A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 14/21 | chr19 | 4690706 | |||||||
chr19:4690769 | G | A | 1 | a0001c0001t0017g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1596+109C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 14/21 | chr19 | 4690769 | |||||||
chr19:4690800 | C | T | 1 | a0001c0003t0011g0299 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1596+78G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 14/21 | chr19 | 4690800 | |||||||
chr19:4690805 | G | A | 30 | a0001c0001t0002g0005 a0001c0001t0002g0028 a0001c0001t0002g0030 others(27): Show |
30 | HG01884.hp2 HG02056.hp1 HG02080.hp2 others(27): Show |
intron_variant | MODIFIER | c.1596+73C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 14/21 | chr19 | 4690805 | |||||||
chr19:4691069 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1517-112G>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4691069 | |||||||
chr19:4691090 | C | T | 1 | a0001c0001t0005g0085 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1517-133G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4691090 | |||||||
chr19:4691345 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1517-388C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4691345 | |||||||
chr19:4691351 | C | T | 1 | a0001c0001t0001g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1517-394G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4691351 | |||||||
chr19:4691473 | CA | C | 29 | a0001c0001t0002g0254 a0001c0001t0002g0255 a0001c0001t0002g0256 others(26): Show |
29 | HG00733.hp1 HG01109.hp1 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.1517-517delT | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4691473 | |||||||
chr19:4691486 | C | A | 4 | a0001c0001t0002g0045 a0001c0001t0002g0051 a0001c0001t0002g0052 others(1): Show |
4 | HG03098.hp1 HG03098.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1517-529G>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4691486 | |||||||
chr19:4691493 | C | A | 4 | a0001c0001t0002g0045 a0001c0001t0002g0051 a0001c0001t0002g0052 others(1): Show |
4 | HG03098.hp1 HG03098.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1517-536G>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4691493 | |||||||
chr19:4691554 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1517-597G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4691554 | |||||||
chr19:4691624 | T | G | 6 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0034 others(3): Show |
6 | HG01891.hp1 HG02109.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1517-667A>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4691624 | |||||||
chr19:4691666 | C | T | 1 | a0001c0001t0002g0003 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1517-709G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4691666 | |||||||
chr19:4691670 | C | CT | 92 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0044 others(89): Show |
92 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(89): Show |
intron_variant | MODIFIER | c.1517-714dupA | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4691670 | |||||||
chr19:4691670 | C | CTT | 19 | a0001c0001t0002g0057 a0001c0001t0002g0232 a0001c0001t0003g0065 others(16): Show |
19 | HG01169.hp2 HG01517.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1517-715_1517-714d others(4): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4691670 | |||||||
chr19:4691923 | C | T | 1 | a0001c0001t0017g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1517-966G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4691923 | |||||||
chr19:4691953 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1517-996G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4691953 | |||||||
chr19:4691997 | A | AG | 6 | a0001c0001t0001g0303 a0001c0001t0003g0101 a0001c0001t0003g0214 others(3): Show |
6 | HG01517.hp1 HG02055.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.1517-1041dupC | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4691997 | |||||||
chr19:4692109 | C | T | 1 | a0001c0013t0001g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1517-1152G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4692109 | |||||||
chr19:4692341 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1517-1384G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4692341 | |||||||
chr19:4692342 | G | C | 99 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0001c0001t0002g0005 others(96): Show |
99 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(96): Show |
intron_variant | MODIFIER | c.1517-1385C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4692342 | |||||||
chr19:4692417 | T | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0306 |
2 | NA18995.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1517-1460A>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4692417 | |||||||
chr19:4692528 | C | T | 1 | a0001c0003t0011g0299 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1517-1571G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4692528 | |||||||
chr19:4692784 | C | T | 1 | a0001c0001t0008g0305 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1517-1827G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4692784 | |||||||
chr19:4693024 | C | T | 1 | a0001c0001t0003g0147 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1516+1637G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4693024 | |||||||
chr19:4693079 | C | A | 1 | a0001c0001t0001g0287 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1516+1582G>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4693079 | |||||||
chr19:4693109 | C | T | 1 | a0001c0001t0001g0263 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1516+1552G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4693109 | |||||||
chr19:4693215 | T | C | 2 | a0001c0001t0003g0113 a0010c0008t0003g0070 |
2 | NA18967.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1516+1446A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4693215 | |||||||
chr19:4693258 | C | T | 3 | a0001c0001t0002g0045 a0001c0001t0002g0051 a0001c0001t0002g0052 |
3 | HG03098.hp1 HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1516+1403G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4693258 | |||||||
chr19:4693266 | C | T | 30 | a0001c0001t0002g0005 a0001c0001t0002g0028 a0001c0001t0002g0030 others(27): Show |
30 | HG01884.hp2 HG02056.hp1 HG02080.hp2 others(27): Show |
intron_variant | MODIFIER | c.1516+1395G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4693266 | |||||||
chr19:4693337 | G | A | 2 | a0001c0001t0001g0170 a0001c0001t0001g0219 |
2 | HG01175.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.1516+1324C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4693337 | |||||||
chr19:4693370 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1516+1291G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4693370 | |||||||
chr19:4693610 | A | AGAATCAG others(15): Show |
1 | a0001c0001t0012g0060 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1516+1029_1516+105 others(26): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4693610 | |||||||
chr19:4693619 | C | T | 2 | a0001c0001t0005g0025 a0001c0001t0005g0026 |
2 | HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1516+1042G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4693619 | |||||||
chr19:4693661 | C | T | 3 | a0001c0001t0001g0270 a0001c0001t0001g0276 a0001c0001t0001g0286 |
3 | HG02717.hp1 HG03130.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1516+1000G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4693661 | |||||||
chr19:4693670 | C | T | 2 | a0001c0001t0001g0236 a0001c0001t0001g0241 |
2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1516+991G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4693670 | |||||||
chr19:4693720 | G | A | 4 | a0001c0001t0002g0045 a0001c0001t0002g0051 a0001c0001t0002g0052 others(1): Show |
4 | HG03098.hp1 HG03098.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1516+941C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4693720 | |||||||
chr19:4693891 | A | G | 2 | a0001c0001t0001g0173 a0001c0001t0001g0188 |
2 | HG01099.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1516+770T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4693891 | |||||||
chr19:4694284 | C | A | 1 | a0001c0001t0004g0177 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1516+377G>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4694284 | |||||||
chr19:4694323 | A | G | 1 | a0001c0001t0001g0097 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1516+338T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4694323 | |||||||
chr19:4694371 | G | A | 5 | a0001c0001t0005g0007 a0001c0001t0005g0025 a0001c0001t0005g0026 others(2): Show |
5 | HG01243.hp1 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1516+290C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4694371 | |||||||
chr19:4694506 | G | GAC | 56 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0001c0001t0002g0003 others(53): Show |
56 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1516+154_1516+155i others(4): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4694506 | |||||||
chr19:4694574 | TG | T | 22 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0033 others(19): Show |
22 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1516+86delC | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4694574 | |||||||
chr19:4694615 | C | T | 1 | a0001c0018t0010g0233 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1516+46G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4694615 | |||||||
chr19:4694618 | G | T | 5 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0034 others(2): Show |
5 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1516+43C>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4694618 | |||||||
chr19:4694627 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1516+34C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4694627 | |||||||
chr19:4694644 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1516+17G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 13/21 | chr19 | 4694644 | |||||||
chr19:4694896 | C | T | 1 | a0001c0001t0017g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1354-73G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 12/21 | chr19 | 4694896 | |||||||
chr19:4695050 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0308 |
2 | NA18966.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1354-227G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 12/21 | chr19 | 4695050 | |||||||
chr19:4695140 | C | A | 1 | a0001c0001t0002g0052 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1353+238G>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 12/21 | chr19 | 4695140 | |||||||
chr19:4695347 | C | A | 2 | a0001c0001t0001g0289 a0001c0001t0001g0290 |
2 | HG01256.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.1353+31G>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 12/21 | chr19 | 4695347 | |||||||
chr19:4695372 | G | T | 47 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0034 others(44): Show |
47 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(44): Show |
splice_region_variant&intron_variant | LOW | c.1353+6C>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 12/21 | chr19 | 4695372 | |||||||
chr19:4695671 | C | T | 1 | a0001c0002t0019g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1176-116G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 11/21 | chr19 | 4695671 | |||||||
chr19:4695809 | AGCG | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(5): Show |
8 | HG02145.hp1 HG02451.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1176-257_1176-255d others(5): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 11/21 | chr19 | 4695809 | |||||||
chr19:4695882 | T | C | 1 | a0001c0003t0002g0144 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1176-327A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 11/21 | chr19 | 4695882 | |||||||
chr19:4695911 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1176-356A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 11/21 | chr19 | 4695911 | |||||||
chr19:4696091 | A | G | 79 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0001c0001t0002g0003 others(76): Show |
79 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.1176-536T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 11/21 | chr19 | 4696091 | |||||||
chr19:4696181 | G | A | 22 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0033 others(19): Show |
22 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1176-626C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 11/21 | chr19 | 4696181 | |||||||
chr19:4696394 | C | T | 2 | a0001c0001t0003g0214 a0001c0009t0001g0271 |
2 | NA18973.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.1176-839G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 11/21 | chr19 | 4696394 | |||||||
chr19:4696397 | G | C | 56 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0001c0001t0002g0003 others(53): Show |
56 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1176-842C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 11/21 | chr19 | 4696397 | |||||||
chr19:4696462 | C | CA | 24 | a0001c0001t0001g0042 a0001c0001t0001g0161 a0001c0001t0001g0163 others(21): Show |
24 | HG01243.hp2 HG01255.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.1176-908dupT | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 11/21 | chr19 | 4696462 | |||||||
chr19:4696498 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1176-943G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 11/21 | chr19 | 4696498 | |||||||
chr19:4696636 | G | GTAATCCC others(3): Show |
1 | a0001c0001t0017g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1175+914_1175+915i others(12): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 11/21 | chr19 | 4696636 | |||||||
chr19:4696684 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1175+867C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 11/21 | chr19 | 4696684 | |||||||
chr19:4696704 | A | G | 56 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0001c0001t0002g0003 others(53): Show |
56 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1175+847T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 11/21 | chr19 | 4696704 | |||||||
chr19:4696760 | T | G | 56 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0001c0001t0002g0003 others(53): Show |
56 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.1175+791A>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 11/21 | chr19 | 4696760 | |||||||
chr19:4696854 | T | C | 1 | a0001c0001t0002g0032 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1175+697A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 11/21 | chr19 | 4696854 | |||||||
chr19:4696867 | C | T | 5 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(2): Show |
5 | HG00323.hp1 HG00738.hp2 HG00741.hp1 others(2): Show |
intron_variant | MODIFIER | c.1175+684G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 11/21 | chr19 | 4696867 | |||||||
chr19:4697098 | C | CA | 6 | a0001c0001t0001g0219 a0001c0001t0002g0045 a0001c0001t0002g0051 others(3): Show |
6 | HG01175.hp1 HG02056.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1175+452dupT | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 11/21 | chr19 | 4697098 | |||||||
chr19:4697185 | T | C | 1 | a0001c0001t0005g0240 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1175+366A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 11/21 | chr19 | 4697185 | |||||||
chr19:4697190 | G | T | 1 | a0001c0001t0001g0196 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1175+361C>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 11/21 | chr19 | 4697190 | |||||||
chr19:4697195 | G | A | 3 | a0001c0001t0001g0119 a0001c0001t0001g0194 a0001c0001t0001g0247 |
3 | HG01106.hp1 HG01433.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1175+356C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 11/21 | chr19 | 4697195 | |||||||
chr19:4697505 | A | G | 22 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0033 others(19): Show |
22 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1175+46T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 11/21 | chr19 | 4697505 | |||||||
chr19:4697745 | C | G | 26 | a0001c0001t0002g0005 a0001c0001t0002g0028 a0001c0001t0002g0030 others(23): Show |
26 | HG01884.hp2 HG02056.hp1 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.1075-94G>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4697745 | |||||||
chr19:4697890 | G | T | 1 | a0001c0001t0016g0296 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1075-239C>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4697890 | |||||||
chr19:4698087 | A | G | 32 | a0001c0001t0002g0131 a0001c0001t0002g0212 a0001c0001t0002g0224 others(29): Show |
32 | HG00733.hp2 HG01168.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.1075-436T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4698087 | |||||||
chr19:4698119 | A | G | 47 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0034 others(44): Show |
47 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.1075-468T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4698119 | |||||||
chr19:4698125 | T | G | 9 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0001c0003t0001g0013 others(6): Show |
9 | HG01255.hp2 HG01891.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1075-474A>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4698125 | |||||||
chr19:4698133 | C | T | 1 | a0001c0001t0003g0113 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1075-482G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4698133 | |||||||
chr19:4698269 | C | T | 1 | a0001c0001t0009g0062 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1075-618G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4698269 | |||||||
chr19:4698326 | C | T | 1 | a0001c0001t0001g0098 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1075-675G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4698326 | |||||||
chr19:4698454 | TA | T | 47 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0034 others(44): Show |
47 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.1075-804delT | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4698454 | |||||||
chr19:4698544 | G | A | 4 | a0001c0002t0002g0006 a0002c0005t0006g0021 a0002c0005t0006g0022 others(1): Show |
4 | HG01891.hp2 HG02258.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1075-893C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4698544 | |||||||
chr19:4698680 | G | T | 2 | a0001c0001t0001g0174 a0001c0001t0001g0227 |
2 | HG00621.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.1075-1029C>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4698680 | |||||||
chr19:4698700 | T | C | 9 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0001c0003t0001g0013 others(6): Show |
9 | HG01255.hp2 HG01891.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1075-1049A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4698700 | |||||||
chr19:4698795 | G | T | 22 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0033 others(19): Show |
22 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1075-1144C>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4698795 | |||||||
chr19:4698804 | G | A | 2 | a0001c0001t0002g0088 a0001c0001t0002g0160 |
2 | HG02273.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.1075-1153C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4698804 | |||||||
chr19:4698806 | A | G | 1 | a0001c0001t0017g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1075-1155T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4698806 | |||||||
chr19:4698916 | T | G | 1 | a0001c0001t0017g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1075-1265A>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4698916 | |||||||
chr19:4698934 | G | A | 7 | a0001c0001t0001g0001 a0001c0001t0001g0073 a0001c0001t0001g0074 others(4): Show |
8 | HG01070.hp2 HG01109.hp2 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.1074+1282C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4698934 | |||||||
chr19:4698940 | C | T | 2 | a0001c0001t0003g0126 a0001c0001t0003g0127 |
2 | HG01884.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1074+1276G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4698940 | |||||||
chr19:4699091 | G | A | 1 | a0001c0001t0017g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1074+1125C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4699091 | |||||||
chr19:4699114 | A | G | 23 | a0001c0001t0017g0234 a0001c0002t0002g0004 a0001c0002t0002g0006 others(20): Show |
23 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.1074+1102T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4699114 | |||||||
chr19:4699158 | C | CA | 27 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0042 others(24): Show |
27 | HG00280.hp2 HG01106.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.1074+1057dupT | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4699158 | |||||||
chr19:4699158 | CA | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0073 a0001c0001t0001g0094 others(95): Show |
99 | HG00609.hp2 HG00733.hp1 HG00733.hp2 others(96): Show |
intron_variant | MODIFIER | c.1074+1057delT | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4699158 | |||||||
chr19:4699158 | CAA | C | 25 | a0001c0001t0001g0196 a0001c0001t0002g0257 a0001c0001t0003g0086 others(22): Show |
25 | HG00597.hp1 HG01109.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.1074+1056_1074+105 others(6): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4699158 | |||||||
chr19:4699228 | T | G | 1 | a0001c0001t0017g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1074+988A>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4699228 | |||||||
chr19:4699459 | A | G | 4 | a0001c0001t0002g0045 a0001c0001t0002g0051 a0001c0001t0002g0052 others(1): Show |
4 | HG03098.hp1 HG03098.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074+757T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4699459 | |||||||
chr19:4699460 | A | G | 1 | a0001c0001t0002g0050 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1074+756T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4699460 | |||||||
chr19:4699564 | C | T | 4 | a0001c0001t0002g0045 a0001c0001t0002g0051 a0001c0001t0002g0052 others(1): Show |
4 | HG03098.hp1 HG03098.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074+652G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4699564 | |||||||
chr19:4699632 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1074+584G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4699632 | |||||||
chr19:4699823 | C | A | 1 | a0001c0001t0003g0101 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1074+393G>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4699823 | |||||||
chr19:4699824 | A | G | 1 | a0001c0001t0003g0101 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1074+392T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4699824 | |||||||
chr19:4699825 | G | C | 1 | a0001c0001t0003g0101 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1074+391C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4699825 | |||||||
chr19:4700014 | G | T | 1 | a0001c0001t0001g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1074+202C>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4700014 | |||||||
chr19:4700026 | C | T | 1 | a0001c0001t0003g0105 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1074+190G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4700026 | |||||||
chr19:4700047 | C | A | 4 | a0001c0001t0002g0045 a0001c0001t0002g0051 a0001c0001t0002g0052 others(1): Show |
4 | HG03098.hp1 HG03098.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1074+169G>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4700047 | |||||||
chr19:4700175 | A | G | 146 | a0001c0001t0001g0220 a0001c0001t0002g0003 a0001c0001t0002g0005 others(143): Show |
146 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(143): Show |
intron_variant | MODIFIER | c.1074+41T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 10/21 | chr19 | 4700175 | |||||||
chr19:4700341 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1013-64G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 9/21 | chr19 | 4700341 | |||||||
chr19:4700348 | C | T | 1 | a0001c0001t0017g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1013-71G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 9/21 | chr19 | 4700348 | |||||||
chr19:4700400 | G | A | 30 | a0001c0001t0002g0005 a0001c0001t0002g0028 a0001c0001t0002g0030 others(27): Show |
30 | HG01884.hp2 HG02056.hp1 HG02080.hp2 others(27): Show |
intron_variant | MODIFIER | c.1013-123C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 9/21 | chr19 | 4700400 | |||||||
chr19:4700452 | G | C | 22 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0033 others(19): Show |
22 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1013-175C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 9/21 | chr19 | 4700452 | |||||||
chr19:4700640 | C | T | 5 | a0001c0001t0005g0007 a0001c0001t0005g0025 a0001c0001t0005g0026 others(2): Show |
5 | HG01243.hp1 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1013-363G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 9/21 | chr19 | 4700640 | |||||||
chr19:4700675 | C | T | 1 | a0001c0002t0002g0129 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1013-398G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 9/21 | chr19 | 4700675 | |||||||
chr19:4700676 | G | A | 1 | a0001c0018t0010g0233 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1013-399C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 9/21 | chr19 | 4700676 | |||||||
chr19:4700735 | G | A | 1 | a0001c0001t0002g0232 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1013-458C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 9/21 | chr19 | 4700735 | |||||||
chr19:4700808 | C | G | 1 | a0001c0001t0001g0097 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1013-531G>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 9/21 | chr19 | 4700808 | |||||||
chr19:4701040 | C | T | 1 | a0001c0001t0003g0150 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1013-763G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 9/21 | chr19 | 4701040 | |||||||
chr19:4701077 | A | G | 1 | a0001c0018t0010g0233 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1013-800T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 9/21 | chr19 | 4701077 | |||||||
chr19:4701120 | C | T | 26 | a0001c0001t0002g0005 a0001c0001t0002g0028 a0001c0001t0002g0030 others(23): Show |
26 | HG01884.hp2 HG02056.hp1 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.1013-843G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 9/21 | chr19 | 4701120 | |||||||
chr19:4701122 | C | T | 1 | a0001c0001t0001g0218 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1013-845G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 9/21 | chr19 | 4701122 | |||||||
chr19:4701139 | T | C | 5 | a0001c0001t0005g0007 a0001c0001t0005g0025 a0001c0001t0005g0026 others(2): Show |
5 | HG01243.hp1 HG02280.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.1013-862A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 9/21 | chr19 | 4701139 | |||||||
chr19:4701233 | C | T | 1 | a0001c0001t0017g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1012+794G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 9/21 | chr19 | 4701233 | |||||||
chr19:4701329 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1012+698T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 9/21 | chr19 | 4701329 | |||||||
chr19:4701436 | C | T | 2 | a0001c0001t0002g0089 a0001c0001t0002g0123 |
2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1012+591G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 9/21 | chr19 | 4701436 | |||||||
chr19:4701469 | A | AAAAC | 13 | a0001c0002t0002g0004 a0001c0002t0002g0033 a0001c0002t0002g0046 others(10): Show |
13 | HG02055.hp2 HG02109.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1012+554_1012+557d others(6): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 9/21 | chr19 | 4701469 | |||||||
chr19:4701577 | G | C | 1 | a0001c0001t0001g0170 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1012+450C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 9/21 | chr19 | 4701577 | |||||||
chr19:4701634 | C | A | 1 | a0001c0001t0002g0057 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1012+393G>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 9/21 | chr19 | 4701634 | |||||||
chr19:4701715 | C | T | 47 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0034 others(44): Show |
47 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.1012+312G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 9/21 | chr19 | 4701715 | |||||||
chr19:4701821 | A | T | 1 | a0001c0001t0002g0041 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1012+206T>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 9/21 | chr19 | 4701821 | |||||||
chr19:4701931 | GCAGCTCA others(15): Show |
G | 1 | a0001c0001t0001g0306 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1012+74_1012+95del others(22): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 9/21 | chr19 | 4701931 | |||||||
chr19:4702305 | T | G | 3 | a0001c0002t0002g0242 a0001c0002t0002g0243 a0001c0002t0002g0244 |
3 | HG02622.hp1 HG02809.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.884-150A>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 8/21 | chr19 | 4702305 | |||||||
chr19:4702387 | A | G | 22 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0033 others(19): Show |
22 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.883+216T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 8/21 | chr19 | 4702387 | |||||||
chr19:4702728 | G | C | 13 | a0001c0002t0002g0004 a0001c0002t0002g0033 a0001c0002t0002g0046 others(10): Show |
13 | HG02055.hp2 HG02109.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.770-12C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702728 | |||||||
chr19:4702836 | G | A | 22 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0033 others(19): Show |
22 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.770-120C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702836 | |||||||
chr19:4702841 | G | GGGGAGGG others(72): Show |
1 | a0001c0001t0003g0101 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.770-126_770-125ins others(79): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(138): Show |
1 | a0001c0001t0001g0248 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.770-126_770-125ins others(145): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(139): Show |
1 | a0001c0001t0001g0276 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.770-126_770-125ins others(146): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(65): Show |
1 | a0001c0001t0003g0083 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.770-126_770-125ins others(72): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(119): Show |
1 | a0001c0001t0002g0171 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.770-126_770-125ins others(126): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(99): Show |
2 | a0001c0001t0002g0050 a0001c0001t0002g0082 |
2 | HG02258.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.770-126_770-125ins others(106): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(109): Show |
3 | a0001c0001t0002g0028 a0001c0001t0002g0100 a0001c0001t0002g0122 |
3 | HG03041.hp2 HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.770-126_770-125ins others(116): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(119): Show |
8 | a0001c0001t0001g0067 a0001c0001t0002g0030 a0001c0001t0002g0031 others(5): Show |
8 | HG02148.hp1 HG02148.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.770-126_770-125ins others(126): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(129): Show |
9 | a0001c0001t0002g0059 a0001c0001t0002g0081 a0001c0001t0002g0088 others(6): Show |
9 | HG02273.hp1 HG02300.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.770-126_770-125ins others(136): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(149): Show |
1 | a0001c0001t0002g0041 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.770-126_770-125ins others(156): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(109): Show |
1 | a0001c0001t0002g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.770-126_770-125ins others(116): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(53): Show |
3 | a0001c0001t0003g0087 a0001c0001t0003g0090 a0001c0001t0003g0150 |
3 | HG02027.hp1 NA18946.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.770-126_770-125ins others(60): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(89): Show |
1 | a0001c0001t0004g0137 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.770-126_770-125ins others(96): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(119): Show |
11 | a0001c0001t0001g0076 a0001c0001t0001g0204 a0001c0001t0002g0005 others(8): Show |
11 | HG00597.hp2 HG01884.hp2 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.770-126_770-125ins others(126): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(129): Show |
28 | a0001c0001t0001g0001 a0001c0001t0001g0073 a0001c0001t0001g0074 others(25): Show |
29 | HG01070.hp2 HG01109.hp2 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.770-126_770-125ins others(136): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(139): Show |
8 | a0001c0001t0001g0027 a0001c0001t0001g0110 a0001c0001t0001g0185 others(5): Show |
8 | HG00280.hp2 HG01891.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.770-126_770-125ins others(146): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(149): Show |
9 | a0001c0001t0001g0159 a0001c0001t0001g0215 a0001c0001t0002g0032 others(6): Show |
9 | HG01081.hp2 HG01168.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.770-126_770-125ins others(156): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(159): Show |
1 | a0001c0001t0004g0138 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.770-126_770-125ins others(166): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(63): Show |
22 | a0001c0001t0002g0232 a0001c0001t0002g0255 a0001c0001t0002g0257 others(19): Show |
22 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.770-126_770-125ins others(70): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(119): Show |
1 | a0001c0001t0001g0125 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.770-126_770-125ins others(126): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(129): Show |
10 | a0001c0001t0001g0077 a0001c0001t0001g0119 a0001c0001t0001g0134 others(7): Show |
10 | HG01106.hp1 HG01433.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.770-126_770-125ins others(136): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(139): Show |
61 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(58): Show |
61 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.770-126_770-125ins others(146): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(149): Show |
37 | a0001c0001t0001g0002 a0001c0001t0001g0117 a0001c0001t0001g0121 others(34): Show |
38 | HG00639.hp2 HG00733.hp2 HG01081.hp1 others(35): Show |
intron_variant | MODIFIER | c.770-126_770-125ins others(156): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(159): Show |
11 | a0001c0001t0001g0071 a0001c0001t0001g0153 a0001c0001t0001g0173 others(8): Show |
11 | HG01255.hp1 HG01433.hp2 HG01516.hp1 others(8): Show |
intron_variant | MODIFIER | c.770-126_770-125ins others(166): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(169): Show |
1 | a0001c0001t0004g0063 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.770-126_770-125ins others(176): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(179): Show |
1 | a0001c0001t0001g0220 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.770-126_770-125ins others(186): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(73): Show |
17 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0034 others(14): Show |
17 | HG01515.hp1 HG01517.hp2 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.770-126_770-125ins others(80): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(139): Show |
4 | a0001c0001t0001g0094 a0001c0001t0001g0303 a0001c0001t0005g0007 others(1): Show |
4 | HG01243.hp1 HG02055.hp1 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.770-126_770-125ins others(146): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(149): Show |
4 | a0001c0001t0001g0151 a0001c0001t0001g0292 a0001c0001t0005g0025 others(1): Show |
4 | HG00639.hp1 HG02976.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.770-126_770-125ins others(156): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(159): Show |
13 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(10): Show |
13 | HG02145.hp1 HG02280.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.770-126_770-125ins others(166): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(169): Show |
2 | a0001c0001t0001g0029 a0001c0001t0004g0091 |
2 | HG02451.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.770-126_770-125ins others(176): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(179): Show |
1 | a0001c0001t0001g0014 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.770-126_770-125ins others(186): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(83): Show |
1 | a0001c0001t0003g0102 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.770-126_770-125ins others(90): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(159): Show |
1 | a0001c0001t0001g0301 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.770-126_770-125ins others(166): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(169): Show |
3 | a0001c0001t0001g0187 a0001c0001t0001g0228 a0001c0015t0001g0309 |
3 | HG02165.hp1 NA18947.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.770-126_770-125ins others(176): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(93): Show |
2 | a0001c0001t0003g0126 a0001c0001t0003g0127 |
2 | HG01884.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.770-126_770-125ins others(100): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(165): Show |
1 | a0001c0001t0017g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.770-126_770-125ins others(172): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGAGGG others(129): Show |
1 | a0001c0001t0001g0167 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.770-126_770-125ins others(136): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702841 | G | GGGGGAGG others(152): Show |
1 | a0001c0009t0001g0271 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.770-126_770-125ins others(159): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702841 | |||||||
chr19:4702846 | G | GGGAGAGG others(89): Show |
1 | a0001c0002t0019g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.770-131_770-130ins others(96): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702846 | |||||||
chr19:4702846 | G | GGGAGAGG others(99): Show |
21 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0033 others(18): Show |
21 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.770-131_770-130ins others(106): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702846 | |||||||
chr19:4702855 | A | AGGGAGAG others(129): Show |
1 | a0001c0001t0002g0109 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.770-140_770-139ins others(136): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702855 | |||||||
chr19:4702859 | A | AGAGGGAG others(150): Show |
1 | a0001c0001t0004g0008 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.770-144_770-143ins others(157): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702859 | |||||||
chr19:4702861 | A | AGGGAGGG others(150): Show |
1 | a0001c0001t0001g0095 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.770-146_770-145ins others(157): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702861 | |||||||
chr19:4702875 | C | T | 1 | a0003c0006t0001g0199 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.770-159G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702875 | |||||||
chr19:4702877 | G | A | 9 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(6): Show |
9 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.770-161C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702877 | |||||||
chr19:4702915 | C | T | 4 | a0001c0001t0002g0015 a0001c0001t0002g0034 a0001c0001t0002g0035 others(1): Show |
4 | HG02109.hp2 HG02280.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.770-199G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4702915 | |||||||
chr19:4703095 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.770-379C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4703095 | |||||||
chr19:4703107 | C | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0216 |
2 | NA18965.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.770-391G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4703107 | |||||||
chr19:4703212 | C | T | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0036 others(77): Show |
82 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(79): Show |
intron_variant | MODIFIER | c.770-496G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4703212 | |||||||
chr19:4703225 | G | T | 1 | a0001c0001t0005g0007 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.770-509C>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4703225 | |||||||
chr19:4703288 | A | G | 1 | a0001c0001t0002g0304 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.770-572T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4703288 | |||||||
chr19:4703343 | G | A | 1 | a0001c0001t0002g0120 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.769+543C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4703343 | |||||||
chr19:4703445 | G | A | 26 | a0001c0001t0002g0005 a0001c0001t0002g0028 a0001c0001t0002g0030 others(23): Show |
26 | HG01884.hp2 HG02056.hp1 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.769+441C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4703445 | |||||||
chr19:4703453 | C | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0188 |
2 | HG01099.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.769+433G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4703453 | |||||||
chr19:4703454 | G | A | 1 | a0001c0001t0017g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.769+432C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4703454 | |||||||
chr19:4703467 | A | C | 1 | a0001c0001t0002g0032 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.769+419T>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4703467 | |||||||
chr19:4703470 | C | CA | 120 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(117): Show |
120 | HG00597.hp1 HG00609.hp2 HG00621.hp1 others(117): Show |
intron_variant | MODIFIER | c.769+415dupT | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4703470 | |||||||
chr19:4703470 | C | CAA | 19 | a0001c0001t0002g0015 a0001c0001t0002g0045 a0001c0001t0002g0212 others(16): Show |
19 | HG01361.hp2 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.769+414_769+415dup others(2): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4703470 | |||||||
chr19:4703470 | CA | C | 6 | a0001c0001t0001g0119 a0001c0001t0001g0153 a0001c0001t0001g0191 others(3): Show |
6 | HG00639.hp2 HG01106.hp1 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.769+415delT | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4703470 | |||||||
chr19:4703503 | G | C | 1 | a0001c0009t0001g0271 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.769+383C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4703503 | |||||||
chr19:4703504 | C | G | 1 | a0001c0009t0001g0271 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.769+382G>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4703504 | |||||||
chr19:4703654 | A | C | 245 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(242): Show |
247 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(244): Show |
intron_variant | MODIFIER | c.769+232T>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4703654 | |||||||
chr19:4703670 | CA | C | 11 | a0001c0001t0001g0020 a0001c0001t0001g0036 a0001c0001t0001g0164 others(8): Show |
11 | HG01168.hp1 HG01168.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.769+215delT | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4703670 | |||||||
chr19:4703681 | AAAAG | A | 22 | a0001c0002t0002g0004 a0001c0002t0002g0006 a0001c0002t0002g0033 others(19): Show |
22 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.769+201_769+204del others(4): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4703681 | |||||||
chr19:4703696 | A | T | 1 | a0001c0001t0001g0241 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.769+190T>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4703696 | |||||||
chr19:4703816 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.769+70C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 7/21 | chr19 | 4703816 | |||||||
chr19:4704876 | G | A | 1 | a0001c0001t0002g0032 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.427-572C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 5/21 | chr19 | 4704876 | |||||||
chr19:4704992 | T | C | 37 | a0001c0001t0002g0032 a0001c0001t0002g0131 a0001c0001t0002g0212 others(34): Show |
37 | HG00733.hp2 HG01168.hp2 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.427-688A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 5/21 | chr19 | 4704992 | |||||||
chr19:4705140 | G | A | 1 | a0001c0001t0002g0032 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.426+718C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 5/21 | chr19 | 4705140 | |||||||
chr19:4705193 | T | TTTATGTT others(13): Show |
1 | a0001c0001t0001g0306 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.426+664_426+665ins others(20): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 5/21 | chr19 | 4705193 | |||||||
chr19:4705194 | A | T | 1 | a0001c0001t0001g0306 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.426+664T>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 5/21 | chr19 | 4705194 | |||||||
chr19:4705203 | T | C | 2 | a0001c0001t0001g0173 a0001c0001t0001g0188 |
2 | HG01099.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.426+655A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 5/21 | chr19 | 4705203 | |||||||
chr19:4705292 | C | T | 1 | a0004c0019t0007g0312 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.426+566G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 5/21 | chr19 | 4705292 | |||||||
chr19:4705496 | A | G | 37 | a0001c0001t0002g0032 a0001c0001t0002g0131 a0001c0001t0002g0212 others(34): Show |
37 | HG00733.hp2 HG01168.hp2 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.426+362T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 5/21 | chr19 | 4705496 | |||||||
chr19:4705544 | C | T | 47 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0034 others(44): Show |
47 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.426+314G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 5/21 | chr19 | 4705544 | |||||||
chr19:4705568 | T | C | 13 | a0001c0001t0002g0005 a0001c0001t0002g0028 a0001c0001t0002g0050 others(10): Show |
13 | HG01243.hp1 HG01884.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.426+290A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 5/21 | chr19 | 4705568 | |||||||
chr19:4705715 | C | T | 1 | a0001c0002t0019g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.426+143G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 5/21 | chr19 | 4705715 | |||||||
chr19:4706086 | C | T | 47 | a0001c0001t0002g0003 a0001c0001t0002g0015 a0001c0001t0002g0034 others(44): Show |
47 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(44): Show |
intron_variant | MODIFIER | c.314-116G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4706086 | |||||||
chr19:4706089 | C | T | 7 | a0001c0001t0003g0084 a0001c0001t0003g0086 a0001c0001t0003g0103 others(4): Show |
7 | NA18944.hp1 NA18946.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.314-119G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4706089 | |||||||
chr19:4706195 | C | T | 2 | a0001c0001t0003g0126 a0001c0001t0003g0127 |
2 | HG01884.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.314-225G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4706195 | |||||||
chr19:4706254 | T | C | 24 | a0001c0001t0002g0005 a0001c0001t0002g0028 a0001c0001t0002g0041 others(21): Show |
24 | HG01884.hp2 HG02056.hp1 HG02080.hp2 others(21): Show |
intron_variant | MODIFIER | c.314-284A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4706254 | |||||||
chr19:4706262 | C | A | 4 | a0001c0001t0003g0079 a0001c0001t0003g0083 a0001c0001t0003g0101 others(1): Show |
4 | NA18947.hp1 NA18953.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.314-292G>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4706262 | |||||||
chr19:4706267 | C | T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0247 |
2 | HG01106.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.314-297G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4706267 | |||||||
chr19:4706268 | G | A | 2 | a0001c0001t0001g0236 a0001c0001t0001g0241 |
2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.314-298C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4706268 | |||||||
chr19:4706330 | C | CA | 106 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(103): Show |
106 | HG00323.hp2 HG00733.hp2 HG01109.hp1 others(103): Show |
intron_variant | MODIFIER | c.314-361dupT | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4706330 | |||||||
chr19:4706330 | C | CAA | 56 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0001c0001t0001g0306 others(53): Show |
56 | HG00597.hp1 HG00609.hp2 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.314-362_314-361dup others(2): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4706330 | |||||||
chr19:4706394 | C | T | 1 | a0001c0001t0002g0249 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.314-424G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4706394 | |||||||
chr19:4706584 | G | C | 9 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0001c0003t0001g0013 others(6): Show |
9 | HG01255.hp2 HG01891.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.314-614C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4706584 | |||||||
chr19:4706788 | C | T | 1 | a0001c0001t0002g0128 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.314-818G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4706788 | |||||||
chr19:4706865 | G | A | 1 | a0001c0001t0004g0011 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.314-895C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4706865 | |||||||
chr19:4706930 | C | G | 1 | a0001c0018t0010g0233 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.314-960G>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4706930 | |||||||
chr19:4706951 | C | T | 4 | a0001c0001t0002g0131 a0001c0001t0002g0212 a0001c0001t0002g0224 others(1): Show |
4 | HG02155.hp2 HG04184.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-981G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4706951 | |||||||
chr19:4706957 | C | G | 1 | a0001c0001t0002g0249 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.314-987G>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4706957 | |||||||
chr19:4706977 | A | C | 30 | a0001c0001t0002g0005 a0001c0001t0002g0028 a0001c0001t0002g0030 others(27): Show |
30 | HG01884.hp2 HG02056.hp1 HG02080.hp2 others(27): Show |
intron_variant | MODIFIER | c.314-1007T>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4706977 | |||||||
chr19:4706983 | G | A | 1 | a0001c0002t0002g0245 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.314-1013C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4706983 | |||||||
chr19:4707044 | G | A | 4 | a0001c0001t0005g0007 a0001c0001t0005g0025 a0001c0001t0005g0026 others(1): Show |
4 | HG01243.hp1 HG02280.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-1074C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4707044 | |||||||
chr19:4707107 | C | T | 7 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(4): Show |
7 | HG02145.hp1 HG02451.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.314-1137G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4707107 | |||||||
chr19:4707108 | G | A | 10 | a0001c0001t0001g0251 a0001c0001t0004g0093 a0001c0001t0004g0140 others(7): Show |
10 | HG01358.hp1 HG01928.hp2 HG01975.hp2 others(7): Show |
intron_variant | MODIFIER | c.314-1138C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4707108 | |||||||
chr19:4707178 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.314-1208T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4707178 | |||||||
chr19:4707198 | T | C | 1 | a0001c0001t0004g0259 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.314-1228A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4707198 | |||||||
chr19:4707257 | G | A | 1 | a0001c0003t0001g0145 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.314-1287C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4707257 | |||||||
chr19:4707460 | T | C | 3 | a0001c0001t0005g0025 a0001c0001t0005g0026 a0001c0001t0005g0085 |
3 | HG02280.hp2 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.314-1490A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4707460 | |||||||
chr19:4707544 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.314-1574G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4707544 | |||||||
chr19:4707614 | C | CT | 87 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0019 others(84): Show |
87 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.314-1645dupA | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4707614 | |||||||
chr19:4707614 | C | CTT | 20 | a0001c0001t0001g0181 a0001c0001t0002g0059 a0001c0001t0002g0260 others(17): Show |
20 | HG00597.hp1 HG00609.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.314-1646_314-1645d others(4): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4707614 | |||||||
chr19:4707614 | CT | C | 40 | a0001c0001t0001g0044 a0001c0001t0002g0005 a0001c0001t0002g0028 others(37): Show |
40 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.314-1645delA | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4707614 | |||||||
chr19:4707614 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0132 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.314-1656_314-1645d others(14): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4707614 | |||||||
chr19:4707700 | A | G | 1 | a0001c0001t0002g0260 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.314-1730T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4707700 | |||||||
chr19:4707787 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.314-1817C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4707787 | |||||||
chr19:4707890 | T | C | 1 | a0001c0001t0017g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.314-1920A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4707890 | |||||||
chr19:4707899 | A | T | 1 | a0001c0001t0002g0225 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.314-1929T>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4707899 | |||||||
chr19:4708090 | C | A | 37 | a0001c0001t0002g0032 a0001c0001t0002g0131 a0001c0001t0002g0212 others(34): Show |
37 | HG00733.hp2 HG01168.hp2 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.314-2120G>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4708090 | |||||||
chr19:4708114 | C | T | 29 | a0001c0001t0002g0005 a0001c0001t0002g0028 a0001c0001t0002g0030 others(26): Show |
29 | HG01884.hp2 HG02056.hp1 HG02080.hp2 others(26): Show |
intron_variant | MODIFIER | c.314-2144G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4708114 | |||||||
chr19:4708218 | C | A | 1 | a0001c0001t0001g0241 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.314-2248G>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4708218 | |||||||
chr19:4708527 | G | A | 2 | a0001c0001t0002g0030 a0001c0001t0002g0031 |
2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.314-2557C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4708527 | |||||||
chr19:4708556 | C | G | 37 | a0001c0001t0002g0032 a0001c0001t0002g0131 a0001c0001t0002g0212 others(34): Show |
37 | HG00733.hp2 HG01168.hp2 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.314-2586G>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4708556 | |||||||
chr19:4708604 | C | T | 3 | a0002c0005t0006g0021 a0002c0005t0006g0022 a0002c0005t0006g0023 |
3 | HG01891.hp2 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.314-2634G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4708604 | |||||||
chr19:4708693 | C | T | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG00738.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.314-2723G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4708693 | |||||||
chr19:4708774 | G | T | 1 | a0001c0001t0002g0225 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.314-2804C>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4708774 | |||||||
chr19:4708800 | G | C | 1 | a0001c0001t0017g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.314-2830C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4708800 | |||||||
chr19:4708944 | G | C | 32 | a0001c0001t0002g0131 a0001c0001t0002g0212 a0001c0001t0002g0224 others(29): Show |
32 | HG00733.hp2 HG01168.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.314-2974C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4708944 | |||||||
chr19:4709020 | C | T | 1 | a0001c0001t0002g0089 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.314-3050G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4709020 | |||||||
chr19:4709074 | C | T | 25 | a0001c0001t0002g0005 a0001c0001t0002g0028 a0001c0001t0002g0030 others(22): Show |
25 | HG01884.hp2 HG02056.hp1 HG02080.hp2 others(22): Show |
intron_variant | MODIFIER | c.314-3104G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4709074 | |||||||
chr19:4709169 | C | T | 28 | a0001c0001t0002g0005 a0001c0001t0002g0028 a0001c0001t0002g0030 others(25): Show |
28 | HG01884.hp2 HG02056.hp1 HG02080.hp2 others(25): Show |
intron_variant | MODIFIER | c.314-3199G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4709169 | |||||||
chr19:4709219 | G | A | 4 | a0001c0001t0005g0007 a0001c0001t0005g0025 a0001c0001t0005g0026 others(1): Show |
4 | HG01243.hp1 HG02280.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.314-3249C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4709219 | |||||||
chr19:4709230 | G | GT | 7 | a0001c0003t0001g0013 a0001c0003t0001g0053 a0001c0003t0001g0143 others(4): Show |
7 | HG01255.hp2 HG01891.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.314-3261dupA | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4709230 | |||||||
chr19:4709230 | G | T | 4 | a0001c0001t0003g0079 a0001c0001t0003g0083 a0001c0001t0003g0101 others(1): Show |
4 | NA18947.hp1 NA18953.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.314-3260C>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4709230 | |||||||
chr19:4709293 | G | A | 22 | a0001c0001t0001g0246 a0001c0002t0002g0004 a0001c0002t0002g0006 others(19): Show |
22 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.314-3323C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4709293 | |||||||
chr19:4709296 | T | C | 1 | a0001c0001t0001g0223 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.314-3326A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4709296 | |||||||
chr19:4709524 | C | T | 1 | a0001c0001t0002g0120 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.314-3554G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4709524 | |||||||
chr19:4709574 | T | G | 1 | a0004c0019t0007g0312 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.314-3604A>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4709574 | |||||||
chr19:4709691 | T | C | 1 | a0001c0001t0017g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.314-3721A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4709691 | |||||||
chr19:4709993 | C | T | 1 | a0001c0001t0002g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.314-4023G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4709993 | |||||||
chr19:4709994 | G | A | 1 | a0001c0001t0003g0069 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.314-4024C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4709994 | |||||||
chr19:4710058 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.313+4023G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4710058 | |||||||
chr19:4710094 | C | G | 2 | a0001c0001t0002g0030 a0001c0001t0002g0031 |
2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.313+3987G>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4710094 | |||||||
chr19:4710423 | G | A | 1 | a0001c0018t0010g0233 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.313+3658C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4710423 | |||||||
chr19:4710504 | G | A | 1 | a0001c0001t0001g0263 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.313+3577C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4710504 | |||||||
chr19:4710633 | G | A | 1 | a0001c0001t0001g0274 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.313+3448C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4710633 | |||||||
chr19:4710723 | G | C | 1 | a0001c0001t0002g0171 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.313+3358C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4710723 | |||||||
chr19:4710747 | G | A | 8 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(5): Show |
8 | HG02145.hp1 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.313+3334C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4710747 | |||||||
chr19:4710802 | C | T | 5 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0001t0001g0306 others(2): Show |
5 | HG00621.hp1 HG02165.hp2 NA18944.hp2 others(2): Show |
intron_variant | MODIFIER | c.313+3279G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4710802 | |||||||
chr19:4710869 | G | T | 1 | a0001c0001t0001g0072 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.313+3212C>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4710869 | |||||||
chr19:4710899 | G | A | 1 | a0001c0001t0017g0234 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.313+3182C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4710899 | |||||||
chr19:4711036 | C | T | 1 | a0001c0001t0004g0252 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.313+3045G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4711036 | |||||||
chr19:4711082 | C | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(230): Show |
235 | HG00280.hp1 HG00323.hp1 HG00597.hp1 others(232): Show |
intron_variant | MODIFIER | c.313+2999G>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4711082 | |||||||
chr19:4711098 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.313+2983G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4711098 | |||||||
chr19:4711099 | G | A | 1 | a0001c0002t0002g0047 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.313+2982C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4711099 | |||||||
chr19:4711296 | G | C | 1 | a0001c0001t0001g0306 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.313+2785C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4711296 | |||||||
chr19:4711329 | CAG | C | 10 | a0001c0002t0002g0004 a0001c0002t0002g0033 a0001c0002t0002g0046 others(7): Show |
10 | HG02109.hp1 HG02486.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.313+2750_313+2751d others(4): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4711329 | |||||||
chr19:4711370 | C | G | 1 | a0001c0001t0001g0183 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.313+2711G>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4711370 | |||||||
chr19:4711443 | T | C | 4 | a0001c0001t0002g0045 a0001c0001t0002g0051 a0001c0001t0002g0052 others(1): Show |
4 | HG03098.hp1 HG03098.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.313+2638A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4711443 | |||||||
chr19:4711708 | A | G | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | NA18965.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.313+2373T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4711708 | |||||||
chr19:4711772 | C | CA | 50 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0066 others(47): Show |
51 | HG00280.hp2 HG00597.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.313+2308dupT | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4711772 | |||||||
chr19:4711772 | C | CAA | 13 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(10): Show |
13 | HG00735.hp1 HG00735.hp2 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.313+2307_313+2308d others(4): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4711772 | |||||||
chr19:4711772 | CA | C | 22 | a0001c0001t0001g0029 a0001c0001t0001g0110 a0001c0001t0001g0182 others(19): Show |
22 | HG00609.hp2 HG01069.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.313+2308delT | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4711772 | |||||||
chr19:4711772 | CAA | C | 26 | a0001c0001t0001g0246 a0001c0001t0002g0030 a0001c0001t0002g0031 others(23): Show |
26 | HG01109.hp1 HG01891.hp2 HG02056.hp1 others(23): Show |
intron_variant | MODIFIER | c.313+2307_313+2308d others(4): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4711772 | |||||||
chr19:4711772 | CAAA | C | 32 | a0001c0001t0002g0005 a0001c0001t0002g0081 a0001c0001t0002g0131 others(29): Show |
32 | HG00733.hp2 HG01168.hp2 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.313+2306_313+2308d others(5): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4711772 | |||||||
chr19:4711772 | CAAAA | C | 7 | a0001c0001t0002g0032 a0001c0001t0002g0225 a0001c0001t0004g0280 others(4): Show |
7 | HG01243.hp1 HG01496.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.313+2305_313+2308d others(6): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4711772 | |||||||
chr19:4711882 | T | C | 1 | a0001c0001t0001g0269 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.313+2199A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4711882 | |||||||
chr19:4711940 | G | C | 1 | a0001c0001t0002g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.313+2141C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4711940 | |||||||
chr19:4712128 | G | C | 1 | a0001c0001t0001g0161 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.313+1953C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4712128 | |||||||
chr19:4712171 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.313+1910C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4712171 | |||||||
chr19:4712186 | T | C | 13 | a0001c0002t0002g0004 a0001c0002t0002g0033 a0001c0002t0002g0046 others(10): Show |
13 | HG02055.hp2 HG02109.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.313+1895A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4712186 | |||||||
chr19:4712624 | G | A | 1 | a0001c0018t0010g0233 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.313+1457C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4712624 | |||||||
chr19:4712706 | G | A | 1 | a0002c0005t0006g0021 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.313+1375C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4712706 | |||||||
chr19:4712818 | T | C | 2 | a0001c0001t0002g0257 a0001c0001t0002g0258 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.313+1263A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4712818 | |||||||
chr19:4712899 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.313+1182G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4712899 | |||||||
chr19:4712940 | C | T | 1 | a0001c0002t0002g0245 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.313+1141G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4712940 | |||||||
chr19:4713058 | A | G | 3 | a0001c0001t0001g0067 a0001c0001t0001g0215 a0001c0001t0001g0248 |
3 | HG01081.hp2 HG02148.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.313+1023T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4713058 | |||||||
chr19:4713064 | G | A | 1 | a0001c0001t0004g0063 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.313+1017C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4713064 | |||||||
chr19:4713144 | C | T | 1 | a0001c0001t0002g0034 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.313+937G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4713144 | |||||||
chr19:4713166 | C | T | 1 | a0001c0018t0010g0233 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.313+915G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4713166 | |||||||
chr19:4713196 | C | T | 1 | a0001c0001t0001g0174 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.313+885G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4713196 | |||||||
chr19:4713234 | C | A | 1 | a0001c0001t0001g0246 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.313+847G>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4713234 | |||||||
chr19:4713260 | C | T | 1 | a0001c0001t0002g0032 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.313+821G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4713260 | |||||||
chr19:4713323 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.313+758G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4713323 | |||||||
chr19:4713375 | C | A | 5 | a0001c0001t0001g0174 a0001c0001t0001g0210 a0001c0001t0001g0211 others(2): Show |
5 | HG00323.hp2 HG00621.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.313+706G>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4713375 | |||||||
chr19:4713418 | G | C | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0042 others(117): Show |
122 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(119): Show |
intron_variant | MODIFIER | c.313+663C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4713418 | |||||||
chr19:4713440 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.313+641G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4713440 | |||||||
chr19:4713456 | C | T | 2 | a0001c0002t0002g0047 a0001c0002t0002g0048 |
2 | HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.313+625G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4713456 | |||||||
chr19:4713535 | G | A | 1 | a0001c0001t0003g0149 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.313+546C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4713535 | |||||||
chr19:4713588 | C | T | 30 | a0001c0001t0001g0180 a0001c0001t0002g0005 a0001c0001t0002g0028 others(27): Show |
30 | HG01884.hp1 HG02132.hp2 HG02145.hp2 others(27): Show |
intron_variant | MODIFIER | c.313+493G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4713588 | |||||||
chr19:4713589 | G | A | 8 | a0001c0001t0001g0078 a0001c0001t0001g0099 a0001c0001t0001g0119 others(5): Show |
8 | HG01070.hp1 HG01099.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.313+492C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4713589 | |||||||
chr19:4713761 | A | C | 12 | a0001c0001t0002g0003 a0001c0001t0002g0032 a0001c0002t0002g0033 others(9): Show |
12 | HG02486.hp1 HG02630.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.313+320T>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4713761 | |||||||
chr19:4713802 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0002g0057 |
2 | HG02109.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.313+279G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4713802 | |||||||
chr19:4713849 | T | C | 5 | a0001c0001t0002g0249 a0001c0002t0002g0054 a0001c0002t0002g0055 others(2): Show |
5 | HG02109.hp1 HG02717.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.313+232A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4713849 | |||||||
chr19:4713879 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.313+202G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4713879 | |||||||
chr19:4713901 | G | A | 1 | a0001c0001t0005g0085 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.313+180C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4713901 | |||||||
chr19:4714032 | T | C | 158 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0016 others(155): Show |
159 | HG00280.hp2 HG00323.hp2 HG00597.hp1 others(156): Show |
intron_variant | MODIFIER | c.313+49A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 4/21 | chr19 | 4714032 | |||||||
chr19:4714398 | A | G | 1 | a0001c0002t0002g0129 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.57-61T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4714398 | |||||||
chr19:4714412 | G | A | 1 | a0001c0001t0003g0150 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.57-75C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4714412 | |||||||
chr19:4714456 | C | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(144): Show |
148 | HG00597.hp1 HG00639.hp2 HG00733.hp1 others(145): Show |
intron_variant | MODIFIER | c.57-119G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4714456 | |||||||
chr19:4714702 | G | C | 3 | a0001c0001t0002g0232 a0001c0001t0017g0234 a0001c0018t0010g0233 |
3 | HG02965.hp2 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.57-365C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4714702 | |||||||
chr19:4714966 | T | G | 1 | a0001c0001t0002g0235 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.57-629A>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4714966 | |||||||
chr19:4715004 | G | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0042 others(99): Show |
103 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.57-667C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4715004 | |||||||
chr19:4715019 | C | CT | 87 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0066 others(84): Show |
87 | HG00597.hp2 HG00733.hp2 HG00735.hp2 others(84): Show |
intron_variant | MODIFIER | c.57-683dupA | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4715019 | |||||||
chr19:4715019 | C | CTT | 81 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(78): Show |
82 | HG00323.hp2 HG00597.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.57-684_57-683dupAA | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4715019 | |||||||
chr19:4715019 | C | CTTT | 27 | a0001c0001t0001g0036 a0001c0001t0001g0068 a0001c0001t0001g0071 others(24): Show |
27 | HG00609.hp2 HG01109.hp2 HG01928.hp1 others(24): Show |
intron_variant | MODIFIER | c.57-685_57-683dupAA others(1): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4715019 | |||||||
chr19:4715019 | CTTT | C | 8 | a0001c0001t0001g0275 a0001c0001t0002g0032 a0001c0001t0002g0255 others(5): Show |
8 | HG00733.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.57-685_57-683delAA others(1): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4715019 | |||||||
chr19:4715019 | CTTTT | C | 11 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0043 others(8): Show |
12 | HG00738.hp2 HG01243.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.57-686_57-683delAA others(2): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4715019 | |||||||
chr19:4715019 | CTTTTT | C | 50 | a0001c0001t0001g0044 a0001c0001t0001g0159 a0001c0001t0001g0264 others(47): Show |
50 | HG00280.hp1 HG00323.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.57-687_57-683delAA others(3): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4715019 | |||||||
chr19:4715019 | CTTTTTT | C | 32 | a0001c0001t0001g0027 a0001c0001t0001g0228 a0001c0001t0001g0236 others(29): Show |
32 | HG00280.hp2 HG01243.hp1 HG01516.hp1 others(29): Show |
intron_variant | MODIFIER | c.57-688_57-683delAA others(4): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4715019 | |||||||
chr19:4715019 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0132 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.57-692_57-683delAA others(8): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4715019 | |||||||
chr19:4715019 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0001g0039 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.57-694_57-683delAA others(10): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4715019 | |||||||
chr19:4715080 | C | T | 3 | a0001c0001t0002g0232 a0001c0001t0017g0234 a0001c0018t0010g0233 |
3 | HG02965.hp2 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.57-743G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4715080 | |||||||
chr19:4715116 | A | T | 226 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(223): Show |
228 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(225): Show |
intron_variant | MODIFIER | c.57-779T>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4715116 | |||||||
chr19:4715174 | C | G | 1 | a0001c0001t0001g0159 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.57-837G>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4715174 | |||||||
chr19:4715234 | G | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(131): Show |
135 | HG00597.hp1 HG00639.hp2 HG00733.hp1 others(132): Show |
intron_variant | MODIFIER | c.57-897C>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4715234 | |||||||
chr19:4715243 | G | A | 7 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(4): Show |
7 | HG00280.hp2 HG01255.hp1 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.57-906C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4715243 | |||||||
chr19:4715293 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0004g0206 |
2 | HG01168.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.57-956C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4715293 | |||||||
chr19:4715395 | C | G | 1 | a0001c0001t0003g0069 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.57-1058G>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4715395 | |||||||
chr19:4715428 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0002g0028 |
2 | HG03041.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.57-1091G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4715428 | |||||||
chr19:4715583 | A | T | 1 | a0001c0002t0002g0033 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.57-1246T>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4715583 | |||||||
chr19:4715589 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.57-1252G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4715589 | |||||||
chr19:4715849 | G | A | 12 | a0001c0001t0002g0045 a0001c0001t0002g0050 a0001c0001t0002g0051 others(9): Show |
12 | HG02109.hp1 HG02258.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.57-1512C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4715849 | |||||||
chr19:4715851 | G | A | 3 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0303 |
3 | HG01069.hp2 HG01934.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.57-1514C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4715851 | |||||||
chr19:4715953 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.57-1616G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4715953 | |||||||
chr19:4715955 | T | C | 12 | a0001c0001t0002g0045 a0001c0001t0002g0050 a0001c0001t0002g0051 others(9): Show |
12 | HG02109.hp1 HG02258.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.57-1618A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4715955 | |||||||
chr19:4716014 | G | A | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0007c0012t0001g0202 |
3 | HG00597.hp2 HG01952.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.57-1677C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4716014 | |||||||
chr19:4716049 | C | T | 1 | a0001c0001t0002g0232 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.57-1712G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4716049 | |||||||
chr19:4716095 | G | A | 2 | a0001c0001t0002g0030 a0001c0001t0002g0031 |
2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.57-1758C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4716095 | |||||||
chr19:4716191 | C | T | 16 | a0001c0001t0002g0032 a0001c0001t0002g0045 a0001c0001t0002g0050 others(13): Show |
16 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.57-1854G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4716191 | |||||||
chr19:4716250 | C | T | 12 | a0001c0001t0002g0045 a0001c0001t0002g0050 a0001c0001t0002g0051 others(9): Show |
12 | HG02109.hp1 HG02258.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.57-1913G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4716250 | |||||||
chr19:4716334 | C | T | 4 | a0001c0001t0002g0032 a0001c0002t0002g0033 a0001c0002t0002g0237 others(1): Show |
4 | HG02055.hp2 HG02895.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.57-1997G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4716334 | |||||||
chr19:4716376 | G | A | 2 | a0001c0001t0002g0304 a0001c0001t0008g0305 |
2 | HG02615.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.57-2039C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4716376 | |||||||
chr19:4716386 | T | C | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(228): Show |
233 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.57-2049A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4716386 | |||||||
chr19:4716409 | A | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(227): Show |
232 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.57-2072T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4716409 | |||||||
chr19:4716419 | T | C | 1 | a0001c0001t0004g0138 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.57-2082A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4716419 | |||||||
chr19:4716420 | G | A | 1 | a0001c0001t0004g0138 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.57-2083C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4716420 | |||||||
chr19:4716423 | A | G | 1 | a0001c0001t0004g0138 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.57-2086T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4716423 | |||||||
chr19:4716439 | C | T | 2 | a0001c0001t0002g0030 a0001c0001t0002g0031 |
2 | HG02451.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.57-2102G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4716439 | |||||||
chr19:4716494 | G | A | 16 | a0001c0001t0002g0032 a0001c0001t0002g0045 a0001c0001t0002g0050 others(13): Show |
16 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.57-2157C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4716494 | |||||||
chr19:4716505 | C | T | 2 | a0001c0001t0001g0272 a0001c0001t0001g0273 |
2 | HG00738.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.57-2168G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4716505 | |||||||
chr19:4716530 | G | A | 10 | a0001c0001t0001g0141 a0001c0001t0001g0142 a0001c0001t0001g0158 others(7): Show |
10 | HG00639.hp2 HG00735.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.57-2193C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4716530 | |||||||
chr19:4716569 | G | A | 4 | a0001c0001t0002g0032 a0001c0002t0002g0033 a0001c0002t0002g0237 others(1): Show |
4 | HG02055.hp2 HG02895.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.57-2232C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4716569 | |||||||
chr19:4716615 | C | T | 5 | a0001c0001t0001g0246 a0001c0002t0002g0242 a0001c0002t0002g0243 others(2): Show |
5 | HG01109.hp1 HG02622.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.57-2278G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4716615 | |||||||
chr19:4716704 | T | C | 4 | a0001c0003t0001g0143 a0001c0003t0001g0145 a0001c0003t0001g0146 others(1): Show |
4 | HG01255.hp2 HG01891.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.57-2367A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4716704 | |||||||
chr19:4716807 | T | C | 3 | a0001c0001t0001g0306 a0001c0001t0001g0308 a0005c0017t0001g0307 |
3 | HG00621.hp1 NA18995.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.57-2470A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4716807 | |||||||
chr19:4716991 | G | A | 1 | a0001c0015t0001g0309 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.57-2654C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4716991 | |||||||
chr19:4717175 | G | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(229): Show |
234 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.56+2676C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4717175 | |||||||
chr19:4717435 | C | T | 14 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0001c0001t0002g0005 others(11): Show |
14 | HG01243.hp1 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.56+2416G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4717435 | |||||||
chr19:4717503 | G | A | 12 | a0001c0001t0002g0045 a0001c0001t0002g0050 a0001c0001t0002g0051 others(9): Show |
12 | HG02109.hp1 HG02258.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.56+2348C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4717503 | |||||||
chr19:4717660 | A | G | 51 | a0001c0001t0001g0002 a0001c0001t0001g0264 a0001c0001t0001g0265 others(48): Show |
52 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.56+2191T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4717660 | |||||||
chr19:4717685 | C | T | 1 | a0001c0001t0002g0032 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.56+2166G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4717685 | |||||||
chr19:4717803 | C | G | 1 | a0001c0001t0001g0066 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.56+2048G>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4717803 | |||||||
chr19:4717828 | G | A | 14 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0001c0001t0002g0005 others(11): Show |
14 | HG01243.hp1 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.56+2023C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4717828 | |||||||
chr19:4717888 | T | A | 1 | a0001c0001t0001g0141 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.56+1963A>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4717888 | |||||||
chr19:4718032 | T | C | 6 | a0001c0001t0001g0027 a0001c0001t0002g0028 a0001c0003t0001g0143 others(3): Show |
6 | HG01255.hp2 HG01891.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.56+1819A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4718032 | |||||||
chr19:4718158 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.56+1693C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4718158 | |||||||
chr19:4718189 | G | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(131): Show |
135 | HG00597.hp1 HG00735.hp2 HG00738.hp2 others(132): Show |
intron_variant | MODIFIER | c.56+1662C>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4718189 | |||||||
chr19:4718212 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.56+1639C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4718212 | |||||||
chr19:4718311 | G | A | 3 | a0001c0001t0002g0034 a0001c0001t0002g0035 a0001c0001t0002g0057 |
3 | HG02109.hp2 HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.56+1540C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4718311 | |||||||
chr19:4718424 | G | A | 2 | a0001c0001t0002g0034 a0001c0001t0002g0035 |
2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.56+1427C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4718424 | |||||||
chr19:4718427 | T | C | 9 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(6): Show |
9 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.56+1424A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4718427 | |||||||
chr19:4718624 | A | G | 1 | a0001c0009t0001g0271 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.56+1227T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4718624 | |||||||
chr19:4718690 | C | T | 11 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0001c0001t0002g0005 others(8): Show |
11 | HG01243.hp1 HG02257.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.56+1161G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4718690 | |||||||
chr19:4718744 | G | A | 7 | a0001c0001t0002g0254 a0001c0001t0002g0255 a0001c0001t0002g0256 others(4): Show |
7 | HG00733.hp1 HG01167.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.56+1107C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4718744 | |||||||
chr19:4718787 | G | A | 9 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0017 others(6): Show |
9 | HG02145.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.56+1064C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4718787 | |||||||
chr19:4718793 | G | A | 5 | a0001c0001t0003g0064 a0001c0001t0003g0065 a0001c0001t0003g0147 others(2): Show |
5 | HG02145.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.56+1058C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4718793 | |||||||
chr19:4719009 | A | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(229): Show |
234 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.56+842T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4719009 | |||||||
chr19:4719013 | C | G | 82 | a0001c0001t0001g0002 a0001c0001t0001g0159 a0001c0001t0001g0236 others(79): Show |
83 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.56+838G>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4719013 | |||||||
chr19:4719111 | C | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0016 others(138): Show |
142 | HG00597.hp1 HG00735.hp2 HG00738.hp2 others(139): Show |
intron_variant | MODIFIER | c.56+740G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4719111 | |||||||
chr19:4719235 | G | A | 4 | a0001c0001t0001g0027 a0001c0001t0002g0028 a0001c0001t0005g0025 others(1): Show |
4 | HG03041.hp1 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.56+616C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4719235 | |||||||
chr19:4719323 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.56+528C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4719323 | |||||||
chr19:4719326 | T | TTAAA | 132 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0037 others(129): Show |
133 | HG00323.hp2 HG00597.hp1 HG00621.hp2 others(130): Show |
intron_variant | MODIFIER | c.56+521_56+524dupTT others(2): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4719326 | |||||||
chr19:4719326 | TTAAA | T | 41 | a0001c0001t0001g0027 a0001c0001t0001g0159 a0001c0001t0001g0161 others(38): Show |
41 | HG00733.hp1 HG00733.hp2 HG00735.hp1 others(38): Show |
intron_variant | MODIFIER | c.56+521_56+524delTT others(2): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4719326 | |||||||
chr19:4719326 | TTAAATAA others(1): Show |
T | 56 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0043 others(53): Show |
57 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.56+517_56+524delTT others(6): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4719326 | |||||||
chr19:4719326 | TTAAATAA others(5): Show |
T | 1 | a0001c0002t0014g0157 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.56+513_56+524delTT others(10): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4719326 | |||||||
chr19:4719326 | TTAAATAA others(9): Show |
T | 1 | a0001c0003t0001g0013 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.56+509_56+524delTT others(14): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4719326 | |||||||
chr19:4719330 | A | T | 1 | a0001c0001t0001g0153 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.56+521T>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4719330 | |||||||
chr19:4719431 | G | A | 57 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0264 others(54): Show |
58 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.56+420C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4719431 | |||||||
chr19:4719473 | G | C | 57 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0264 others(54): Show |
58 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.56+378C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4719473 | |||||||
chr19:4719608 | G | A | 1 | a0001c0001t0002g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.56+243C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4719608 | |||||||
chr19:4719688 | C | T | 1 | a0001c0004t0003g0040 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.56+163G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4719688 | |||||||
chr19:4719704 | C | T | 3 | a0001c0001t0002g0232 a0001c0001t0017g0234 a0001c0018t0010g0233 |
3 | HG02965.hp2 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.56+147G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4719704 | |||||||
chr19:4719822 | C | T | 4 | a0001c0001t0001g0027 a0001c0001t0002g0028 a0001c0001t0005g0025 others(1): Show |
4 | HG03041.hp1 HG03041.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.56+29G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 3/21 | chr19 | 4719822 | |||||||
chr19:4720019 | C | CCCT | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(194): Show |
199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-35-81_-35-79dupAG others(1): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4720019 | |||||||
chr19:4720030 | G | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(194): Show |
199 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.-35-89C>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4720030 | |||||||
chr19:4720040 | G | GC | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(188): Show |
193 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.-35-100dupG | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4720040 | |||||||
chr19:4720108 | G | C | 2 | a0001c0001t0002g0032 a0001c0002t0002g0033 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-35-167C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4720108 | |||||||
chr19:4720118 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-35-177G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4720118 | |||||||
chr19:4720120 | GGAGGTTC others(55): Show |
G | 1 | a0001c0001t0001g0248 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-35-241_-35-180del others(62): Show |
DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4720120 | |||||||
chr19:4720147 | G | A | 1 | a0001c0001t0005g0007 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-35-206C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4720147 | |||||||
chr19:4720329 | G | A | 2 | a0001c0001t0002g0032 a0001c0002t0002g0033 |
2 | HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-35-388C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4720329 | |||||||
chr19:4720511 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(192): Show |
197 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.-35-570A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4720511 | |||||||
chr19:4720520 | G | A | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(188): Show |
193 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.-35-579C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4720520 | |||||||
chr19:4720522 | G | T | 191 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(188): Show |
193 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.-35-581C>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4720522 | |||||||
chr19:4720544 | C | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(1): Show |
4 | NA18965.hp1 NA18966.hp1 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.-35-603G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4720544 | |||||||
chr19:4720549 | A | G | 2 | a0001c0001t0001g0155 a0008c0021t0001g0154 |
2 | HG01515.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.-35-608T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4720549 | |||||||
chr19:4720570 | T | A | 1 | a0001c0001t0001g0153 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-35-629A>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4720570 | |||||||
chr19:4720584 | T | C | 1 | a0001c0001t0001g0153 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-35-643A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4720584 | |||||||
chr19:4720586 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-35-645G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4720586 | |||||||
chr19:4720599 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0003g0150 |
2 | NA18946.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-35-658C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4720599 | |||||||
chr19:4720689 | G | C | 1 | a0001c0001t0001g0029 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-35-748C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4720689 | |||||||
chr19:4720764 | C | A | 1 | a0001c0001t0001g0229 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-35-823G>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4720764 | |||||||
chr19:4720791 | C | A | 1 | a0001c0013t0001g0230 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-35-850G>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4720791 | |||||||
chr19:4720947 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-35-1006C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4720947 | |||||||
chr19:4720948 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-35-1007T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4720948 | |||||||
chr19:4721061 | C | T | 3 | a0001c0002t0002g0242 a0001c0002t0002g0243 a0001c0002t0002g0244 |
3 | HG02622.hp1 HG02809.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-35-1120G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4721061 | |||||||
chr19:4721068 | C | A | 1 | a0001c0002t0002g0033 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-35-1127G>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4721068 | |||||||
chr19:4721190 | C | T | 13 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0001c0001t0002g0005 others(10): Show |
13 | HG01243.hp1 HG02055.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.-35-1249G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4721190 | |||||||
chr19:4721194 | A | C | 1 | a0001c0001t0001g0248 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-35-1253T>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4721194 | |||||||
chr19:4721210 | A | G | 2 | a0001c0001t0002g0249 a0001c0002t0002g0004 |
2 | HG03098.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-35-1269T>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4721210 | |||||||
chr19:4721334 | C | T | 2 | a0001c0001t0002g0034 a0001c0001t0002g0035 |
2 | HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-36+1165G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4721334 | |||||||
chr19:4721390 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-36+1109C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4721390 | |||||||
chr19:4721400 | G | C | 4 | a0001c0001t0002g0030 a0001c0001t0002g0031 a0001c0001t0002g0032 others(1): Show |
4 | HG02451.hp1 HG02895.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-36+1099C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4721400 | |||||||
chr19:4721504 | G | T | 1 | a0001c0001t0001g0153 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-36+995C>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4721504 | |||||||
chr19:4721548 | A | T | 1 | a0001c0001t0001g0153 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-36+951T>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4721548 | |||||||
chr19:4721833 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-36+666C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4721833 | |||||||
chr19:4721915 | G | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0036 a0001c0001t0001g0037 others(124): Show |
128 | HG00597.hp1 HG00735.hp2 HG00738.hp2 others(125): Show |
intron_variant | MODIFIER | c.-36+584C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4721915 | |||||||
chr19:4721979 | C | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0014 others(207): Show |
212 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.-36+520G>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4721979 | |||||||
chr19:4722194 | C | T | 5 | a0001c0001t0004g0008 a0001c0001t0004g0009 a0001c0001t0004g0010 others(2): Show |
5 | HG01168.hp2 HG01169.hp2 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-36+305G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4722194 | |||||||
chr19:4722263 | T | C | 1 | a0001c0001t0001g0248 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-36+236A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4722263 | |||||||
chr19:4722264 | T | C | 1 | a0001c0001t0001g0248 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-36+235A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4722264 | |||||||
chr19:4722265 | C | T | 1 | a0001c0001t0001g0248 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-36+234G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4722265 | |||||||
chr19:4722301 | G | A | 18 | a0001c0001t0001g0236 a0001c0001t0001g0241 a0001c0001t0001g0246 others(15): Show |
18 | HG01109.hp1 HG01243.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-36+198C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4722301 | |||||||
chr19:4722311 | G | C | 1 | a0001c0001t0001g0247 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-36+188C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4722311 | |||||||
chr19:4722351 | A | C | 4 | a0001c0001t0001g0266 a0001c0001t0001g0267 a0001c0001t0001g0268 others(1): Show |
4 | HG00280.hp2 HG01255.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.-36+148T>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4722351 | |||||||
chr19:4722396 | T | C | 13 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0002g0249 others(10): Show |
13 | HG00733.hp1 HG00733.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.-36+103A>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 2/21 | chr19 | 4722396 | |||||||
chr19:4722600 | G | C | 1 | a0001c0001t0001g0248 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-88-49C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 1/21 | chr19 | 4722600 | |||||||
chr19:4723037 | C | T | 3 | a0001c0001t0002g0005 a0001c0001t0005g0007 a0001c0002t0002g0006 |
3 | HG01243.hp1 HG02258.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.-88-486G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 1/21 | chr19 | 4723037 | |||||||
chr19:4723146 | G | C | 1 | a0001c0001t0002g0260 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-89+528C>G | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 1/21 | chr19 | 4723146 | |||||||
chr19:4723261 | T | G | 13 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0002g0249 others(10): Show |
13 | HG00733.hp1 HG00733.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.-89+413A>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 1/21 | chr19 | 4723261 | |||||||
chr19:4723283 | T | G | 1 | a0001c0001t0001g0261 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-89+391A>C | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 1/21 | chr19 | 4723283 | |||||||
chr19:4723342 | A | T | 1 | a0001c0002t0002g0004 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-89+332T>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 1/21 | chr19 | 4723342 | |||||||
chr19:4723445 | G | A | 1 | a0001c0001t0002g0262 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-89+229C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 1/21 | chr19 | 4723445 | |||||||
chr19:4723541 | C | T | 2 | a0001c0001t0001g0264 a0001c0001t0001g0265 |
2 | HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.-89+133G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 1/21 | chr19 | 4723541 | |||||||
chr19:4723547 | C | T | 1 | a0001c0001t0002g0003 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-89+127G>A | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 1/21 | chr19 | 4723547 | |||||||
chr19:4723594 | G | A | 1 | a0001c0001t0001g0263 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-89+80C>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 1/21 | chr19 | 4723594 | |||||||
chr19:4723658 | C | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0264 a0001c0001t0001g0265 others(46): Show |
50 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.-89+16G>T | DPP9 | ENSG00000142002.19 | transcript | ENST00000262960.14 | protein_coding | 1/21 | chr19 | 4723658 |