Item | Value |
---|---|
geneid | 2683 |
ensemblid | ENSG00000086062.13 |
hgncid | 924 |
symbol | B4GALT1 |
name | beta-1,4-galactosyltransferase 1 |
refseq_nuc | NM_001497.4 |
refseq_prot | NP_001488.2 |
ensembl_nuc | ENST00000379731.5 |
ensembl_prot | ENSP00000369055.4 |
mane_status | MANE Select |
chr | chr9 |
start | 33110642 |
end | 33167336 |
strand | - |
ver | v1.2 |
region | chr9:33110642-33167336 |
region5000 | chr9:33105642-33172336 |
regionname0 | B4GALT1_chr9_33110642_33167336 |
regionname5000 | B4GALT1_chr9_33105642_33172336 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 398 | 360 | 88 | 68 | 147 | 13 | 42 | 117 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | MRLRE others(393): Show |
chr9 | 33105642 | 33172336 |
a0002 | 0/0 | 398 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | MRLRE others(393): Show |
chr9 | 33105642 | 33172336 |
a0003 | 0/0 | 398 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | MRLRE others(393): Show |
chr9 | 33105642 | 33172336 |
a0004 | 0/0 | 398 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | MRLRE others(393): Show |
chr9 | 33105642 | 33172336 |
a0005 | 0/0 | 398 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | MRLRE others(393): Show |
chr9 | 33105642 | 33172336 |
a0006 | 0/0 | 398 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | MRLRE others(393): Show |
chr9 | 33105642 | 33172336 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1194 | 339 | 84 | 67 | 133 | 12 | 42 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | ATGAG others(1189): Show |
chr9 | 33105642 | 33172336 | ||
a0001c0002 | 0/1 | 1194 | 21 | 4 | 1 | 14 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | ATGAG others(1189): Show |
chr9 | 33105642 | 33172336 | ||
a0002c0003 | 0/0 | 1194 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | ATGAG others(1189): Show |
chr9 | 33105642 | 33172336 | ||
a0003c0007 | 0/0 | 1194 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | ATGAG others(1189): Show |
chr9 | 33105642 | 33172336 | ||
a0004c0005 | 0/0 | 1194 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | ATGAG others(1189): Show |
chr9 | 33105642 | 33172336 | ||
a0005c0006 | 0/0 | 1194 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | ATGAG others(1189): Show |
chr9 | 33105642 | 33172336 | ||
a0006c0004 | 0/0 | 1194 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | ATGAG others(1189): Show |
chr9 | 33105642 | 33172336 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4172 | 86 | 7 | 26 | 32 | 5 | 16 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4167): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0002 | 0/0 | 4176 | 78 | 16 | 7 | 38 | 3 | 14 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4171): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0003 | 0/0 | 4167 | 32 | 0 | 7 | 21 | 0 | 4 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4162): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0004 | 0/0 | 4176 | 16 | 7 | 8 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4171): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0005 | 0/0 | 4176 | 14 | 4 | 1 | 7 | 1 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4171): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0006 | 0/0 | 4176 | 12 | 8 | 1 | 2 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4171): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0007 | 0/0 | 4177 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4172): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0008 | 0/0 | 4174 | 7 | 7 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4169): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0009 | 0/0 | 4176 | 7 | 6 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4171): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0010 | 0/0 | 4174 | 6 | 0 | 0 | 5 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4169): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0011 | 0/0 | 4176 | 5 | 0 | 0 | 5 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4171): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0013 | 0/0 | 4176 | 4 | 4 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4171): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0014 | 0/0 | 4161 | 4 | 0 | 0 | 4 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4156): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0015 | 0/0 | 4173 | 4 | 0 | 1 | 2 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4168): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0016 | 0/0 | 4176 | 4 | 4 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4171): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0017 | 0/0 | 4174 | 3 | 0 | 0 | 3 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4169): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0018 | 0/0 | 4176 | 3 | 2 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4171): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0020 | 0/0 | 4176 | 3 | 2 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4171): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0021 | 0/0 | 4176 | 3 | 1 | 2 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4171): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0022 | 0/0 | 4175 | 3 | 0 | 3 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4170): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0023 | 0/0 | 4172 | 3 | 0 | 3 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4167): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0024 | 0/0 | 4177 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4172): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0025 | 0/0 | 4174 | 2 | 0 | 0 | 0 | 0 | 2 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4169): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0026 | 0/0 | 4176 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4171): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0028 | 0/0 | 4174 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4169): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0029 | 0/0 | 4175 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4170): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0030 | 0/0 | 4175 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4170): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0031 | 0/0 | 4176 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4171): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0032 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4162): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0034 | 0/0 | 4176 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4171): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0035 | 0/0 | 4176 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4171): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0037 | 0/0 | 4176 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4171): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0038 | 0/0 | 4176 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4171): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0039 | 0/0 | 4172 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4167): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0040 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4168): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0041 | 0/0 | 4174 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4169): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0042 | 0/0 | 4172 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4167): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0044 | 0/0 | 4173 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4168): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0045 | 0/0 | 4174 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4169): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0046 | 0/0 | 4177 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4172): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0047 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4162): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0048 | 0/0 | 4172 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4167): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0049 | 0/0 | 4176 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4171): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0050 | 0/0 | 4167 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4162): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0051 | 0/0 | 4167 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4162): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0052 | 0/0 | 4174 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4169): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0053 | 0/0 | 4177 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4172): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0054 | 0/0 | 4177 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4172): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0055 | 0/0 | 4176 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4171): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0056 | 0/0 | 4176 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4171): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0057 | 0/0 | 4166 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4161): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0058 | 1/0 | 4176 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4171): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0059 | 0/0 | 4175 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4170): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0060 | 0/0 | 4174 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4169): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0061 | 0/0 | 4172 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4167): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0062 | 0/0 | 4172 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4167): Show |
chr9 | 33105642 | 33172336 |
a0001c0001t0063 | 0/0 | 4173 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4168): Show |
chr9 | 33105642 | 33172336 |
a0001c0002t0007 | 0/0 | 4177 | 11 | 4 | 1 | 6 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4172): Show |
chr9 | 33105642 | 33172336 |
a0001c0002t0012 | 0/0 | 4177 | 4 | 0 | 0 | 4 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4172): Show |
chr9 | 33105642 | 33172336 |
a0001c0002t0019 | 0/0 | 4178 | 3 | 0 | 0 | 2 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4173): Show |
chr9 | 33105642 | 33172336 |
a0001c0002t0024 | 0/1 | 4177 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4172): Show |
chr9 | 33105642 | 33172336 |
a0001c0002t0033 | 0/0 | 4176 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4171): Show |
chr9 | 33105642 | 33172336 |
a0001c0002t0036 | 0/0 | 4178 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4173): Show |
chr9 | 33105642 | 33172336 |
a0002c0003t0027 | 0/0 | 4176 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4171): Show |
chr9 | 33105642 | 33172336 |
a0003c0007t0002 | 0/0 | 4176 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4171): Show |
chr9 | 33105642 | 33172336 |
a0004c0005t0043 | 0/0 | 4173 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4168): Show |
chr9 | 33105642 | 33172336 |
a0005c0006t0001 | 0/0 | 4172 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4167): Show |
chr9 | 33105642 | 33172336 |
a0006c0004t0002 | 0/0 | 4176 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | GCTCC others(4171): Show |
chr9 | 33105642 | 33172336 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0003g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0004g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0004g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0004g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0004g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0004g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0004g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0004g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0005g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0005g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0005g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0005g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0005g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0005g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0005g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0005g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0005g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0005g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0005g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0005g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0006g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0006g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0006g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0006g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0006g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0006g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0006g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0006g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0006g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0006g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0006g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0007g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0008g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0008g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0008g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0008g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0008g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0008g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0008g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0009g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0009g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0009g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0009g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0009g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0009g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0009g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0010g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0010g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0010g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0010g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0010g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0011g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0011g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0011g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0011g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0011g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0013g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0013g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0013g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0013g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0014g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0014g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0014g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0015g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0015g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0015g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0015g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0016g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0016g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0016g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0016g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0017g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0017g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0017g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0018g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0018g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0018g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0020g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0020g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0020g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0021g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0021g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0021g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0022g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0022g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0022g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0023g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0023g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0023g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0024g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0025g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0026g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0026g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0028g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0028g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0029g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0029g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0030g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0030g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0031g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0032g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0034g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0035g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0037g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0038g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0039g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0040g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0041g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0042g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0044g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0045g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0046g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0047g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0048g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0049g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0050g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0051g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0052g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0053g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0054g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0055g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0056g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0057g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0058g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0059g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0060g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0061g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0062g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0001t0063g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0002t0007g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0002t0007g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0002t0007g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0002t0007g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0002t0007g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0002t0007g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0002t0007g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0002t0007g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0002t0007g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0002t0007g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0002t0007g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0002t0012g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0002t0012g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0002t0012g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0002t0012g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0002t0019g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0002t0019g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0002t0019g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0002t0024g0179 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0002t0033g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0001c0002t0036g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0002c0003t0027g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0003c0007t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0004c0005t0043g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0005c0006t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
a0006c0004t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0067 | EUR | GBR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | GBR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG00280 | hp1 | a0001 | c0001 | t0038 | g0170 | EUR | FIN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG00280 | hp2 | a0001 | c0001 | t0005 | g0033 | EUR | FIN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0076 | EUR | FIN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0249 | EUR | FIN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG00544 | hp1 | a0001 | c0002 | t0007 | g0185 | EAS | CHS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | CHS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | CHS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG00597 | hp1 | a0001 | c0001 | t0017 | g0283 | EAS | CHS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0347 | EAS | CHS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | CHS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | CHS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG00673 | hp1 | a0001 | c0001 | t0035 | g0252 | EAS | CHS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | CHS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG00733 | hp1 | a0001 | c0001 | t0005 | g0024 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0079 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG00735 | hp2 | a0001 | c0001 | t0023 | g0350 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0161 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG00741 | hp2 | a0001 | c0001 | t0015 | g0146 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0317 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01070 | hp2 | a0001 | c0001 | t0004 | g0010 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0010 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01074 | hp1 | a0001 | c0001 | t0020 | g0176 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01081 | hp1 | a0001 | c0001 | t0048 | g0116 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01081 | hp2 | a0001 | c0001 | t0021 | g0292 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0129 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0245 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01106 | hp2 | a0001 | c0001 | t0056 | g0337 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01167 | hp2 | a0001 | c0001 | t0055 | g0164 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01168 | hp2 | a0001 | c0001 | t0004 | g0159 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0160 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01175 | hp1 | a0001 | c0001 | t0006 | g0342 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01192 | hp2 | a0001 | c0001 | t0018 | g0168 | AMR | PUR | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01257 | hp1 | a0001 | c0002 | t0007 | g0180 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0130 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0131 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01358 | hp2 | a0001 | c0001 | t0022 | g0023 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0217 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01361 | hp2 | a0001 | c0001 | t0004 | g0162 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01496 | hp1 | a0001 | c0001 | t0009 | g0037 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01496 | hp2 | a0001 | c0001 | t0049 | g0281 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01515 | hp1 | a0001 | c0001 | t0060 | g0290 | EUR | IBS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0221 | EUR | IBS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0220 | EUR | IBS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0272 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01884 | hp2 | a0001 | c0001 | t0008 | g0345 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01891 | hp2 | a0001 | c0001 | t0016 | g0155 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0140 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01934 | hp2 | a0001 | c0001 | t0022 | g0021 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0135 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01978 | hp1 | a0001 | c0001 | t0021 | g0291 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01978 | hp2 | a0001 | c0001 | t0022 | g0022 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01993 | hp1 | a0001 | c0001 | t0023 | g0351 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0128 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02055 | hp1 | a0001 | c0001 | t0046 | g0327 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02055 | hp2 | a0003 | c0007 | t0002 | g0348 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02071 | hp1 | a0001 | c0001 | t0006 | g0064 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02071 | hp2 | a0001 | c0001 | t0034 | g0258 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02080 | hp1 | a0001 | c0001 | t0015 | g0141 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02145 | hp1 | a0001 | c0001 | t0021 | g0289 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02165 | hp1 | a0001 | c0002 | t0007 | g0187 | EAS | CDX | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | CDX | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02257 | hp1 | a0001 | c0001 | t0057 | g0294 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0276 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02258 | hp1 | a0001 | c0001 | t0018 | g0167 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02258 | hp2 | a0001 | c0002 | t0007 | g0288 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02280 | hp1 | a0001 | c0001 | t0008 | g0331 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02280 | hp2 | a0001 | c0001 | t0016 | g0053 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02293 | hp1 | a0001 | c0001 | t0023 | g0349 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02293 | hp2 | a0001 | c0001 | t0054 | g0333 | AMR | PEL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02451 | hp2 | a0001 | c0001 | t0006 | g0296 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02523 | hp1 | a0001 | c0001 | t0042 | g0133 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | KHV | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02572 | hp1 | a0001 | c0001 | t0041 | g0338 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0344 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0311 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02615 | hp1 | a0001 | c0001 | t0006 | g0323 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02615 | hp2 | a0001 | c0001 | t0028 | g0017 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02622 | hp1 | a0001 | c0001 | t0008 | g0302 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02622 | hp2 | a0001 | c0001 | t0009 | g0041 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0172 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0279 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02647 | hp2 | a0001 | c0001 | t0020 | g0175 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02683 | hp1 | a0001 | c0001 | t0005 | g0334 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02683 | hp2 | a0001 | c0001 | t0003 | g0298 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02698 | hp1 | a0001 | c0001 | t0010 | g0068 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02717 | hp1 | a0001 | c0001 | t0016 | g0156 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02717 | hp2 | a0001 | c0001 | t0030 | g0301 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0286 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02738 | hp1 | a0001 | c0001 | t0039 | g0061 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02809 | hp1 | a0001 | c0001 | t0030 | g0299 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02809 | hp2 | a0001 | c0001 | t0009 | g0042 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02818 | hp1 | a0001 | c0001 | t0009 | g0044 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02895 | hp1 | a0001 | c0001 | t0008 | g0325 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02895 | hp2 | a0001 | c0001 | t0040 | g0158 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02896 | hp1 | a0001 | c0001 | t0006 | g0332 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02896 | hp2 | a0002 | c0003 | t0027 | g0011 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02897 | hp1 | a0002 | c0003 | t0027 | g0011 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02897 | hp2 | a0001 | c0001 | t0008 | g0326 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0263 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02965 | hp1 | a0001 | c0001 | t0006 | g0343 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02965 | hp2 | a0001 | c0002 | t0007 | g0191 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02970 | hp1 | a0001 | c0001 | t0062 | g0173 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0268 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02976 | hp1 | a0001 | c0001 | t0006 | g0038 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02976 | hp2 | a0001 | c0001 | t0045 | g0035 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03041 | hp1 | a0001 | c0001 | t0020 | g0174 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03041 | hp2 | a0001 | c0001 | t0008 | g0335 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0275 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03195 | hp1 | a0001 | c0002 | t0007 | g0190 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03195 | hp2 | a0001 | c0001 | t0006 | g0336 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03209 | hp1 | a0001 | c0001 | t0007 | g0108 | AFR | MSL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | MSL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0212 | AFR | MSL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0236 | AFR | MSL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0320 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03453 | hp1 | a0001 | c0001 | t0009 | g0036 | AFR | MSL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03453 | hp2 | a0001 | c0001 | t0006 | g0330 | AFR | MSL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | MSL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03486 | hp2 | a0001 | c0001 | t0008 | g0346 | AFR | MSL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0233 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03491 | hp1 | a0001 | c0001 | t0025 | g0002 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03491 | hp2 | a0001 | c0001 | t0006 | g0049 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0235 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03492 | hp2 | a0001 | c0001 | t0025 | g0002 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0277 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | ESN | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03540 | hp1 | a0001 | c0001 | t0051 | g0054 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0329 | AFR | GWD | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | MSL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | MSL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0227 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0295 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0303 | SAS | PJL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0234 | SAS | BEB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | BEB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | BEB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0237 | SAS | BEB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | BEB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0244 | SAS | BEB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03942 | hp1 | a0001 | c0001 | t0063 | g0081 | SAS | BEB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0270 | SAS | BEB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0226 | SAS | STU | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | STU | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | STU | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0282 | SAS | STU | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0253 | SAS | STU | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18522 | hp1 | a0001 | c0001 | t0013 | g0127 | AFR | YRI | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0328 | AFR | YRI | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18612 | hp1 | a0001 | c0001 | t0044 | g0132 | EAS | CHB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18612 | hp2 | a0001 | c0002 | t0007 | g0186 | EAS | CHB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18747 | hp1 | a0001 | c0001 | t0050 | g0318 | EAS | CHB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | CHB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0278 | AFR | YRI | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0300 | AFR | YRI | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18940 | hp2 | a0001 | c0002 | t0019 | g0241 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18945 | hp2 | a0001 | c0001 | t0011 | g0255 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18946 | hp1 | a0001 | c0001 | t0005 | g0209 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18946 | hp2 | a0001 | c0001 | t0047 | g0107 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18947 | hp1 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18950 | hp1 | a0001 | c0001 | t0005 | g0032 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0134 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18952 | hp1 | a0001 | c0001 | t0010 | g0020 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18954 | hp1 | a0001 | c0001 | t0011 | g0242 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18959 | hp1 | a0001 | c0001 | t0010 | g0027 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18961 | hp1 | a0001 | c0001 | t0010 | g0003 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18962 | hp1 | a0001 | c0002 | t0007 | g0184 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18964 | hp2 | a0001 | c0001 | t0061 | g0125 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0319 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18972 | hp1 | a0001 | c0001 | t0053 | g0196 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18974 | hp2 | a0001 | c0001 | t0005 | g0030 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18978 | hp2 | a0001 | c0002 | t0036 | g0193 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0316 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18980 | hp1 | a0001 | c0001 | t0031 | g0199 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18988 | hp1 | a0001 | c0001 | t0011 | g0262 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18990 | hp2 | a0005 | c0006 | t0001 | g0091 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18991 | hp1 | a0001 | c0001 | t0005 | g0026 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18992 | hp1 | a0001 | c0001 | t0014 | g0007 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0306 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18995 | hp1 | a0001 | c0001 | t0052 | g0018 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0304 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18998 | hp1 | a0001 | c0002 | t0007 | g0189 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18999 | hp1 | a0001 | c0001 | t0005 | g0025 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19000 | hp1 | a0001 | c0001 | t0014 | g0051 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19002 | hp1 | a0001 | c0001 | t0010 | g0003 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19006 | hp1 | a0001 | c0002 | t0012 | g0285 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19006 | hp2 | a0001 | c0001 | t0014 | g0007 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0257 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19010 | hp2 | a0001 | c0001 | t0005 | g0029 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19030 | hp1 | a0001 | c0001 | t0013 | g0139 | AFR | LWK | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19030 | hp2 | a0001 | c0001 | t0013 | g0324 | AFR | LWK | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0280 | AFR | LWK | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0322 | AFR | LWK | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19054 | hp1 | a0001 | c0001 | t0014 | g0104 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19057 | hp2 | a0001 | c0001 | t0017 | g0077 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19060 | hp1 | a0001 | c0001 | t0005 | g0031 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19060 | hp2 | a0001 | c0001 | t0006 | g0267 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19063 | hp1 | a0001 | c0002 | t0007 | g0229 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19066 | hp2 | a0001 | c0002 | t0012 | g0177 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19068 | hp1 | a0001 | c0001 | t0026 | g0321 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19072 | hp1 | a0001 | c0002 | t0012 | g0178 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19072 | hp2 | a0001 | c0001 | t0037 | g0224 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19074 | hp1 | a0001 | c0001 | t0010 | g0028 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19074 | hp2 | a0001 | c0002 | t0033 | g0182 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19078 | hp1 | a0001 | c0001 | t0026 | g0102 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19078 | hp2 | a0001 | c0001 | t0011 | g0261 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19079 | hp2 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19081 | hp2 | a0001 | c0002 | t0012 | g0183 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19082 | hp2 | a0001 | c0002 | t0019 | g0188 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19084 | hp1 | a0001 | c0001 | t0015 | g0103 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19085 | hp1 | a0001 | c0001 | t0032 | g0309 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19086 | hp1 | a0001 | c0001 | t0011 | g0254 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19091 | hp1 | a0001 | c0001 | t0017 | g0284 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0339 | AFR | YRI | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA19240 | hp2 | a0001 | c0001 | t0028 | g0016 | AFR | YRI | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA20129 | hp1 | a0001 | c0001 | t0059 | g0043 | AFR | ASW | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA20129 | hp2 | a0001 | c0001 | t0024 | g0109 | AFR | ASW | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA20752 | hp1 | a0006 | c0004 | t0002 | g0216 | EUR | TSI | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0166 | EUR | TSI | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA20805 | hp1 | a0001 | c0002 | t0019 | g0192 | EUR | TSI | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0143 | EUR | TSI | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0198 | SAS | GIH | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA20905 | hp2 | a0001 | c0001 | t0015 | g0052 | SAS | GIH | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG01123 | hp2 | a0001 | c0001 | t0004 | g0165 | AMR | CLM | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02486 | hp1 | a0001 | c0001 | t0009 | g0040 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02486 | hp2 | a0001 | c0002 | t0007 | g0181 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02559 | hp1 | a0001 | c0001 | t0029 | g0340 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG02559 | hp2 | a0004 | c0005 | t0043 | g0287 | AFR | ACB | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03471 | hp1 | a0001 | c0001 | t0009 | g0045 | AFR | MSL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG03471 | hp2 | a0001 | c0001 | t0016 | g0157 | AFR | MSL | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG06807 | hp1 | a0001 | c0001 | t0018 | g0169 | AFR | USA | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0293 | AFR | USA | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | USA | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA20300 | hp2 | a0001 | c0001 | t0029 | g0341 | AFR | USA | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0163 | AFR | LWK | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
NA21309 | hp2 | a0001 | c0001 | t0013 | g0138 | AFR | LWK | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
homoSapiens | chm13v2 | a0001 | c0002 | t0024 | g0179 | REF | REF | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
homoSapiens | grch38p0 | a0001 | c0001 | t0058 | g0039 | REF | REF | B4GALT1_chr9_33105642_33172336 | B4GALT1 | chr9 | 33105642 | 33172336 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:33113461 | G | A | 1 | a0006 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.1190C>T | p.Pro397Leu | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1357/4176 | 1190/1197 | 397/398 | chr9 | 33113461 | |||
chr9:33116058 | G | C | 1 | a0002 | 2 | HG02896.hp2 HG02897.hp1 |
missense_variant | MODERATE | c.892C>G | p.Leu298Val | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/6 | 1059/4176 | 892/1197 | 298/398 | chr9 | 33116058 | |||
chr9:33120479 | G | C | 1 | a0004 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.776C>G | p.Ala259Gly | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/6 | 943/4176 | 776/1197 | 259/398 | chr9 | 33120479 | |||
chr9:33135266 | G | A | 1 | a0005 | 1 | NA18990.hp2 | missense_variant | MODERATE | c.571C>T | p.Leu191Phe | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/6 | 738/4176 | 571/1197 | 191/398 | chr9 | 33135266 | |||
chr9:33166911 | G | A | 1 | a0003 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.259C>T | p.Pro87Ser | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/6 | 426/4176 | 259/1197 | 87/398 | chr9 | 33166911 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:33135240 | G | A | 1 | a0001c0002 | 20 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(17): Show |
synonymous_variant | LOW | c.597C>T | p.His199His | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/6 | 764/4176 | 597/1197 | 199/398 | chr9 | 33135240 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:33110695 | A | C | 4 | a0001c0001t0010 a0001c0001t0025 a0001c0001t0028 others(1): Show |
11 | HG02615.hp2 HG02698.hp1 HG03491.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2759T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2759 | chr9 | 33110695 | ||||||
chr9:33110725 | G | A | 2 | a0001c0001t0042 a0001c0001t0044 |
2 | HG02523.hp1 NA18612.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2729C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2729 | chr9 | 33110725 | ||||||
chr9:33110841 | C | T | 11 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0018 others(8): Show |
34 | HG00544.hp1 HG01192.hp2 HG01257.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2613G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2613 | chr9 | 33110841 | ||||||
chr9:33110948 | TCA | T | 1 | a0001c0001t0017 | 3 | HG00597.hp1 NA19057.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2504_*2505delTG | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2504 | chr9 | 33110948 | ||||||
chr9:33110996 | G | A | 1 | a0001c0001t0035 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2458C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2458 | chr9 | 33110996 | ||||||
chr9:33111013 | C | T | 1 | a0001c0001t0011 | 5 | NA18945.hp2 NA18954.hp1 NA18988.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2441G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2441 | chr9 | 33111013 | ||||||
chr9:33111049 | A | AC | 8 | a0001c0001t0007 a0001c0001t0024 a0001c0001t0053 others(5): Show |
23 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2404dupG | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2404 | chr9 | 33111049 | ||||||
chr9:33111052 | C | T | 1 | a0001c0001t0034 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2402G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2402 | chr9 | 33111052 | ||||||
chr9:33111173 | C | T | 1 | a0001c0001t0008 | 7 | HG01884.hp2 HG02280.hp1 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2281G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2281 | chr9 | 33111173 | ||||||
chr9:33111185 | G | C | 1 | a0001c0001t0051 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2269C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2269 | chr9 | 33111185 | ||||||
chr9:33111201 | C | T | 2 | a0001c0001t0021 a0001c0001t0060 |
4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2253G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2253 | chr9 | 33111201 | ||||||
chr9:33111250 | C | CA | 4 | a0001c0001t0046 a0001c0001t0054 a0001c0002t0019 others(1): Show |
6 | HG02055.hp1 HG02293.hp2 NA18940.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2203dupT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2203 | chr9 | 33111250 | ||||||
chr9:33111250 | CA | C | 4 | a0001c0001t0029 a0001c0001t0030 a0001c0001t0059 others(1): Show |
6 | HG02559.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2203delT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2203 | chr9 | 33111250 | ||||||
chr9:33111250 | CAA | C | 8 | a0001c0001t0008 a0001c0001t0010 a0001c0001t0025 others(5): Show |
21 | HG01515.hp1 HG01884.hp2 HG02280.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2202_*2203delTT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2202 | chr9 | 33111250 | ||||||
chr9:33111250 | CAAA | C | 5 | a0001c0001t0015 a0001c0001t0040 a0001c0001t0044 others(2): Show |
8 | HG00741.hp2 HG02080.hp1 HG02559.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2201_*2203delTTT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2201 | chr9 | 33111250 | ||||||
chr9:33111250 | CAAAA | C | 8 | a0001c0001t0001 a0001c0001t0023 a0001c0001t0039 others(5): Show |
95 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*2200_*2203delTTTT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2200 | chr9 | 33111250 | ||||||
chr9:33111250 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0057 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2194_*2203delTTTT others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2194 | chr9 | 33111250 | ||||||
chr9:33111250 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0014 | 4 | NA18992.hp1 NA19000.hp1 NA19006.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2189_*2203delTTTT others(11): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2189 | chr9 | 33111250 | ||||||
chr9:33111269 | A | C | 5 | a0001c0001t0004 a0001c0001t0013 a0001c0001t0016 others(2): Show |
26 | HG00280.hp1 HG00733.hp2 HG00738.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2185T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2185 | chr9 | 33111269 | ||||||
chr9:33111270 | AAAAAAAA others(2): Show |
A | 5 | a0001c0001t0003 a0001c0001t0032 a0001c0001t0047 others(2): Show |
36 | HG00597.hp2 HG01070.hp1 HG01099.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2175_*2183delGTTT others(5): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2175 | chr9 | 33111270 | ||||||
chr9:33111276 | A | AAAAAAAA others(33): Show |
1 | a0001c0001t0021 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2177_*2178insGTTT others(36): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2177 | chr9 | 33111276 | ||||||
chr9:33111276 | A | AAAAAAAA others(25): Show |
1 | a0001c0001t0021 | 1 | HG01978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2177_*2178insGTTG others(28): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2177 | chr9 | 33111276 | ||||||
chr9:33111276 | A | C | 1 | a0001c0001t0060 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2178T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2178 | chr9 | 33111276 | ||||||
chr9:33111276 | AAAC | A | 13 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(10): Show |
81 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*2175_*2177delGTT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2175 | chr9 | 33111276 | ||||||
chr9:33111277 | AAC | A | 3 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0011 |
17 | HG00609.hp1 HG00733.hp1 HG01361.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2175_*2176delGT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2175 | chr9 | 33111277 | ||||||
chr9:33111279 | C | A | 1 | a0001c0001t0002 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2175G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2175 | chr9 | 33111279 | ||||||
chr9:33111350 | A | G | 6 | a0001c0001t0003 a0001c0001t0026 a0001c0001t0032 others(3): Show |
38 | HG00597.hp2 HG01070.hp1 HG01099.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2104T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2104 | chr9 | 33111350 | ||||||
chr9:33111413 | C | T | 9 | a0001c0001t0003 a0001c0001t0020 a0001c0001t0021 others(6): Show |
45 | HG00597.hp2 HG01070.hp1 HG01074.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*2041G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 2041 | chr9 | 33111413 | ||||||
chr9:33111563 | GA | G | 8 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0026 others(5): Show |
44 | HG00597.hp2 HG01070.hp1 HG01099.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1890delT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1890 | chr9 | 33111563 | ||||||
chr9:33111593 | G | A | 1 | a0001c0001t0052 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1861C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1861 | chr9 | 33111593 | ||||||
chr9:33111688 | G | A | 3 | a0001c0001t0020 a0001c0001t0021 a0001c0001t0060 |
7 | HG01074.hp1 HG01081.hp2 HG01515.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1766C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1766 | chr9 | 33111688 | ||||||
chr9:33111716 | T | G | 2 | a0001c0001t0021 a0001c0001t0060 |
4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1738A>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1738 | chr9 | 33111716 | ||||||
chr9:33111766 | G | A | 2 | a0001c0001t0021 a0001c0001t0060 |
4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1688C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1688 | chr9 | 33111766 | ||||||
chr9:33111778 | G | GA | 8 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0026 others(5): Show |
44 | HG00597.hp2 HG01070.hp1 HG01099.hp1 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1675dupT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1675 | chr9 | 33111778 | ||||||
chr9:33111790 | T | C | 11 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0020 others(8): Show |
51 | HG00597.hp2 HG01070.hp1 HG01074.hp1 others(48): Show |
3_prime_UTR_variant | MODIFIER | c.*1664A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1664 | chr9 | 33111790 | ||||||
chr9:33111826 | A | T | 1 | a0001c0001t0050 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1628T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1628 | chr9 | 33111826 | ||||||
chr9:33111909 | G | A | 1 | a0001c0001t0048 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1545C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1545 | chr9 | 33111909 | ||||||
chr9:33111954 | C | T | 1 | a0001c0001t0028 | 2 | HG02615.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1500G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1500 | chr9 | 33111954 | ||||||
chr9:33111955 | G | A | 3 | a0001c0001t0020 a0001c0001t0021 a0001c0001t0060 |
7 | HG01074.hp1 HG01081.hp2 HG01515.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1499C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1499 | chr9 | 33111955 | ||||||
chr9:33112084 | C | T | 1 | a0001c0001t0049 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1370G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1370 | chr9 | 33112084 | ||||||
chr9:33112440 | T | C | 2 | a0001c0001t0021 a0001c0001t0060 |
4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1014A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 1014 | chr9 | 33112440 | ||||||
chr9:33112575 | A | G | 4 | a0001c0001t0010 a0001c0001t0025 a0001c0001t0028 others(1): Show |
11 | HG02615.hp2 HG02698.hp1 HG03491.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*879T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 879 | chr9 | 33112575 | ||||||
chr9:33112625 | A | C | 10 | a0001c0001t0003 a0001c0001t0016 a0001c0001t0018 others(7): Show |
49 | HG00597.hp2 HG01070.hp1 HG01099.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*829T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 829 | chr9 | 33112625 | ||||||
chr9:33112634 | A | C | 1 | a0001c0001t0031 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*820T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 820 | chr9 | 33112634 | ||||||
chr9:33112977 | G | A | 1 | a0001c0001t0037 | 1 | NA19072.hp2 | 3_prime_UTR_variant | MODIFIER | c.*477C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 477 | chr9 | 33112977 | ||||||
chr9:33113000 | T | A | 1 | a0001c0001t0055 | 1 | HG01167.hp2 | 3_prime_UTR_variant | MODIFIER | c.*454A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 454 | chr9 | 33113000 | ||||||
chr9:33113068 | G | A | 4 | a0001c0001t0020 a0001c0001t0021 a0001c0001t0059 others(1): Show |
8 | HG01074.hp1 HG01081.hp2 HG01515.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*386C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 386 | chr9 | 33113068 | ||||||
chr9:33113071 | T | C | 1 | a0001c0001t0056 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*383A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 383 | chr9 | 33113071 | ||||||
chr9:33113123 | G | A | 45 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(42): Show |
230 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*331C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 331 | chr9 | 33113123 | ||||||
chr9:33113186 | A | G | 2 | a0001c0001t0040 a0001c0001t0041 |
2 | HG02572.hp1 HG02895.hp2 |
3_prime_UTR_variant | MODIFIER | c.*268T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 268 | chr9 | 33113186 | ||||||
chr9:33113198 | G | T | 59 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(56): Show |
346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
3_prime_UTR_variant | MODIFIER | c.*256C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 256 | chr9 | 33113198 | ||||||
chr9:33113207 | CT | C | 1 | a0001c0001t0022 | 3 | HG01358.hp2 HG01934.hp2 HG01978.hp2 |
3_prime_UTR_variant | MODIFIER | c.*246delA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 246 | chr9 | 33113207 | ||||||
chr9:33113235 | G | T | 1 | a0001c0001t0039 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*219C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 219 | chr9 | 33113235 | ||||||
chr9:33113285 | G | A | 1 | a0001c0001t0061 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*169C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 169 | chr9 | 33113285 | ||||||
chr9:33113300 | C | T | 1 | a0001c0001t0038 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*154G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 154 | chr9 | 33113300 | ||||||
chr9:33113301 | G | A | 2 | a0001c0001t0062 a0001c0001t0063 |
2 | HG02970.hp1 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*153C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 153 | chr9 | 33113301 | ||||||
chr9:33113324 | C | T | 13 | a0001c0001t0002 a0001c0001t0011 a0001c0001t0017 others(10): Show |
99 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*130G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 6/6 | 130 | chr9 | 33113324 | ||||||
chr9:33167229 | G | A | 1 | a0001c0001t0023 | 3 | HG00735.hp2 HG01993.hp1 HG02293.hp1 |
5_prime_UTR_variant | MODIFIER | c.-60C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/6 | 60 | chr9 | 33167229 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:33113714 | C | G | 3 | a0001c0001t0004g0300 a0001c0001t0020g0174 a0001c0001t0020g0176 |
3 | HG01074.hp1 HG03041.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1064+60G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 5/5 | chr9 | 33113714 | |||||||
chr9:33113742 | G | C | 8 | a0001c0001t0006g0343 a0001c0001t0008g0302 a0001c0001t0008g0325 others(5): Show |
8 | HG01884.hp2 HG02280.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1064+32C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 5/5 | chr9 | 33113742 | |||||||
chr9:33113769 | T | A | 1 | a0001c0001t0003g0317 | 1 | HG01070.hp1 | splice_region_variant&intron_variant | LOW | c.1064+5A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 5/5 | chr9 | 33113769 | |||||||
chr9:33113890 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.960-12T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33113890 | |||||||
chr9:33113906 | T | C | 1 | a0001c0001t0059g0043 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.960-28A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33113906 | |||||||
chr9:33113972 | C | T | 11 | a0001c0001t0016g0053 a0001c0001t0016g0155 a0001c0001t0016g0156 others(8): Show |
12 | HG01081.hp2 HG01515.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.960-94G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33113972 | |||||||
chr9:33114029 | T | A | 1 | a0001c0001t0001g0087 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.960-151A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33114029 | |||||||
chr9:33114084 | G | A | 29 | a0001c0001t0003g0046 a0001c0001t0003g0063 a0001c0001t0003g0128 others(26): Show |
29 | HG01070.hp1 HG01074.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.960-206C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33114084 | |||||||
chr9:33114121 | G | A | 1 | a0001c0001t0059g0043 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.960-243C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33114121 | |||||||
chr9:33114283 | G | T | 2 | a0001c0001t0002g0226 a0001c0001t0002g0295 |
2 | HG03669.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.960-405C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33114283 | |||||||
chr9:33114547 | G | GTC | 303 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(300): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.960-671_960-670dup others(2): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33114547 | |||||||
chr9:33114846 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.960-968G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33114846 | |||||||
chr9:33114921 | T | C | 1 | a0001c0001t0006g0343 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.960-1043A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33114921 | |||||||
chr9:33114934 | C | CA | 4 | a0001c0001t0021g0289 a0001c0001t0021g0291 a0001c0001t0021g0292 others(1): Show |
4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.959+1056dupT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33114934 | |||||||
chr9:33115109 | A | C | 1 | a0001c0001t0057g0294 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.959+882T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33115109 | |||||||
chr9:33115168 | G | T | 303 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(300): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.959+823C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33115168 | |||||||
chr9:33115170 | G | C | 1 | a0001c0002t0033g0182 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.959+821C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33115170 | |||||||
chr9:33115503 | G | T | 303 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(300): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.959+488C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33115503 | |||||||
chr9:33115522 | G | A | 1 | a0001c0001t0003g0297 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.959+469C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33115522 | |||||||
chr9:33115558 | A | G | 294 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(291): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.959+433T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33115558 | |||||||
chr9:33115582 | C | T | 5 | a0001c0001t0002g0197 a0001c0001t0002g0219 a0001c0001t0002g0246 others(2): Show |
5 | NA18994.hp2 NA19012.hp1 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.959+409G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33115582 | |||||||
chr9:33115856 | C | T | 1 | a0001c0001t0051g0054 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.959+135G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33115856 | |||||||
chr9:33115962 | G | T | 1 | a0001c0001t0004g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.959+29C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33115962 | |||||||
chr9:33115969 | A | G | 2 | a0001c0001t0001g0055 a0001c0001t0049g0281 |
2 | HG01255.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.959+22T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33115969 | |||||||
chr9:33115972 | T | C | 1 | a0001c0001t0025g0002 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.959+19A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 4/5 | chr9 | 33115972 | |||||||
chr9:33116146 | T | A | 1 | a0001c0002t0019g0241 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.837-33A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116146 | |||||||
chr9:33116240 | AT | A | 302 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(299): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.837-128delA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116240 | |||||||
chr9:33116256 | G | A | 1 | a0001c0001t0050g0318 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.837-143C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116256 | |||||||
chr9:33116388 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.837-275G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116388 | |||||||
chr9:33116458 | G | A | 1 | a0001c0001t0002g0231 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.837-345C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116458 | |||||||
chr9:33116468 | G | A | 1 | a0001c0001t0006g0323 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.837-355C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116468 | |||||||
chr9:33116500 | T | C | 294 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(291): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.837-387A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116500 | |||||||
chr9:33116504 | A | G | 302 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(299): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.837-391T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116504 | |||||||
chr9:33116516 | C | A | 5 | a0001c0001t0016g0053 a0001c0001t0016g0155 a0001c0001t0016g0156 others(2): Show |
6 | HG01891.hp2 HG02280.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.837-403G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116516 | |||||||
chr9:33116516 | C | T | 4 | a0001c0001t0020g0174 a0001c0001t0020g0175 a0001c0001t0020g0176 others(1): Show |
4 | HG01074.hp1 HG02647.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.837-403G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116516 | |||||||
chr9:33116519 | A | C | 4 | a0001c0001t0021g0289 a0001c0001t0021g0291 a0001c0001t0021g0292 others(1): Show |
4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.837-406T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116519 | |||||||
chr9:33116521 | C | CT | 66 | a0001c0001t0001g0055 a0001c0001t0002g0249 a0001c0001t0002g0274 others(63): Show |
70 | HG00280.hp1 HG00323.hp2 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.837-409dupA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116521 | |||||||
chr9:33116521 | C | CTT | 126 | a0001c0001t0001g0076 a0001c0001t0001g0080 a0001c0001t0001g0088 others(123): Show |
129 | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.837-410_837-409dup others(2): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116521 | |||||||
chr9:33116521 | C | CTTT | 101 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): Show |
106 | HG00140.hp1 HG00558.hp1 HG00642.hp1 others(103): Show |
intron_variant | MODIFIER | c.837-411_837-409dup others(3): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116521 | |||||||
chr9:33116709 | G | C | 1 | a0001c0001t0026g0321 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.837-596C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116709 | |||||||
chr9:33116789 | C | A | 2 | a0001c0001t0007g0108 a0001c0001t0024g0109 |
2 | HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.837-676G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116789 | |||||||
chr9:33116943 | G | C | 105 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(102): Show |
108 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(105): Show |
intron_variant | MODIFIER | c.837-830C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33116943 | |||||||
chr9:33117496 | A | G | 1 | a0001c0001t0051g0054 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.837-1383T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33117496 | |||||||
chr9:33117526 | C | T | 117 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
124 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.837-1413G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33117526 | |||||||
chr9:33117573 | C | T | 1 | a0001c0001t0051g0054 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.837-1460G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33117573 | |||||||
chr9:33117702 | A | C | 2 | a0001c0001t0001g0070 a0001c0001t0006g0064 |
2 | HG02071.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.837-1589T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33117702 | |||||||
chr9:33117775 | T | C | 340 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(337): Show |
355 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.837-1662A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33117775 | |||||||
chr9:33117784 | C | T | 1 | a0001c0001t0004g0172 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.837-1671G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33117784 | |||||||
chr9:33117800 | C | G | 9 | a0001c0001t0010g0003 a0001c0001t0010g0020 a0001c0001t0010g0027 others(6): Show |
11 | HG02615.hp2 HG02698.hp1 HG03491.hp1 others(8): Show |
intron_variant | MODIFIER | c.837-1687G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33117800 | |||||||
chr9:33117920 | A | G | 1 | a0001c0001t0002g0208 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.837-1807T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33117920 | |||||||
chr9:33117956 | C | T | 63 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0195 others(60): Show |
65 | HG00323.hp2 HG00544.hp2 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.837-1843G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33117956 | |||||||
chr9:33117967 | C | T | 221 | a0001c0001t0001g0055 a0001c0001t0002g0012 a0001c0001t0002g0013 others(218): Show |
230 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(227): Show |
intron_variant | MODIFIER | c.837-1854G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33117967 | |||||||
chr9:33118112 | G | C | 29 | a0001c0001t0001g0055 a0001c0001t0004g0009 a0001c0001t0004g0010 others(26): Show |
31 | HG00280.hp1 HG00733.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.837-1999C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118112 | |||||||
chr9:33118113 | T | C | 113 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(110): Show |
119 | HG00140.hp1 HG00323.hp1 HG00597.hp2 others(116): Show |
intron_variant | MODIFIER | c.837-2000A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118113 | |||||||
chr9:33118260 | T | A | 3 | a0001c0001t0003g0298 a0001c0001t0003g0303 a0001c0001t0003g0320 |
3 | HG02683.hp2 HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.837-2147A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118260 | |||||||
chr9:33118271 | G | T | 1 | a0004c0005t0043g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.836+2148C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118271 | |||||||
chr9:33118301 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0119 |
2 | HG03834.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.836+2118C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118301 | |||||||
chr9:33118319 | A | G | 56 | a0001c0001t0001g0005 a0001c0001t0001g0171 a0001c0001t0001g0314 others(53): Show |
60 | HG00597.hp2 HG01070.hp1 HG01099.hp1 others(57): Show |
intron_variant | MODIFIER | c.836+2100T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118319 | |||||||
chr9:33118325 | G | A | 2 | a0001c0001t0006g0322 a0001c0001t0006g0323 |
2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.836+2094C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118325 | |||||||
chr9:33118389 | G | C | 111 | a0001c0001t0001g0008 a0001c0001t0001g0057 a0001c0001t0001g0059 others(108): Show |
116 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.836+2030C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118389 | |||||||
chr9:33118412 | C | T | 340 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(337): Show |
355 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.836+2007G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118412 | |||||||
chr9:33118504 | A | AT | 21 | a0001c0001t0005g0024 a0001c0001t0005g0025 a0001c0001t0005g0026 others(18): Show |
23 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.836+1914dupA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118504 | |||||||
chr9:33118603 | A | G | 32 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(29): Show |
32 | HG01106.hp2 HG01175.hp1 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.836+1816T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118603 | |||||||
chr9:33118741 | A | G | 1 | a0001c0001t0057g0294 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.836+1678T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118741 | |||||||
chr9:33118760 | A | G | 1 | a0001c0001t0010g0020 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.836+1659T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118760 | |||||||
chr9:33118857 | T | C | 22 | a0001c0001t0037g0224 a0001c0001t0053g0196 a0001c0002t0007g0180 others(19): Show |
22 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(19): Show |
intron_variant | MODIFIER | c.836+1562A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118857 | |||||||
chr9:33118860 | GT | G | 22 | a0001c0001t0001g0019 a0001c0001t0005g0024 a0001c0001t0005g0025 others(19): Show |
24 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.836+1558delA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118860 | |||||||
chr9:33118898 | G | GT | 195 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0171 others(192): Show |
202 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.836+1520dupA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118898 | |||||||
chr9:33118906 | A | G | 195 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0171 others(192): Show |
202 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.836+1513T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118906 | |||||||
chr9:33118958 | T | C | 1 | a0004c0005t0043g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.836+1461A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33118958 | |||||||
chr9:33119082 | G | A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 |
3 | HG01891.hp1 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.836+1337C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33119082 | |||||||
chr9:33119122 | A | G | 1 | a0001c0001t0003g0223 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.836+1297T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33119122 | |||||||
chr9:33119243 | C | T | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.836+1176G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33119243 | |||||||
chr9:33119256 | AC | A | 22 | a0001c0001t0037g0224 a0001c0001t0053g0196 a0001c0002t0007g0180 others(19): Show |
22 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(19): Show |
intron_variant | MODIFIER | c.836+1162delG | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33119256 | |||||||
chr9:33119315 | C | T | 1 | a0002c0003t0027g0011 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.836+1104G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33119315 | |||||||
chr9:33119585 | T | A | 93 | a0001c0001t0001g0200 a0001c0001t0002g0012 a0001c0001t0002g0013 others(90): Show |
96 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.836+834A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33119585 | |||||||
chr9:33119702 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.836+717G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33119702 | |||||||
chr9:33119820 | A | G | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.836+599T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33119820 | |||||||
chr9:33119964 | G | T | 4 | a0001c0001t0021g0289 a0001c0001t0021g0291 a0001c0001t0021g0292 others(1): Show |
4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.836+455C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33119964 | |||||||
chr9:33120108 | C | T | 1 | a0001c0001t0003g0304 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.836+311G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33120108 | |||||||
chr9:33120115 | C | G | 2 | a0001c0001t0002g0195 a0001c0001t0002g0204 |
2 | NA18966.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.836+304G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33120115 | |||||||
chr9:33120125 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.836+294C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33120125 | |||||||
chr9:33120204 | A | G | 1 | a0001c0001t0002g0260 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.836+215T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33120204 | |||||||
chr9:33120205 | A | G | 115 | a0001c0001t0001g0200 a0001c0001t0002g0012 a0001c0001t0002g0013 others(112): Show |
118 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.836+214T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33120205 | |||||||
chr9:33120206 | A | G | 167 | a0001c0001t0001g0019 a0001c0001t0001g0105 a0001c0001t0001g0200 others(164): Show |
172 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(169): Show |
intron_variant | MODIFIER | c.836+213T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33120206 | |||||||
chr9:33120213 | A | G | 37 | a0001c0001t0001g0314 a0001c0001t0003g0001 a0001c0001t0003g0297 others(34): Show |
41 | HG00280.hp1 HG00597.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.836+206T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33120213 | |||||||
chr9:33120263 | T | C | 26 | a0001c0001t0001g0055 a0001c0001t0001g0171 a0001c0001t0004g0009 others(23): Show |
28 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.836+156A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 3/5 | chr9 | 33120263 | |||||||
chr9:33120645 | A | G | 1 | a0001c0001t0002g0275 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.649-39T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33120645 | |||||||
chr9:33120708 | A | G | 93 | a0001c0001t0001g0200 a0001c0001t0002g0012 a0001c0001t0002g0013 others(90): Show |
96 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.649-102T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33120708 | |||||||
chr9:33120752 | G | C | 1 | a0001c0001t0003g0317 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.649-146C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33120752 | |||||||
chr9:33120767 | T | C | 20 | a0001c0001t0037g0224 a0001c0001t0053g0196 a0001c0002t0007g0180 others(17): Show |
20 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(17): Show |
intron_variant | MODIFIER | c.649-161A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33120767 | |||||||
chr9:33120768 | G | C | 1 | a0001c0001t0002g0210 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.649-162C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33120768 | |||||||
chr9:33121035 | G | A | 2 | a0001c0002t0012g0183 a0001c0002t0033g0182 |
2 | NA19074.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.649-429C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33121035 | |||||||
chr9:33121174 | T | A | 2 | a0001c0001t0029g0340 a0001c0001t0029g0341 |
2 | HG02559.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.649-568A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33121174 | |||||||
chr9:33121183 | C | G | 1 | a0001c0001t0051g0054 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.649-577G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33121183 | |||||||
chr9:33121482 | C | T | 115 | a0001c0001t0001g0200 a0001c0001t0002g0012 a0001c0001t0002g0013 others(112): Show |
118 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.649-876G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33121482 | |||||||
chr9:33121487 | C | T | 1 | a0001c0001t0003g0130 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.649-881G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33121487 | |||||||
chr9:33121526 | C | CT | 7 | a0001c0001t0001g0078 a0001c0001t0001g0147 a0001c0001t0009g0036 others(4): Show |
7 | HG00642.hp1 HG01081.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.649-921dupA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33121526 | |||||||
chr9:33121526 | CT | C | 29 | a0001c0001t0001g0055 a0001c0001t0001g0171 a0001c0001t0001g0314 others(26): Show |
32 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.649-921delA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33121526 | |||||||
chr9:33121526 | CTTT | C | 24 | a0001c0001t0002g0259 a0001c0001t0002g0273 a0001c0001t0037g0224 others(21): Show |
24 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(21): Show |
intron_variant | MODIFIER | c.649-923_649-921del others(3): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33121526 | |||||||
chr9:33121526 | CTTTT | C | 139 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(136): Show |
144 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.649-924_649-921del others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33121526 | |||||||
chr9:33121537 | T | G | 1 | a0001c0001t0006g0064 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.649-931A>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33121537 | |||||||
chr9:33121546 | T | A | 2 | a0001c0001t0001g0074 a0001c0001t0001g0152 |
2 | HG03654.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.649-940A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33121546 | |||||||
chr9:33121572 | G | A | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.649-966C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33121572 | |||||||
chr9:33121978 | A | G | 1 | a0001c0001t0002g0260 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.649-1372T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33121978 | |||||||
chr9:33122026 | C | A | 93 | a0001c0001t0001g0200 a0001c0001t0002g0012 a0001c0001t0002g0013 others(90): Show |
96 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(93): Show |
intron_variant | MODIFIER | c.649-1420G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122026 | |||||||
chr9:33122128 | G | C | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 |
3 | HG01891.hp1 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.649-1522C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122128 | |||||||
chr9:33122135 | C | T | 3 | a0001c0001t0008g0302 a0001c0001t0030g0299 a0001c0001t0030g0301 |
3 | HG02622.hp1 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.649-1529G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122135 | |||||||
chr9:33122159 | T | C | 27 | a0001c0001t0001g0055 a0001c0001t0001g0171 a0001c0001t0004g0009 others(24): Show |
30 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.649-1553A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122159 | |||||||
chr9:33122214 | C | A | 23 | a0001c0001t0001g0055 a0001c0001t0001g0171 a0001c0001t0004g0009 others(20): Show |
25 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.649-1608G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122214 | |||||||
chr9:33122259 | T | C | 341 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(338): Show |
356 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.649-1653A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122259 | |||||||
chr9:33122307 | T | C | 1 | a0004c0005t0043g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.649-1701A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122307 | |||||||
chr9:33122372 | T | A | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.649-1766A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122372 | |||||||
chr9:33122462 | G | A | 29 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0171 others(26): Show |
31 | HG00280.hp1 HG00280.hp2 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.649-1856C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122462 | |||||||
chr9:33122511 | AAAAT | A | 159 | a0001c0001t0001g0019 a0001c0001t0001g0098 a0001c0001t0001g0200 others(156): Show |
166 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(163): Show |
intron_variant | MODIFIER | c.649-1909_649-1906d others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122511 | |||||||
chr9:33122628 | T | C | 191 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0171 others(188): Show |
199 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.649-2022A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122628 | |||||||
chr9:33122647 | G | C | 168 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(165): Show |
173 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(170): Show |
intron_variant | MODIFIER | c.649-2041C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122647 | |||||||
chr9:33122696 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.649-2090C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122696 | |||||||
chr9:33122776 | T | C | 3 | a0001c0001t0020g0174 a0001c0001t0020g0175 a0001c0001t0020g0176 |
3 | HG01074.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.649-2170A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33122776 | |||||||
chr9:33123000 | C | T | 1 | a0001c0001t0045g0035 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.649-2394G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123000 | |||||||
chr9:33123015 | A | G | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.649-2409T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123015 | |||||||
chr9:33123106 | C | T | 1 | a0001c0001t0001g0008 | 2 | NA18971.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.649-2500G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123106 | |||||||
chr9:33123108 | T | A | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.649-2502A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123108 | |||||||
chr9:33123132 | G | T | 1 | a0004c0005t0043g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.649-2526C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123132 | |||||||
chr9:33123135 | G | C | 25 | a0001c0001t0001g0171 a0001c0001t0004g0009 a0001c0001t0004g0010 others(22): Show |
28 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.649-2529C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123135 | |||||||
chr9:33123276 | T | A | 1 | a0002c0003t0027g0011 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.649-2670A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123276 | |||||||
chr9:33123277 | C | CA | 133 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(130): Show |
140 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.649-2672dupT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123277 | |||||||
chr9:33123277 | C | CAA | 29 | a0001c0001t0001g0062 a0001c0001t0001g0065 a0001c0001t0001g0066 others(26): Show |
31 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.649-2673_649-2672d others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123277 | |||||||
chr9:33123277 | CA | C | 42 | a0001c0001t0002g0213 a0001c0001t0002g0215 a0001c0001t0002g0233 others(39): Show |
42 | HG01074.hp1 HG01106.hp2 HG01175.hp1 others(39): Show |
intron_variant | MODIFIER | c.649-2672delT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123277 | |||||||
chr9:33123277 | CAA | C | 118 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(115): Show |
123 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.649-2673_649-2672d others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123277 | |||||||
chr9:33123277 | CAAAAAAA others(7): Show |
C | 4 | a0001c0001t0021g0289 a0001c0001t0021g0291 a0001c0001t0021g0292 others(1): Show |
4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.649-2685_649-2672d others(16): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123277 | |||||||
chr9:33123388 | A | G | 190 | a0001c0001t0001g0019 a0001c0001t0001g0171 a0001c0001t0001g0200 others(187): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.649-2782T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123388 | |||||||
chr9:33123466 | G | A | 166 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(163): Show |
171 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.649-2860C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123466 | |||||||
chr9:33123629 | A | G | 169 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(166): Show |
174 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.649-3023T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123629 | |||||||
chr9:33123853 | C | T | 4 | a0001c0001t0021g0289 a0001c0001t0021g0291 a0001c0001t0021g0292 others(1): Show |
4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.649-3247G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33123853 | |||||||
chr9:33124044 | T | C | 191 | a0001c0001t0001g0019 a0001c0001t0001g0171 a0001c0001t0001g0200 others(188): Show |
199 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.649-3438A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33124044 | |||||||
chr9:33124163 | T | C | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.649-3557A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33124163 | |||||||
chr9:33124319 | T | C | 21 | a0001c0001t0037g0224 a0001c0002t0007g0180 a0001c0002t0007g0181 others(18): Show |
21 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(18): Show |
intron_variant | MODIFIER | c.649-3713A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33124319 | |||||||
chr9:33124567 | C | T | 1 | a0001c0001t0045g0035 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.649-3961G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33124567 | |||||||
chr9:33124636 | A | G | 117 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
122 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.649-4030T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33124636 | |||||||
chr9:33124686 | G | A | 1 | a0001c0001t0006g0267 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.649-4080C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33124686 | |||||||
chr9:33124874 | T | C | 115 | a0001c0001t0001g0200 a0001c0001t0002g0012 a0001c0001t0002g0013 others(112): Show |
118 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.649-4268A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33124874 | |||||||
chr9:33125002 | T | C | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.649-4396A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33125002 | |||||||
chr9:33125029 | G | C | 1 | a0002c0003t0027g0011 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.649-4423C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33125029 | |||||||
chr9:33125281 | G | A | 118 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
123 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.649-4675C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33125281 | |||||||
chr9:33125361 | C | T | 20 | a0001c0001t0001g0019 a0001c0001t0005g0024 a0001c0001t0005g0025 others(17): Show |
22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.649-4755G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33125361 | |||||||
chr9:33125487 | C | A | 1 | a0001c0002t0007g0181 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.649-4881G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33125487 | |||||||
chr9:33125659 | C | A | 1 | a0001c0001t0002g0269 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.649-5053G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33125659 | |||||||
chr9:33125659 | CGA | C | 70 | a0001c0001t0001g0008 a0001c0001t0001g0034 a0001c0001t0001g0047 others(67): Show |
72 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(69): Show |
intron_variant | MODIFIER | c.649-5055_649-5054d others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33125659 | |||||||
chr9:33125806 | T | C | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.649-5200A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33125806 | |||||||
chr9:33125944 | A | C | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.649-5338T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33125944 | |||||||
chr9:33126012 | T | C | 1 | a0001c0001t0045g0035 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.649-5406A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126012 | |||||||
chr9:33126095 | G | A | 2 | a0001c0001t0005g0334 a0002c0003t0027g0011 |
3 | HG02683.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.649-5489C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126095 | |||||||
chr9:33126186 | C | A | 20 | a0001c0002t0007g0180 a0001c0002t0007g0181 a0001c0002t0007g0184 others(17): Show |
20 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(17): Show |
intron_variant | MODIFIER | c.649-5580G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126186 | |||||||
chr9:33126226 | T | C | 20 | a0001c0001t0001g0019 a0001c0001t0005g0024 a0001c0001t0005g0025 others(17): Show |
22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.649-5620A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126226 | |||||||
chr9:33126348 | C | G | 341 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(338): Show |
356 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.649-5742G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126348 | |||||||
chr9:33126365 | A | T | 30 | a0001c0001t0004g0300 a0001c0001t0005g0328 a0001c0001t0005g0329 others(27): Show |
30 | HG01106.hp2 HG01175.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.649-5759T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126365 | |||||||
chr9:33126394 | T | C | 3 | a0001c0001t0020g0174 a0001c0001t0020g0175 a0001c0001t0020g0176 |
3 | HG01074.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.649-5788A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126394 | |||||||
chr9:33126396 | T | C | 1 | a0001c0001t0004g0079 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.649-5790A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126396 | |||||||
chr9:33126439 | T | A | 24 | a0001c0001t0001g0171 a0001c0001t0004g0009 a0001c0001t0004g0010 others(21): Show |
26 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.649-5833A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126439 | |||||||
chr9:33126572 | A | G | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.649-5966T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126572 | |||||||
chr9:33126594 | A | AAACATTG others(32): Show |
1 | a0004c0005t0043g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.649-5989_649-5988i others(41): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | |||||||
chr9:33126594 | A | AAACATTG others(110): Show |
1 | a0001c0001t0001g0117 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.649-5989_649-5988i others(119): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | |||||||
chr9:33126594 | A | AAACATTG others(149): Show |
1 | a0001c0001t0001g0115 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.649-5989_649-5988i others(158): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | |||||||
chr9:33126594 | A | AAACATTG others(188): Show |
1 | a0001c0001t0001g0118 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.649-5989_649-5988i others(197): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | |||||||
chr9:33126594 | A | AAACATTG others(188): Show |
1 | a0001c0001t0001g0050 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.649-5989_649-5988i others(197): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | |||||||
chr9:33126594 | A | AAACATTG others(149): Show |
2 | a0001c0001t0002g0058 a0001c0001t0062g0173 |
2 | HG00609.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.649-5989_649-5988i others(158): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | |||||||
chr9:33126594 | A | AAACATTG others(149): Show |
4 | a0001c0001t0001g0047 a0001c0001t0001g0124 a0001c0001t0006g0049 others(1): Show |
4 | HG03239.hp1 HG03491.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.649-5989_649-5988i others(158): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | |||||||
chr9:33126594 | A | AAACATTG others(149): Show |
4 | a0001c0001t0001g0171 a0001c0001t0018g0167 a0001c0001t0018g0168 others(1): Show |
4 | HG01192.hp2 HG02258.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.649-5989_649-5988i others(158): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | |||||||
chr9:33126594 | A | AAACATTG others(32): Show |
69 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(66): Show |
74 | HG00323.hp1 HG00597.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.649-6027_649-5989d others(41): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | |||||||
chr9:33126594 | A | AAACATTG others(71): Show |
8 | a0001c0001t0001g0055 a0001c0001t0021g0289 a0001c0001t0021g0291 others(5): Show |
8 | HG01081.hp2 HG01255.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.649-5989_649-5988i others(80): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | |||||||
chr9:33126594 | A | AAACATTG others(344): Show |
1 | a0002c0003t0027g0011 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.649-5989_649-5988i others(353): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | |||||||
chr9:33126594 | A | AAACATTG others(305): Show |
1 | a0001c0001t0020g0176 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.649-5989_649-5988i others(314): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | |||||||
chr9:33126594 | A | AAACATTG others(149): Show |
3 | a0001c0001t0016g0156 a0001c0001t0016g0157 a0001c0001t0040g0158 |
3 | HG02717.hp1 HG02895.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.649-5989_649-5988i others(158): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | |||||||
chr9:33126594 | A | AAACATTG others(188): Show |
1 | a0001c0001t0016g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.649-5989_649-5988i others(197): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | |||||||
chr9:33126594 | A | AAACATTG others(266): Show |
1 | a0001c0001t0020g0175 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.649-5989_649-5988i others(275): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | |||||||
chr9:33126594 | A | AAACATTG others(305): Show |
1 | a0001c0001t0020g0174 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.649-5989_649-5988i others(314): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126594 | |||||||
chr9:33126610 | T | G | 11 | a0001c0001t0001g0047 a0001c0001t0001g0050 a0001c0001t0001g0115 others(8): Show |
11 | HG00609.hp2 HG01123.hp1 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.649-6004A>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126610 | |||||||
chr9:33126610 | T | TGTTAACC others(149): Show |
3 | a0001c0001t0001g0089 a0001c0001t0001g0142 a0001c0001t0042g0133 |
3 | HG02523.hp1 HG02698.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.649-6005_649-6004i others(158): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126610 | |||||||
chr9:33126610 | T | TGTTAACC others(188): Show |
1 | a0001c0001t0001g0112 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.649-6005_649-6004i others(197): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126610 | |||||||
chr9:33126610 | T | TGTTAACC others(149): Show |
2 | a0001c0001t0001g0126 a0001c0001t0003g0015 |
2 | HG00558.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.649-6005_649-6004i others(158): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126610 | |||||||
chr9:33126610 | T | TGTTAACC others(168): Show |
1 | a0001c0001t0001g0143 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.649-6005_649-6004i others(177): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126610 | |||||||
chr9:33126610 | T | TGTTAACC others(110): Show |
3 | a0001c0001t0023g0349 a0001c0001t0023g0350 a0001c0001t0023g0351 |
3 | HG00735.hp2 HG01993.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.649-6005_649-6004i others(119): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126610 | |||||||
chr9:33126610 | T | TGTTAACC others(149): Show |
7 | a0001c0001t0001g0056 a0001c0001t0001g0119 a0001c0001t0001g0149 others(4): Show |
7 | HG00735.hp1 HG00741.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.649-6005_649-6004i others(158): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126610 | |||||||
chr9:33126610 | T | TGTTAACC others(149): Show |
41 | a0001c0001t0001g0034 a0001c0001t0001g0048 a0001c0001t0001g0057 others(38): Show |
42 | HG00642.hp2 HG01074.hp2 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.649-6005_649-6004i others(158): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126610 | |||||||
chr9:33126610 | T | TGTTAACC others(188): Show |
5 | a0001c0001t0001g0008 a0001c0001t0001g0106 a0001c0001t0001g0144 others(2): Show |
6 | HG01981.hp2 HG02135.hp2 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.649-6005_649-6004i others(197): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126610 | |||||||
chr9:33126610 | T | TGTTAACC others(149): Show |
10 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0159 others(7): Show |
12 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(9): Show |
intron_variant | MODIFIER | c.649-6005_649-6004i others(158): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126610 | |||||||
chr9:33126649 | T | TGTTAACC others(149): Show |
1 | a0001c0001t0001g0111 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.649-6044_649-6043i others(158): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126649 | |||||||
chr9:33126955 | T | G | 1 | a0001c0001t0001g0110 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.649-6349A>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126955 | |||||||
chr9:33126960 | TTTTG | T | 24 | a0001c0001t0001g0171 a0001c0001t0004g0009 a0001c0001t0004g0010 others(21): Show |
26 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.649-6358_649-6355d others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33126960 | |||||||
chr9:33127000 | C | T | 1 | a0001c0001t0009g0040 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.649-6394G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127000 | |||||||
chr9:33127001 | G | A | 5 | a0001c0001t0001g0111 a0001c0001t0016g0155 a0001c0001t0016g0156 others(2): Show |
5 | HG00140.hp2 HG01891.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.649-6395C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127001 | |||||||
chr9:33127023 | G | A | 24 | a0001c0001t0001g0171 a0001c0001t0004g0009 a0001c0001t0004g0010 others(21): Show |
26 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.649-6417C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127023 | |||||||
chr9:33127048 | G | A | 1 | a0004c0005t0043g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.649-6442C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127048 | |||||||
chr9:33127061 | A | C | 1 | a0002c0003t0027g0011 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.649-6455T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127061 | |||||||
chr9:33127122 | C | A | 1 | a0001c0001t0044g0132 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.649-6516G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127122 | |||||||
chr9:33127154 | G | A | 23 | a0001c0001t0001g0314 a0001c0001t0003g0001 a0001c0001t0003g0297 others(20): Show |
25 | HG00597.hp2 HG01070.hp1 HG02602.hp2 others(22): Show |
intron_variant | MODIFIER | c.649-6548C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127154 | |||||||
chr9:33127157 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0051g0054 |
2 | HG01255.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.649-6551C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127157 | |||||||
chr9:33127180 | G | C | 3 | a0001c0001t0001g0055 a0001c0001t0016g0053 a0001c0001t0051g0054 |
3 | HG01255.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.649-6574C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127180 | |||||||
chr9:33127185 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.649-6579C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127185 | |||||||
chr9:33127185 | G | C | 3 | a0001c0001t0001g0055 a0001c0001t0016g0053 a0001c0001t0051g0054 |
3 | HG01255.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.649-6579C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127185 | |||||||
chr9:33127198 | A | C | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 |
3 | HG01891.hp1 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.649-6592T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127198 | |||||||
chr9:33127206 | G | C | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 |
3 | HG01891.hp1 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.649-6600C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127206 | |||||||
chr9:33127215 | G | A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 |
3 | HG01891.hp1 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.649-6609C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127215 | |||||||
chr9:33127226 | G | A | 1 | a0002c0003t0027g0011 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.649-6620C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127226 | |||||||
chr9:33127228 | A | C | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 |
3 | HG01891.hp1 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.649-6622T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127228 | |||||||
chr9:33127253 | A | G | 341 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(338): Show |
356 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.649-6647T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127253 | |||||||
chr9:33127349 | G | A | 2 | a0001c0001t0028g0016 a0001c0001t0028g0017 |
2 | HG02615.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.649-6743C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127349 | |||||||
chr9:33127642 | G | A | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.649-7036C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127642 | |||||||
chr9:33127685 | C | A | 1 | a0001c0001t0002g0208 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.649-7079G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127685 | |||||||
chr9:33127688 | C | T | 4 | a0001c0001t0021g0289 a0001c0001t0021g0291 a0001c0001t0021g0292 others(1): Show |
4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.649-7082G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127688 | |||||||
chr9:33127744 | T | A | 1 | a0001c0001t0061g0125 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.649-7138A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127744 | |||||||
chr9:33127788 | C | T | 18 | a0001c0002t0007g0180 a0001c0002t0007g0181 a0001c0002t0007g0184 others(15): Show |
18 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(15): Show |
intron_variant | MODIFIER | c.649-7182G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127788 | |||||||
chr9:33127866 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0002g0265 |
3 | HG00558.hp2 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.649-7260C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33127866 | |||||||
chr9:33128023 | A | G | 115 | a0001c0001t0001g0200 a0001c0001t0002g0012 a0001c0001t0002g0013 others(112): Show |
118 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.648+7166T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33128023 | |||||||
chr9:33128053 | C | T | 11 | a0001c0001t0002g0208 a0001c0001t0002g0240 a0001c0001t0002g0243 others(8): Show |
11 | HG00673.hp2 HG02071.hp2 NA18945.hp2 others(8): Show |
intron_variant | MODIFIER | c.648+7136G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33128053 | |||||||
chr9:33128078 | G | A | 117 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
122 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.648+7111C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33128078 | |||||||
chr9:33128181 | T | A | 3 | a0001c0001t0001g0120 a0001c0001t0001g0137 a0001c0001t0048g0116 |
3 | HG01081.hp1 HG01099.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.648+7008A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33128181 | |||||||
chr9:33128431 | A | G | 195 | a0001c0001t0001g0019 a0001c0001t0001g0171 a0001c0001t0001g0200 others(192): Show |
203 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.648+6758T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33128431 | |||||||
chr9:33128619 | G | A | 30 | a0001c0001t0001g0171 a0001c0001t0004g0009 a0001c0001t0004g0010 others(27): Show |
33 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.648+6570C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33128619 | |||||||
chr9:33128660 | C | A | 30 | a0001c0001t0004g0300 a0001c0001t0005g0328 a0001c0001t0005g0329 others(27): Show |
30 | HG01106.hp2 HG01175.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.648+6529G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33128660 | |||||||
chr9:33128765 | C | T | 1 | a0001c0001t0008g0346 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.648+6424G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33128765 | |||||||
chr9:33129126 | C | A | 1 | a0001c0001t0051g0054 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.648+6063G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33129126 | |||||||
chr9:33129144 | T | C | 341 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(338): Show |
356 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.648+6045A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33129144 | |||||||
chr9:33129433 | C | T | 1 | a0001c0002t0007g0189 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.648+5756G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33129433 | |||||||
chr9:33129583 | T | C | 2 | a0001c0001t0005g0209 a0001c0001t0037g0224 |
2 | NA18946.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.648+5606A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33129583 | |||||||
chr9:33129609 | A | G | 195 | a0001c0001t0001g0019 a0001c0001t0001g0171 a0001c0001t0001g0200 others(192): Show |
203 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.648+5580T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33129609 | |||||||
chr9:33129627 | G | A | 1 | a0001c0001t0002g0266 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.648+5562C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33129627 | |||||||
chr9:33129841 | A | G | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.648+5348T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33129841 | |||||||
chr9:33129846 | G | T | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.648+5343C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33129846 | |||||||
chr9:33129898 | G | A | 1 | a0001c0001t0002g0266 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.648+5291C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33129898 | |||||||
chr9:33130166 | C | G | 1 | a0001c0001t0001g0314 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.648+5023G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130166 | |||||||
chr9:33130220 | C | T | 1 | a0001c0001t0004g0079 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.648+4969G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130220 | |||||||
chr9:33130291 | G | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0119 |
2 | HG03834.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.648+4898C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130291 | |||||||
chr9:33130297 | G | A | 2 | a0001c0001t0013g0138 a0001c0001t0013g0139 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.648+4892C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130297 | |||||||
chr9:33130327 | T | C | 3 | a0001c0001t0001g0060 a0001c0001t0001g0087 a0001c0001t0004g0079 |
3 | HG00733.hp2 HG01175.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.648+4862A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130327 | |||||||
chr9:33130411 | G | A | 8 | a0001c0001t0006g0296 a0001c0001t0006g0322 a0001c0001t0006g0323 others(5): Show |
8 | HG02055.hp1 HG02451.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.648+4778C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130411 | |||||||
chr9:33130434 | T | C | 1 | a0001c0001t0009g0042 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.648+4755A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130434 | |||||||
chr9:33130487 | A | C | 22 | a0001c0001t0001g0171 a0001c0001t0004g0009 a0001c0001t0004g0010 others(19): Show |
25 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.648+4702T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130487 | |||||||
chr9:33130488 | G | A | 10 | a0001c0001t0004g0010 a0001c0001t0004g0159 a0001c0001t0004g0160 others(7): Show |
11 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.648+4701C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130488 | |||||||
chr9:33130550 | T | TTCAATAT others(2045): Show |
1 | a0001c0002t0012g0183 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2054): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(1715): Show |
1 | a0001c0001t0005g0328 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.648+4638_648+4639i others(1724): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2041): Show |
2 | a0001c0001t0005g0339 a0001c0001t0054g0333 |
2 | HG02293.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2050): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2041): Show |
2 | a0001c0001t0006g0322 a0001c0001t0006g0323 |
2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2050): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2041): Show |
17 | a0001c0001t0005g0329 a0001c0001t0005g0334 a0001c0001t0005g0344 others(14): Show |
17 | HG01106.hp2 HG01884.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2050): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2044): Show |
1 | a0001c0001t0013g0324 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2053): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2042): Show |
1 | a0001c0001t0046g0327 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2051): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(1993): Show |
4 | a0001c0001t0004g0300 a0001c0001t0008g0302 a0001c0001t0030g0299 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2002): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2042): Show |
2 | a0001c0001t0006g0342 a0001c0001t0008g0346 |
2 | HG01175.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2051): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2044): Show |
1 | a0001c0001t0002g0260 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2053): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2027): Show |
1 | a0001c0001t0005g0033 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2036): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2044): Show |
2 | a0001c0002t0007g0191 a0001c0002t0007g0229 |
2 | HG02965.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2053): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2045): Show |
12 | a0001c0001t0002g0194 a0001c0001t0002g0221 a0001c0001t0002g0225 others(9): Show |
12 | HG00558.hp2 HG00673.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2054): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2046): Show |
2 | a0001c0001t0002g0244 a0001c0001t0002g0295 |
2 | HG03669.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2055): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2046): Show |
1 | a0001c0001t0017g0284 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2055): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2047): Show |
1 | a0001c0001t0017g0283 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2056): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2029): Show |
2 | a0001c0001t0001g0019 a0001c0001t0005g0024 |
2 | HG00733.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2038): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2028): Show |
3 | a0001c0001t0005g0025 a0001c0001t0010g0027 a0001c0001t0022g0023 |
3 | HG01358.hp2 NA18959.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2037): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2028): Show |
2 | a0001c0001t0005g0029 a0001c0001t0005g0030 |
2 | NA18974.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2037): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2029): Show |
1 | a0001c0001t0022g0021 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2038): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2029): Show |
1 | a0001c0001t0022g0022 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2038): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(1975): Show |
2 | a0001c0001t0005g0031 a0001c0001t0005g0032 |
2 | NA18950.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(1984): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2045): Show |
1 | a0001c0002t0007g0190 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2054): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2059): Show |
5 | a0001c0001t0002g0197 a0001c0001t0002g0219 a0001c0001t0002g0246 others(2): Show |
5 | NA18994.hp2 NA19012.hp1 NA19063.hp2 others(2): Show |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2068): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2046): Show |
1 | a0001c0001t0002g0214 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2055): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2045): Show |
16 | a0001c0001t0002g0230 a0001c0002t0007g0180 a0001c0002t0007g0181 others(13): Show |
16 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2054): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2046): Show |
1 | a0001c0001t0002g0271 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2055): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2047): Show |
1 | a0001c0001t0002g0232 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2056): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2046): Show |
1 | a0001c0001t0002g0014 | 2 | HG02109.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2055): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2046): Show |
1 | a0001c0001t0011g0242 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2055): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2046): Show |
51 | a0001c0001t0001g0200 a0001c0001t0002g0012 a0001c0001t0002g0013 others(48): Show |
53 | HG00323.hp2 HG00544.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2055): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2049): Show |
1 | a0001c0001t0002g0215 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2058): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2048): Show |
1 | a0001c0001t0002g0234 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2057): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2048): Show |
1 | a0001c0001t0002g0211 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2057): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2048): Show |
1 | a0001c0001t0002g0275 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2057): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2047): Show |
1 | a0001c0001t0002g0204 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2056): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2047): Show |
2 | a0001c0001t0002g0240 a0001c0001t0002g0279 |
2 | HG02647.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2056): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(1997): Show |
2 | a0001c0001t0002g0212 a0001c0001t0002g0222 |
2 | HG02451.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2006): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2046): Show |
1 | a0001c0002t0019g0188 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2055): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2029): Show |
3 | a0001c0001t0025g0002 a0001c0001t0028g0016 a0001c0001t0028g0017 |
4 | HG02615.hp2 HG03491.hp1 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2038): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2029): Show |
1 | a0001c0001t0010g0028 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2038): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2030): Show |
1 | a0001c0001t0005g0026 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2039): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2048): Show |
1 | a0001c0001t0011g0254 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2057): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2047): Show |
2 | a0001c0001t0011g0255 a0001c0001t0011g0262 |
2 | NA18945.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2056): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2047): Show |
2 | a0001c0001t0002g0248 a0001c0001t0006g0267 |
2 | NA19060.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2056): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2048): Show |
1 | a0001c0001t0002g0274 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2057): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2053): Show |
1 | a0001c0001t0011g0261 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.648+4638_648+4639i others(2062): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130550 | T | TTCAATAT others(2029): Show |
3 | a0001c0001t0010g0003 a0001c0001t0010g0020 a0001c0001t0052g0018 |
4 | NA18952.hp1 NA18961.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.648+4638_648+4639i others(2038): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130550 | |||||||
chr9:33130603 | G | A | 1 | a0001c0001t0003g0305 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.648+4586C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130603 | |||||||
chr9:33130639 | A | G | 1 | a0001c0001t0015g0103 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.648+4550T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130639 | |||||||
chr9:33130642 | A | G | 25 | a0001c0001t0001g0171 a0001c0001t0004g0009 a0001c0001t0004g0010 others(22): Show |
28 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.648+4547T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130642 | |||||||
chr9:33130683 | A | G | 1 | a0003c0007t0002g0348 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.648+4506T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130683 | |||||||
chr9:33130723 | C | T | 3 | a0001c0001t0001g0047 a0001c0001t0001g0050 a0001c0001t0006g0049 |
3 | HG03239.hp1 HG03491.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.648+4466G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130723 | |||||||
chr9:33130765 | T | C | 25 | a0001c0001t0001g0171 a0001c0001t0004g0009 a0001c0001t0004g0010 others(22): Show |
28 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.648+4424A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130765 | |||||||
chr9:33130879 | A | G | 143 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(140): Show |
150 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.648+4310T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130879 | |||||||
chr9:33130879 | AGAAGCAG others(6): Show |
A | 20 | a0001c0001t0001g0019 a0001c0001t0005g0024 a0001c0001t0005g0025 others(17): Show |
22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.648+4297_648+4309d others(15): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130879 | |||||||
chr9:33130981 | T | C | 1 | a0001c0001t0001g0293 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.648+4208A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33130981 | |||||||
chr9:33131025 | A | T | 1 | a0001c0001t0005g0024 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.648+4164T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33131025 | |||||||
chr9:33131306 | A | G | 1 | a0004c0005t0043g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.648+3883T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33131306 | |||||||
chr9:33131421 | G | A | 23 | a0001c0001t0001g0314 a0001c0001t0003g0001 a0001c0001t0003g0297 others(20): Show |
25 | HG00597.hp2 HG01070.hp1 HG02602.hp2 others(22): Show |
intron_variant | MODIFIER | c.648+3768C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33131421 | |||||||
chr9:33131473 | C | A | 1 | a0001c0001t0002g0226 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.648+3716G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33131473 | |||||||
chr9:33131593 | T | A | 13 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0159 others(10): Show |
15 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.648+3596A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33131593 | |||||||
chr9:33131653 | G | A | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.648+3536C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33131653 | |||||||
chr9:33131961 | T | C | 1 | a0001c0001t0057g0294 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.648+3228A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33131961 | |||||||
chr9:33132046 | A | G | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.648+3143T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33132046 | |||||||
chr9:33132136 | A | G | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.648+3053T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33132136 | |||||||
chr9:33132217 | T | TG | 95 | a0001c0001t0001g0200 a0001c0001t0002g0012 a0001c0001t0002g0013 others(92): Show |
98 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.648+2971dupC | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33132217 | |||||||
chr9:33132356 | C | T | 95 | a0001c0001t0001g0200 a0001c0001t0002g0012 a0001c0001t0002g0013 others(92): Show |
98 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.648+2833G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33132356 | |||||||
chr9:33132494 | G | A | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.648+2695C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33132494 | |||||||
chr9:33132520 | G | C | 25 | a0001c0001t0001g0171 a0001c0001t0004g0009 a0001c0001t0004g0010 others(22): Show |
28 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.648+2669C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33132520 | |||||||
chr9:33132572 | C | T | 2 | a0001c0001t0010g0068 a0001c0001t0023g0351 |
2 | HG01993.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.648+2617G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33132572 | |||||||
chr9:33132644 | G | C | 1 | a0001c0001t0002g0280 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.648+2545C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33132644 | |||||||
chr9:33132661 | T | C | 15 | a0001c0001t0001g0062 a0001c0001t0001g0065 a0001c0001t0001g0066 others(12): Show |
15 | HG01192.hp1 HG01952.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.648+2528A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33132661 | |||||||
chr9:33132790 | G | A | 17 | a0001c0001t0001g0171 a0001c0001t0004g0009 a0001c0001t0004g0010 others(14): Show |
19 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.648+2399C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33132790 | |||||||
chr9:33132841 | A | C | 1 | a0001c0001t0009g0045 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.648+2348T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33132841 | |||||||
chr9:33132876 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0072 |
2 | HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.648+2313G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33132876 | |||||||
chr9:33132966 | G | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0153 |
2 | HG02735.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.648+2223C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33132966 | |||||||
chr9:33133043 | C | T | 1 | a0001c0001t0059g0043 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.648+2146G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33133043 | |||||||
chr9:33133132 | A | T | 1 | a0001c0001t0001g0056 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.648+2057T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33133132 | |||||||
chr9:33133193 | G | A | 20 | a0001c0001t0001g0019 a0001c0001t0005g0024 a0001c0001t0005g0025 others(17): Show |
22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.648+1996C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33133193 | |||||||
chr9:33133296 | G | A | 1 | a0001c0001t0057g0294 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.648+1893C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33133296 | |||||||
chr9:33133415 | T | C | 4 | a0001c0001t0001g0171 a0001c0001t0018g0167 a0001c0001t0018g0168 others(1): Show |
4 | HG01192.hp2 HG02258.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.648+1774A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33133415 | |||||||
chr9:33133429 | G | A | 2 | a0001c0002t0007g0184 a0001c0002t0007g0187 |
2 | HG02165.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.648+1760C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33133429 | |||||||
chr9:33133807 | CA | C | 72 | a0001c0001t0001g0008 a0001c0001t0001g0034 a0001c0001t0001g0047 others(69): Show |
74 | HG00140.hp2 HG00558.hp1 HG00609.hp2 others(71): Show |
intron_variant | MODIFIER | c.648+1381delT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33133807 | |||||||
chr9:33133814 | T | C | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.648+1375A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33133814 | |||||||
chr9:33133835 | C | T | 3 | a0001c0001t0008g0302 a0001c0001t0030g0299 a0001c0001t0030g0301 |
3 | HG02622.hp1 HG02717.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.648+1354G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33133835 | |||||||
chr9:33133991 | C | G | 1 | a0001c0001t0057g0294 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.648+1198G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33133991 | |||||||
chr9:33134030 | C | T | 2 | a0001c0001t0003g0134 a0001c0001t0026g0102 |
2 | NA18951.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.648+1159G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33134030 | |||||||
chr9:33134149 | G | A | 4 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | NA18946.hp2 NA18948.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.648+1040C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33134149 | |||||||
chr9:33134200 | G | C | 1 | a0004c0005t0043g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.648+989C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33134200 | |||||||
chr9:33134245 | C | T | 1 | a0001c0001t0002g0198 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.648+944G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33134245 | |||||||
chr9:33134325 | G | T | 30 | a0001c0001t0004g0300 a0001c0001t0005g0328 a0001c0001t0005g0329 others(27): Show |
30 | HG01106.hp2 HG01175.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.648+864C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33134325 | |||||||
chr9:33134619 | C | T | 20 | a0001c0001t0001g0019 a0001c0001t0005g0024 a0001c0001t0005g0025 others(17): Show |
22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.648+570G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33134619 | |||||||
chr9:33134772 | G | A | 341 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(338): Show |
356 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.648+417C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33134772 | |||||||
chr9:33134794 | T | C | 1 | a0001c0001t0002g0248 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.648+395A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33134794 | |||||||
chr9:33134864 | A | T | 1 | a0001c0001t0001g0056 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.648+325T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33134864 | |||||||
chr9:33135037 | T | C | 1 | a0001c0001t0001g0293 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.648+152A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33135037 | |||||||
chr9:33135087 | G | A | 163 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(160): Show |
168 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(165): Show |
intron_variant | MODIFIER | c.648+102C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33135087 | |||||||
chr9:33135156 | CA | C | 4 | a0001c0001t0016g0155 a0001c0001t0016g0156 a0001c0001t0016g0157 others(1): Show |
4 | HG01891.hp2 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.648+32delT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 2/5 | chr9 | 33135156 | |||||||
chr9:33135439 | G | A | 1 | a0001c0002t0012g0183 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.413-15C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135439 | |||||||
chr9:33135466 | C | G | 1 | a0001c0001t0004g0300 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.413-42G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135466 | |||||||
chr9:33135539 | G | A | 20 | a0001c0001t0001g0019 a0001c0001t0005g0024 a0001c0001t0005g0025 others(17): Show |
22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.413-115C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135539 | |||||||
chr9:33135636 | T | C | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.413-212A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135636 | |||||||
chr9:33135661 | C | G | 1 | a0001c0001t0010g0068 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.413-237G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135661 | |||||||
chr9:33135809 | G | C | 1 | a0001c0001t0003g0303 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.413-385C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135809 | |||||||
chr9:33135835 | C | T | 1 | a0001c0001t0005g0344 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.413-411G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135835 | |||||||
chr9:33135889 | A | AAG | 33 | a0001c0001t0001g0200 a0001c0001t0002g0197 a0001c0001t0002g0208 others(30): Show |
33 | HG00673.hp2 HG00733.hp1 HG01175.hp1 others(30): Show |
intron_variant | MODIFIER | c.413-467_413-466dup others(2): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135889 | |||||||
chr9:33135890 | A | AGAGT | 9 | a0001c0001t0002g0269 a0001c0001t0002g0286 a0001c0001t0005g0328 others(6): Show |
9 | HG01106.hp2 HG02572.hp2 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.413-467_413-466ins others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135890 | |||||||
chr9:33135890 | A | AGAGTGT | 3 | a0001c0001t0002g0225 a0001c0001t0002g0234 a0001c0001t0029g0340 |
3 | HG02132.hp2 HG02559.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.413-467_413-466ins others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135890 | |||||||
chr9:33135890 | A | AGTGTGT | 5 | a0001c0001t0001g0171 a0001c0001t0004g0166 a0001c0001t0038g0170 others(2): Show |
5 | HG00280.hp1 HG01167.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.413-472_413-467dup others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135890 | |||||||
chr9:33135890 | A | AGTGTGTG others(1): Show |
7 | a0001c0001t0004g0161 a0001c0001t0004g0162 a0001c0001t0004g0163 others(4): Show |
7 | HG00738.hp2 HG01123.hp2 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.413-474_413-467dup others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135890 | |||||||
chr9:33135890 | A | AGTGTGTG others(3): Show |
1 | a0001c0001t0016g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.413-476_413-467dup others(10): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135890 | |||||||
chr9:33135890 | A | AGTGTGTG others(5): Show |
1 | a0001c0001t0016g0157 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.413-478_413-467dup others(12): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135890 | |||||||
chr9:33135890 | A | AGTGTGTG others(7): Show |
2 | a0001c0001t0004g0160 a0001c0001t0018g0167 |
2 | HG01169.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.413-480_413-467dup others(14): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135890 | |||||||
chr9:33135890 | A | AGTGTGTG others(9): Show |
2 | a0001c0001t0004g0159 a0001c0001t0018g0169 |
2 | HG01168.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.413-482_413-467dup others(16): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135890 | |||||||
chr9:33135892 | T | A | 120 | a0001c0001t0001g0019 a0001c0001t0002g0012 a0001c0001t0002g0013 others(117): Show |
125 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.413-468A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135892 | |||||||
chr9:33135897 | GTGTGTGT others(7): Show |
G | 1 | a0001c0001t0002g0198 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.413-487_413-474del others(14): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135897 | |||||||
chr9:33135901 | GTGTGTGT others(3): Show |
G | 1 | a0001c0001t0029g0341 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.413-487_413-478del others(10): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135901 | |||||||
chr9:33135905 | G | GTGTGTGT others(1): Show |
17 | a0001c0001t0001g0008 a0001c0001t0001g0048 a0001c0001t0001g0059 others(14): Show |
19 | HG00140.hp2 HG00609.hp2 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.413-482_413-481ins others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135905 | |||||||
chr9:33135905 | G | GTGTGTGT others(5): Show |
1 | a0001c0001t0001g0121 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.413-482_413-481ins others(12): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135905 | |||||||
chr9:33135907 | G | GTGTGTA | 4 | a0001c0001t0001g0057 a0001c0001t0001g0143 a0001c0001t0001g0145 others(1): Show |
4 | HG00642.hp2 HG00741.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.413-484_413-483ins others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135907 | |||||||
chr9:33135907 | GTGTA | G | 9 | a0001c0001t0002g0270 a0001c0001t0008g0346 a0001c0001t0021g0289 others(6): Show |
9 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(6): Show |
intron_variant | MODIFIER | c.413-487_413-484del others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135907 | |||||||
chr9:33135909 | GTA | G | 47 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0195 others(44): Show |
49 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.413-487_413-486del others(2): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135909 | |||||||
chr9:33135911 | A | ATG | 3 | a0001c0001t0001g0096 a0001c0001t0001g0117 a0001c0001t0015g0141 |
3 | HG01346.hp2 HG02080.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.413-489_413-488dup others(2): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135911 | |||||||
chr9:33135911 | A | ATGTG | 4 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
4 | HG01891.hp1 HG02818.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-491_413-488dup others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135911 | |||||||
chr9:33135911 | A | ATGTGTG | 69 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(66): Show |
72 | HG00558.hp1 HG00642.hp1 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.413-493_413-488dup others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135911 | |||||||
chr9:33135911 | A | ATGTGTGT others(1): Show |
19 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0001g0065 others(16): Show |
19 | HG00140.hp1 HG00323.hp1 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.413-495_413-488dup others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135911 | |||||||
chr9:33135911 | A | G | 158 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0048 others(155): Show |
166 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.413-487T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33135911 | |||||||
chr9:33136235 | T | G | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.413-811A>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33136235 | |||||||
chr9:33136419 | G | A | 195 | a0001c0001t0001g0019 a0001c0001t0001g0171 a0001c0001t0001g0200 others(192): Show |
203 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.413-995C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33136419 | |||||||
chr9:33136430 | G | C | 2 | a0001c0001t0004g0263 a0001c0001t0004g0272 |
2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.413-1006C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33136430 | |||||||
chr9:33136518 | T | A | 25 | a0001c0001t0001g0171 a0001c0001t0004g0009 a0001c0001t0004g0010 others(22): Show |
28 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.413-1094A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33136518 | |||||||
chr9:33136538 | G | A | 21 | a0001c0001t0001g0019 a0001c0001t0002g0213 a0001c0001t0005g0024 others(18): Show |
23 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.413-1114C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33136538 | |||||||
chr9:33136548 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.413-1124G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33136548 | |||||||
chr9:33136830 | C | T | 1 | a0001c0001t0002g0244 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.413-1406G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33136830 | |||||||
chr9:33136908 | G | C | 26 | a0001c0001t0005g0328 a0001c0001t0005g0329 a0001c0001t0005g0334 others(23): Show |
26 | HG01106.hp2 HG01175.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.413-1484C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33136908 | |||||||
chr9:33136917 | G | A | 1 | a0004c0005t0043g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.413-1493C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33136917 | |||||||
chr9:33136990 | ACC | A | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.413-1568_413-1567d others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33136990 | |||||||
chr9:33137006 | C | T | 2 | a0001c0001t0028g0016 a0001c0001t0028g0017 |
2 | HG02615.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.413-1582G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33137006 | |||||||
chr9:33137305 | C | T | 190 | a0001c0001t0001g0019 a0001c0001t0001g0171 a0001c0001t0001g0200 others(187): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.413-1881G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33137305 | |||||||
chr9:33137423 | A | C | 1 | a0001c0001t0041g0338 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.413-1999T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33137423 | |||||||
chr9:33137461 | C | T | 30 | a0001c0001t0004g0300 a0001c0001t0005g0328 a0001c0001t0005g0329 others(27): Show |
30 | HG01106.hp2 HG01175.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.413-2037G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33137461 | |||||||
chr9:33137598 | A | C | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.413-2174T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33137598 | |||||||
chr9:33137647 | CTTAGA | C | 145 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(142): Show |
152 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.413-2228_413-2224d others(7): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33137647 | |||||||
chr9:33137794 | A | G | 1 | a0001c0001t0045g0035 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.413-2370T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33137794 | |||||||
chr9:33137851 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.413-2427C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33137851 | |||||||
chr9:33138029 | G | A | 1 | a0001c0001t0004g0079 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.413-2605C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33138029 | |||||||
chr9:33138117 | T | C | 341 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(338): Show |
356 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.413-2693A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33138117 | |||||||
chr9:33138156 | C | A | 2 | a0001c0001t0013g0138 a0001c0001t0013g0139 |
2 | NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.413-2732G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33138156 | |||||||
chr9:33138221 | C | T | 4 | a0001c0001t0021g0289 a0001c0001t0021g0291 a0001c0001t0021g0292 others(1): Show |
4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-2797G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33138221 | |||||||
chr9:33138249 | G | A | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.413-2825C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33138249 | |||||||
chr9:33138354 | A | T | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.413-2930T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33138354 | |||||||
chr9:33138777 | T | C | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.413-3353A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33138777 | |||||||
chr9:33138807 | A | T | 1 | a0001c0001t0001g0067 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.413-3383T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33138807 | |||||||
chr9:33138927 | C | T | 25 | a0001c0001t0001g0171 a0001c0001t0004g0009 a0001c0001t0004g0010 others(22): Show |
28 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.413-3503G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33138927 | |||||||
chr9:33138935 | C | T | 2 | a0001c0001t0021g0289 a0001c0001t0060g0290 |
2 | HG01515.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.413-3511G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33138935 | |||||||
chr9:33138975 | T | TAC | 4 | a0001c0001t0001g0120 a0001c0001t0001g0137 a0001c0001t0003g0129 others(1): Show |
4 | HG01081.hp1 HG01099.hp1 HG01099.hp2 others(1): Show |
intron_variant | MODIFIER | c.413-3553_413-3552d others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33138975 | |||||||
chr9:33139049 | C | T | 1 | a0001c0001t0002g0256 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.413-3625G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33139049 | |||||||
chr9:33139239 | T | C | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.413-3815A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33139239 | |||||||
chr9:33139455 | C | T | 115 | a0001c0001t0001g0200 a0001c0001t0002g0012 a0001c0001t0002g0013 others(112): Show |
118 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.413-4031G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33139455 | |||||||
chr9:33139620 | T | C | 20 | a0001c0001t0001g0019 a0001c0001t0005g0024 a0001c0001t0005g0025 others(17): Show |
22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.413-4196A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33139620 | |||||||
chr9:33139793 | T | G | 1 | a0004c0005t0043g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.413-4369A>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33139793 | |||||||
chr9:33140218 | C | G | 1 | a0001c0001t0003g0320 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.413-4794G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140218 | |||||||
chr9:33140246 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.413-4822A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140246 | |||||||
chr9:33140249 | T | C | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 |
3 | HG01891.hp1 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.413-4825A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140249 | |||||||
chr9:33140354 | A | C | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.413-4930T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140354 | |||||||
chr9:33140366 | G | C | 1 | a0001c0001t0001g0171 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.413-4942C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140366 | |||||||
chr9:33140478 | AT | A | 142 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(139): Show |
149 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.413-5055delA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140478 | |||||||
chr9:33140495 | TA | T | 163 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(160): Show |
168 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(165): Show |
intron_variant | MODIFIER | c.413-5072delT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140495 | |||||||
chr9:33140599 | G | A | 1 | a0004c0005t0043g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.413-5175C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140599 | |||||||
chr9:33140664 | G | A | 1 | a0001c0001t0002g0202 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.413-5240C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140664 | |||||||
chr9:33140753 | C | T | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 |
3 | HG01891.hp1 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.413-5329G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140753 | |||||||
chr9:33140767 | A | C | 1 | a0001c0001t0002g0237 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.413-5343T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140767 | |||||||
chr9:33140791 | C | G | 117 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
122 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.413-5367G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140791 | |||||||
chr9:33140945 | G | A | 1 | a0001c0001t0003g0315 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.413-5521C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140945 | |||||||
chr9:33140978 | G | A | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.413-5554C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33140978 | |||||||
chr9:33141231 | A | G | 190 | a0001c0001t0001g0019 a0001c0001t0001g0171 a0001c0001t0001g0200 others(187): Show |
198 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.413-5807T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33141231 | |||||||
chr9:33141252 | C | T | 20 | a0001c0001t0001g0019 a0001c0001t0005g0024 a0001c0001t0005g0025 others(17): Show |
22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.413-5828G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33141252 | |||||||
chr9:33141322 | A | G | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.413-5898T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33141322 | |||||||
chr9:33141379 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.413-5955C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33141379 | |||||||
chr9:33141473 | C | T | 2 | a0001c0001t0002g0213 a0001c0001t0002g0236 |
2 | HG03225.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.413-6049G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33141473 | |||||||
chr9:33141574 | A | G | 1 | a0001c0001t0010g0028 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.413-6150T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33141574 | |||||||
chr9:33141605 | T | C | 230 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0171 others(227): Show |
240 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.413-6181A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33141605 | |||||||
chr9:33141754 | G | A | 230 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0171 others(227): Show |
240 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.413-6330C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33141754 | |||||||
chr9:33141793 | C | T | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.413-6369G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33141793 | |||||||
chr9:33141907 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.413-6483C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33141907 | |||||||
chr9:33141916 | G | A | 1 | a0001c0001t0003g0312 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.413-6492C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33141916 | |||||||
chr9:33142007 | G | A | 27 | a0001c0001t0001g0314 a0001c0001t0003g0001 a0001c0001t0003g0297 others(24): Show |
29 | HG00597.hp2 HG01070.hp1 HG02602.hp2 others(26): Show |
intron_variant | MODIFIER | c.413-6583C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33142007 | |||||||
chr9:33142172 | G | A | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.413-6748C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33142172 | |||||||
chr9:33142260 | C | A | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.413-6836G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33142260 | |||||||
chr9:33142414 | G | A | 230 | a0001c0001t0001g0019 a0001c0001t0001g0055 a0001c0001t0001g0171 others(227): Show |
240 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(237): Show |
intron_variant | MODIFIER | c.413-6990C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33142414 | |||||||
chr9:33142648 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.413-7224C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33142648 | |||||||
chr9:33142730 | G | A | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.413-7306C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33142730 | |||||||
chr9:33143006 | G | A | 21 | a0001c0001t0001g0171 a0001c0001t0004g0009 a0001c0001t0004g0010 others(18): Show |
23 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.413-7582C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33143006 | |||||||
chr9:33143027 | C | G | 1 | a0001c0001t0017g0284 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.413-7603G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33143027 | |||||||
chr9:33143059 | C | T | 1 | a0001c0001t0018g0168 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.413-7635G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33143059 | |||||||
chr9:33143265 | T | G | 1 | a0001c0001t0051g0054 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.413-7841A>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33143265 | |||||||
chr9:33143579 | T | C | 1 | a0001c0002t0007g0191 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.413-8155A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33143579 | |||||||
chr9:33143735 | G | C | 20 | a0001c0001t0001g0019 a0001c0001t0005g0024 a0001c0001t0005g0025 others(17): Show |
22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.413-8311C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33143735 | |||||||
chr9:33143824 | T | C | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.413-8400A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33143824 | |||||||
chr9:33143881 | C | CT | 187 | a0001c0001t0001g0019 a0001c0001t0001g0171 a0001c0001t0001g0200 others(184): Show |
195 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.413-8458dupA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33143881 | |||||||
chr9:33143936 | G | C | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 |
3 | HG01891.hp1 HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.413-8512C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33143936 | |||||||
chr9:33144142 | C | T | 1 | a0004c0005t0043g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.413-8718G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33144142 | |||||||
chr9:33144170 | C | A | 1 | a0001c0001t0047g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.413-8746G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33144170 | |||||||
chr9:33144338 | G | A | 2 | a0001c0001t0007g0108 a0001c0001t0024g0109 |
2 | HG03209.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.413-8914C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33144338 | |||||||
chr9:33144425 | G | A | 1 | a0002c0003t0027g0011 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.413-9001C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33144425 | |||||||
chr9:33144605 | C | G | 2 | a0001c0001t0001g0076 a0001c0001t0001g0078 |
2 | HG00323.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.413-9181G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33144605 | |||||||
chr9:33144659 | T | C | 1 | a0001c0001t0059g0043 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.413-9235A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33144659 | |||||||
chr9:33144697 | G | A | 1 | a0001c0001t0003g0320 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.413-9273C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33144697 | |||||||
chr9:33144780 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.413-9356C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33144780 | |||||||
chr9:33144811 | C | T | 165 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(162): Show |
170 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(167): Show |
intron_variant | MODIFIER | c.413-9387G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33144811 | |||||||
chr9:33144877 | G | A | 1 | a0001c0001t0016g0157 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.413-9453C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33144877 | |||||||
chr9:33144935 | G | A | 4 | a0001c0001t0021g0289 a0001c0001t0021g0291 a0001c0001t0021g0292 others(1): Show |
4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-9511C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33144935 | |||||||
chr9:33144937 | G | C | 3 | a0001c0001t0001g0055 a0001c0001t0016g0053 a0001c0001t0051g0054 |
3 | HG01255.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.413-9513C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33144937 | |||||||
chr9:33145083 | G | A | 13 | a0001c0001t0001g0096 a0001c0001t0001g0149 a0001c0001t0001g0151 others(10): Show |
13 | HG01099.hp1 HG01261.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.413-9659C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33145083 | |||||||
chr9:33145545 | T | C | 218 | a0001c0001t0001g0019 a0001c0001t0001g0171 a0001c0001t0001g0200 others(215): Show |
228 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(225): Show |
intron_variant | MODIFIER | c.413-10121A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33145545 | |||||||
chr9:33145550 | C | T | 1 | a0001c0001t0044g0132 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.413-10126G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33145550 | |||||||
chr9:33145574 | G | T | 1 | a0001c0001t0001g0137 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.413-10150C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33145574 | |||||||
chr9:33145649 | C | CA | 188 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0001g0314 others(185): Show |
196 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(193): Show |
intron_variant | MODIFIER | c.413-10226dupT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33145649 | |||||||
chr9:33145805 | G | T | 1 | a0001c0001t0003g0303 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.413-10381C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33145805 | |||||||
chr9:33146177 | T | C | 3 | a0001c0001t0001g0055 a0001c0001t0016g0053 a0001c0001t0051g0054 |
3 | HG01255.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.413-10753A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33146177 | |||||||
chr9:33146245 | T | A | 1 | a0004c0005t0043g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.413-10821A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33146245 | |||||||
chr9:33146305 | T | C | 1 | a0002c0003t0027g0011 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.413-10881A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33146305 | |||||||
chr9:33146395 | C | A | 210 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0001g0314 others(207): Show |
220 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.413-10971G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33146395 | |||||||
chr9:33146403 | T | A | 210 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0001g0314 others(207): Show |
220 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.413-10979A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33146403 | |||||||
chr9:33146530 | T | C | 213 | a0001c0001t0001g0019 a0001c0001t0001g0171 a0001c0001t0001g0200 others(210): Show |
223 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.413-11106A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33146530 | |||||||
chr9:33146697 | CT | C | 307 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(304): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(316): Show |
intron_variant | MODIFIER | c.413-11274delA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33146697 | |||||||
chr9:33146697 | CTT | C | 26 | a0001c0001t0001g0171 a0001c0001t0004g0009 a0001c0001t0004g0010 others(23): Show |
29 | HG00280.hp1 HG00733.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.413-11275_413-1127 others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33146697 | |||||||
chr9:33146819 | G | C | 1 | a0001c0001t0003g0297 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.413-11395C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33146819 | |||||||
chr9:33146876 | T | G | 1 | a0001c0001t0057g0294 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.413-11452A>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33146876 | |||||||
chr9:33147007 | T | C | 3 | a0001c0001t0020g0174 a0001c0001t0020g0175 a0001c0001t0020g0176 |
3 | HG01074.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.413-11583A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147007 | |||||||
chr9:33147105 | A | G | 13 | a0001c0001t0004g0009 a0001c0001t0004g0010 a0001c0001t0004g0159 others(10): Show |
15 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.413-11681T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147105 | |||||||
chr9:33147245 | CT | C | 18 | a0001c0001t0001g0055 a0001c0001t0001g0076 a0001c0001t0001g0078 others(15): Show |
18 | HG00323.hp1 HG01081.hp2 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.413-11822delA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147245 | |||||||
chr9:33147245 | CTT | C | 209 | a0001c0001t0001g0019 a0001c0001t0001g0171 a0001c0001t0001g0200 others(206): Show |
219 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(216): Show |
intron_variant | MODIFIER | c.413-11823_413-1182 others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147245 | |||||||
chr9:33147257 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.413-11833A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147257 | |||||||
chr9:33147388 | C | T | 3 | a0001c0001t0013g0127 a0001c0001t0013g0138 a0001c0001t0013g0139 |
3 | NA18522.hp1 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.413-11964G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147388 | |||||||
chr9:33147433 | G | C | 3 | a0001c0001t0020g0174 a0001c0001t0020g0175 a0001c0001t0020g0176 |
3 | HG01074.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.413-12009C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147433 | |||||||
chr9:33147481 | G | A | 188 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0001g0314 others(185): Show |
195 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(192): Show |
intron_variant | MODIFIER | c.413-12057C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147481 | |||||||
chr9:33147529 | GAGCC | G | 97 | a0001c0001t0001g0200 a0001c0001t0002g0012 a0001c0001t0002g0013 others(94): Show |
100 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.413-12109_413-1210 others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147529 | |||||||
chr9:33147534 | C | G | 97 | a0001c0001t0001g0200 a0001c0001t0002g0012 a0001c0001t0002g0013 others(94): Show |
100 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.413-12110G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147534 | |||||||
chr9:33147646 | C | T | 1 | a0001c0002t0007g0185 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.413-12222G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147646 | |||||||
chr9:33147860 | T | C | 213 | a0001c0001t0001g0019 a0001c0001t0001g0171 a0001c0001t0001g0200 others(210): Show |
223 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.413-12436A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147860 | |||||||
chr9:33147864 | T | C | 1 | a0001c0001t0059g0043 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.413-12440A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147864 | |||||||
chr9:33147993 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.413-12569G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33147993 | |||||||
chr9:33148001 | T | C | 3 | a0001c0001t0005g0344 a0001c0001t0006g0342 a0001c0001t0006g0343 |
3 | HG01175.hp1 HG02572.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.413-12577A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148001 | |||||||
chr9:33148035 | TA | T | 4 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
5 | HG01891.hp1 HG02818.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.413-12612delT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148035 | |||||||
chr9:33148139 | G | A | 2 | a0001c0001t0002g0277 a0001c0001t0002g0278 |
2 | HG03516.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.413-12715C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148139 | |||||||
chr9:33148148 | C | G | 1 | a0001c0001t0016g0157 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.413-12724G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148148 | |||||||
chr9:33148300 | T | C | 25 | a0001c0001t0001g0171 a0001c0001t0004g0009 a0001c0001t0004g0010 others(22): Show |
28 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.413-12876A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148300 | |||||||
chr9:33148554 | G | A | 188 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0001g0314 others(185): Show |
195 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(192): Show |
intron_variant | MODIFIER | c.413-13130C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148554 | |||||||
chr9:33148633 | G | A | 24 | a0001c0001t0001g0171 a0001c0001t0004g0009 a0001c0001t0004g0010 others(21): Show |
26 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.413-13209C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148633 | |||||||
chr9:33148804 | T | TAA | 7 | a0001c0001t0002g0195 a0001c0001t0002g0218 a0001c0001t0002g0222 others(4): Show |
7 | HG01975.hp1 HG02451.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.413-13382_413-1338 others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148804 | |||||||
chr9:33148804 | T | TAAA | 167 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0001g0314 others(164): Show |
174 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.413-13383_413-1338 others(7): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148804 | |||||||
chr9:33148804 | T | TAAAA | 11 | a0001c0001t0002g0257 a0001c0001t0004g0300 a0001c0001t0005g0334 others(8): Show |
11 | HG01106.hp2 HG01496.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.413-13384_413-1338 others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148804 | |||||||
chr9:33148804 | T | TAAAAAA | 19 | a0001c0001t0001g0171 a0001c0001t0004g0009 a0001c0001t0004g0010 others(16): Show |
21 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.413-13386_413-1338 others(10): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148804 | |||||||
chr9:33148804 | T | TAAAAAAA | 6 | a0001c0001t0004g0162 a0001c0001t0016g0155 a0001c0001t0016g0156 others(3): Show |
7 | HG01361.hp2 HG01891.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.413-13387_413-1338 others(11): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148804 | |||||||
chr9:33148824 | C | T | 4 | a0001c0001t0021g0289 a0001c0001t0021g0291 a0001c0001t0021g0292 others(1): Show |
4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-13400G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148824 | |||||||
chr9:33148836 | T | C | 213 | a0001c0001t0001g0019 a0001c0001t0001g0171 a0001c0001t0001g0200 others(210): Show |
223 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.413-13412A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33148836 | |||||||
chr9:33149061 | C | T | 2 | a0001c0001t0018g0167 a0001c0001t0018g0169 |
2 | HG02258.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.413-13637G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33149061 | |||||||
chr9:33149186 | T | C | 25 | a0001c0001t0001g0171 a0001c0001t0004g0009 a0001c0001t0004g0010 others(22): Show |
28 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.413-13762A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33149186 | |||||||
chr9:33149194 | A | T | 1 | a0001c0001t0001g0122 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.413-13770T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33149194 | |||||||
chr9:33149200 | TA | T | 194 | a0001c0001t0001g0019 a0001c0001t0001g0075 a0001c0001t0001g0200 others(191): Show |
201 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(198): Show |
intron_variant | MODIFIER | c.413-13777delT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33149200 | |||||||
chr9:33149209 | A | G | 115 | a0001c0001t0001g0200 a0001c0001t0002g0012 a0001c0001t0002g0013 others(112): Show |
118 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.413-13785T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33149209 | |||||||
chr9:33149269 | A | T | 1 | a0001c0001t0001g0112 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.413-13845T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33149269 | |||||||
chr9:33149270 | A | T | 331 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(328): Show |
346 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(343): Show |
intron_variant | MODIFIER | c.413-13846T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33149270 | |||||||
chr9:33149342 | G | A | 20 | a0001c0001t0001g0019 a0001c0001t0005g0024 a0001c0001t0005g0025 others(17): Show |
22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.413-13918C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33149342 | |||||||
chr9:33149367 | G | A | 30 | a0001c0001t0004g0300 a0001c0001t0005g0328 a0001c0001t0005g0329 others(27): Show |
30 | HG01106.hp2 HG01175.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.413-13943C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33149367 | |||||||
chr9:33150047 | T | C | 23 | a0001c0001t0001g0314 a0001c0001t0003g0001 a0001c0001t0003g0297 others(20): Show |
25 | HG00597.hp2 HG01070.hp1 HG02602.hp2 others(22): Show |
intron_variant | MODIFIER | c.413-14623A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150047 | |||||||
chr9:33150049 | C | T | 5 | a0001c0001t0001g0090 a0001c0001t0001g0097 a0001c0001t0001g0099 others(2): Show |
5 | HG01952.hp2 NA18962.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.413-14625G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150049 | |||||||
chr9:33150126 | TATATAG | T | 27 | a0001c0001t0001g0055 a0001c0001t0001g0171 a0001c0001t0004g0009 others(24): Show |
29 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.413-14708_413-1470 others(10): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150126 | |||||||
chr9:33150142 | T | TATACACA others(15): Show |
21 | a0001c0001t0001g0019 a0001c0001t0005g0024 a0001c0001t0005g0025 others(18): Show |
24 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.413-14719_413-1471 others(26): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150142 | |||||||
chr9:33150144 | G | GATATATA others(21): Show |
191 | a0001c0001t0001g0171 a0001c0001t0001g0200 a0001c0001t0001g0314 others(188): Show |
198 | HG00280.hp1 HG00323.hp2 HG00544.hp1 others(195): Show |
intron_variant | MODIFIER | c.413-14721_413-1472 others(32): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150144 | |||||||
chr9:33150144 | G | T | 21 | a0001c0001t0001g0019 a0001c0001t0005g0024 a0001c0001t0005g0025 others(18): Show |
24 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(21): Show |
intron_variant | MODIFIER | c.413-14720C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150144 | |||||||
chr9:33150152 | C | CACACATA others(19): Show |
2 | a0001c0002t0007g0184 a0001c0002t0007g0187 |
2 | HG02165.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.413-14729_413-1472 others(30): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150152 | |||||||
chr9:33150159 | A | T | 3 | a0001c0001t0020g0174 a0001c0001t0020g0175 a0001c0001t0020g0176 |
3 | HG01074.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.413-14735T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150159 | |||||||
chr9:33150162 | T | C | 2 | a0001c0002t0007g0184 a0001c0002t0007g0187 |
2 | HG02165.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.413-14738A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150162 | |||||||
chr9:33150168 | T | TGA | 21 | a0001c0001t0001g0048 a0001c0001t0002g0208 a0001c0001t0002g0238 others(18): Show |
21 | HG00323.hp2 HG00673.hp1 HG00673.hp2 others(18): Show |
intron_variant | MODIFIER | c.413-14746_413-1474 others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150168 | |||||||
chr9:33150233 | T | TAC | 119 | a0001c0001t0001g0019 a0001c0001t0001g0080 a0001c0001t0001g0098 others(116): Show |
123 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.413-14811_413-1481 others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150233 | |||||||
chr9:33150233 | T | TACAC | 84 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(81): Show |
87 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(84): Show |
intron_variant | MODIFIER | c.413-14813_413-1481 others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150233 | |||||||
chr9:33150233 | T | TACACAC | 81 | a0001c0001t0001g0034 a0001c0001t0001g0047 a0001c0001t0001g0048 others(78): Show |
84 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.413-14815_413-1481 others(10): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150233 | |||||||
chr9:33150233 | T | TACACACA others(1): Show |
14 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0095 others(11): Show |
15 | HG01099.hp1 HG01358.hp1 HG01928.hp1 others(12): Show |
intron_variant | MODIFIER | c.413-14817_413-1481 others(12): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150233 | |||||||
chr9:33150233 | T | TACACACA others(3): Show |
4 | a0001c0001t0001g0121 a0001c0001t0001g0136 a0001c0001t0003g0130 others(1): Show |
4 | HG01070.hp1 HG01074.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.413-14819_413-1481 others(14): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150233 | |||||||
chr9:33150233 | TAC | T | 9 | a0001c0001t0002g0198 a0001c0001t0002g0232 a0001c0001t0016g0155 others(6): Show |
11 | HG01891.hp2 HG02559.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.413-14811_413-1481 others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150233 | |||||||
chr9:33150233 | TACAC | T | 18 | a0001c0001t0004g0010 a0001c0001t0004g0159 a0001c0001t0004g0160 others(15): Show |
19 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.413-14813_413-1481 others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150233 | |||||||
chr9:33150233 | TACACAC | T | 4 | a0001c0001t0001g0171 a0001c0001t0004g0009 a0001c0001t0018g0167 others(1): Show |
5 | HG01192.hp2 HG02109.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.413-14815_413-1481 others(10): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150233 | |||||||
chr9:33150267 | G | C | 1 | a0001c0001t0001g0080 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.413-14843C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150267 | |||||||
chr9:33150270 | C | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0080 |
2 | HG00642.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.413-14846G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150270 | |||||||
chr9:33150271 | G | A | 4 | a0001c0001t0004g0300 a0001c0001t0008g0302 a0001c0001t0030g0299 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-14847C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150271 | |||||||
chr9:33150272 | A | C | 1 | a0001c0001t0001g0080 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.413-14848T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150272 | |||||||
chr9:33150320 | C | T | 3 | a0001c0001t0020g0174 a0001c0001t0020g0175 a0001c0001t0020g0176 |
3 | HG01074.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.413-14896G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150320 | |||||||
chr9:33150411 | T | TA | 213 | a0001c0001t0001g0019 a0001c0001t0001g0171 a0001c0001t0001g0200 others(210): Show |
223 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.413-14988dupT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150411 | |||||||
chr9:33150552 | G | A | 4 | a0001c0001t0001g0171 a0001c0001t0018g0167 a0001c0001t0018g0168 others(1): Show |
4 | HG01192.hp2 HG02258.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.413-15128C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150552 | |||||||
chr9:33150606 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.413-15182T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150606 | |||||||
chr9:33150719 | A | G | 1 | a0004c0005t0043g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.413-15295T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150719 | |||||||
chr9:33150764 | T | C | 1 | a0001c0001t0003g0319 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.413-15340A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150764 | |||||||
chr9:33150845 | G | A | 341 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(338): Show |
356 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.413-15421C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150845 | |||||||
chr9:33150973 | AGAAG | A | 115 | a0001c0001t0001g0200 a0001c0001t0002g0012 a0001c0001t0002g0013 others(112): Show |
118 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.413-15553_413-1555 others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33150973 | |||||||
chr9:33151098 | G | A | 4 | a0001c0001t0016g0155 a0001c0001t0016g0156 a0001c0001t0016g0157 others(1): Show |
4 | HG01891.hp2 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.412+15660C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33151098 | |||||||
chr9:33151237 | T | G | 1 | a0001c0001t0050g0318 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.412+15521A>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33151237 | |||||||
chr9:33151417 | C | T | 20 | a0001c0001t0001g0019 a0001c0001t0005g0024 a0001c0001t0005g0025 others(17): Show |
22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.412+15341G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33151417 | |||||||
chr9:33151492 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.412+15266G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33151492 | |||||||
chr9:33151858 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.412+14900T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33151858 | |||||||
chr9:33152122 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.412+14636A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152122 | |||||||
chr9:33152134 | G | A | 4 | a0001c0001t0016g0155 a0001c0001t0016g0156 a0001c0001t0016g0157 others(1): Show |
4 | HG01891.hp2 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.412+14624C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152134 | |||||||
chr9:33152241 | T | G | 1 | a0001c0001t0061g0125 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.412+14517A>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152241 | |||||||
chr9:33152309 | A | AATAAC | 39 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(36): Show |
43 | HG00140.hp1 HG00323.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.412+14444_412+1444 others(9): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152309 | |||||||
chr9:33152309 | A | AATAACAT others(3): Show |
15 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0083 others(12): Show |
15 | HG01099.hp1 HG01167.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.412+14439_412+1444 others(14): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152309 | |||||||
chr9:33152309 | A | AATAACAT others(8): Show |
3 | a0001c0001t0001g0082 a0001c0001t0003g0128 a0001c0001t0006g0064 |
3 | HG01993.hp2 HG02071.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.412+14434_412+1444 others(19): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152309 | |||||||
chr9:33152309 | AATAAC | A | 23 | a0001c0001t0001g0059 a0001c0001t0001g0094 a0001c0001t0001g0095 others(20): Show |
23 | HG00140.hp2 HG00735.hp2 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.412+14444_412+1444 others(9): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152309 | |||||||
chr9:33152309 | AATAACAT others(3): Show |
A | 8 | a0001c0001t0001g0144 a0001c0001t0001g0147 a0001c0001t0015g0141 others(5): Show |
8 | HG00642.hp1 HG01993.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.412+14439_412+1444 others(14): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152309 | |||||||
chr9:33152309 | AATAACAT others(8): Show |
A | 3 | a0001c0001t0020g0174 a0001c0001t0020g0175 a0001c0001t0020g0176 |
3 | HG01074.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.412+14434_412+1444 others(19): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152309 | |||||||
chr9:33152339 | CAT | C | 115 | a0001c0001t0001g0200 a0001c0001t0002g0012 a0001c0001t0002g0013 others(112): Show |
118 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.412+14417_412+1441 others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152339 | |||||||
chr9:33152351 | TAACATAA others(12): Show |
T | 3 | a0001c0001t0005g0328 a0001c0001t0005g0329 a0001c0001t0006g0332 |
3 | HG02896.hp1 HG03540.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.412+14388_412+1440 others(23): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152351 | |||||||
chr9:33152356 | TAACATAA others(7): Show |
T | 4 | a0001c0001t0003g0297 a0001c0001t0003g0307 a0001c0001t0003g0310 others(1): Show |
4 | NA18947.hp1 NA19070.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.412+14388_412+1440 others(18): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152356 | |||||||
chr9:33152356 | TAACATAA others(8): Show |
T | 1 | a0001c0001t0001g0080 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.412+14387_412+1440 others(19): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152356 | |||||||
chr9:33152361 | TAACATAA others(2): Show |
T | 40 | a0001c0001t0001g0314 a0001c0001t0003g0001 a0001c0001t0003g0298 others(37): Show |
43 | HG00280.hp2 HG00597.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.412+14388_412+1439 others(13): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152361 | |||||||
chr9:33152361 | TAACATAA others(3): Show |
T | 1 | a0001c0001t0001g0060 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.412+14387_412+1439 others(14): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152361 | |||||||
chr9:33152366 | TAACA | T | 135 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(132): Show |
139 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(136): Show |
intron_variant | MODIFIER | c.412+14388_412+1439 others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152366 | |||||||
chr9:33152370 | A | AT | 6 | a0001c0001t0002g0232 a0001c0001t0003g0316 a0001c0001t0005g0031 others(3): Show |
6 | NA18747.hp1 NA18950.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.412+14387_412+1438 others(5): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152370 | |||||||
chr9:33152371 | A | T | 36 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(33): Show |
39 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.412+14387T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152371 | |||||||
chr9:33152400 | AAAG | A | 4 | a0001c0001t0004g0300 a0001c0001t0008g0302 a0001c0001t0030g0299 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+14355_412+1435 others(7): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152400 | |||||||
chr9:33152453 | A | G | 2 | a0001c0001t0010g0003 a0001c0001t0052g0018 |
3 | NA18961.hp1 NA18995.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.412+14305T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152453 | |||||||
chr9:33152556 | T | TA | 6 | a0001c0001t0001g0171 a0001c0001t0002g0228 a0001c0001t0003g0306 others(3): Show |
6 | HG02258.hp1 HG02622.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.412+14201dupT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152556 | |||||||
chr9:33152624 | C | T | 67 | a0001c0001t0001g0200 a0001c0001t0002g0012 a0001c0001t0002g0013 others(64): Show |
69 | HG00323.hp2 HG00544.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.412+14134G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33152624 | |||||||
chr9:33153020 | A | G | 5 | a0001c0001t0011g0242 a0001c0001t0011g0254 a0001c0001t0011g0255 others(2): Show |
5 | NA18945.hp2 NA18954.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.412+13738T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33153020 | |||||||
chr9:33153088 | G | A | 4 | a0001c0001t0001g0171 a0001c0001t0018g0167 a0001c0001t0018g0168 others(1): Show |
4 | HG01192.hp2 HG02258.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+13670C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33153088 | |||||||
chr9:33153275 | G | A | 7 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0117 others(4): Show |
7 | HG01081.hp1 HG01099.hp2 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.412+13483C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33153275 | |||||||
chr9:33153529 | G | T | 115 | a0001c0001t0001g0200 a0001c0001t0002g0012 a0001c0001t0002g0013 others(112): Show |
118 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(115): Show |
intron_variant | MODIFIER | c.412+13229C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33153529 | |||||||
chr9:33153708 | G | A | 53 | a0001c0001t0001g0314 a0001c0001t0003g0001 a0001c0001t0003g0297 others(50): Show |
55 | HG00597.hp2 HG01070.hp1 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.412+13050C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33153708 | |||||||
chr9:33153767 | T | G | 1 | a0001c0001t0009g0044 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.412+12991A>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33153767 | |||||||
chr9:33153871 | C | A | 1 | a0001c0001t0003g0317 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.412+12887G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33153871 | |||||||
chr9:33153900 | G | A | 1 | a0001c0001t0002g0280 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.412+12858C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33153900 | |||||||
chr9:33153912 | C | G | 1 | a0002c0003t0027g0011 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.412+12846G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33153912 | |||||||
chr9:33154002 | G | GGA | 11 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0082 others(8): Show |
11 | HG01192.hp1 HG01952.hp1 HG01981.hp1 others(8): Show |
intron_variant | MODIFIER | c.412+12754_412+1275 others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154002 | |||||||
chr9:33154018 | A | G | 1 | a0001c0001t0002g0264 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.412+12740T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154018 | |||||||
chr9:33154019 | G | A | 1 | a0001c0001t0002g0264 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.412+12739C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154019 | |||||||
chr9:33154019 | GAGGA | G | 4 | a0001c0001t0004g0300 a0001c0001t0008g0302 a0001c0001t0030g0299 others(1): Show |
4 | HG02622.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+12735_412+1273 others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154019 | |||||||
chr9:33154031 | A | AAGGG | 27 | a0001c0001t0002g0014 a0001c0001t0002g0194 a0001c0001t0002g0205 others(24): Show |
28 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.412+12723_412+1272 others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154031 | |||||||
chr9:33154031 | A | G | 1 | a0001c0001t0002g0264 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.412+12727T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154031 | |||||||
chr9:33154031 | AAGGG | A | 110 | a0001c0001t0001g0019 a0001c0001t0001g0119 a0001c0001t0001g0171 others(107): Show |
115 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(112): Show |
intron_variant | MODIFIER | c.412+12723_412+1272 others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154031 | |||||||
chr9:33154031 | AAGGGAGG others(5): Show |
A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0057 others(5): Show |
10 | HG00642.hp2 HG01081.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.412+12715_412+1272 others(16): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154031 | |||||||
chr9:33154110 | C | T | 4 | a0001c0001t0021g0289 a0001c0001t0021g0291 a0001c0001t0021g0292 others(1): Show |
4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+12648G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154110 | |||||||
chr9:33154187 | T | C | 1 | a0001c0002t0007g0186 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.412+12571A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154187 | |||||||
chr9:33154410 | T | C | 2 | a0001c0002t0007g0229 a0001c0002t0019g0241 |
2 | NA18940.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.412+12348A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154410 | |||||||
chr9:33154481 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.412+12277G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154481 | |||||||
chr9:33154578 | C | A | 1 | a0001c0001t0002g0282 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.412+12180G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154578 | |||||||
chr9:33154592 | C | T | 340 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(337): Show |
355 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(352): Show |
intron_variant | MODIFIER | c.412+12166G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154592 | |||||||
chr9:33154796 | T | A | 1 | a0001c0001t0001g0171 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.412+11962A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33154796 | |||||||
chr9:33155427 | T | C | 17 | a0001c0002t0007g0180 a0001c0002t0007g0181 a0001c0002t0007g0184 others(14): Show |
17 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(14): Show |
intron_variant | MODIFIER | c.412+11331A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33155427 | |||||||
chr9:33155630 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.412+11128A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33155630 | |||||||
chr9:33155678 | C | G | 2 | a0001c0002t0012g0177 a0001c0002t0012g0178 |
2 | NA19066.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.412+11080G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33155678 | |||||||
chr9:33155957 | C | T | 27 | a0001c0001t0001g0314 a0001c0001t0003g0001 a0001c0001t0003g0297 others(24): Show |
29 | HG00597.hp2 HG01070.hp1 HG02602.hp2 others(26): Show |
intron_variant | MODIFIER | c.412+10801G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33155957 | |||||||
chr9:33156166 | C | T | 1 | a0001c0001t0016g0053 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.412+10592G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33156166 | |||||||
chr9:33156674 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.412+10084T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33156674 | |||||||
chr9:33156723 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.412+10035C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33156723 | |||||||
chr9:33156741 | G | A | 6 | a0001c0001t0002g0251 a0001c0001t0002g0264 a0001c0001t0002g0265 others(3): Show |
6 | HG00558.hp2 HG00597.hp1 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.412+10017C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33156741 | |||||||
chr9:33157063 | T | TAC | 29 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0001g0096 others(26): Show |
31 | HG00280.hp2 HG00558.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.412+9693_412+9694d others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | |||||||
chr9:33157063 | T | TACAC | 8 | a0001c0001t0004g0172 a0001c0001t0008g0325 a0001c0001t0008g0326 others(5): Show |
8 | HG01891.hp2 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.412+9691_412+9694d others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | |||||||
chr9:33157063 | T | TACACAC | 10 | a0001c0001t0001g0006 a0001c0001t0001g0055 a0001c0001t0002g0211 others(7): Show |
12 | HG01167.hp1 HG01169.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.412+9689_412+9694d others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | |||||||
chr9:33157063 | T | TACACACA others(1): Show |
12 | a0001c0001t0003g0317 a0001c0001t0005g0328 a0001c0001t0005g0329 others(9): Show |
13 | HG01070.hp1 HG01884.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.412+9687_412+9694d others(10): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | |||||||
chr9:33157063 | T | TACACACA others(3): Show |
17 | a0001c0001t0002g0210 a0001c0001t0002g0266 a0001c0001t0003g0308 others(14): Show |
17 | HG01496.hp2 HG02293.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.412+9685_412+9694d others(12): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | |||||||
chr9:33157063 | T | TACACACA others(5): Show |
25 | a0001c0001t0001g0171 a0001c0001t0002g0212 a0001c0001t0002g0222 others(22): Show |
25 | HG00544.hp1 HG01106.hp2 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.412+9683_412+9694d others(14): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | |||||||
chr9:33157063 | T | TACACACA others(7): Show |
21 | a0001c0001t0002g0014 a0001c0001t0002g0194 a0001c0001t0002g0202 others(18): Show |
24 | HG00597.hp2 HG00741.hp1 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.412+9681_412+9694d others(16): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | |||||||
chr9:33157063 | T | TACACACA others(9): Show |
13 | a0001c0001t0001g0314 a0001c0001t0002g0230 a0001c0001t0002g0231 others(10): Show |
13 | HG02257.hp2 HG02630.hp1 HG02683.hp2 others(10): Show |
intron_variant | MODIFIER | c.412+9679_412+9694d others(18): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | |||||||
chr9:33157063 | T | TACACACA others(11): Show |
18 | a0001c0001t0002g0203 a0001c0001t0002g0215 a0001c0001t0002g0217 others(15): Show |
18 | HG01261.hp1 HG01361.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.412+9677_412+9694d others(20): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | |||||||
chr9:33157063 | T | TACACACA others(13): Show |
10 | a0001c0001t0002g0012 a0001c0001t0002g0198 a0001c0001t0002g0204 others(7): Show |
11 | HG00544.hp2 HG01975.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.412+9675_412+9694d others(22): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | |||||||
chr9:33157063 | T | TACACACA others(15): Show |
20 | a0001c0001t0001g0200 a0001c0001t0002g0195 a0001c0001t0002g0197 others(17): Show |
20 | HG00323.hp2 HG00609.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.412+9673_412+9694d others(24): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | |||||||
chr9:33157063 | T | TACACACA others(17): Show |
12 | a0001c0001t0002g0207 a0001c0001t0002g0253 a0001c0001t0002g0256 others(9): Show |
12 | HG01884.hp1 HG02071.hp2 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.412+9671_412+9694d others(26): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | |||||||
chr9:33157063 | T | TACACACA others(19): Show |
8 | a0001c0001t0002g0013 a0001c0001t0002g0273 a0001c0001t0002g0274 others(5): Show |
9 | HG01069.hp2 HG01071.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.412+9669_412+9694d others(28): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | |||||||
chr9:33157063 | T | TACACACA others(21): Show |
3 | a0001c0001t0002g0264 a0001c0001t0017g0283 a0001c0001t0020g0175 |
3 | HG00597.hp1 HG02027.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.412+9667_412+9694d others(30): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | |||||||
chr9:33157063 | T | TACACACA others(23): Show |
2 | a0001c0001t0017g0284 a0003c0007t0002g0348 |
2 | HG02055.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.412+9665_412+9694d others(32): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | |||||||
chr9:33157063 | T | TACACACA others(25): Show |
1 | a0001c0001t0020g0176 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.412+9663_412+9694d others(34): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | |||||||
chr9:33157063 | T | TACACACA others(27): Show |
1 | a0001c0001t0002g0265 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.412+9661_412+9694d others(36): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | |||||||
chr9:33157063 | T | TCACACAC others(18): Show |
1 | a0001c0001t0002g0260 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.412+9694_412+9695i others(27): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | |||||||
chr9:33157063 | TAC | T | 95 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(92): Show |
99 | HG00140.hp1 HG00140.hp2 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.412+9693_412+9694d others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | |||||||
chr9:33157063 | TACACACA others(5): Show |
T | 10 | a0001c0001t0004g0010 a0001c0001t0004g0159 a0001c0001t0004g0160 others(7): Show |
11 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(8): Show |
intron_variant | MODIFIER | c.412+9683_412+9694d others(14): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | |||||||
chr9:33157063 | TACACACA others(9): Show |
T | 1 | a0004c0005t0043g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.412+9679_412+9694d others(18): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157063 | |||||||
chr9:33157101 | C | CACACACA others(16): Show |
1 | a0001c0001t0002g0201 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.412+9656_412+9657i others(25): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157101 | |||||||
chr9:33157121 | T | TAC | 88 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0034 others(85): Show |
92 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.412+9635_412+9636d others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157121 | |||||||
chr9:33157121 | T | TACAC | 62 | a0001c0001t0001g0005 a0001c0001t0001g0057 a0001c0001t0001g0082 others(59): Show |
63 | HG00642.hp2 HG00741.hp1 HG01074.hp2 others(60): Show |
intron_variant | MODIFIER | c.412+9633_412+9636d others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157121 | |||||||
chr9:33157121 | T | TACACAC | 83 | a0001c0001t0001g0006 a0001c0001t0001g0086 a0001c0001t0001g0087 others(80): Show |
86 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.412+9631_412+9636d others(8): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157121 | |||||||
chr9:33157121 | T | TACACACA others(1): Show |
53 | a0001c0001t0001g0200 a0001c0001t0002g0012 a0001c0001t0002g0194 others(50): Show |
55 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.412+9629_412+9636d others(10): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157121 | |||||||
chr9:33157121 | T | TACACACA others(3): Show |
19 | a0001c0001t0001g0019 a0001c0001t0002g0014 a0001c0001t0002g0275 others(16): Show |
21 | HG00280.hp1 HG01358.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.412+9627_412+9636d others(12): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157121 | |||||||
chr9:33157121 | T | TACACACA others(5): Show |
7 | a0001c0001t0001g0171 a0001c0001t0002g0282 a0001c0001t0003g0317 others(4): Show |
8 | HG00733.hp1 HG01070.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.412+9625_412+9636d others(14): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157121 | |||||||
chr9:33157121 | T | TACACACA others(7): Show |
2 | a0001c0001t0005g0026 a0001c0001t0016g0157 |
2 | HG03471.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.412+9623_412+9636d others(16): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157121 | |||||||
chr9:33157121 | T | TACACACA others(9): Show |
3 | a0001c0001t0004g0172 a0001c0001t0010g0027 a0001c0001t0016g0053 |
3 | HG02280.hp2 HG02630.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.412+9621_412+9636d others(18): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157121 | |||||||
chr9:33157121 | T | TACACACA others(11): Show |
1 | a0001c0001t0051g0054 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.412+9619_412+9636d others(20): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157121 | |||||||
chr9:33157121 | T | TACACACA others(13): Show |
2 | a0001c0001t0001g0055 a0001c0001t0010g0028 |
2 | HG01255.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.412+9617_412+9636d others(22): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157121 | |||||||
chr9:33157121 | T | TACACACA others(15): Show |
1 | a0001c0001t0040g0158 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.412+9615_412+9636d others(24): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157121 | |||||||
chr9:33157121 | TAC | T | 5 | a0001c0001t0001g0060 a0001c0001t0001g0090 a0001c0001t0023g0349 others(2): Show |
5 | HG01175.hp2 HG02293.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.412+9635_412+9636d others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157121 | |||||||
chr9:33157303 | T | C | 1 | a0001c0001t0002g0197 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.412+9455A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157303 | |||||||
chr9:33157421 | G | T | 214 | a0001c0001t0001g0019 a0001c0001t0001g0171 a0001c0001t0001g0200 others(211): Show |
224 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.412+9337C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157421 | |||||||
chr9:33157594 | A | C | 23 | a0001c0001t0001g0314 a0001c0001t0003g0001 a0001c0001t0003g0297 others(20): Show |
25 | HG00597.hp2 HG01070.hp1 HG02602.hp2 others(22): Show |
intron_variant | MODIFIER | c.412+9164T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157594 | |||||||
chr9:33157636 | T | C | 4 | a0001c0001t0021g0289 a0001c0001t0021g0291 a0001c0001t0021g0292 others(1): Show |
4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+9122A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157636 | |||||||
chr9:33157654 | T | C | 23 | a0001c0001t0001g0314 a0001c0001t0003g0001 a0001c0001t0003g0297 others(20): Show |
25 | HG00597.hp2 HG01070.hp1 HG02602.hp2 others(22): Show |
intron_variant | MODIFIER | c.412+9104A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157654 | |||||||
chr9:33157658 | G | T | 2 | a0001c0001t0006g0322 a0001c0001t0006g0323 |
2 | HG02615.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.412+9100C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157658 | |||||||
chr9:33157717 | TA | T | 153 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
160 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.412+9040delT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157717 | |||||||
chr9:33157853 | G | T | 1 | a0002c0003t0027g0011 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.412+8905C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33157853 | |||||||
chr9:33158282 | G | A | 341 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(338): Show |
356 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(353): Show |
intron_variant | MODIFIER | c.412+8476C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33158282 | |||||||
chr9:33158342 | A | G | 1 | a0001c0002t0012g0285 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.412+8416T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33158342 | |||||||
chr9:33158401 | T | C | 17 | a0001c0002t0007g0180 a0001c0002t0007g0181 a0001c0002t0007g0184 others(14): Show |
17 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(14): Show |
intron_variant | MODIFIER | c.412+8357A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33158401 | |||||||
chr9:33158559 | G | A | 20 | a0001c0001t0001g0019 a0001c0001t0005g0024 a0001c0001t0005g0025 others(17): Show |
22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.412+8199C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33158559 | |||||||
chr9:33158579 | G | A | 53 | a0001c0001t0001g0314 a0001c0001t0003g0001 a0001c0001t0003g0297 others(50): Show |
55 | HG00597.hp2 HG01070.hp1 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.412+8179C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33158579 | |||||||
chr9:33158673 | G | A | 2 | a0001c0001t0001g0147 a0001c0001t0015g0146 |
2 | HG00642.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.412+8085C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33158673 | |||||||
chr9:33158678 | G | T | 2 | a0001c0002t0012g0177 a0001c0002t0012g0178 |
2 | NA19066.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.412+8080C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33158678 | |||||||
chr9:33158703 | G | A | 1 | a0001c0001t0045g0035 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.412+8055C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33158703 | |||||||
chr9:33159747 | G | A | 5 | a0001c0001t0005g0029 a0001c0001t0005g0030 a0001c0001t0005g0031 others(2): Show |
5 | HG00280.hp2 NA18950.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.412+7011C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33159747 | |||||||
chr9:33160119 | A | G | 9 | a0001c0001t0002g0012 a0001c0001t0002g0195 a0001c0001t0002g0201 others(6): Show |
10 | HG00544.hp2 HG00609.hp1 HG02027.hp1 others(7): Show |
intron_variant | MODIFIER | c.412+6639T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33160119 | |||||||
chr9:33160248 | CT | C | 24 | a0001c0001t0001g0171 a0001c0001t0004g0009 a0001c0001t0004g0010 others(21): Show |
26 | HG00280.hp1 HG00738.hp2 HG01070.hp2 others(23): Show |
intron_variant | MODIFIER | c.412+6509delA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33160248 | |||||||
chr9:33160613 | A | G | 39 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(36): Show |
42 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.412+6145T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33160613 | |||||||
chr9:33160689 | C | T | 1 | a0001c0001t0001g0200 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.412+6069G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33160689 | |||||||
chr9:33160714 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.412+6044G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33160714 | |||||||
chr9:33160781 | A | T | 4 | a0001c0001t0021g0289 a0001c0001t0021g0291 a0001c0001t0021g0292 others(1): Show |
4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+5977T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33160781 | |||||||
chr9:33160976 | C | A | 1 | a0001c0001t0045g0035 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.412+5782G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33160976 | |||||||
chr9:33161005 | T | C | 1 | a0001c0001t0005g0344 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.412+5753A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33161005 | |||||||
chr9:33161021 | T | TTC | 138 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(135): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.412+5735_412+5736d others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33161021 | |||||||
chr9:33161021 | T | TTCTC | 11 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG00642.hp1 HG00741.hp2 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.412+5733_412+5736d others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33161021 | |||||||
chr9:33161080 | C | A | 1 | a0001c0001t0009g0044 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.412+5678G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33161080 | |||||||
chr9:33161179 | C | G | 5 | a0001c0001t0016g0155 a0001c0001t0016g0156 a0001c0001t0016g0157 others(2): Show |
6 | HG01891.hp2 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.412+5579G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33161179 | |||||||
chr9:33161223 | G | A | 1 | a0001c0001t0008g0346 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.412+5535C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33161223 | |||||||
chr9:33161443 | T | G | 1 | a0001c0001t0001g0148 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.412+5315A>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33161443 | |||||||
chr9:33161545 | G | A | 1 | a0001c0002t0019g0192 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.412+5213C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33161545 | |||||||
chr9:33161833 | G | C | 4 | a0001c0001t0021g0289 a0001c0001t0021g0291 a0001c0001t0021g0292 others(1): Show |
4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+4925C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33161833 | |||||||
chr9:33161840 | A | G | 1 | a0001c0001t0031g0199 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.412+4918T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33161840 | |||||||
chr9:33161891 | T | C | 1 | a0001c0001t0050g0318 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.412+4867A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33161891 | |||||||
chr9:33162258 | AGTTTCTG others(15): Show |
A | 1 | a0001c0001t0001g0088 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+4478_412+4499d others(24): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162258 | |||||||
chr9:33162281 | A | C | 1 | a0001c0001t0001g0088 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+4477T>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162281 | |||||||
chr9:33162283 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+4475T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162283 | |||||||
chr9:33162294 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+4464T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162294 | |||||||
chr9:33162390 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.412+4368G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162390 | |||||||
chr9:33162437 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.412+4321C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162437 | |||||||
chr9:33162463 | T | A | 1 | a0001c0001t0001g0088 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+4295A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162463 | |||||||
chr9:33162528 | C | A | 1 | a0001c0001t0001g0088 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+4230G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162528 | |||||||
chr9:33162574 | C | G | 1 | a0001c0001t0001g0088 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+4184G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162574 | |||||||
chr9:33162575 | G | C | 1 | a0001c0001t0001g0088 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+4183C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162575 | |||||||
chr9:33162716 | T | A | 1 | a0001c0001t0001g0088 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+4042A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162716 | |||||||
chr9:33162799 | A | G | 1 | a0001c0001t0025g0002 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.412+3959T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162799 | |||||||
chr9:33162902 | G | T | 1 | a0001c0001t0001g0088 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+3856C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162902 | |||||||
chr9:33162941 | G | T | 1 | a0001c0001t0001g0088 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+3817C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162941 | |||||||
chr9:33162961 | A | T | 1 | a0001c0001t0001g0088 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+3797T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162961 | |||||||
chr9:33162973 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.412+3785C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33162973 | |||||||
chr9:33163048 | T | TCCAC | 3 | a0001c0001t0002g0280 a0001c0001t0002g0282 a0001c0001t0049g0281 |
3 | HG01496.hp2 HG04204.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.412+3706_412+3709d others(6): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163048 | |||||||
chr9:33163061 | G | A | 39 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(36): Show |
42 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.412+3697C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163061 | |||||||
chr9:33163067 | T | A | 1 | a0001c0001t0001g0088 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+3691A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163067 | |||||||
chr9:33163076 | T | A | 1 | a0001c0001t0001g0088 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+3682A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163076 | |||||||
chr9:33163083 | C | G | 1 | a0001c0001t0001g0089 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.412+3675G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163083 | |||||||
chr9:33163149 | C | A | 1 | a0001c0001t0001g0088 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+3609G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163149 | |||||||
chr9:33163150 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+3608A>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163150 | |||||||
chr9:33163151 | G | C | 1 | a0001c0001t0001g0088 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+3607C>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163151 | |||||||
chr9:33163152 | C | A | 1 | a0001c0001t0001g0088 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+3606G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163152 | |||||||
chr9:33163193 | C | G | 1 | a0001c0001t0001g0088 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+3565G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163193 | |||||||
chr9:33163194 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.412+3564A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163194 | |||||||
chr9:33163273 | A | G | 213 | a0001c0001t0001g0019 a0001c0001t0001g0171 a0001c0001t0001g0200 others(210): Show |
223 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.412+3485T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163273 | |||||||
chr9:33163300 | C | T | 20 | a0001c0001t0001g0019 a0001c0001t0005g0024 a0001c0001t0005g0025 others(17): Show |
22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.412+3458G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163300 | |||||||
chr9:33163388 | C | T | 3 | a0001c0001t0020g0174 a0001c0001t0020g0175 a0001c0001t0020g0176 |
3 | HG01074.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.412+3370G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163388 | |||||||
chr9:33163481 | C | G | 5 | a0001c0001t0016g0155 a0001c0001t0016g0156 a0001c0001t0016g0157 others(2): Show |
6 | HG01891.hp2 HG02717.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.412+3277G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163481 | |||||||
chr9:33163488 | G | T | 112 | a0001c0001t0001g0200 a0001c0001t0002g0012 a0001c0001t0002g0013 others(109): Show |
115 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(112): Show |
intron_variant | MODIFIER | c.412+3270C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163488 | |||||||
chr9:33163509 | G | A | 1 | a0001c0001t0003g0319 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.412+3249C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163509 | |||||||
chr9:33163525 | C | G | 39 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(36): Show |
42 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.412+3233G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163525 | |||||||
chr9:33163542 | C | G | 1 | a0001c0001t0026g0321 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.412+3216G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163542 | |||||||
chr9:33163558 | C | G | 1 | a0001c0001t0026g0321 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.412+3200G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163558 | |||||||
chr9:33163625 | T | C | 2 | a0001c0001t0001g0149 a0001c0001t0001g0151 |
2 | NA18988.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.412+3133A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163625 | |||||||
chr9:33163667 | C | T | 17 | a0001c0002t0007g0180 a0001c0002t0007g0181 a0001c0002t0007g0184 others(14): Show |
17 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(14): Show |
intron_variant | MODIFIER | c.412+3091G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163667 | |||||||
chr9:33163668 | G | T | 1 | a0001c0001t0002g0198 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.412+3090C>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163668 | |||||||
chr9:33163773 | C | G | 2 | a0001c0001t0001g0059 a0001c0001t0002g0058 |
2 | HG00609.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.412+2985G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163773 | |||||||
chr9:33163811 | T | C | 3 | a0001c0001t0020g0174 a0001c0001t0020g0175 a0001c0001t0020g0176 |
3 | HG01074.hp1 HG02647.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.412+2947A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163811 | |||||||
chr9:33163886 | C | A | 1 | a0001c0002t0036g0193 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.412+2872G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163886 | |||||||
chr9:33163964 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.412+2794G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33163964 | |||||||
chr9:33164078 | C | T | 4 | a0001c0001t0016g0155 a0001c0001t0016g0156 a0001c0001t0016g0157 others(1): Show |
4 | HG01891.hp2 HG02717.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.412+2680G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33164078 | |||||||
chr9:33164118 | T | A | 20 | a0001c0001t0001g0019 a0001c0001t0005g0024 a0001c0001t0005g0025 others(17): Show |
22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.412+2640A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33164118 | |||||||
chr9:33164157 | T | C | 1 | a0001c0001t0009g0045 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.412+2601A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33164157 | |||||||
chr9:33164529 | T | A | 20 | a0001c0001t0001g0019 a0001c0001t0005g0024 a0001c0001t0005g0025 others(17): Show |
22 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(19): Show |
intron_variant | MODIFIER | c.412+2229A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33164529 | |||||||
chr9:33164669 | T | A | 53 | a0001c0001t0001g0314 a0001c0001t0003g0001 a0001c0001t0003g0297 others(50): Show |
55 | HG00597.hp2 HG01070.hp1 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.412+2089A>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33164669 | |||||||
chr9:33164676 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.412+2082G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33164676 | |||||||
chr9:33164679 | G | A | 118 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
123 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.412+2079C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33164679 | |||||||
chr9:33164736 | C | T | 2 | a0001c0001t0003g0298 a0001c0001t0003g0320 |
2 | HG02683.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.412+2022G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33164736 | |||||||
chr9:33164960 | G | A | 1 | a0001c0001t0003g0320 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.412+1798C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33164960 | |||||||
chr9:33164970 | AT | A | 117 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
123 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.412+1787delA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33164970 | |||||||
chr9:33164970 | ATT | A | 185 | a0001c0001t0001g0019 a0001c0001t0001g0150 a0001c0001t0001g0151 others(182): Show |
194 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.412+1786_412+1787d others(4): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33164970 | |||||||
chr9:33164970 | ATTT | A | 28 | a0001c0001t0002g0286 a0001c0001t0005g0328 a0001c0001t0005g0329 others(25): Show |
28 | HG01106.hp2 HG01175.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.412+1785_412+1787d others(5): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33164970 | |||||||
chr9:33165227 | C | G | 1 | a0001c0001t0002g0295 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.412+1531G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33165227 | |||||||
chr9:33165239 | A | AT | 17 | a0001c0002t0007g0180 a0001c0002t0007g0181 a0001c0002t0007g0184 others(14): Show |
17 | HG00544.hp1 HG01257.hp1 HG02165.hp1 others(14): Show |
intron_variant | MODIFIER | c.412+1518dupA | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33165239 | |||||||
chr9:33165285 | T | C | 3 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0154 |
3 | HG01928.hp2 HG03654.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.412+1473A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33165285 | |||||||
chr9:33165307 | T | TA | 136 | a0001c0001t0001g0019 a0001c0001t0001g0200 a0001c0001t0002g0012 others(133): Show |
142 | HG00280.hp2 HG00323.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.412+1450dupT | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33165307 | |||||||
chr9:33165374 | C | T | 53 | a0001c0001t0001g0314 a0001c0001t0003g0001 a0001c0001t0003g0297 others(50): Show |
55 | HG00597.hp2 HG01070.hp1 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.412+1384G>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33165374 | |||||||
chr9:33165454 | A | T | 1 | a0001c0001t0003g0015 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.412+1304T>A | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33165454 | |||||||
chr9:33165646 | T | C | 1 | a0001c0001t0003g0347 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.412+1112A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33165646 | |||||||
chr9:33165691 | A | G | 1 | a0001c0001t0045g0035 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.412+1067T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33165691 | |||||||
chr9:33165836 | C | G | 1 | a0001c0001t0001g0034 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.412+922G>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33165836 | |||||||
chr9:33165987 | A | G | 214 | a0001c0001t0001g0019 a0001c0001t0001g0171 a0001c0001t0001g0200 others(211): Show |
224 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.412+771T>C | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33165987 | |||||||
chr9:33166236 | T | C | 213 | a0001c0001t0001g0019 a0001c0001t0001g0171 a0001c0001t0001g0200 others(210): Show |
223 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.412+522A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33166236 | |||||||
chr9:33166271 | ATCAGGAG others(10): Show |
A | 1 | a0004c0005t0043g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.412+470_412+486del others(17): Show |
B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33166271 | |||||||
chr9:33166350 | G | A | 1 | a0001c0002t0007g0288 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.412+408C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33166350 | |||||||
chr9:33166617 | T | C | 4 | a0001c0001t0021g0289 a0001c0001t0021g0291 a0001c0001t0021g0292 others(1): Show |
4 | HG01081.hp2 HG01515.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.412+141A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33166617 | |||||||
chr9:33166643 | G | A | 1 | a0001c0001t0001g0293 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.412+115C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33166643 | |||||||
chr9:33166649 | G | A | 1 | a0001c0001t0057g0294 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.412+109C>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33166649 | |||||||
chr9:33166664 | T | C | 1 | a0001c0001t0002g0295 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.412+94A>G | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33166664 | |||||||
chr9:33166713 | C | CG | 21 | a0001c0001t0001g0019 a0001c0001t0003g0015 a0001c0001t0005g0024 others(18): Show |
23 | HG00280.hp2 HG00733.hp1 HG01358.hp2 others(20): Show |
intron_variant | MODIFIER | c.412+44dupC | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33166713 | |||||||
chr9:33166747 | C | A | 53 | a0001c0001t0001g0314 a0001c0001t0003g0001 a0001c0001t0003g0297 others(50): Show |
55 | HG00597.hp2 HG01070.hp1 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.412+11G>T | B4GALT1 | ENSG00000086062.13 | transcript | ENST00000379731.5 | protein_coding | 1/5 | chr9 | 33166747 |