Item | Value |
---|---|
geneid | 4254 |
ensemblid | ENSG00000049130.16 |
hgncid | 6343 |
symbol | KITLG |
name | KIT ligand |
refseq_nuc | NM_000899.5 |
refseq_prot | NP_000890.1 |
ensembl_nuc | ENST00000644744.1 |
ensembl_prot | ENSP00000495951.1 |
mane_status | MANE Select |
chr | chr12 |
start | 88492793 |
end | 88580471 |
strand | - |
ver | v1.2 |
region | chr12:88492793-88580471 |
region5000 | chr12:88487793-88585471 |
regionname0 | KITLG_chr12_88492793_88580471 |
regionname5000 | KITLG_chr12_88487793_88585471 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 273 | 239 | 84 | 24 | 107 | 6 | 16 | 89 | KITLG_chr12_88487793_88585471 | KITLG | MKKTQ others(268): Show |
chr12 | 88487793 | 88585471 |
a0002 | 0/0 | 273 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | MKKTQ others(268): Show |
chr12 | 88487793 | 88585471 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 819 | 235 | 80 | 24 | 107 | 6 | 16 | KITLG_chr12_88487793_88585471 | KITLG | ATGAA others(814): Show |
chr12 | 88487793 | 88585471 | ||
a0001c0002 | 0/0 | 819 | 4 | 4 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | ATGAA others(814): Show |
chr12 | 88487793 | 88585471 | ||
a0002c0003 | 0/0 | 819 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | ATGAA others(814): Show |
chr12 | 88487793 | 88585471 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 5441 | 64 | 9 | 9 | 38 | 2 | 5 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0002 | 1/0 | 5441 | 53 | 22 | 4 | 20 | 1 | 5 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0003 | 0/0 | 5441 | 44 | 6 | 1 | 36 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0004 | 0/0 | 5441 | 15 | 3 | 5 | 5 | 1 | 1 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0005 | 0/0 | 5441 | 9 | 9 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0006 | 0/0 | 5441 | 6 | 0 | 0 | 6 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0007 | 0/0 | 5441 | 6 | 5 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0008 | 0/0 | 5441 | 4 | 0 | 2 | 0 | 1 | 1 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0009 | 0/0 | 5441 | 4 | 4 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0010 | 0/0 | 5441 | 4 | 4 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0011 | 0/0 | 5441 | 2 | 1 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0012 | 0/0 | 5441 | 2 | 2 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0013 | 0/0 | 5441 | 2 | 2 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0014 | 0/0 | 5441 | 2 | 2 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0015 | 0/0 | 5441 | 2 | 2 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0016 | 0/0 | 5441 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0017 | 0/0 | 5441 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0018 | 0/0 | 5441 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0019 | 0/0 | 5441 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0020 | 0/0 | 5441 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0021 | 0/0 | 5441 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0022 | 0/0 | 5441 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0023 | 0/0 | 5441 | 1 | 0 | 0 | 0 | 1 | 0 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0024 | 0/0 | 5441 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0025 | 0/0 | 5441 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0026 | 0/0 | 5441 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0027 | 0/0 | 5441 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0028 | 0/0 | 5441 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0029 | 0/0 | 5441 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0030 | 0/0 | 5441 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0001t0031 | 0/0 | 5441 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0001c0002t0002 | 0/0 | 5441 | 4 | 4 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
a0002c0003t0001 | 0/0 | 5441 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | GCTTC others(5436): Show |
chr12 | 88487793 | 88585471 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0157 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0011 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0100 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0005g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0005g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0005g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0006g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0006g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0006g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0006g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0007g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0007g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0007g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0007g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0007g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0007g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0008g0004 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0008g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0009g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0010g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0010g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0010g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0011g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0011g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0012g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0012g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0013g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0013g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0014g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0015g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0015g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0016g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0017g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0018g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0019g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0020g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0021g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0022g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0023g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0024g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0025g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0026g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0027g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0028g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0029g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0030g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0001t0031g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0001c0002t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
a0002c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0008 | g0191 | EUR | GBR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00099 | hp2 | a0001 | c0001 | t0004 | g0046 | EUR | GBR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0011 | EUR | FIN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0166 | EUR | FIN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | CHS | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | CHS | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | CHS | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | CHS | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | CHS | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00738 | hp2 | a0001 | c0001 | t0008 | g0004 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG00741 | hp2 | a0001 | c0001 | t0003 | g0125 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0049 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01106 | hp2 | a0001 | c0001 | t0004 | g0039 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01175 | hp1 | a0001 | c0001 | t0004 | g0042 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01192 | hp2 | a0001 | c0001 | t0011 | g0035 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01346 | hp1 | a0001 | c0001 | t0018 | g0181 | AMR | CLM | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01346 | hp2 | a0001 | c0001 | t0004 | g0038 | AMR | CLM | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01496 | hp1 | a0001 | c0001 | t0008 | g0004 | AMR | CLM | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01496 | hp2 | a0001 | c0001 | t0004 | g0045 | AMR | CLM | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0176 | EUR | IBS | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01517 | hp2 | a0001 | c0001 | t0023 | g0041 | EUR | IBS | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01891 | hp2 | a0001 | c0001 | t0031 | g0219 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | PEL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02055 | hp1 | a0001 | c0001 | t0015 | g0216 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | KHV | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02083 | hp1 | a0001 | c0001 | t0021 | g0206 | EAS | KHV | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02145 | hp1 | a0001 | c0001 | t0013 | g0110 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CDX | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | CDX | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02257 | hp1 | a0001 | c0001 | t0007 | g0200 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02257 | hp2 | a0001 | c0001 | t0015 | g0217 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02280 | hp1 | a0001 | c0001 | t0011 | g0124 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02280 | hp2 | a0001 | c0001 | t0005 | g0075 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02300 | hp2 | a0001 | c0001 | t0019 | g0023 | AMR | PEL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02451 | hp2 | a0001 | c0001 | t0014 | g0010 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02615 | hp1 | a0001 | c0001 | t0013 | g0067 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0153 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02622 | hp1 | a0001 | c0001 | t0022 | g0027 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02622 | hp2 | a0001 | c0001 | t0009 | g0048 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02630 | hp1 | a0001 | c0001 | t0007 | g0204 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02647 | hp1 | a0001 | c0001 | t0005 | g0131 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02647 | hp2 | a0001 | c0002 | t0002 | g0061 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0097 | SAS | PJL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0096 | SAS | PJL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02809 | hp1 | a0001 | c0001 | t0025 | g0140 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0134 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0129 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02896 | hp2 | a0001 | c0001 | t0007 | g0202 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02922 | hp1 | a0001 | c0001 | t0014 | g0010 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02965 | hp1 | a0001 | c0002 | t0002 | g0148 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02965 | hp2 | a0001 | c0002 | t0002 | g0037 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02970 | hp2 | a0001 | c0001 | t0009 | g0044 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0150 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03098 | hp1 | a0001 | c0001 | t0016 | g0018 | AFR | MSL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03098 | hp2 | a0001 | c0001 | t0009 | g0047 | AFR | MSL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03130 | hp1 | a0001 | c0001 | t0029 | g0142 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03130 | hp2 | a0001 | c0001 | t0010 | g0006 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03139 | hp2 | a0001 | c0001 | t0009 | g0057 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0203 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03209 | hp1 | a0001 | c0001 | t0026 | g0036 | AFR | MSL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0138 | AFR | MSL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0135 | AFR | MSL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03225 | hp2 | a0001 | c0001 | t0005 | g0154 | AFR | MSL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03453 | hp1 | a0001 | c0001 | t0010 | g0112 | AFR | MSL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03453 | hp2 | a0001 | c0001 | t0028 | g0151 | AFR | MSL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03516 | hp1 | a0001 | c0001 | t0010 | g0006 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0116 | AFR | ESN | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0152 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0139 | AFR | MSL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03579 | hp2 | a0001 | c0001 | t0005 | g0053 | AFR | MSL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03688 | hp1 | a0001 | c0001 | t0017 | g0040 | SAS | STU | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | STU | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03704 | hp1 | a0001 | c0001 | t0004 | g0043 | SAS | PJL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0127 | SAS | BEB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03834 | hp2 | a0001 | c0001 | t0008 | g0004 | SAS | BEB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0128 | SAS | STU | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0064 | SAS | STU | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG04184 | hp1 | a0001 | c0001 | t0007 | g0199 | SAS | BEB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0058 | SAS | BEB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | STU | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG04228 | hp2 | a0001 | c0001 | t0024 | g0050 | SAS | STU | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | CHB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18906 | hp1 | a0001 | c0001 | t0012 | g0072 | AFR | YRI | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0141 | AFR | YRI | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18939 | hp2 | a0002 | c0003 | t0001 | g0192 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18949 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18949 | hp2 | a0001 | c0001 | t0004 | g0215 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0056 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0093 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18973 | hp2 | a0001 | c0001 | t0006 | g0015 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18975 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18982 | hp1 | a0001 | c0001 | t0020 | g0194 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0086 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18990 | hp1 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19002 | hp2 | a0001 | c0001 | t0006 | g0017 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0213 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19005 | hp2 | a0001 | c0001 | t0006 | g0016 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19007 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0104 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19030 | hp1 | a0001 | c0002 | t0002 | g0059 | AFR | LWK | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0130 | AFR | LWK | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | LWK | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | LWK | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19058 | hp2 | a0001 | c0001 | t0004 | g0212 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0094 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19083 | hp2 | a0001 | c0001 | t0004 | g0214 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19091 | hp1 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0218 | AFR | YRI | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA19240 | hp2 | a0001 | c0001 | t0027 | g0144 | AFR | YRI | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ASW | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA20129 | hp2 | a0001 | c0001 | t0030 | g0120 | AFR | ASW | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02486 | hp2 | a0001 | c0001 | t0010 | g0119 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG02559 | hp2 | a0001 | c0001 | t0012 | g0052 | AFR | ACB | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0143 | AFR | MSL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | MSL | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0210 | AFR | USA | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | USA | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0085 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA18955 | hp2 | a0001 | c0001 | t0006 | g0003 | EAS | JPT | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | USA | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | USA | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | LWK | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
NA21309 | hp2 | a0001 | c0001 | t0007 | g0063 | AFR | LWK | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0157 | REF | REF | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0100 | REF | REF | KITLG_chr12_88487793_88585471 | KITLG | chr12 | 88487793 | 88585471 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:88532473 | T | C | 1 | a0002 | 1 | NA18939.hp2 | missense_variant | MODERATE | c.160A>G | p.Thr54Ala | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/10 | 353/5441 | 160/822 | 54/273 | chr12 | 88532473 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:88518847 | G | A | 1 | a0001c0002 | 4 | HG02647.hp2 HG02965.hp1 HG02965.hp2 others(1): Show |
synonymous_variant | LOW | c.213C>T | p.Ser71Ser | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 4/10 | 406/5441 | 213/822 | 71/273 | chr12 | 88518847 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:88492845 | T | C | 1 | a0001c0001t0020 | 1 | NA18982.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4374A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 12351 | chr12 | 88492845 | ||||||
chr12:88493147 | A | G | 1 | a0001c0001t0015 | 2 | HG02055.hp1 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4072T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 12049 | chr12 | 88493147 | ||||||
chr12:88493176 | T | A | 1 | a0001c0001t0013 | 2 | HG02145.hp1 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4043A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 12020 | chr12 | 88493176 | ||||||
chr12:88493186 | T | C | 6 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0017 others(3): Show |
23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*4033A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 12010 | chr12 | 88493186 | ||||||
chr12:88493300 | T | C | 1 | a0001c0001t0024 | 1 | HG04228.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3919A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 11896 | chr12 | 88493300 | ||||||
chr12:88493509 | A | T | 1 | a0001c0001t0026 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3710T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 11687 | chr12 | 88493509 | ||||||
chr12:88493512 | T | C | 8 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(5): Show |
83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*3707A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 11684 | chr12 | 88493512 | ||||||
chr12:88493594 | T | G | 1 | a0001c0001t0027 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3625A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 11602 | chr12 | 88493594 | ||||||
chr12:88493624 | C | A | 1 | a0001c0001t0028 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3595G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 11572 | chr12 | 88493624 | ||||||
chr12:88493947 | G | T | 6 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0017 others(3): Show |
23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3272C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 11249 | chr12 | 88493947 | ||||||
chr12:88494114 | T | C | 3 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0028 |
47 | HG00741.hp2 HG02451.hp2 HG02615.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*3105A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 11082 | chr12 | 88494114 | ||||||
chr12:88494242 | C | A | 1 | a0001c0001t0014 | 2 | HG02451.hp2 HG02922.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2977G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 10954 | chr12 | 88494242 | ||||||
chr12:88494438 | T | C | 6 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0017 others(3): Show |
23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2781A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 10758 | chr12 | 88494438 | ||||||
chr12:88494470 | T | C | 7 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(4): Show |
77 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*2749A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 10726 | chr12 | 88494470 | ||||||
chr12:88494674 | T | G | 1 | a0001c0001t0025 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2545A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 10522 | chr12 | 88494674 | ||||||
chr12:88494693 | A | C | 1 | a0001c0001t0012 | 2 | HG02559.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2526T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 10503 | chr12 | 88494693 | ||||||
chr12:88494714 | T | C | 1 | a0001c0001t0008 | 4 | HG00099.hp1 HG00738.hp2 HG01496.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2505A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 10482 | chr12 | 88494714 | ||||||
chr12:88494904 | C | A | 1 | a0001c0001t0021 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2315G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 10292 | chr12 | 88494904 | ||||||
chr12:88494976 | T | C | 1 | a0001c0001t0015 | 2 | HG02055.hp1 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2243A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 10220 | chr12 | 88494976 | ||||||
chr12:88495184 | T | C | 1 | a0001c0001t0011 | 2 | HG01192.hp2 HG02280.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2035A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 10012 | chr12 | 88495184 | ||||||
chr12:88495246 | A | G | 1 | a0001c0001t0010 | 4 | HG02486.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1973T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 9950 | chr12 | 88495246 | ||||||
chr12:88495593 | C | T | 1 | a0001c0001t0029 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1626G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 9603 | chr12 | 88495593 | ||||||
chr12:88495960 | C | T | 1 | a0001c0001t0019 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1259G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 9236 | chr12 | 88495960 | ||||||
chr12:88496121 | A | C | 1 | a0001c0001t0009 | 4 | HG02622.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1098T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 9075 | chr12 | 88496121 | ||||||
chr12:88496200 | A | T | 8 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(5): Show |
83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*1019T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 8996 | chr12 | 88496200 | ||||||
chr12:88496206 | A | T | 1 | a0001c0001t0023 | 1 | HG01517.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1013T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 8990 | chr12 | 88496206 | ||||||
chr12:88496214 | G | A | 1 | a0001c0001t0022 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1005C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 8982 | chr12 | 88496214 | ||||||
chr12:88496381 | G | A | 2 | a0001c0001t0005 a0001c0001t0029 |
10 | HG02280.hp2 HG02647.hp1 HG02895.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*838C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 8815 | chr12 | 88496381 | ||||||
chr12:88496584 | G | T | 1 | a0001c0001t0018 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*635C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 8612 | chr12 | 88496584 | ||||||
chr12:88496744 | C | T | 20 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(17): Show |
113 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*475G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 8452 | chr12 | 88496744 | ||||||
chr12:88496804 | C | G | 6 | a0001c0001t0004 a0001c0001t0009 a0001c0001t0017 others(3): Show |
23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*415G>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 8392 | chr12 | 88496804 | ||||||
chr12:88496894 | A | G | 11 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0007 others(8): Show |
86 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*325T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 8302 | chr12 | 88496894 | ||||||
chr12:88496912 | G | A | 1 | a0001c0001t0030 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*307C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 8284 | chr12 | 88496912 | ||||||
chr12:88497126 | A | T | 1 | a0001c0001t0017 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*93T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 10/10 | 8070 | chr12 | 88497126 | ||||||
chr12:88580422 | C | T | 1 | a0001c0001t0016 | 1 | HG03098.hp1 | 5_prime_UTR_variant | MODIFIER | c.-144G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/10 | 144 | chr12 | 88580422 | ||||||
chr12:88580425 | T | C | 1 | a0001c0001t0031 | 1 | HG01891.hp2 | 5_prime_UTR_variant | MODIFIER | c.-147A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/10 | 147 | chr12 | 88580425 | ||||||
chr12:88580435 | A | G | 1 | a0001c0001t0006 | 6 | NA18955.hp2 NA18973.hp2 NA18975.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-157T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/10 | 157 | chr12 | 88580435 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:88497297 | G | A | 5 | a0001c0001t0002g0007 a0001c0001t0002g0121 a0001c0001t0002g0122 others(2): Show |
6 | NA18944.hp2 NA18964.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.*38-116C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88497297 | |||||||
chr12:88497327 | T | C | 1 | a0001c0001t0005g0143 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.*38-146A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88497327 | |||||||
chr12:88497396 | A | G | 1 | a0001c0001t0002g0026 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.*38-215T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88497396 | |||||||
chr12:88497451 | G | T | 17 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(14): Show |
17 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.*38-270C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88497451 | |||||||
chr12:88497671 | A | G | 1 | a0001c0001t0004g0039 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.*38-490T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88497671 | |||||||
chr12:88497676 | C | T | 23 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(20): Show |
23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.*38-495G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88497676 | |||||||
chr12:88497885 | C | T | 2 | a0001c0001t0026g0036 a0001c0001t0027g0144 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.*38-704G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88497885 | |||||||
chr12:88497931 | C | T | 1 | a0001c0001t0007g0200 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.*38-750G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88497931 | |||||||
chr12:88497940 | A | G | 4 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0109 others(1): Show |
4 | NA18974.hp1 NA18981.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.*38-759T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88497940 | |||||||
chr12:88497999 | T | A | 23 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(20): Show |
23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.*38-818A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88497999 | |||||||
chr12:88498543 | A | G | 2 | a0001c0001t0026g0036 a0001c0001t0027g0144 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.*38-1362T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88498543 | |||||||
chr12:88498579 | G | C | 2 | a0001c0001t0011g0035 a0001c0001t0011g0124 |
2 | HG01192.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.*38-1398C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88498579 | |||||||
chr12:88498838 | C | CA | 28 | a0001c0001t0003g0002 a0001c0001t0003g0005 a0001c0001t0003g0055 others(25): Show |
32 | HG00741.hp2 NA18747.hp1 NA18943.hp1 others(29): Show |
intron_variant | MODIFIER | c.*38-1658dupT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88498838 | |||||||
chr12:88498855 | C | A | 6 | a0001c0001t0002g0074 a0001c0001t0002g0096 a0001c0001t0002g0097 others(3): Show |
6 | HG02071.hp1 HG02559.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.*38-1674G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88498855 | |||||||
chr12:88498903 | G | C | 1 | a0001c0001t0013g0067 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.*38-1722C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88498903 | |||||||
chr12:88498956 | C | T | 1 | a0001c0001t0009g0044 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.*38-1775G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88498956 | |||||||
chr12:88499344 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.*38-2163G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88499344 | |||||||
chr12:88499359 | T | C | 1 | a0001c0001t0012g0052 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.*38-2178A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88499359 | |||||||
chr12:88499482 | G | A | 23 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(20): Show |
23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.*38-2301C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88499482 | |||||||
chr12:88499684 | G | A | 2 | a0001c0001t0005g0053 a0001c0001t0005g0075 |
2 | HG02280.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.*38-2503C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88499684 | |||||||
chr12:88500111 | A | C | 2 | a0001c0001t0011g0035 a0001c0001t0011g0124 |
2 | HG01192.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.*38-2930T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88500111 | |||||||
chr12:88500215 | C | T | 3 | a0001c0001t0010g0006 a0001c0001t0010g0112 a0001c0001t0010g0119 |
4 | HG02486.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.*38-3034G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88500215 | |||||||
chr12:88500309 | T | C | 2 | a0001c0001t0002g0034 a0001c0001t0002g0069 |
2 | HG03041.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.*38-3128A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88500309 | |||||||
chr12:88500391 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.*38-3210C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88500391 | |||||||
chr12:88500445 | T | A | 1 | a0001c0001t0022g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.*38-3264A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88500445 | |||||||
chr12:88500718 | A | G | 23 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(20): Show |
23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.*38-3537T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88500718 | |||||||
chr12:88501000 | G | A | 1 | a0001c0001t0005g0218 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.*38-3819C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88501000 | |||||||
chr12:88501107 | G | T | 1 | a0001c0001t0002g0096 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.*38-3926C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88501107 | |||||||
chr12:88501316 | C | T | 2 | a0001c0001t0008g0004 a0001c0001t0008g0191 |
4 | HG00099.hp1 HG00738.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.*37+3843G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88501316 | |||||||
chr12:88501529 | C | T | 3 | a0001c0001t0010g0006 a0001c0001t0010g0112 a0001c0001t0010g0119 |
4 | HG02486.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.*37+3630G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88501529 | |||||||
chr12:88501934 | C | T | 1 | a0001c0002t0002g0037 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.*37+3225G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88501934 | |||||||
chr12:88502333 | T | C | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.*37+2826A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88502333 | |||||||
chr12:88502344 | C | A | 1 | a0001c0001t0002g0097 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.*37+2815G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88502344 | |||||||
chr12:88502716 | T | C | 1 | a0001c0001t0011g0035 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.*37+2443A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88502716 | |||||||
chr12:88502817 | A | G | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG01243.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.*37+2342T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88502817 | |||||||
chr12:88502907 | G | GA | 199 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(196): Show |
218 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(215): Show |
intron_variant | MODIFIER | c.*37+2251dupT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88502907 | |||||||
chr12:88503415 | T | C | 6 | a0001c0001t0005g0053 a0001c0001t0005g0075 a0001c0001t0005g0116 others(3): Show |
6 | HG02280.hp2 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.*37+1744A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88503415 | |||||||
chr12:88503446 | A | G | 3 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0099 |
3 | HG02145.hp2 HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.*37+1713T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88503446 | |||||||
chr12:88503556 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.*37+1603T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88503556 | |||||||
chr12:88504448 | C | T | 1 | a0001c0001t0002g0099 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.*37+711G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88504448 | |||||||
chr12:88504449 | G | A | 1 | a0001c0001t0002g0025 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.*37+710C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88504449 | |||||||
chr12:88504470 | C | A | 10 | a0001c0001t0005g0053 a0001c0001t0005g0075 a0001c0001t0005g0116 others(7): Show |
10 | HG02280.hp2 HG02647.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.*37+689G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88504470 | |||||||
chr12:88504685 | C | A | 1 | a0001c0001t0004g0043 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.*37+474G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88504685 | |||||||
chr12:88504863 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.*37+296G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88504863 | |||||||
chr12:88504864 | G | T | 23 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(20): Show |
23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.*37+295C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88504864 | |||||||
chr12:88504993 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.*37+166T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 9/9 | chr12 | 88504993 | |||||||
chr12:88506199 | A | T | 1 | a0001c0001t0006g0017 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.782+112T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 8/9 | chr12 | 88506199 | |||||||
chr12:88506260 | G | A | 1 | a0001c0001t0002g0122 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.782+51C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 8/9 | chr12 | 88506260 | |||||||
chr12:88506469 | G | T | 23 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(20): Show |
23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.715-91C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 7/9 | chr12 | 88506469 | |||||||
chr12:88506757 | A | C | 1 | a0001c0001t0010g0119 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.714+271T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 7/9 | chr12 | 88506757 | |||||||
chr12:88507270 | A | G | 1 | a0001c0001t0002g0097 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.605-133T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88507270 | |||||||
chr12:88507877 | A | C | 1 | a0001c0001t0003g0073 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.605-740T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88507877 | |||||||
chr12:88507916 | G | A | 1 | a0001c0001t0022g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.605-779C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88507916 | |||||||
chr12:88508025 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.605-888T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88508025 | |||||||
chr12:88508223 | A | G | 3 | a0001c0001t0007g0202 a0001c0001t0007g0203 a0001c0001t0007g0204 |
3 | HG02630.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.605-1086T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88508223 | |||||||
chr12:88508264 | G | A | 2 | a0001c0001t0001g0175 a0001c0001t0001g0188 |
2 | HG00639.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.605-1127C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88508264 | |||||||
chr12:88508556 | C | CGT | 60 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0164 others(57): Show |
65 | HG00099.hp2 HG00323.hp2 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.605-1421_605-1420d others(4): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88508556 | |||||||
chr12:88508556 | C | CGTGT | 22 | a0001c0001t0002g0051 a0001c0001t0002g0054 a0001c0001t0002g0060 others(19): Show |
22 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(19): Show |
intron_variant | MODIFIER | c.605-1423_605-1420d others(6): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88508556 | |||||||
chr12:88508556 | C | CGTGTGT | 3 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0137 |
3 | HG01243.hp1 HG02572.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.605-1425_605-1420d others(8): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88508556 | |||||||
chr12:88508556 | CGT | C | 3 | a0001c0001t0001g0171 a0001c0001t0001g0173 a0001c0001t0014g0010 |
4 | HG01975.hp1 HG02451.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.605-1421_605-1420d others(4): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88508556 | |||||||
chr12:88508595 | G | C | 10 | a0001c0001t0005g0053 a0001c0001t0005g0075 a0001c0001t0005g0116 others(7): Show |
10 | HG02280.hp2 HG02647.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.605-1458C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88508595 | |||||||
chr12:88508632 | C | T | 1 | a0001c0001t0026g0036 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.605-1495G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88508632 | |||||||
chr12:88508677 | T | C | 1 | a0001c0001t0005g0075 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.605-1540A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88508677 | |||||||
chr12:88508963 | A | G | 1 | a0001c0001t0022g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.605-1826T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88508963 | |||||||
chr12:88508984 | T | A | 1 | a0001c0001t0004g0043 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.605-1847A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88508984 | |||||||
chr12:88509202 | A | G | 1 | a0001c0001t0003g0086 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.605-2065T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88509202 | |||||||
chr12:88509711 | T | C | 2 | a0001c0001t0001g0167 a0001c0001t0001g0190 |
2 | HG02083.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.605-2574A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88509711 | |||||||
chr12:88509825 | T | C | 8 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0030 others(5): Show |
8 | HG00639.hp2 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.605-2688A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88509825 | |||||||
chr12:88510154 | C | T | 204 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(201): Show |
223 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.605-3017G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88510154 | |||||||
chr12:88510512 | A | G | 4 | a0001c0001t0009g0044 a0001c0001t0009g0047 a0001c0001t0009g0048 others(1): Show |
4 | HG02622.hp2 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.605-3375T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88510512 | |||||||
chr12:88510779 | T | C | 1 | a0001c0001t0002g0011 | 2 | HG00323.hp1 HG00738.hp1 |
intron_variant | MODIFIER | c.605-3642A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88510779 | |||||||
chr12:88510987 | C | T | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.605-3850G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88510987 | |||||||
chr12:88511906 | C | T | 1 | a0001c0001t0016g0018 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.604+3628G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88511906 | |||||||
chr12:88512071 | T | A | 1 | a0001c0001t0001g0145 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.604+3463A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88512071 | |||||||
chr12:88512127 | A | G | 2 | a0001c0001t0003g0005 a0001c0001t0003g0118 |
3 | NA18975.hp2 NA19068.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.604+3407T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88512127 | |||||||
chr12:88512192 | G | A | 1 | a0001c0001t0001g0014 | 2 | NA18961.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.604+3342C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88512192 | |||||||
chr12:88512982 | C | T | 1 | a0001c0001t0002g0070 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.604+2552G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88512982 | |||||||
chr12:88513012 | C | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(68): Show |
83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.604+2522G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88513012 | |||||||
chr12:88513051 | T | C | 1 | a0001c0001t0002g0134 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.604+2483A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88513051 | |||||||
chr12:88513525 | T | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(212): Show |
236 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.604+2009A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88513525 | |||||||
chr12:88513628 | A | G | 1 | a0001c0001t0026g0036 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.604+1906T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88513628 | |||||||
chr12:88513786 | A | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(72): Show |
87 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.604+1748T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88513786 | |||||||
chr12:88513987 | A | C | 3 | a0001c0001t0002g0051 a0001c0001t0012g0052 a0001c0001t0012g0072 |
3 | HG02559.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.604+1547T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88513987 | |||||||
chr12:88514028 | C | A | 1 | a0001c0001t0022g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.604+1506G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88514028 | |||||||
chr12:88514092 | T | C | 1 | a0001c0001t0002g0134 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.604+1442A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88514092 | |||||||
chr12:88515008 | A | C | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.604+526T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88515008 | |||||||
chr12:88515072 | T | C | 6 | a0001c0001t0002g0034 a0001c0001t0002g0069 a0001c0001t0002g0134 others(3): Show |
6 | HG01243.hp1 HG02572.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.604+462A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88515072 | |||||||
chr12:88515213 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.604+321G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 6/9 | chr12 | 88515213 | |||||||
chr12:88516530 | C | T | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.364-40G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 4/9 | chr12 | 88516530 | |||||||
chr12:88516693 | G | T | 1 | a0001c0001t0001g0176 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.364-203C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 4/9 | chr12 | 88516693 | |||||||
chr12:88516840 | G | GA | 26 | a0001c0001t0001g0014 a0001c0001t0003g0082 a0001c0001t0003g0092 others(23): Show |
27 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(24): Show |
intron_variant | MODIFIER | c.364-351dupT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 4/9 | chr12 | 88516840 | |||||||
chr12:88516857 | C | A | 1 | a0001c0001t0001g0209 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.364-367G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 4/9 | chr12 | 88516857 | |||||||
chr12:88517009 | A | C | 1 | a0001c0001t0026g0036 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.364-519T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 4/9 | chr12 | 88517009 | |||||||
chr12:88517043 | AC | A | 23 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(20): Show |
23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.364-554delG | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 4/9 | chr12 | 88517043 | |||||||
chr12:88517181 | A | C | 1 | a0001c0001t0007g0200 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.364-691T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 4/9 | chr12 | 88517181 | |||||||
chr12:88517245 | G | C | 23 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(20): Show |
23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.364-755C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 4/9 | chr12 | 88517245 | |||||||
chr12:88517985 | C | A | 1 | a0001c0001t0002g0101 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.363+712G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 4/9 | chr12 | 88517985 | |||||||
chr12:88518681 | A | T | 7 | a0001c0001t0003g0009 a0001c0001t0003g0020 a0001c0001t0003g0150 others(4): Show |
9 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.363+16T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 4/9 | chr12 | 88518681 | |||||||
chr12:88519123 | A | G | 1 | a0001c0001t0003g0020 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.193-256T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88519123 | |||||||
chr12:88519409 | C | G | 1 | a0001c0001t0001g0182 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.193-542G>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88519409 | |||||||
chr12:88519640 | A | G | 23 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(20): Show |
23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.193-773T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88519640 | |||||||
chr12:88519714 | C | G | 26 | a0001c0001t0002g0034 a0001c0001t0002g0054 a0001c0001t0002g0060 others(23): Show |
26 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(23): Show |
intron_variant | MODIFIER | c.193-847G>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88519714 | |||||||
chr12:88519827 | C | T | 23 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(20): Show |
23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.193-960G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88519827 | |||||||
chr12:88519844 | G | A | 1 | a0001c0001t0003g0094 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.193-977C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88519844 | |||||||
chr12:88519863 | A | G | 1 | a0001c0001t0016g0018 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.193-996T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88519863 | |||||||
chr12:88519890 | C | T | 3 | a0001c0001t0010g0006 a0001c0001t0010g0112 a0001c0001t0010g0119 |
4 | HG02486.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-1023G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88519890 | |||||||
chr12:88520296 | G | T | 1 | a0001c0001t0001g0179 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.193-1429C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88520296 | |||||||
chr12:88520533 | T | C | 1 | a0001c0001t0007g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.193-1666A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88520533 | |||||||
chr12:88520670 | G | T | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.193-1803C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88520670 | |||||||
chr12:88520809 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.193-1942A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88520809 | |||||||
chr12:88520972 | G | A | 1 | a0001c0001t0005g0218 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.193-2105C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88520972 | |||||||
chr12:88521023 | G | A | 5 | a0001c0001t0002g0007 a0001c0001t0002g0121 a0001c0001t0002g0122 others(2): Show |
6 | NA18944.hp2 NA18964.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.193-2156C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88521023 | |||||||
chr12:88521381 | G | T | 1 | a0001c0001t0001g0209 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.193-2514C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88521381 | |||||||
chr12:88521386 | G | A | 63 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(60): Show |
75 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.193-2519C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88521386 | |||||||
chr12:88521466 | C | T | 1 | a0001c0001t0011g0035 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.193-2599G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88521466 | |||||||
chr12:88521467 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.193-2600C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88521467 | |||||||
chr12:88521686 | T | C | 3 | a0001c0001t0002g0051 a0001c0001t0012g0052 a0001c0001t0012g0072 |
3 | HG02559.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.193-2819A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88521686 | |||||||
chr12:88521785 | C | T | 3 | a0001c0001t0004g0138 a0001c0001t0004g0139 a0001c0001t0025g0140 |
3 | HG02809.hp1 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.193-2918G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88521785 | |||||||
chr12:88521810 | C | A | 1 | a0001c0001t0002g0134 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.193-2943G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88521810 | |||||||
chr12:88522058 | G | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(111): Show |
126 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(123): Show |
intron_variant | MODIFIER | c.193-3191C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88522058 | |||||||
chr12:88522269 | C | T | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.193-3402G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88522269 | |||||||
chr12:88522426 | CT | C | 110 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0002g0028 others(107): Show |
118 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.193-3560delA | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88522426 | |||||||
chr12:88522426 | CTT | C | 90 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(87): Show |
101 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.193-3561_193-3560d others(4): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88522426 | |||||||
chr12:88522455 | C | T | 1 | a0001c0001t0003g0152 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.193-3588G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88522455 | |||||||
chr12:88522473 | G | T | 1 | a0001c0001t0022g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.193-3606C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88522473 | |||||||
chr12:88522531 | G | C | 27 | a0001c0001t0002g0034 a0001c0001t0002g0054 a0001c0001t0002g0060 others(24): Show |
28 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(25): Show |
intron_variant | MODIFIER | c.193-3664C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88522531 | |||||||
chr12:88522569 | G | A | 1 | a0001c0001t0002g0066 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.193-3702C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88522569 | |||||||
chr12:88522577 | G | A | 1 | a0001c0001t0022g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.193-3710C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88522577 | |||||||
chr12:88522734 | C | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0201 |
2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.193-3867G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88522734 | |||||||
chr12:88522838 | A | G | 2 | a0001c0001t0013g0067 a0001c0001t0013g0110 |
2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.193-3971T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88522838 | |||||||
chr12:88522907 | T | A | 1 | a0001c0001t0002g0074 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.193-4040A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88522907 | |||||||
chr12:88523770 | C | T | 1 | a0001c0001t0027g0144 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.193-4903G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88523770 | |||||||
chr12:88523807 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.193-4940A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88523807 | |||||||
chr12:88523903 | T | C | 3 | a0001c0001t0002g0051 a0001c0001t0012g0052 a0001c0001t0012g0072 |
3 | HG02559.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.193-5036A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88523903 | |||||||
chr12:88524191 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.193-5324A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88524191 | |||||||
chr12:88524426 | G | A | 2 | a0001c0001t0002g0130 a0001c0001t0002g0133 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.193-5559C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88524426 | |||||||
chr12:88524628 | A | T | 1 | a0001c0001t0003g0058 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.193-5761T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88524628 | |||||||
chr12:88524663 | G | C | 23 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(20): Show |
23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.193-5796C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88524663 | |||||||
chr12:88524806 | T | C | 23 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(20): Show |
23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.193-5939A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88524806 | |||||||
chr12:88524850 | C | T | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.193-5983G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88524850 | |||||||
chr12:88524956 | C | T | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.193-6089G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88524956 | |||||||
chr12:88524966 | T | G | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(68): Show |
83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.193-6099A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88524966 | |||||||
chr12:88525042 | T | C | 1 | a0001c0001t0022g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.193-6175A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88525042 | |||||||
chr12:88525072 | A | G | 23 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(20): Show |
23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.193-6205T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88525072 | |||||||
chr12:88525128 | C | T | 3 | a0001c0001t0010g0006 a0001c0001t0010g0112 a0001c0001t0010g0119 |
4 | HG02486.hp2 HG03130.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-6261G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88525128 | |||||||
chr12:88525255 | G | A | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.193-6388C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88525255 | |||||||
chr12:88525277 | T | C | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.193-6410A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88525277 | |||||||
chr12:88525542 | A | G | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.193-6675T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88525542 | |||||||
chr12:88525572 | GTTA | G | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.193-6708_193-6706d others(5): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88525572 | |||||||
chr12:88525678 | C | A | 1 | a0001c0001t0001g0014 | 2 | NA18961.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.192+6763G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88525678 | |||||||
chr12:88525706 | T | C | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+6735A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88525706 | |||||||
chr12:88525819 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.192+6622G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88525819 | |||||||
chr12:88526159 | G | T | 2 | a0001c0001t0011g0035 a0001c0001t0011g0124 |
2 | HG01192.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.192+6282C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88526159 | |||||||
chr12:88526242 | A | G | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+6199T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88526242 | |||||||
chr12:88526446 | T | C | 2 | a0001c0001t0026g0036 a0001c0001t0027g0144 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+5995A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88526446 | |||||||
chr12:88526659 | A | C | 1 | a0001c0001t0001g0196 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.192+5782T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88526659 | |||||||
chr12:88526863 | C | CT | 10 | a0001c0001t0002g0051 a0001c0001t0002g0064 a0001c0001t0002g0099 others(7): Show |
10 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.192+5577dupA | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88526863 | |||||||
chr12:88526863 | CT | C | 80 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(77): Show |
92 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.192+5577delA | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88526863 | |||||||
chr12:88526863 | CTTTTT | C | 23 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(20): Show |
23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+5573_192+5577d others(7): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88526863 | |||||||
chr12:88526914 | C | G | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+5527G>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88526914 | |||||||
chr12:88526982 | T | C | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+5459A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88526982 | |||||||
chr12:88526995 | A | G | 1 | a0001c0002t0002g0148 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.192+5446T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88526995 | |||||||
chr12:88526998 | AGCTGGGA others(12): Show |
A | 1 | a0001c0001t0002g0134 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.192+5424_192+5442d others(21): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88526998 | |||||||
chr12:88527087 | C | A | 23 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(20): Show |
23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+5354G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88527087 | |||||||
chr12:88527105 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.192+5336A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88527105 | |||||||
chr12:88527177 | C | T | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+5264G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88527177 | |||||||
chr12:88527184 | G | T | 1 | a0001c0001t0001g0145 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.192+5257C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88527184 | |||||||
chr12:88527340 | C | G | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+5101G>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88527340 | |||||||
chr12:88527439 | A | G | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+5002T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88527439 | |||||||
chr12:88527452 | G | A | 1 | a0001c0001t0030g0120 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.192+4989C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88527452 | |||||||
chr12:88527540 | C | T | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+4901G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88527540 | |||||||
chr12:88527609 | G | T | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+4832C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88527609 | |||||||
chr12:88527617 | G | A | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+4824C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88527617 | |||||||
chr12:88527640 | T | C | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+4801A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88527640 | |||||||
chr12:88527783 | A | G | 2 | a0001c0001t0026g0036 a0001c0001t0027g0144 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+4658T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88527783 | |||||||
chr12:88528184 | C | T | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+4257G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88528184 | |||||||
chr12:88528314 | T | A | 1 | a0001c0001t0003g0058 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.192+4127A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88528314 | |||||||
chr12:88528829 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0193 a0001c0001t0001g0197 |
3 | HG00597.hp1 NA18944.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.192+3612A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88528829 | |||||||
chr12:88528837 | T | A | 4 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(1): Show |
4 | HG01243.hp1 HG02572.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+3604A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88528837 | |||||||
chr12:88528878 | G | A | 1 | a0001c0001t0003g0089 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.192+3563C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88528878 | |||||||
chr12:88528947 | T | C | 1 | a0001c0001t0012g0072 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.192+3494A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88528947 | |||||||
chr12:88529012 | T | C | 3 | a0001c0001t0007g0202 a0001c0001t0007g0203 a0001c0001t0007g0204 |
3 | HG02630.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.192+3429A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88529012 | |||||||
chr12:88529089 | C | T | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+3352G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88529089 | |||||||
chr12:88529160 | A | T | 1 | a0001c0001t0003g0080 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.192+3281T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88529160 | |||||||
chr12:88529197 | A | T | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+3244T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88529197 | |||||||
chr12:88529446 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.192+2995C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88529446 | |||||||
chr12:88529860 | T | C | 1 | a0001c0001t0022g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.192+2581A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88529860 | |||||||
chr12:88529934 | A | C | 1 | a0001c0001t0007g0200 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.192+2507T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88529934 | |||||||
chr12:88530243 | A | T | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+2198T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88530243 | |||||||
chr12:88530290 | C | G | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(112): Show |
127 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.192+2151G>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88530290 | |||||||
chr12:88530351 | C | A | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+2090G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88530351 | |||||||
chr12:88530538 | A | G | 2 | a0001c0001t0011g0035 a0001c0001t0011g0124 |
2 | HG01192.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.192+1903T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88530538 | |||||||
chr12:88530559 | G | GT | 3 | a0001c0001t0002g0074 a0001c0001t0002g0096 a0001c0001t0002g0097 |
3 | HG02071.hp1 HG02683.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.192+1881dupA | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88530559 | |||||||
chr12:88530676 | C | T | 3 | a0001c0001t0002g0054 a0001c0001t0002g0062 a0001c0001t0002g0105 |
3 | HG00423.hp1 HG00597.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.192+1765G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88530676 | |||||||
chr12:88530714 | A | G | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+1727T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88530714 | |||||||
chr12:88530887 | C | A | 1 | a0001c0001t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.192+1554G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88530887 | |||||||
chr12:88530975 | T | A | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+1466A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88530975 | |||||||
chr12:88531013 | T | C | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+1428A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88531013 | |||||||
chr12:88531295 | A | C | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+1146T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88531295 | |||||||
chr12:88531377 | A | T | 1 | a0001c0001t0001g0165 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.192+1064T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88531377 | |||||||
chr12:88531436 | T | C | 23 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(20): Show |
23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+1005A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88531436 | |||||||
chr12:88531600 | CTTG | C | 4 | a0001c0001t0003g0009 a0001c0001t0003g0152 a0001c0001t0003g0153 others(1): Show |
5 | HG02615.hp2 HG02630.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+838_192+840del others(3): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88531600 | |||||||
chr12:88531660 | T | C | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+781A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88531660 | |||||||
chr12:88531718 | CT | C | 23 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(20): Show |
23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+722delA | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88531718 | |||||||
chr12:88531819 | C | T | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+622G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88531819 | |||||||
chr12:88531895 | C | T | 4 | a0001c0001t0005g0141 a0001c0001t0005g0143 a0001c0001t0005g0154 others(1): Show |
4 | HG03130.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+546G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88531895 | |||||||
chr12:88531906 | G | A | 2 | a0001c0001t0015g0216 a0001c0001t0015g0217 |
2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.192+535C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88531906 | |||||||
chr12:88532102 | T | C | 3 | a0001c0001t0002g0051 a0001c0001t0012g0052 a0001c0001t0012g0072 |
3 | HG02559.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.192+339A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88532102 | |||||||
chr12:88532174 | G | T | 1 | a0001c0001t0001g0183 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.192+267C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88532174 | |||||||
chr12:88532196 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(112): Show |
127 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.192+245A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88532196 | |||||||
chr12:88532213 | A | C | 2 | a0001c0001t0003g0084 a0001c0001t0003g0147 |
2 | NA18969.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.192+228T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88532213 | |||||||
chr12:88532295 | C | T | 24 | a0001c0001t0002g0070 a0001c0001t0004g0038 a0001c0001t0004g0039 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+146G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 3/9 | chr12 | 88532295 | |||||||
chr12:88532513 | C | CA | 25 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(22): Show |
25 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-11dupT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88532513 | |||||||
chr12:88532663 | C | A | 2 | a0001c0001t0026g0036 a0001c0001t0027g0144 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.130-160G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88532663 | |||||||
chr12:88532688 | A | T | 3 | a0001c0001t0004g0211 a0001c0001t0004g0212 a0001c0001t0004g0215 |
3 | NA18949.hp2 NA19058.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.130-185T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88532688 | |||||||
chr12:88532828 | T | C | 1 | a0001c0001t0031g0219 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.130-325A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88532828 | |||||||
chr12:88532945 | T | A | 6 | a0001c0001t0004g0210 a0001c0001t0004g0211 a0001c0001t0004g0212 others(3): Show |
6 | HG06807.hp1 NA18949.hp2 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.130-442A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88532945 | |||||||
chr12:88533010 | C | T | 25 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(22): Show |
25 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-507G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88533010 | |||||||
chr12:88533052 | C | T | 2 | a0001c0001t0011g0035 a0001c0001t0011g0124 |
2 | HG01192.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.130-549G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88533052 | |||||||
chr12:88533070 | AC | A | 6 | a0001c0001t0002g0113 a0001c0001t0010g0006 a0001c0001t0010g0112 others(3): Show |
7 | HG02486.hp2 HG02970.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.130-568delG | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88533070 | |||||||
chr12:88533224 | T | G | 1 | a0001c0001t0001g0207 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.130-721A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88533224 | |||||||
chr12:88533258 | G | C | 2 | a0001c0001t0021g0206 a0001c0001t0022g0027 |
2 | HG02083.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.130-755C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88533258 | |||||||
chr12:88533469 | G | A | 2 | a0001c0001t0011g0035 a0001c0001t0011g0124 |
2 | HG01192.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.130-966C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88533469 | |||||||
chr12:88533538 | T | C | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.130-1035A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88533538 | |||||||
chr12:88533579 | C | T | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.130-1076G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88533579 | |||||||
chr12:88533592 | T | C | 3 | a0001c0001t0004g0138 a0001c0001t0004g0139 a0001c0001t0025g0140 |
3 | HG02809.hp1 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.130-1089A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88533592 | |||||||
chr12:88533635 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.130-1132A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88533635 | |||||||
chr12:88533733 | C | T | 1 | a0001c0001t0015g0216 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.130-1230G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88533733 | |||||||
chr12:88533926 | G | T | 1 | a0001c0001t0026g0036 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130-1423C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88533926 | |||||||
chr12:88534071 | G | T | 1 | a0001c0001t0001g0159 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.130-1568C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88534071 | |||||||
chr12:88534232 | G | A | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.130-1729C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88534232 | |||||||
chr12:88534342 | C | T | 1 | a0001c0001t0002g0060 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.130-1839G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88534342 | |||||||
chr12:88534605 | G | A | 2 | a0001c0001t0021g0206 a0001c0001t0022g0027 |
2 | HG02083.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.130-2102C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88534605 | |||||||
chr12:88534736 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.130-2233C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88534736 | |||||||
chr12:88534976 | T | C | 1 | a0001c0001t0002g0031 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.130-2473A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88534976 | |||||||
chr12:88534984 | C | T | 2 | a0001c0001t0021g0206 a0001c0001t0022g0027 |
2 | HG02083.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.130-2481G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88534984 | |||||||
chr12:88535009 | G | A | 1 | a0001c0001t0002g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.130-2506C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88535009 | |||||||
chr12:88535079 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.130-2576G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88535079 | |||||||
chr12:88535249 | T | C | 25 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(22): Show |
25 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-2746A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88535249 | |||||||
chr12:88535489 | C | T | 4 | a0001c0001t0002g0028 a0001c0001t0002g0032 a0001c0001t0002g0114 others(1): Show |
4 | HG00639.hp2 HG02055.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.130-2986G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88535489 | |||||||
chr12:88535490 | G | A | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.130-2987C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88535490 | |||||||
chr12:88535571 | A | C | 25 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(22): Show |
25 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-3068T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88535571 | |||||||
chr12:88535847 | T | C | 8 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0030 others(5): Show |
8 | HG00639.hp2 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.130-3344A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88535847 | |||||||
chr12:88535971 | C | A | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.130-3468G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88535971 | |||||||
chr12:88536157 | C | T | 1 | a0001c0001t0022g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.130-3654G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88536157 | |||||||
chr12:88536301 | T | C | 25 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(22): Show |
25 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-3798A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88536301 | |||||||
chr12:88536427 | C | T | 2 | a0001c0001t0001g0160 a0001c0001t0001g0180 |
2 | HG02155.hp2 NA18951.hp2 |
intron_variant | MODIFIER | c.130-3924G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88536427 | |||||||
chr12:88536838 | T | C | 3 | a0001c0001t0004g0138 a0001c0001t0004g0139 a0001c0001t0025g0140 |
3 | HG02809.hp1 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.130-4335A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88536838 | |||||||
chr12:88536846 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.130-4343G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88536846 | |||||||
chr12:88536851 | C | T | 1 | a0001c0001t0005g0218 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.130-4348G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88536851 | |||||||
chr12:88536949 | T | C | 25 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(22): Show |
25 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-4446A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88536949 | |||||||
chr12:88536961 | A | G | 1 | a0001c0001t0007g0199 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.130-4458T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88536961 | |||||||
chr12:88537020 | C | T | 1 | a0001c0001t0002g0030 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.130-4517G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88537020 | |||||||
chr12:88537198 | G | A | 1 | a0001c0001t0004g0213 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.130-4695C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88537198 | |||||||
chr12:88537218 | C | T | 4 | a0001c0001t0007g0199 a0001c0001t0007g0202 a0001c0001t0007g0203 others(1): Show |
4 | HG02630.hp1 HG02896.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-4715G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88537218 | |||||||
chr12:88537229 | C | T | 1 | a0001c0001t0011g0124 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.130-4726G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88537229 | |||||||
chr12:88537303 | A | C | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.130-4800T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88537303 | |||||||
chr12:88537421 | A | T | 1 | a0001c0001t0022g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.130-4918T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88537421 | |||||||
chr12:88537654 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.130-5151T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88537654 | |||||||
chr12:88537655 | C | A | 4 | a0001c0001t0001g0163 a0001c0001t0001g0169 a0001c0001t0001g0170 others(1): Show |
4 | HG00408.hp1 HG02071.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.130-5152G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88537655 | |||||||
chr12:88537675 | G | GA | 7 | a0001c0001t0002g0032 a0001c0001t0002g0074 a0001c0001t0002g0096 others(4): Show |
7 | HG02071.hp1 HG02559.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.130-5173dupT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88537675 | |||||||
chr12:88537755 | T | C | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.130-5252A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88537755 | |||||||
chr12:88538105 | T | G | 25 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(22): Show |
25 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-5602A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88538105 | |||||||
chr12:88538258 | C | A | 25 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(22): Show |
25 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-5755G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88538258 | |||||||
chr12:88538469 | C | T | 25 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(22): Show |
25 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-5966G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88538469 | |||||||
chr12:88538587 | T | C | 25 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(22): Show |
25 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-6084A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88538587 | |||||||
chr12:88538606 | T | C | 1 | a0001c0001t0022g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.130-6103A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88538606 | |||||||
chr12:88538762 | T | C | 1 | a0001c0001t0002g0031 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.130-6259A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88538762 | |||||||
chr12:88538895 | T | A | 1 | a0001c0001t0002g0128 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.130-6392A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88538895 | |||||||
chr12:88538947 | T | C | 25 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(22): Show |
25 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.130-6444A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88538947 | |||||||
chr12:88539027 | C | G | 24 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(21): Show |
24 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.130-6524G>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88539027 | |||||||
chr12:88539227 | G | A | 2 | a0001c0001t0015g0216 a0001c0001t0015g0217 |
2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.129+6525C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88539227 | |||||||
chr12:88539564 | G | A | 23 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(20): Show |
23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.129+6188C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88539564 | |||||||
chr12:88539602 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.129+6150A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88539602 | |||||||
chr12:88539692 | T | C | 25 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(22): Show |
25 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.129+6060A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88539692 | |||||||
chr12:88539774 | A | T | 1 | a0001c0001t0002g0066 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.129+5978T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88539774 | |||||||
chr12:88539866 | A | G | 1 | a0001c0001t0002g0134 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.129+5886T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88539866 | |||||||
chr12:88539873 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.129+5879G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88539873 | |||||||
chr12:88539936 | T | C | 1 | a0001c0001t0007g0200 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.129+5816A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88539936 | |||||||
chr12:88539967 | G | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(115): Show |
130 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.129+5785C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88539967 | |||||||
chr12:88540099 | C | T | 1 | a0001c0001t0002g0066 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.129+5653G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88540099 | |||||||
chr12:88540252 | A | T | 1 | a0001c0001t0002g0101 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.129+5500T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88540252 | |||||||
chr12:88540334 | A | G | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.129+5418T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88540334 | |||||||
chr12:88540430 | T | A | 1 | a0001c0001t0022g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.129+5322A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88540430 | |||||||
chr12:88540594 | G | A | 1 | a0001c0001t0002g0070 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.129+5158C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88540594 | |||||||
chr12:88540936 | C | T | 3 | a0001c0001t0002g0025 a0001c0001t0002g0026 a0001c0001t0002g0099 |
3 | HG02145.hp2 HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.129+4816G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88540936 | |||||||
chr12:88541112 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.129+4640T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88541112 | |||||||
chr12:88541274 | C | T | 1 | a0001c0001t0003g0079 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.129+4478G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88541274 | |||||||
chr12:88541359 | T | A | 1 | a0001c0001t0001g0190 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.129+4393A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88541359 | |||||||
chr12:88541460 | A | G | 34 | a0001c0001t0002g0158 a0001c0001t0003g0002 a0001c0001t0003g0005 others(31): Show |
38 | HG00741.hp2 HG04184.hp2 NA18747.hp1 others(35): Show |
intron_variant | MODIFIER | c.129+4292T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88541460 | |||||||
chr12:88541794 | T | C | 3 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 |
3 | HG01243.hp2 HG01975.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.129+3958A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88541794 | |||||||
chr12:88541815 | T | G | 1 | a0001c0001t0002g0097 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.129+3937A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88541815 | |||||||
chr12:88541816 | T | TA | 29 | a0001c0001t0002g0134 a0001c0001t0002g0136 a0001c0001t0002g0137 others(26): Show |
29 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.129+3935dupT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88541816 | |||||||
chr12:88541817 | A | T | 1 | a0001c0001t0027g0144 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.129+3935T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88541817 | |||||||
chr12:88541852 | G | T | 112 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(109): Show |
124 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.129+3900C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88541852 | |||||||
chr12:88541866 | G | A | 2 | a0001c0001t0002g0130 a0001c0001t0002g0133 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.129+3886C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88541866 | |||||||
chr12:88542035 | A | G | 2 | a0001c0001t0002g0065 a0001c0001t0002g0071 |
2 | HG00438.hp2 HG00544.hp1 |
intron_variant | MODIFIER | c.129+3717T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88542035 | |||||||
chr12:88542300 | C | A | 23 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(20): Show |
23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.129+3452G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88542300 | |||||||
chr12:88542766 | T | A | 1 | a0001c0001t0001g0190 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.129+2986A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88542766 | |||||||
chr12:88542871 | G | A | 214 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(211): Show |
235 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.129+2881C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88542871 | |||||||
chr12:88543160 | G | C | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.129+2592C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88543160 | |||||||
chr12:88543927 | T | G | 3 | a0001c0001t0001g0024 a0001c0001t0001g0174 a0001c0001t0019g0023 |
3 | HG01099.hp1 HG02300.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.129+1825A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88543927 | |||||||
chr12:88543947 | C | T | 3 | a0001c0001t0021g0206 a0001c0001t0026g0036 a0001c0001t0027g0144 |
3 | HG02083.hp1 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.129+1805G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88543947 | |||||||
chr12:88544017 | G | A | 3 | a0001c0001t0021g0206 a0001c0001t0026g0036 a0001c0001t0027g0144 |
3 | HG02083.hp1 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.129+1735C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88544017 | |||||||
chr12:88544053 | C | T | 7 | a0001c0001t0003g0009 a0001c0001t0003g0020 a0001c0001t0003g0150 others(4): Show |
9 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.129+1699G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88544053 | |||||||
chr12:88544200 | G | A | 3 | a0001c0001t0021g0206 a0001c0001t0026g0036 a0001c0001t0027g0144 |
3 | HG02083.hp1 HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.129+1552C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88544200 | |||||||
chr12:88544487 | A | C | 1 | a0001c0001t0001g0160 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.129+1265T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88544487 | |||||||
chr12:88544511 | T | TA | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(68): Show |
83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.129+1240dupT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88544511 | |||||||
chr12:88544512 | A | T | 1 | a0001c0001t0004g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.129+1240T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88544512 | |||||||
chr12:88544517 | A | C | 1 | a0001c0001t0027g0144 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.129+1235T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88544517 | |||||||
chr12:88544527 | C | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0197 |
2 | NA18944.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.129+1225G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88544527 | |||||||
chr12:88544741 | A | G | 6 | a0001c0001t0004g0210 a0001c0001t0004g0211 a0001c0001t0004g0212 others(3): Show |
6 | HG06807.hp1 NA18949.hp2 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.129+1011T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88544741 | |||||||
chr12:88544785 | A | G | 62 | a0001c0001t0002g0034 a0001c0001t0002g0054 a0001c0001t0002g0060 others(59): Show |
66 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(63): Show |
intron_variant | MODIFIER | c.129+967T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88544785 | |||||||
chr12:88544883 | A | C | 2 | a0001c0001t0015g0216 a0001c0001t0015g0217 |
2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.129+869T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88544883 | |||||||
chr12:88545100 | A | T | 26 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(23): Show |
26 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.129+652T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88545100 | |||||||
chr12:88545242 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.129+510C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88545242 | |||||||
chr12:88545266 | C | G | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.129+486G>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88545266 | |||||||
chr12:88545298 | C | T | 23 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(20): Show |
23 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.129+454G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88545298 | |||||||
chr12:88545356 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(115): Show |
130 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.129+396T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88545356 | |||||||
chr12:88545570 | A | G | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.129+182T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88545570 | |||||||
chr12:88545714 | T | C | 3 | a0001c0001t0002g0051 a0001c0001t0012g0052 a0001c0001t0012g0072 |
3 | HG02559.hp2 HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.129+38A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 2/9 | chr12 | 88545714 | |||||||
chr12:88545934 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.16-69A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88545934 | |||||||
chr12:88545984 | A | T | 1 | a0001c0001t0002g0111 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.16-119T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88545984 | |||||||
chr12:88546002 | C | T | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-137G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88546002 | |||||||
chr12:88546013 | T | C | 3 | a0001c0001t0002g0054 a0001c0001t0002g0062 a0001c0001t0002g0105 |
3 | HG00423.hp1 HG00597.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.16-148A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88546013 | |||||||
chr12:88546152 | T | A | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.16-287A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88546152 | |||||||
chr12:88546380 | G | A | 2 | a0001c0001t0001g0175 a0001c0001t0001g0188 |
2 | HG00639.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.16-515C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88546380 | |||||||
chr12:88546496 | T | G | 1 | a0001c0001t0022g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.16-631A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88546496 | |||||||
chr12:88546551 | T | C | 2 | a0001c0001t0026g0036 a0001c0001t0027g0144 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.16-686A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88546551 | |||||||
chr12:88546574 | T | A | 1 | a0001c0001t0001g0076 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.16-709A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88546574 | |||||||
chr12:88546729 | T | A | 1 | a0001c0001t0003g0125 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.16-864A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88546729 | |||||||
chr12:88546735 | T | C | 2 | a0001c0001t0026g0036 a0001c0001t0027g0144 |
2 | HG03209.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.16-870A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88546735 | |||||||
chr12:88546928 | C | A | 3 | a0001c0001t0007g0202 a0001c0001t0007g0203 a0001c0001t0007g0204 |
3 | HG02630.hp1 HG02896.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.16-1063G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88546928 | |||||||
chr12:88546944 | A | G | 1 | a0001c0001t0011g0035 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.16-1079T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88546944 | |||||||
chr12:88547234 | T | C | 17 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(14): Show |
17 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.16-1369A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88547234 | |||||||
chr12:88547365 | C | A | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-1500G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88547365 | |||||||
chr12:88547437 | C | T | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-1572G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88547437 | |||||||
chr12:88547781 | C | T | 1 | a0001c0001t0001g0021 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.16-1916G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88547781 | |||||||
chr12:88547827 | G | A | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-1962C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88547827 | |||||||
chr12:88547846 | A | C | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-1981T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88547846 | |||||||
chr12:88547873 | C | T | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-2008G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88547873 | |||||||
chr12:88548026 | T | C | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-2161A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88548026 | |||||||
chr12:88548182 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.16-2317C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88548182 | |||||||
chr12:88548379 | G | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(69): Show |
84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.16-2514C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88548379 | |||||||
chr12:88548385 | C | T | 1 | a0001c0001t0016g0018 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.16-2520G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88548385 | |||||||
chr12:88548411 | G | A | 10 | a0001c0001t0004g0210 a0001c0001t0004g0211 a0001c0001t0004g0212 others(7): Show |
10 | HG02965.hp2 HG03209.hp1 HG06807.hp1 others(7): Show |
intron_variant | MODIFIER | c.16-2546C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88548411 | |||||||
chr12:88548454 | CAA | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(72): Show |
87 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.16-2591_16-2590del others(2): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88548454 | |||||||
chr12:88548577 | G | A | 4 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0109 others(1): Show |
4 | NA18974.hp1 NA18981.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-2712C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88548577 | |||||||
chr12:88548605 | T | C | 2 | a0001c0001t0001g0189 a0001c0001t0020g0194 |
2 | NA18982.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.16-2740A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88548605 | |||||||
chr12:88548964 | A | T | 22 | a0001c0001t0002g0034 a0001c0001t0002g0054 a0001c0001t0002g0060 others(19): Show |
22 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(19): Show |
intron_variant | MODIFIER | c.16-3099T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88548964 | |||||||
chr12:88549076 | G | A | 7 | a0001c0001t0003g0009 a0001c0001t0003g0020 a0001c0001t0003g0150 others(4): Show |
9 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.16-3211C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88549076 | |||||||
chr12:88549203 | G | A | 27 | a0001c0001t0003g0002 a0001c0001t0003g0005 a0001c0001t0003g0055 others(24): Show |
31 | HG00741.hp2 NA18747.hp1 NA18943.hp1 others(28): Show |
intron_variant | MODIFIER | c.16-3338C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88549203 | |||||||
chr12:88549226 | C | T | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-3361G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88549226 | |||||||
chr12:88549372 | A | C | 10 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0025 others(7): Show |
12 | HG00323.hp1 HG00738.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.16-3507T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88549372 | |||||||
chr12:88549546 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(72): Show |
87 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.16-3681C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88549546 | |||||||
chr12:88549758 | C | A | 2 | a0001c0001t0011g0035 a0001c0001t0011g0124 |
2 | HG01192.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.16-3893G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88549758 | |||||||
chr12:88549777 | A | G | 1 | a0001c0001t0004g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.16-3912T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88549777 | |||||||
chr12:88549819 | C | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(72): Show |
87 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.16-3954G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88549819 | |||||||
chr12:88549820 | G | T | 5 | a0001c0001t0003g0079 a0001c0001t0003g0080 a0001c0001t0003g0081 others(2): Show |
5 | NA18951.hp1 NA18953.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-3955C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88549820 | |||||||
chr12:88549982 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(72): Show |
87 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.16-4117C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88549982 | |||||||
chr12:88549990 | T | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(72): Show |
87 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.16-4125A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88549990 | |||||||
chr12:88550016 | T | C | 17 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(14): Show |
17 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.16-4151A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88550016 | |||||||
chr12:88550022 | C | T | 10 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0025 others(7): Show |
12 | HG00323.hp1 HG00738.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.16-4157G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88550022 | |||||||
chr12:88550113 | T | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(72): Show |
87 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.16-4248A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88550113 | |||||||
chr12:88550232 | A | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(72): Show |
87 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.16-4367T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88550232 | |||||||
chr12:88550426 | TAGG | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(72): Show |
87 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.16-4564_16-4562del others(3): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88550426 | |||||||
chr12:88550445 | A | G | 1 | a0001c0001t0002g0132 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.16-4580T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88550445 | |||||||
chr12:88550741 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(72): Show |
87 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.16-4876C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88550741 | |||||||
chr12:88550986 | T | A | 4 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0109 others(1): Show |
4 | NA18974.hp1 NA18981.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-5121A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88550986 | |||||||
chr12:88551359 | C | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(72): Show |
87 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.16-5494G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88551359 | |||||||
chr12:88551691 | C | G | 4 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(1): Show |
4 | HG01243.hp1 HG02572.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-5826G>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88551691 | |||||||
chr12:88551705 | CACA | C | 2 | a0001c0001t0011g0035 a0001c0001t0011g0124 |
2 | HG01192.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.16-5843_16-5841del others(3): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88551705 | |||||||
chr12:88551709 | A | G | 1 | a0001c0002t0002g0059 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.16-5844T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88551709 | |||||||
chr12:88551742 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.16-5877C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88551742 | |||||||
chr12:88551948 | T | C | 2 | a0001c0001t0003g0093 a0001c0001t0003g0098 |
2 | NA18967.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.16-6083A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88551948 | |||||||
chr12:88552002 | G | C | 1 | a0001c0001t0003g0152 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.16-6137C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88552002 | |||||||
chr12:88552175 | AAT | A | 2 | a0001c0001t0002g0130 a0001c0001t0002g0133 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.16-6312_16-6311del others(2): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88552175 | |||||||
chr12:88552176 | A | AT | 19 | a0001c0001t0001g0179 a0001c0001t0001g0185 a0001c0001t0001g0208 others(16): Show |
19 | HG01192.hp2 HG01243.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.16-6312dupA | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88552176 | |||||||
chr12:88552176 | AT | A | 9 | a0001c0001t0001g0159 a0001c0001t0002g0051 a0001c0001t0002g0127 others(6): Show |
9 | HG02280.hp1 HG02809.hp1 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.16-6312delA | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88552176 | |||||||
chr12:88552350 | C | CT | 5 | a0001c0001t0003g0009 a0001c0001t0003g0150 a0001c0001t0003g0152 others(2): Show |
6 | HG02615.hp2 HG02630.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.16-6486dupA | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88552350 | |||||||
chr12:88552350 | CT | C | 7 | a0001c0001t0002g0113 a0001c0001t0010g0006 a0001c0001t0010g0112 others(4): Show |
8 | HG02083.hp1 HG02486.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.16-6486delA | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88552350 | |||||||
chr12:88552416 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.16-6551G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88552416 | |||||||
chr12:88552549 | T | C | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-6684A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88552549 | |||||||
chr12:88552560 | T | C | 2 | a0001c0001t0003g0094 a0001c0001t0003g0095 |
2 | NA18984.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.16-6695A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88552560 | |||||||
chr12:88552592 | T | C | 6 | a0001c0001t0005g0053 a0001c0001t0005g0075 a0001c0001t0005g0116 others(3): Show |
6 | HG02280.hp2 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-6727A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88552592 | |||||||
chr12:88552685 | T | C | 22 | a0001c0001t0002g0034 a0001c0001t0002g0054 a0001c0001t0002g0060 others(19): Show |
22 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(19): Show |
intron_variant | MODIFIER | c.16-6820A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88552685 | |||||||
chr12:88552763 | A | T | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(72): Show |
87 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.16-6898T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88552763 | |||||||
chr12:88552881 | C | A | 1 | a0001c0001t0002g0101 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.16-7016G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88552881 | |||||||
chr12:88553000 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(72): Show |
87 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.16-7135C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88553000 | |||||||
chr12:88553010 | C | T | 204 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(201): Show |
223 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.16-7145G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88553010 | |||||||
chr12:88553094 | A | G | 91 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(88): Show |
103 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.16-7229T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88553094 | |||||||
chr12:88553346 | A | G | 10 | a0001c0001t0004g0210 a0001c0001t0004g0211 a0001c0001t0004g0212 others(7): Show |
10 | HG02965.hp2 HG03209.hp1 HG06807.hp1 others(7): Show |
intron_variant | MODIFIER | c.16-7481T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88553346 | |||||||
chr12:88553620 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(194): Show |
216 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.16-7755G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88553620 | |||||||
chr12:88553659 | A | G | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(72): Show |
87 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.16-7794T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88553659 | |||||||
chr12:88553792 | T | G | 2 | a0001c0001t0011g0035 a0001c0001t0011g0124 |
2 | HG01192.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.16-7927A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88553792 | |||||||
chr12:88553821 | T | C | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-7956A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88553821 | |||||||
chr12:88553970 | T | C | 2 | a0001c0001t0002g0028 a0001c0001t0002g0032 |
2 | HG02572.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.16-8105A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88553970 | |||||||
chr12:88554201 | T | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(194): Show |
216 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(213): Show |
intron_variant | MODIFIER | c.16-8336A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88554201 | |||||||
chr12:88554348 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.16-8483A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88554348 | |||||||
chr12:88554355 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.16-8490G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88554355 | |||||||
chr12:88554874 | G | C | 1 | a0001c0001t0002g0025 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.16-9009C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88554874 | |||||||
chr12:88554926 | T | C | 16 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(13): Show |
16 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.16-9061A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88554926 | |||||||
chr12:88554990 | T | C | 1 | a0001c0001t0003g0073 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.16-9125A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88554990 | |||||||
chr12:88555084 | A | C | 1 | a0001c0001t0002g0111 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.16-9219T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88555084 | |||||||
chr12:88555095 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(70): Show |
85 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.16-9230C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88555095 | |||||||
chr12:88555149 | C | T | 2 | a0001c0001t0026g0036 a0001c0002t0002g0037 |
2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.16-9284G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88555149 | |||||||
chr12:88555347 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(70): Show |
85 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.16-9482C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88555347 | |||||||
chr12:88555738 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(70): Show |
85 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.16-9873C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88555738 | |||||||
chr12:88555767 | G | A | 4 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(1): Show |
4 | HG01517.hp1 HG02683.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-9902C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88555767 | |||||||
chr12:88555849 | A | T | 1 | a0001c0001t0011g0035 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.16-9984T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88555849 | |||||||
chr12:88555997 | G | T | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-10132C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88555997 | |||||||
chr12:88556218 | C | CA | 85 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(82): Show |
97 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.16-10354dupT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88556218 | |||||||
chr12:88556218 | CA | C | 11 | a0001c0001t0002g0064 a0001c0001t0005g0053 a0001c0001t0005g0075 others(8): Show |
11 | HG02280.hp2 HG02647.hp1 HG02895.hp2 others(8): Show |
intron_variant | MODIFIER | c.16-10354delT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88556218 | |||||||
chr12:88556250 | T | C | 16 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(13): Show |
16 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.16-10385A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88556250 | |||||||
chr12:88556296 | G | T | 10 | a0001c0001t0002g0007 a0001c0001t0002g0011 a0001c0001t0002g0025 others(7): Show |
12 | HG00323.hp1 HG00738.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.16-10431C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88556296 | |||||||
chr12:88556401 | G | A | 1 | a0001c0001t0003g0150 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.16-10536C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88556401 | |||||||
chr12:88556540 | C | T | 5 | a0001c0001t0002g0007 a0001c0001t0002g0121 a0001c0001t0002g0122 others(2): Show |
6 | NA18944.hp2 NA18964.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-10675G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88556540 | |||||||
chr12:88556683 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.16-10818C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88556683 | |||||||
chr12:88556802 | G | T | 2 | a0001c0001t0015g0216 a0001c0001t0015g0217 |
2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.16-10937C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88556802 | |||||||
chr12:88556874 | C | A | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-11009G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88556874 | |||||||
chr12:88557098 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.16-11233C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88557098 | |||||||
chr12:88557102 | T | C | 1 | a0001c0001t0001g0182 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.16-11237A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88557102 | |||||||
chr12:88557610 | A | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(193): Show |
215 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(212): Show |
intron_variant | MODIFIER | c.16-11745T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88557610 | |||||||
chr12:88557708 | C | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(67): Show |
82 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.16-11843G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88557708 | |||||||
chr12:88557769 | G | A | 1 | a0001c0001t0018g0181 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.16-11904C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88557769 | |||||||
chr12:88557799 | G | T | 5 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0005g0116 others(2): Show |
5 | HG00639.hp2 HG02055.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.16-11934C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88557799 | |||||||
chr12:88557856 | T | C | 84 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(81): Show |
96 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.16-11991A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88557856 | |||||||
chr12:88557970 | C | T | 2 | a0001c0001t0002g0051 a0001c0001t0012g0052 |
2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.16-12105G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88557970 | |||||||
chr12:88558072 | A | G | 1 | a0001c0001t0002g0101 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.16-12207T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88558072 | |||||||
chr12:88558245 | TTAAATAA others(1): Show |
T | 13 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0005g0053 others(10): Show |
13 | HG00639.hp2 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.16-12388_16-12381d others(10): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88558245 | |||||||
chr12:88558373 | T | A | 1 | a0001c0001t0001g0182 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.16-12508A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88558373 | |||||||
chr12:88558485 | C | G | 7 | a0001c0001t0003g0009 a0001c0001t0003g0020 a0001c0001t0003g0150 others(4): Show |
9 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.16-12620G>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88558485 | |||||||
chr12:88558552 | T | C | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-12687A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88558552 | |||||||
chr12:88558650 | T | A | 4 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(1): Show |
4 | HG01243.hp1 HG02572.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-12785A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88558650 | |||||||
chr12:88558752 | G | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(68): Show |
83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.16-12887C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88558752 | |||||||
chr12:88558812 | G | C | 7 | a0001c0001t0003g0009 a0001c0001t0003g0020 a0001c0001t0003g0150 others(4): Show |
9 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.16-12947C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88558812 | |||||||
chr12:88558838 | A | C | 7 | a0001c0001t0003g0009 a0001c0001t0003g0020 a0001c0001t0003g0150 others(4): Show |
9 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.16-12973T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88558838 | |||||||
chr12:88559066 | G | A | 1 | a0001c0001t0011g0035 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.16-13201C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88559066 | |||||||
chr12:88559171 | C | T | 4 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(1): Show |
4 | HG01243.hp1 HG02572.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-13306G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88559171 | |||||||
chr12:88559315 | G | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(68): Show |
83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.16-13450C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88559315 | |||||||
chr12:88559489 | G | A | 1 | a0001c0001t0002g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.16-13624C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88559489 | |||||||
chr12:88559547 | A | G | 3 | a0001c0001t0005g0141 a0001c0001t0005g0143 a0001c0001t0029g0142 |
3 | HG03130.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.16-13682T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88559547 | |||||||
chr12:88559549 | C | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(68): Show |
83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.16-13684G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88559549 | |||||||
chr12:88559622 | C | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(68): Show |
83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.16-13757G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88559622 | |||||||
chr12:88559784 | C | A | 70 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(67): Show |
82 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.16-13919G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88559784 | |||||||
chr12:88559882 | A | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(69): Show |
84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.16-14017T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88559882 | |||||||
chr12:88560182 | G | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(68): Show |
83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.16-14317C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88560182 | |||||||
chr12:88560497 | G | A | 13 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0005g0053 others(10): Show |
13 | HG00639.hp2 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.16-14632C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88560497 | |||||||
chr12:88560518 | G | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(68): Show |
83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.16-14653C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88560518 | |||||||
chr12:88560917 | G | A | 1 | a0001c0001t0002g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.16-15052C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88560917 | |||||||
chr12:88560964 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.16-15099A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88560964 | |||||||
chr12:88560967 | C | CA | 19 | a0001c0001t0002g0033 a0001c0001t0002g0071 a0001c0001t0002g0113 others(16): Show |
19 | HG00438.hp2 HG02280.hp2 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.16-15103dupT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88560967 | |||||||
chr12:88560967 | CA | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(72): Show |
87 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.16-15103delT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88560967 | |||||||
chr12:88560989 | A | G | 3 | a0001c0001t0001g0145 a0001c0001t0002g0126 a0001c0001t0011g0124 |
3 | HG02280.hp1 HG02896.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.16-15124T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88560989 | |||||||
chr12:88560990 | A | G | 1 | a0001c0001t0003g0095 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.16-15125T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88560990 | |||||||
chr12:88561052 | G | T | 1 | a0001c0001t0003g0095 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.16-15187C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88561052 | |||||||
chr12:88561535 | T | C | 4 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(1): Show |
4 | HG01243.hp1 HG02572.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.16-15670A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88561535 | |||||||
chr12:88561672 | C | A | 1 | a0001c0001t0011g0124 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.16-15807G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88561672 | |||||||
chr12:88561692 | G | A | 63 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(60): Show |
75 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.16-15827C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88561692 | |||||||
chr12:88561783 | G | T | 2 | a0001c0001t0001g0076 a0001c0001t0003g0077 |
2 | HG00438.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.16-15918C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88561783 | |||||||
chr12:88561865 | C | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(68): Show |
83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.16-16000G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88561865 | |||||||
chr12:88561898 | A | G | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.16-16033T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88561898 | |||||||
chr12:88561952 | TATCAC | T | 215 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(212): Show |
236 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(233): Show |
intron_variant | MODIFIER | c.16-16092_16-16088d others(7): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88561952 | |||||||
chr12:88562562 | G | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(68): Show |
83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.16-16697C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88562562 | |||||||
chr12:88562623 | T | G | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(68): Show |
83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.16-16758A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88562623 | |||||||
chr12:88562775 | C | A | 1 | a0001c0001t0004g0138 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.16-16910G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88562775 | |||||||
chr12:88562833 | G | A | 6 | a0001c0001t0002g0074 a0001c0001t0002g0096 a0001c0001t0002g0097 others(3): Show |
6 | HG02071.hp1 HG02559.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-16968C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88562833 | |||||||
chr12:88562848 | T | C | 204 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(201): Show |
223 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.16-16983A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88562848 | |||||||
chr12:88562970 | A | G | 2 | a0001c0001t0005g0129 a0001c0001t0005g0131 |
2 | HG02647.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.16-17105T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88562970 | |||||||
chr12:88562979 | C | T | 4 | a0001c0001t0002g0106 a0001c0001t0002g0107 a0001c0001t0002g0109 others(1): Show |
4 | NA18974.hp1 NA18981.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-17114G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88562979 | |||||||
chr12:88563089 | A | C | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.15+17175T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88563089 | |||||||
chr12:88563381 | C | A | 2 | a0001c0001t0003g0094 a0001c0001t0003g0095 |
2 | NA18984.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.15+16883G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88563381 | |||||||
chr12:88563575 | A | C | 97 | a0001c0001t0001g0076 a0001c0001t0002g0034 a0001c0001t0002g0051 others(94): Show |
104 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.15+16689T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88563575 | |||||||
chr12:88563591 | G | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(68): Show |
83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.15+16673C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88563591 | |||||||
chr12:88563671 | G | C | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.15+16593C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88563671 | |||||||
chr12:88563699 | A | G | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(68): Show |
83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.15+16565T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88563699 | |||||||
chr12:88563962 | C | CA | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(68): Show |
83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.15+16301dupT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88563962 | |||||||
chr12:88564085 | T | G | 2 | a0001c0001t0002g0130 a0001c0001t0002g0133 |
2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.15+16179A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88564085 | |||||||
chr12:88564103 | G | A | 7 | a0001c0001t0003g0009 a0001c0001t0003g0020 a0001c0001t0003g0150 others(4): Show |
9 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+16161C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88564103 | |||||||
chr12:88564333 | G | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(68): Show |
83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.15+15931C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88564333 | |||||||
chr12:88564390 | C | CTGTT | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(68): Show |
83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.15+15873_15+15874i others(6): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88564390 | |||||||
chr12:88564432 | G | A | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.15+15832C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88564432 | |||||||
chr12:88564573 | C | T | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(68): Show |
83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.15+15691G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88564573 | |||||||
chr12:88564742 | T | TA | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(68): Show |
83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.15+15521dupT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88564742 | |||||||
chr12:88565004 | C | T | 1 | a0001c0001t0004g0211 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.15+15260G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88565004 | |||||||
chr12:88565119 | T | C | 1 | a0001c0001t0003g0095 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.15+15145A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88565119 | |||||||
chr12:88565223 | T | C | 1 | a0001c0001t0004g0046 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.15+15041A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88565223 | |||||||
chr12:88565355 | GGTGGCTC others(6): Show |
G | 1 | a0001c0001t0001g0190 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.15+14896_15+14908d others(15): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88565355 | |||||||
chr12:88565622 | TAAAC | T | 9 | a0001c0001t0002g0051 a0001c0001t0003g0009 a0001c0001t0003g0020 others(6): Show |
11 | HG02451.hp2 HG02559.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.15+14638_15+14641d others(6): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88565622 | |||||||
chr12:88565660 | G | A | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(68): Show |
83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.15+14604C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88565660 | |||||||
chr12:88565733 | G | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(68): Show |
83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.15+14531C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88565733 | |||||||
chr12:88565991 | G | C | 1 | a0001c0001t0008g0191 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.15+14273C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88565991 | |||||||
chr12:88566072 | T | C | 71 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(68): Show |
83 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.15+14192A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88566072 | |||||||
chr12:88566083 | A | G | 1 | a0001c0001t0028g0151 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.15+14181T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88566083 | |||||||
chr12:88566115 | C | T | 14 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(11): Show |
14 | HG01243.hp1 HG02572.hp2 HG02895.hp1 others(11): Show |
intron_variant | MODIFIER | c.15+14149G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88566115 | |||||||
chr12:88566580 | G | A | 2 | a0001c0001t0015g0216 a0001c0001t0015g0217 |
2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.15+13684C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88566580 | |||||||
chr12:88566615 | T | C | 1 | a0001c0001t0012g0052 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.15+13649A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88566615 | |||||||
chr12:88566668 | C | T | 1 | a0001c0001t0002g0029 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.15+13596G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88566668 | |||||||
chr12:88566931 | T | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(82): Show |
98 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.15+13333A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88566931 | |||||||
chr12:88566950 | C | T | 72 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(69): Show |
85 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.15+13314G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88566950 | |||||||
chr12:88567259 | C | T | 14 | a0001c0001t0002g0114 a0001c0001t0002g0115 a0001c0001t0005g0053 others(11): Show |
14 | HG00639.hp2 HG01891.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.15+13005G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88567259 | |||||||
chr12:88567672 | A | G | 1 | a0001c0001t0007g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.15+12592T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88567672 | |||||||
chr12:88567688 | T | C | 1 | a0001c0001t0022g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.15+12576A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88567688 | |||||||
chr12:88567936 | A | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(82): Show |
98 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.15+12328T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88567936 | |||||||
chr12:88567972 | A | C | 1 | a0001c0001t0001g0162 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.15+12292T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88567972 | |||||||
chr12:88567975 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(82): Show |
98 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.15+12289G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88567975 | |||||||
chr12:88568075 | T | C | 2 | a0001c0001t0015g0216 a0001c0001t0015g0217 |
2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.15+12189A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568075 | |||||||
chr12:88568102 | TA | T | 214 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(211): Show |
235 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.15+12161delT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568102 | |||||||
chr12:88568134 | G | A | 6 | a0001c0001t0002g0074 a0001c0001t0002g0096 a0001c0001t0002g0097 others(3): Show |
6 | HG02071.hp1 HG02559.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+12130C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568134 | |||||||
chr12:88568234 | T | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(82): Show |
98 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.15+12030A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568234 | |||||||
chr12:88568280 | C | CATTT | 68 | a0001c0001t0001g0076 a0001c0001t0002g0026 a0001c0001t0002g0051 others(65): Show |
73 | HG00408.hp2 HG00438.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.15+11980_15+11983d others(6): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568280 | |||||||
chr12:88568280 | C | CATTTATT others(1): Show |
9 | a0001c0001t0002g0074 a0001c0001t0002g0113 a0001c0001t0002g0134 others(6): Show |
9 | HG02071.hp1 HG02257.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.15+11976_15+11983d others(10): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568280 | |||||||
chr12:88568280 | C | CATTTATT others(5): Show |
1 | a0001c0001t0004g0210 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.15+11972_15+11983d others(14): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568280 | |||||||
chr12:88568280 | CATTT | C | 7 | a0001c0001t0003g0009 a0001c0001t0003g0102 a0001c0001t0003g0150 others(4): Show |
9 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+11980_15+11983d others(6): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568280 | |||||||
chr12:88568280 | CATTTATT others(1): Show |
C | 3 | a0001c0001t0005g0218 a0001c0001t0012g0072 a0001c0002t0002g0148 |
3 | HG02965.hp1 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.15+11976_15+11983d others(10): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568280 | |||||||
chr12:88568280 | CATTTATT others(9): Show |
C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(82): Show |
98 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.15+11968_15+11983d others(18): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568280 | |||||||
chr12:88568284 | T | C | 1 | a0001c0001t0003g0020 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.15+11980A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568284 | |||||||
chr12:88568562 | A | C | 10 | a0001c0001t0004g0210 a0001c0001t0004g0211 a0001c0001t0004g0212 others(7): Show |
10 | HG02965.hp2 HG03209.hp1 HG06807.hp1 others(7): Show |
intron_variant | MODIFIER | c.15+11702T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568562 | |||||||
chr12:88568588 | C | T | 1 | a0001c0001t0002g0111 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.15+11676G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568588 | |||||||
chr12:88568765 | A | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(82): Show |
98 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.15+11499T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568765 | |||||||
chr12:88568904 | A | C | 13 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(10): Show |
13 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.15+11360T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568904 | |||||||
chr12:88568982 | T | A | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.15+11282A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88568982 | |||||||
chr12:88569176 | G | A | 1 | a0001c0001t0004g0215 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.15+11088C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88569176 | |||||||
chr12:88569186 | C | T | 1 | a0001c0001t0001g0205 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.15+11078G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88569186 | |||||||
chr12:88569666 | C | T | 1 | a0001c0001t0002g0158 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.15+10598G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88569666 | |||||||
chr12:88569830 | A | G | 1 | a0001c0001t0002g0105 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.15+10434T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88569830 | |||||||
chr12:88569942 | C | T | 1 | a0001c0001t0001g0161 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.15+10322G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88569942 | |||||||
chr12:88569969 | G | C | 85 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(82): Show |
98 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.15+10295C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88569969 | |||||||
chr12:88569999 | A | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(82): Show |
98 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.15+10265T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88569999 | |||||||
chr12:88570058 | T | C | 2 | a0001c0001t0009g0047 a0001c0001t0009g0048 |
2 | HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.15+10206A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88570058 | |||||||
chr12:88570522 | A | C | 1 | a0001c0001t0027g0144 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.15+9742T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88570522 | |||||||
chr12:88570533 | A | G | 2 | a0001c0001t0026g0036 a0001c0002t0002g0037 |
2 | HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.15+9731T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88570533 | |||||||
chr12:88570537 | C | CA | 85 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(82): Show |
98 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.15+9726dupT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88570537 | |||||||
chr12:88570540 | A | C | 1 | a0001c0001t0011g0035 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.15+9724T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88570540 | |||||||
chr12:88570598 | T | C | 4 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(1): Show |
4 | HG01243.hp1 HG02572.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+9666A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88570598 | |||||||
chr12:88570603 | G | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0197 |
2 | NA18944.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.15+9661C>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88570603 | |||||||
chr12:88570627 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.15+9637C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88570627 | |||||||
chr12:88570683 | C | G | 21 | a0001c0001t0002g0034 a0001c0001t0002g0054 a0001c0001t0002g0060 others(18): Show |
21 | HG00408.hp2 HG00423.hp1 HG00438.hp2 others(18): Show |
intron_variant | MODIFIER | c.15+9581G>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88570683 | |||||||
chr12:88570805 | A | G | 4 | a0001c0001t0002g0134 a0001c0001t0002g0135 a0001c0001t0002g0136 others(1): Show |
4 | HG01243.hp1 HG02572.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+9459T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88570805 | |||||||
chr12:88570809 | G | A | 1 | a0001c0001t0003g0104 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.15+9455C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88570809 | |||||||
chr12:88570868 | A | G | 1 | a0001c0001t0026g0036 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.15+9396T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88570868 | |||||||
chr12:88571060 | G | A | 1 | a0001c0001t0031g0219 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.15+9204C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88571060 | |||||||
chr12:88571195 | C | T | 1 | a0001c0001t0001g0160 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.15+9069G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88571195 | |||||||
chr12:88571347 | T | G | 3 | a0001c0001t0005g0141 a0001c0001t0005g0143 a0001c0001t0029g0142 |
3 | HG03130.hp1 HG03471.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.15+8917A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88571347 | |||||||
chr12:88571763 | C | T | 2 | a0001c0001t0002g0051 a0001c0001t0012g0052 |
2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.15+8501G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88571763 | |||||||
chr12:88572338 | A | T | 1 | a0001c0001t0022g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.15+7926T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572338 | |||||||
chr12:88572424 | C | A | 1 | a0002c0003t0001g0192 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.15+7840G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572424 | |||||||
chr12:88572594 | A | ATT | 6 | a0001c0001t0004g0210 a0001c0001t0004g0211 a0001c0001t0004g0212 others(3): Show |
6 | HG06807.hp1 NA18949.hp2 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+7668_15+7669dup others(2): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572594 | |||||||
chr12:88572595 | T | A | 1 | a0001c0001t0003g0153 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.15+7669A>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572595 | |||||||
chr12:88572595 | T | TTA | 99 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(96): Show |
114 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.15+7667_15+7668dup others(2): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572595 | |||||||
chr12:88572595 | T | TTATA | 15 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0145 others(12): Show |
16 | HG00597.hp1 HG01099.hp2 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.15+7665_15+7668dup others(4): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572595 | |||||||
chr12:88572595 | T | TTATATA | 8 | a0001c0001t0001g0195 a0001c0001t0001g0196 a0001c0001t0002g0134 others(5): Show |
8 | HG00544.hp2 HG01243.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+7663_15+7668dup others(6): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572595 | |||||||
chr12:88572595 | T | TTATATAT others(1): Show |
6 | a0001c0001t0001g0197 a0001c0001t0002g0026 a0001c0001t0004g0138 others(3): Show |
6 | HG02630.hp1 HG02809.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+7661_15+7668dup others(8): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572595 | |||||||
chr12:88572595 | TTA | T | 9 | a0001c0001t0002g0028 a0001c0001t0002g0054 a0001c0001t0003g0055 others(6): Show |
9 | HG00423.hp1 HG01192.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+7667_15+7668del others(2): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572595 | |||||||
chr12:88572595 | TTATA | T | 2 | a0001c0001t0002g0158 a0001c0001t0005g0053 |
2 | HG03579.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.15+7665_15+7668del others(4): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572595 | |||||||
chr12:88572595 | TTATATA | T | 2 | a0001c0001t0002g0051 a0001c0001t0012g0052 |
2 | HG02559.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.15+7663_15+7668del others(6): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572595 | |||||||
chr12:88572597 | A | T | 1 | a0001c0001t0027g0144 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.15+7667T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572597 | |||||||
chr12:88572599 | A | T | 3 | a0001c0001t0011g0035 a0001c0001t0026g0036 a0001c0002t0002g0037 |
3 | HG01192.hp2 HG02965.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.15+7665T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572599 | |||||||
chr12:88572624 | G | A | 7 | a0001c0001t0003g0009 a0001c0001t0003g0020 a0001c0001t0003g0150 others(4): Show |
9 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+7640C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572624 | |||||||
chr12:88572636 | T | G | 73 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(70): Show |
86 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.15+7628A>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88572636 | |||||||
chr12:88573011 | A | G | 1 | a0001c0001t0001g0145 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.15+7253T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88573011 | |||||||
chr12:88573230 | C | T | 64 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(61): Show |
77 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.15+7034G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88573230 | |||||||
chr12:88573504 | C | G | 1 | a0001c0001t0011g0035 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.15+6760G>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88573504 | |||||||
chr12:88573520 | ATT | A | 4 | a0001c0001t0005g0141 a0001c0001t0005g0143 a0001c0001t0005g0154 others(1): Show |
4 | HG03130.hp1 HG03225.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+6742_15+6743del others(2): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88573520 | |||||||
chr12:88573599 | G | C | 1 | a0001c0001t0027g0144 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.15+6665C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88573599 | |||||||
chr12:88573829 | C | A | 1 | a0001c0001t0001g0014 | 2 | NA18961.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.15+6435G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88573829 | |||||||
chr12:88573931 | C | A | 6 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0030 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+6333G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88573931 | |||||||
chr12:88574065 | CT | C | 75 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(72): Show |
88 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.15+6198delA | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88574065 | |||||||
chr12:88574080 | A | T | 16 | a0001c0001t0004g0038 a0001c0001t0004g0039 a0001c0001t0004g0042 others(13): Show |
16 | HG00099.hp2 HG01099.hp2 HG01106.hp2 others(13): Show |
intron_variant | MODIFIER | c.15+6184T>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88574080 | |||||||
chr12:88574114 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.15+6150A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88574114 | |||||||
chr12:88574180 | G | A | 2 | a0001c0001t0003g0020 a0001c0001t0014g0010 |
3 | HG02451.hp2 HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.15+6084C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88574180 | |||||||
chr12:88574285 | TAAAAGAA others(7): Show |
T | 1 | a0001c0001t0001g0156 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.15+5965_15+5978del others(14): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88574285 | |||||||
chr12:88574290 | GA | G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0012 others(67): Show |
83 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.15+5973delT | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88574290 | |||||||
chr12:88574299 | A | G | 1 | a0001c0001t0007g0063 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.15+5965T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88574299 | |||||||
chr12:88575902 | T | C | 1 | a0001c0001t0021g0206 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.15+4362A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88575902 | |||||||
chr12:88575965 | C | T | 1 | a0001c0001t0002g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.15+4299G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88575965 | |||||||
chr12:88576131 | G | A | 7 | a0001c0001t0003g0009 a0001c0001t0003g0020 a0001c0001t0003g0150 others(4): Show |
9 | HG02451.hp2 HG02615.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+4133C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88576131 | |||||||
chr12:88576275 | T | C | 1 | a0001c0001t0022g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.15+3989A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88576275 | |||||||
chr12:88577277 | T | C | 1 | a0001c0001t0005g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.15+2987A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88577277 | |||||||
chr12:88577528 | A | C | 1 | a0001c0001t0001g0155 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.15+2736T>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88577528 | |||||||
chr12:88577641 | CAG | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(66): Show |
81 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.15+2621_15+2622del others(2): Show |
KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88577641 | |||||||
chr12:88578622 | T | C | 1 | a0001c0001t0001g0207 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.15+1642A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88578622 | |||||||
chr12:88578955 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.15+1309A>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88578955 | |||||||
chr12:88578992 | G | A | 1 | a0001c0001t0001g0209 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.15+1272C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88578992 | |||||||
chr12:88579003 | C | G | 6 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0030 others(3): Show |
6 | HG02258.hp1 HG02572.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+1261G>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88579003 | |||||||
chr12:88579445 | C | T | 1 | a0001c0001t0022g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.15+819G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88579445 | |||||||
chr12:88579525 | C | T | 2 | a0001c0001t0002g0025 a0001c0001t0002g0026 |
2 | HG02809.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.15+739G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88579525 | |||||||
chr12:88579955 | A | G | 8 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0024 others(5): Show |
10 | HG01099.hp1 HG02300.hp2 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.15+309T>C | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88579955 | |||||||
chr12:88580079 | C | T | 1 | a0001c0001t0003g0020 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.15+185G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88580079 | |||||||
chr12:88580084 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.15+180G>A | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88580084 | |||||||
chr12:88580091 | G | A | 6 | a0001c0001t0004g0210 a0001c0001t0004g0211 a0001c0001t0004g0212 others(3): Show |
6 | HG06807.hp1 NA18949.hp2 NA19004.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+173C>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88580091 | |||||||
chr12:88580174 | C | A | 2 | a0001c0001t0015g0216 a0001c0001t0015g0217 |
2 | HG02055.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.15+90G>T | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88580174 | |||||||
chr12:88580212 | G | C | 1 | a0001c0001t0005g0218 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.15+52C>G | KITLG | ENSG00000049130.16 | transcript | ENST00000644744.1 | protein_coding | 1/9 | chr12 | 88580212 |