Item | Value |
---|---|
geneid | 338707 |
ensemblid | ENSG00000182272.12 |
hgncid | 26315 |
symbol | B4GALNT4 |
name | beta-1,4-N-acetyl-galactosaminyltransferase 4 |
refseq_nuc | NM_178537.5 |
refseq_prot | NP_848632.2 |
ensembl_nuc | ENST00000329962.11 |
ensembl_prot | ENSP00000328277.6 |
mane_status | MANE Select |
chr | chr11 |
start | 369499 |
end | 382117 |
strand | + |
ver | v1.2 |
region | chr11:369499-382117 |
region5000 | chr11:364499-387117 |
regionname0 | B4GALNT4_chr11_369499_382117 |
regionname5000 | B4GALNT4_chr11_364499_387117 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1039 | 82 | 13 | 30 | 20 | 5 | 12 | 11 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | MPRLP others(1034): Show |
chr11 | 364499 | 387117 |
a0002 | 0/0 | 1039 | 58 | 16 | 13 | 19 | 3 | 7 | 13 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | MPRLP others(1034): Show |
chr11 | 364499 | 387117 |
a0003 | 0/0 | 403 | 7 | 2 | 2 | 2 | 0 | 1 | 2 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | MPRLP others(398): Show |
chr11 | 364499 | 387117 |
a0004 | 0/0 | 1039 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | MPRLP others(1034): Show |
chr11 | 364499 | 387117 |
a0005 | 0/0 | 403 | 4 | 0 | 1 | 2 | 0 | 1 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | MPRLP others(398): Show |
chr11 | 364499 | 387117 |
a0006 | 0/0 | 974 | 4 | 1 | 2 | 0 | 0 | 1 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | MPRLP others(969): Show |
chr11 | 364499 | 387117 |
a0007 | 0/0 | 974 | 3 | 2 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | MPRLP others(969): Show |
chr11 | 364499 | 387117 |
a0008 | 0/0 | 1039 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | MPRLP others(1034): Show |
chr11 | 364499 | 387117 |
a0009 | 0/0 | 1039 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | MPRLP others(1034): Show |
chr11 | 364499 | 387117 |
a0010 | 0/0 | 1039 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | MPRLP others(1034): Show |
chr11 | 364499 | 387117 |
a0011 | 0/0 | 1039 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | MPRLP others(1034): Show |
chr11 | 364499 | 387117 |
a0012 | 0/0 | 76 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | MPRLP others(71): Show |
chr11 | 364499 | 387117 |
a0013 | 0/0 | 1039 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | MPRLP others(1034): Show |
chr11 | 364499 | 387117 |
a0014 | 0/0 | 1039 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | MPRLP others(1034): Show |
chr11 | 364499 | 387117 |
a0015 | 0/0 | 1039 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | MPRLP others(1034): Show |
chr11 | 364499 | 387117 |
a0016 | 0/0 | 1039 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | MPRLP others(1034): Show |
chr11 | 364499 | 387117 |
a0017 | 0/0 | 403 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | MPRLP others(398): Show |
chr11 | 364499 | 387117 |
a0018 | 0/0 | 974 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | MPRLP others(969): Show |
chr11 | 364499 | 387117 |
a0019 | 0/0 | 1031 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | MPRLP others(1026): Show |
chr11 | 364499 | 387117 |
a0020 | 0/0 | 969 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | MPRLP others(964): Show |
chr11 | 364499 | 387117 |
a0021 | 0/0 | 1039 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | MPRLP others(1034): Show |
chr11 | 364499 | 387117 |
a0022 | 0/0 | 1039 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | MPRLP others(1034): Show |
chr11 | 364499 | 387117 |
a0023 | 0/0 | 1039 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | MPRLP others(1034): Show |
chr11 | 364499 | 387117 |
a0024 | 0/0 | 1039 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | MPRLP others(1034): Show |
chr11 | 364499 | 387117 |
a0025 | 0/0 | 1039 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | MPRLP others(1034): Show |
chr11 | 364499 | 387117 |
a0026 | 0/0 | 1044 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | MPRLP others(1039): Show |
chr11 | 364499 | 387117 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 3117 | 59 | 10 | 20 | 18 | 3 | 6 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0001c0003 | 0/0 | 3117 | 15 | 3 | 5 | 2 | 1 | 4 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0001c0005 | 0/0 | 3117 | 5 | 0 | 4 | 0 | 1 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0001c0016 | 0/0 | 3117 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0001c0024 | 0/0 | 3117 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0001c0026 | 0/0 | 3117 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0002c0002 | 0/0 | 3117 | 40 | 6 | 11 | 14 | 3 | 6 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0002c0004 | 0/0 | 3117 | 6 | 5 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0002c0008 | 0/0 | 3117 | 4 | 0 | 1 | 3 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0002c0009 | 0/0 | 3117 | 4 | 3 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0002c0033 | 0/0 | 3117 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0002c0035 | 0/0 | 3117 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0002c0037 | 0/0 | 3117 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0002c0038 | 0/0 | 3117 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0003c0006 | 0/0 | 3118 | 5 | 1 | 1 | 2 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3113): Show |
chr11 | 364499 | 387117 | ||
a0003c0036 | 0/0 | 3118 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3113): Show |
chr11 | 364499 | 387117 | ||
a0003c0039 | 0/0 | 3118 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3113): Show |
chr11 | 364499 | 387117 | ||
a0004c0014 | 0/0 | 3117 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0004c0042 | 0/0 | 3117 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0004c0043 | 0/0 | 3117 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0004c0044 | 0/0 | 3117 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0005c0010 | 0/0 | 3118 | 3 | 0 | 1 | 2 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3113): Show |
chr11 | 364499 | 387117 | ||
a0005c0023 | 0/0 | 3119 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3114): Show |
chr11 | 364499 | 387117 | ||
a0006c0007 | 0/0 | 3118 | 4 | 1 | 2 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3113): Show |
chr11 | 364499 | 387117 | ||
a0007c0011 | 0/0 | 3118 | 3 | 2 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3113): Show |
chr11 | 364499 | 387117 | ||
a0008c0013 | 0/0 | 3117 | 2 | 1 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0009c0012 | 0/0 | 3117 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0010c0017 | 0/0 | 3117 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0011c0022 | 0/0 | 3117 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0012c0040 | 0/0 | 3106 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3101): Show |
chr11 | 364499 | 387117 | ||
a0013c0020 | 0/0 | 3117 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0014c0030 | 0/0 | 3117 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0015c0041 | 0/0 | 3117 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0016c0027 | 0/0 | 3117 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0017c0031 | 0/0 | 3118 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3113): Show |
chr11 | 364499 | 387117 | ||
a0018c0029 | 0/0 | 3118 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3113): Show |
chr11 | 364499 | 387117 | ||
a0019c0018 | 0/0 | 3093 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3088): Show |
chr11 | 364499 | 387117 | ||
a0020c0032 | 0/0 | 3103 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3098): Show |
chr11 | 364499 | 387117 | ||
a0021c0019 | 0/0 | 3117 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0022c0015 | 0/0 | 3117 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0023c0034 | 0/0 | 3117 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0024c0021 | 0/0 | 3117 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0025c0028 | 0/0 | 3117 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3112): Show |
chr11 | 364499 | 387117 | ||
a0026c0025 | 0/0 | 3132 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | ATGCC others(3127): Show |
chr11 | 364499 | 387117 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3750 | 52 | 4 | 19 | 18 | 3 | 6 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0001c0001t0002 | 0/0 | 3757 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3752): Show |
chr11 | 364499 | 387117 |
a0001c0001t0003 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0001c0001t0004 | 0/0 | 3757 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3752): Show |
chr11 | 364499 | 387117 |
a0001c0001t0005 | 0/0 | 3750 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0001c0001t0007 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0001c0003t0001 | 0/0 | 3750 | 5 | 0 | 0 | 2 | 0 | 3 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0001c0003t0002 | 0/0 | 3757 | 6 | 0 | 4 | 0 | 1 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3752): Show |
chr11 | 364499 | 387117 |
a0001c0003t0003 | 0/0 | 3750 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0001c0003t0004 | 0/0 | 3757 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3752): Show |
chr11 | 364499 | 387117 |
a0001c0005t0002 | 0/0 | 3757 | 5 | 0 | 4 | 0 | 1 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3752): Show |
chr11 | 364499 | 387117 |
a0001c0016t0001 | 0/0 | 3750 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0001c0024t0003 | 0/0 | 3750 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0001c0026t0002 | 0/0 | 3757 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3752): Show |
chr11 | 364499 | 387117 |
a0002c0002t0001 | 0/0 | 3750 | 38 | 6 | 10 | 14 | 3 | 5 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0002c0002t0003 | 0/0 | 3750 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0002c0002t0006 | 0/0 | 3750 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0002c0004t0001 | 0/0 | 3750 | 4 | 3 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0002c0004t0002 | 0/0 | 3757 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3752): Show |
chr11 | 364499 | 387117 |
a0002c0008t0001 | 0/0 | 3750 | 4 | 0 | 1 | 3 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0002c0009t0001 | 0/0 | 3750 | 4 | 3 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0002c0033t0001 | 0/0 | 3750 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0002c0035t0001 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0002c0037t0001 | 0/0 | 3750 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0002c0038t0003 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0003c0006t0001 | 0/0 | 3751 | 5 | 1 | 1 | 2 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3746): Show |
chr11 | 364499 | 387117 |
a0003c0036t0001 | 0/0 | 3751 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3746): Show |
chr11 | 364499 | 387117 |
a0003c0039t0001 | 0/0 | 3751 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3746): Show |
chr11 | 364499 | 387117 |
a0004c0014t0002 | 0/0 | 3757 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3752): Show |
chr11 | 364499 | 387117 |
a0004c0042t0001 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0004c0043t0001 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0004c0044t0001 | 0/0 | 3750 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0005c0010t0001 | 0/0 | 3751 | 3 | 0 | 1 | 2 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3746): Show |
chr11 | 364499 | 387117 |
a0005c0023t0001 | 0/0 | 3752 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3747): Show |
chr11 | 364499 | 387117 |
a0006c0007t0001 | 0/0 | 3751 | 4 | 1 | 2 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3746): Show |
chr11 | 364499 | 387117 |
a0007c0011t0001 | 0/0 | 3751 | 3 | 2 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3746): Show |
chr11 | 364499 | 387117 |
a0008c0013t0001 | 0/0 | 3750 | 2 | 1 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0009c0012t0001 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0009c0012t0003 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0010c0017t0001 | 0/0 | 3750 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0011c0022t0001 | 0/0 | 3750 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0012c0040t0001 | 0/0 | 3739 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3734): Show |
chr11 | 364499 | 387117 |
a0013c0020t0001 | 0/0 | 3750 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0014c0030t0004 | 0/0 | 3757 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3752): Show |
chr11 | 364499 | 387117 |
a0015c0041t0001 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0016c0027t0001 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0017c0031t0004 | 0/0 | 3758 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3753): Show |
chr11 | 364499 | 387117 |
a0018c0029t0004 | 0/0 | 3758 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3753): Show |
chr11 | 364499 | 387117 |
a0019c0018t0001 | 0/0 | 3726 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3721): Show |
chr11 | 364499 | 387117 |
a0020c0032t0001 | 0/0 | 3736 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3731): Show |
chr11 | 364499 | 387117 |
a0021c0019t0001 | 0/0 | 3750 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0022c0015t0001 | 0/0 | 3750 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0023c0034t0001 | 0/0 | 3750 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0024c0021t0001 | 0/0 | 3750 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0025c0028t0001 | 0/0 | 3750 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3745): Show |
chr11 | 364499 | 387117 |
a0026c0025t0003 | 0/0 | 3765 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | GATCC others(3760): Show |
chr11 | 364499 | 387117 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0006 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0115 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0005g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0005g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0001t0007g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0003t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0003t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0003t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0003t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0003t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0003t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0003t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0003t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0003t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0003t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0003t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0003t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0005t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0005t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0005t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0005t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0005t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0016t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0024t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0001c0026t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0002t0006g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0004t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0004t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0004t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0004t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0004t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0008t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0008t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0008t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0008t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0009t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0009t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0009t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0009t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0033t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0035t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0037t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0002c0038t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0003c0006t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0003c0006t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0003c0006t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0003c0006t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0003c0006t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0003c0036t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0003c0039t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0004c0014t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0004c0014t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0004c0042t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0004c0043t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0004c0044t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0005c0010t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0005c0010t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0005c0010t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0005c0023t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0006c0007t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0006c0007t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0006c0007t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0006c0007t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0007c0011t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0007c0011t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0007c0011t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0008c0013t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0008c0013t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0009c0012t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0009c0012t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0010c0017t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0011c0022t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0012c0040t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0013c0020t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0014c0030t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0015c0041t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0016c0027t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0017c0031t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0018c0029t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0019c0018t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0020c0032t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0021c0019t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0022c0015t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0023c0034t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0024c0021t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0025c0028t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
a0026c0025t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0152 | EUR | GBR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0142 | EUR | GBR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0124 | EUR | GBR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | FIN | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG00323 | hp2 | a0001 | c0005 | t0002 | g0107 | EUR | FIN | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG00408 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | CHS | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG00438 | hp1 | a0005 | c0010 | t0001 | g0174 | EAS | CHS | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG00438 | hp2 | a0002 | c0008 | t0001 | g0089 | EAS | CHS | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG00544 | hp1 | a0007 | c0011 | t0001 | g0158 | EAS | CHS | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG00544 | hp2 | a0005 | c0010 | t0001 | g0037 | EAS | CHS | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG00639 | hp2 | a0010 | c0017 | t0001 | g0086 | AMR | PUR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG00642 | hp1 | a0001 | c0024 | t0003 | g0022 | AMR | PUR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0082 | AMR | PUR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG00738 | hp1 | a0011 | c0022 | t0001 | g0126 | AMR | PUR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01070 | hp1 | a0001 | c0005 | t0002 | g0131 | AMR | PUR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0140 | AMR | PUR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0143 | AMR | PUR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01074 | hp2 | a0001 | c0003 | t0002 | g0025 | AMR | PUR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01106 | hp1 | a0003 | c0036 | t0001 | g0079 | AMR | PUR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01106 | hp2 | a0001 | c0003 | t0003 | g0018 | AMR | PUR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01243 | hp1 | a0002 | c0004 | t0001 | g0176 | AMR | PUR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01243 | hp2 | a0004 | c0044 | t0001 | g0032 | AMR | PUR | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01255 | hp1 | a0006 | c0007 | t0001 | g0175 | AMR | CLM | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0162 | AMR | CLM | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | CLM | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01346 | hp1 | a0002 | c0008 | t0001 | g0081 | AMR | CLM | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01346 | hp2 | a0001 | c0003 | t0002 | g0024 | AMR | CLM | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0141 | AMR | CLM | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01361 | hp1 | a0005 | c0010 | t0001 | g0109 | AMR | CLM | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01361 | hp2 | a0002 | c0002 | t0006 | g0076 | AMR | CLM | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01433 | hp1 | a0008 | c0013 | t0001 | g0057 | AMR | CLM | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | ACB | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01891 | hp2 | a0001 | c0001 | t0007 | g0006 | AFR | ACB | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0008 | AMR | PEL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01934 | hp2 | a0001 | c0005 | t0002 | g0108 | AMR | PEL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01952 | hp1 | a0001 | c0005 | t0002 | g0116 | AMR | PEL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01952 | hp2 | a0006 | c0007 | t0001 | g0041 | AMR | PEL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01975 | hp1 | a0001 | c0005 | t0002 | g0117 | AMR | PEL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01975 | hp2 | a0012 | c0040 | t0001 | g0007 | AMR | PEL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0157 | AMR | PEL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01978 | hp2 | a0013 | c0020 | t0001 | g0046 | AMR | PEL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | PEL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | PEL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02040 | hp2 | a0002 | c0033 | t0001 | g0070 | EAS | KHV | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02080 | hp1 | a0001 | c0003 | t0001 | g0091 | EAS | KHV | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02080 | hp2 | a0001 | c0003 | t0001 | g0097 | EAS | KHV | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0145 | EAS | KHV | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02132 | hp2 | a0002 | c0009 | t0001 | g0177 | EAS | KHV | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02148 | hp2 | a0003 | c0006 | t0001 | g0154 | AMR | PEL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02258 | hp1 | a0002 | c0004 | t0001 | g0001 | AFR | ACB | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02258 | hp2 | a0002 | c0004 | t0001 | g0001 | AFR | ACB | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02273 | hp2 | a0001 | c0003 | t0002 | g0026 | AMR | PEL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0146 | AMR | PEL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02300 | hp2 | a0001 | c0003 | t0002 | g0164 | AMR | PEL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02630 | hp1 | a0008 | c0013 | t0001 | g0059 | AFR | GWD | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02630 | hp2 | a0001 | c0003 | t0004 | g0014 | AFR | GWD | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02683 | hp1 | a0002 | c0002 | t0003 | g0153 | SAS | PJL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02683 | hp2 | a0001 | c0026 | t0002 | g0049 | SAS | PJL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02723 | hp1 | a0014 | c0030 | t0004 | g0011 | AFR | GWD | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0073 | AFR | GWD | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0067 | AFR | GWD | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0169 | AFR | GWD | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0061 | AFR | ESN | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02976 | hp1 | a0002 | c0035 | t0001 | g0071 | AFR | ESN | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02976 | hp2 | a0002 | c0009 | t0001 | g0166 | AFR | ESN | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03041 | hp1 | a0015 | c0041 | t0001 | g0030 | AFR | GWD | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03041 | hp2 | a0009 | c0012 | t0003 | g0023 | AFR | GWD | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03098 | hp1 | a0006 | c0007 | t0001 | g0132 | AFR | MSL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | MSL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03130 | hp1 | a0016 | c0027 | t0001 | g0015 | AFR | ESN | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03130 | hp2 | a0001 | c0001 | t0005 | g0172 | AFR | ESN | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0074 | AFR | ESN | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03139 | hp2 | a0017 | c0031 | t0004 | g0012 | AFR | ESN | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03195 | hp1 | a0004 | c0043 | t0001 | g0028 | AFR | ESN | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03195 | hp2 | a0002 | c0009 | t0001 | g0168 | AFR | ESN | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03225 | hp1 | a0004 | c0042 | t0001 | g0031 | AFR | MSL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03225 | hp2 | a0003 | c0039 | t0001 | g0058 | AFR | MSL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03239 | hp1 | a0001 | c0003 | t0001 | g0136 | SAS | PJL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03239 | hp2 | a0002 | c0037 | t0001 | g0156 | SAS | PJL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03453 | hp1 | a0003 | c0006 | t0001 | g0078 | AFR | MSL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | MSL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03486 | hp1 | a0002 | c0004 | t0002 | g0084 | AFR | MSL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03486 | hp2 | a0018 | c0029 | t0004 | g0053 | AFR | MSL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03490 | hp1 | a0019 | c0018 | t0001 | g0139 | SAS | PJL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03490 | hp2 | a0020 | c0032 | t0001 | g0147 | SAS | PJL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03516 | hp1 | a0002 | c0004 | t0002 | g0085 | AFR | ESN | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03516 | hp2 | a0007 | c0011 | t0001 | g0068 | AFR | ESN | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03540 | hp1 | a0001 | c0003 | t0004 | g0017 | AFR | GWD | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0072 | AFR | GWD | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03579 | hp2 | a0002 | c0002 | t0001 | g0080 | AFR | MSL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03669 | hp2 | a0006 | c0007 | t0001 | g0122 | SAS | PJL | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03688 | hp1 | a0001 | c0003 | t0001 | g0106 | SAS | STU | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | STU | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03831 | hp1 | a0002 | c0002 | t0001 | g0063 | SAS | BEB | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03831 | hp2 | a0001 | c0003 | t0001 | g0129 | SAS | BEB | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03834 | hp1 | a0001 | c0016 | t0001 | g0104 | SAS | BEB | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03834 | hp2 | a0003 | c0006 | t0001 | g0065 | SAS | BEB | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03927 | hp1 | a0002 | c0002 | t0001 | g0155 | SAS | BEB | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG03927 | hp2 | a0005 | c0023 | t0001 | g0125 | SAS | BEB | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0149 | SAS | STU | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0055 | SAS | STU | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0064 | SAS | STU | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | STU | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA18522 | hp1 | a0004 | c0014 | t0002 | g0051 | AFR | YRI | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA18522 | hp2 | a0001 | c0003 | t0004 | g0050 | AFR | YRI | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | CHB | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHB | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA18947 | hp2 | a0003 | c0006 | t0001 | g0077 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA18963 | hp1 | a0021 | c0019 | t0001 | g0033 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA18963 | hp2 | a0002 | c0002 | t0001 | g0160 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA18970 | hp1 | a0002 | c0008 | t0001 | g0148 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA19005 | hp2 | a0022 | c0015 | t0001 | g0040 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA19007 | hp1 | a0023 | c0034 | t0001 | g0090 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA19012 | hp1 | a0024 | c0021 | t0001 | g0096 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA19057 | hp1 | a0002 | c0008 | t0001 | g0144 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA19057 | hp2 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA19085 | hp1 | a0003 | c0006 | t0001 | g0133 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA19240 | hp1 | a0025 | c0028 | t0001 | g0052 | AFR | YRI | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA19240 | hp2 | a0002 | c0038 | t0003 | g0020 | AFR | YRI | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0066 | EUR | TSI | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA20805 | hp2 | a0001 | c0003 | t0002 | g0047 | EUR | TSI | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | GIH | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA20905 | hp2 | a0001 | c0003 | t0002 | g0027 | SAS | GIH | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02109 | hp1 | a0009 | c0012 | t0001 | g0103 | AFR | ACB | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02109 | hp2 | a0002 | c0009 | t0001 | g0013 | AFR | ACB | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02559 | hp1 | a0004 | c0014 | t0002 | g0029 | AFR | ACB | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0171 | AFR | ACB | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | USA | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
HG06807 | hp2 | a0007 | c0011 | t0001 | g0150 | AFR | USA | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA21309 | hp1 | a0026 | c0025 | t0003 | g0021 | AFR | LWK | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
NA21309 | hp2 | a0002 | c0004 | t0001 | g0056 | AFR | LWK | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0115 | REF | REF | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0006 | REF | REF | B4GALNT4_chr11_364499_387117 | B4GALNT4 | chr11 | 364499 | 387117 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:372157 | C | T | 9 | a0002 a0003 a0004 others(6): Show |
79 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(76): Show |
missense_variant | MODERATE | c.200C>T | p.Ala67Val | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 2/20 | 505/3750 | 200/3120 | 67/1039 | chr11 | 372157 | |||
chr11:372169 | A | G | 4 | a0004 a0014 a0015 others(1): Show |
8 | HG01243.hp2 HG02559.hp1 HG02723.hp1 others(5): Show |
missense_variant | MODERATE | c.212A>G | p.Gln71Arg | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 2/20 | 517/3750 | 212/3120 | 71/1039 | chr11 | 372169 | |||
chr11:372179 | GGACTCCA others(4): Show |
G | 1 | a0012 | 1 | HG01975.hp2 | frameshift_variant | HIGH | c.225_235delCTCCAGTG others(3): Show |
p.Asp75fs | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 2/20 | 530/3750 | 225/3120 | 75/1039 | INFO_REALIGN_3_PRIME | chr11 | 372179 | ||
chr11:372613 | T | TCCTCCCT others(101): Show |
1 | a0002 | 1 | NA19057.hp1 | disruptive_inframe_insertion | MODERATE | c.293_294insCGCTGGGA others(100): Show |
p.Gly98_Ala99insAlaG others(104): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 3/20 | 599/3750 | 294/3120 | 98/1039 | INFO_REALIGN_3_PRIME | chr11 | 372613 | ||
chr11:372669 | G | T | 3 | a0016 a0018 a0025 |
3 | HG03130.hp1 HG03486.hp2 NA19240.hp1 |
missense_variant | MODERATE | c.263G>T | p.Gly88Val | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 3/20 | 568/3750 | 263/3120 | 88/1039 | chr11 | 372669 | |||
chr11:372672 | G | A | 1 | a0022 | 1 | NA19005.hp2 | missense_variant | MODERATE | c.266G>A | p.Arg89Gln | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 3/20 | 571/3750 | 266/3120 | 89/1039 | chr11 | 372672 | |||
chr11:373492 | G | A | 1 | a0016 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.680G>A | p.Ser227Asn | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 7/20 | 985/3750 | 680/3120 | 227/1039 | chr11 | 373492 | |||
chr11:373494 | TCCCAGGT others(8): Show |
T | 1 | a0020 | 1 | HG03490.hp2 | conservative_inframe_deletion | MODERATE | c.685_699delCAGGTGTC others(7): Show |
p.Gln229_Pro233del | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 7/20 | 990/3750 | 685/3120 | 229/1039 | INFO_REALIGN_3_PRIME | chr11 | 373494 | ||
chr11:375699 | T | TG | 3 | a0003 a0005 a0017 |
12 | HG00438.hp1 HG00544.hp2 HG01106.hp1 others(9): Show |
frameshift_variant | HIGH | c.918dupG | p.Arg307fs | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 10/20 | 1224/3750 | 919/3120 | 307/1039 | INFO_REALIGN_3_PRIME | chr11 | 375699 | ||
chr11:375877 | A | C | 1 | a0011 | 1 | HG00738.hp1 | missense_variant | MODERATE | c.1016A>C | p.Asn339Thr | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 11/20 | 1321/3750 | 1016/3120 | 339/1039 | chr11 | 375877 | |||
chr11:376331 | T | A | 1 | a0010 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.1277T>A | p.Phe426Tyr | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 13/20 | 1582/3750 | 1277/3120 | 426/1039 | chr11 | 376331 | |||
chr11:376343 | A | G | 4 | a0003 a0008 a0009 others(1): Show |
6 | HG01433.hp1 HG02109.hp1 HG02630.hp1 others(3): Show |
missense_variant | MODERATE | c.1289A>G | p.Asn430Ser | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 13/20 | 1594/3750 | 1289/3120 | 430/1039 | chr11 | 376343 | |||
chr11:376489 | A | G | 1 | a0024 | 1 | NA19012.hp1 | missense_variant | MODERATE | c.1366A>G | p.Arg456Gly | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/20 | 1671/3750 | 1366/3120 | 456/1039 | chr11 | 376489 | |||
chr11:376571 | G | C | 1 | a0015 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.1448G>C | p.Arg483Pro | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/20 | 1753/3750 | 1448/3120 | 483/1039 | chr11 | 376571 | |||
chr11:376627 | C | G | 1 | a0021 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.1504C>G | p.Arg502Gly | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/20 | 1809/3750 | 1504/3120 | 502/1039 | chr11 | 376627 | |||
chr11:376628 | G | C | 1 | a0021 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.1505G>C | p.Arg502Pro | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/20 | 1810/3750 | 1505/3120 | 502/1039 | chr11 | 376628 | |||
chr11:376914 | A | T | 1 | a0013 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.1791A>T | p.Gln597His | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/20 | 2096/3750 | 1791/3120 | 597/1039 | chr11 | 376914 | |||
chr11:377066 | A | C | 1 | a0014 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.1943A>C | p.Glu648Ala | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/20 | 2248/3750 | 1943/3120 | 648/1039 | chr11 | 377066 | |||
chr11:377086 | CCGGGCGA others(17): Show |
C | 1 | a0019 | 1 | HG03490.hp1 | disruptive_inframe_deletion | MODERATE | c.1964_1987delCGGGCG others(18): Show |
p.Pro655_Asp663delin others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/20 | 2269/3750 | 1964/3120 | 655/1039 | chr11 | 377086 | |||
chr11:377132 | C | G | 1 | a0013 | 1 | HG01978.hp2 | missense_variant | MODERATE | c.2009C>G | p.Pro670Arg | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/20 | 2314/3750 | 2009/3120 | 670/1039 | chr11 | 377132 | |||
chr11:379511 | C | CG | 5 | a0005 a0006 a0007 others(2): Show |
10 | HG00544.hp1 HG01255.hp1 HG01952.hp2 others(7): Show |
frameshift_variant | HIGH | c.2303dupG | p.Gly769fs | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 15/20 | 2609/3750 | 2304/3120 | 768/1039 | INFO_REALIGN_3_PRIME | chr11 | 379511 | ||
chr11:379599 | C | T | 1 | a0023 | 1 | NA19007.hp1 | missense_variant | MODERATE | c.2386C>T | p.Pro796Ser | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 15/20 | 2691/3750 | 2386/3120 | 796/1039 | chr11 | 379599 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:372700 | G | C | 16 | a0002c0002 a0002c0004 a0002c0008 others(13): Show |
70 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(67): Show |
synonymous_variant | LOW | c.294G>C | p.Gly98Gly | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 3/20 | 599/3750 | 294/3120 | 98/1039 | chr11 | 372700 | |||
chr11:373061 | C | T | 1 | a0004c0043 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.480C>T | p.Pro160Pro | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 5/20 | 785/3750 | 480/3120 | 160/1039 | chr11 | 373061 | |||
chr11:373079 | A | G | 1 | a0001c0026 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.498A>G | p.Gly166Gly | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 5/20 | 803/3750 | 498/3120 | 166/1039 | chr11 | 373079 | |||
chr11:373499 | G | A | 3 | a0016c0027 a0018c0029 a0025c0028 |
3 | HG03130.hp1 HG03486.hp2 NA19240.hp1 |
synonymous_variant | LOW | c.687G>A | p.Gln229Gln | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 7/20 | 992/3750 | 687/3120 | 229/1039 | chr11 | 373499 | |||
chr11:373759 | C | T | 1 | a0016c0027 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.714C>T | p.Ala238Ala | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/20 | 1019/3750 | 714/3120 | 238/1039 | chr11 | 373759 | |||
chr11:373804 | C | T | 1 | a0002c0037 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.759C>T | p.Arg253Arg | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/20 | 1064/3750 | 759/3120 | 253/1039 | chr11 | 373804 | |||
chr11:373810 | G | A | 1 | a0002c0033 | 1 | HG02040.hp2 | synonymous_variant | LOW | c.765G>A | p.Ser255Ser | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/20 | 1070/3750 | 765/3120 | 255/1039 | chr11 | 373810 | |||
chr11:375496 | C | T | 1 | a0001c0024 | 1 | HG00642.hp1 | synonymous_variant | LOW | c.819C>T | p.Val273Val | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 9/20 | 1124/3750 | 819/3120 | 273/1039 | chr11 | 375496 | |||
chr11:375700 | G | A | 1 | a0001c0016 | 1 | HG03834.hp1 | synonymous_variant | LOW | c.912G>A | p.Val304Val | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 10/20 | 1217/3750 | 912/3120 | 304/1039 | chr11 | 375700 | |||
chr11:376497 | C | G | 1 | a0013c0020 | 1 | HG01978.hp2 | synonymous_variant | LOW | c.1374C>G | p.Gly458Gly | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/20 | 1679/3750 | 1374/3120 | 458/1039 | chr11 | 376497 | |||
chr11:377139 | C | A | 4 | a0002c0004 a0004c0014 a0004c0043 others(1): Show |
10 | HG01243.hp1 HG01243.hp2 HG02258.hp1 others(7): Show |
synonymous_variant | LOW | c.2016C>A | p.Leu672Leu | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/20 | 2321/3750 | 2016/3120 | 672/1039 | chr11 | 377139 | |||
chr11:377139 | C | G | 1 | a0019c0018 | 1 | HG03490.hp1 | synonymous_variant | LOW | c.2016C>G | p.Leu672Leu | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/20 | 2321/3750 | 2016/3120 | 672/1039 | chr11 | 377139 | |||
chr11:379598 | A | G | 26 | a0001c0003 a0001c0024 a0002c0002 others(23): Show |
93 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(90): Show |
synonymous_variant | LOW | c.2385A>G | p.Glu795Glu | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 15/20 | 2690/3750 | 2385/3120 | 795/1039 | chr11 | 379598 | |||
chr11:380014 | G | C | 1 | a0022c0015 | 1 | NA19005.hp2 | synonymous_variant | LOW | c.2637G>C | p.Leu879Leu | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 16/20 | 2942/3750 | 2637/3120 | 879/1039 | chr11 | 380014 | |||
chr11:380315 | C | T | 2 | a0001c0005 a0011c0022 |
6 | HG00323.hp2 HG00738.hp1 HG01070.hp1 others(3): Show |
synonymous_variant | LOW | c.2739C>T | p.Leu913Leu | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 18/20 | 3044/3750 | 2739/3120 | 913/1039 | chr11 | 380315 | |||
chr11:380390 | C | T | 1 | a0002c0035 | 1 | HG02976.hp1 | synonymous_variant | LOW | c.2814C>T | p.Ala938Ala | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 18/20 | 3119/3750 | 2814/3120 | 938/1039 | chr11 | 380390 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:369514 | C | CTCCGCGG | 11 | a0001c0001t0002 a0001c0001t0004 a0001c0003t0002 others(8): Show |
24 | HG00323.hp2 HG01070.hp1 HG01074.hp2 others(21): Show |
5_prime_UTR_variant | MODIFIER | c.-290_-289insTCCGCG others(1): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/20 | 289 | chr11 | 369514 | ||||||
chr11:369725 | G | A | 1 | a0002c0002t0006 | 1 | HG01361.hp2 | 5_prime_UTR_variant | MODIFIER | c.-79G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/20 | 79 | chr11 | 369725 | ||||||
chr11:369796 | C | A | 12 | a0001c0001t0003 a0001c0001t0004 a0001c0003t0003 others(9): Show |
14 | HG00642.hp1 HG01106.hp2 HG01891.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-8C>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/20 | 8 | chr11 | 369796 | ||||||
chr11:381816 | C | T | 1 | a0001c0001t0005 | 3 | HG02559.hp2 HG02886.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*24C>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 20/20 | 24 | chr11 | 381816 | ||||||
chr11:381866 | C | T | 1 | a0001c0001t0007 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*74C>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 20/20 | 74 | chr11 | 381866 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:369967 | G | GGGCGCGG others(11): Show |
1 | a0002c0009t0001g0177 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.151+26_151+27insGG others(16): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 369967 | ||||||
chr11:369967 | G | GGGGCGCG others(12): Show |
1 | a0002c0002t0001g0178 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.151+15_151+16insGC others(17): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 369967 | ||||||
chr11:369967 | GGGCGCGG others(20): Show |
G | 6 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0010 others(3): Show |
6 | HG01258.hp2 HG01934.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.151+36_151+62delGG others(25): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 369967 | ||||||
chr11:369981 | C | CG | 6 | a0001c0001t0001g0094 a0001c0001t0001g0123 a0001c0003t0001g0097 others(3): Show |
6 | HG00735.hp2 HG01255.hp2 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.151+33dupG | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 369981 | ||||||
chr11:369990 | G | C | 2 | a0002c0002t0001g0178 a0002c0009t0001g0177 |
2 | HG00408.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.151+36G>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 369990 | |||||||
chr11:369990 | GGGGCGGC others(20): Show |
G | 1 | a0001c0003t0004g0050 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.151+58_151+84delGG others(25): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 369990 | ||||||
chr11:369994 | C | CGGCGCGG others(2): Show |
28 | a0001c0003t0001g0091 a0002c0002t0001g0054 a0002c0002t0001g0055 others(25): Show |
28 | HG00140.hp1 HG00733.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.151+58_151+66dupGG others(7): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 369994 | ||||||
chr11:369994 | C | CGGCGCGG others(74): Show |
1 | a0002c0002t0001g0072 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.151+66_151+67insGG others(79): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 369994 | ||||||
chr11:369994 | C | G | 2 | a0002c0002t0001g0178 a0002c0009t0001g0177 |
2 | HG00408.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.151+40C>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 369994 | |||||||
chr11:369999 | C | CGGGGGGC others(3): Show |
1 | a0003c0006t0001g0133 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.151+51_151+60dupGC others(8): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 369999 | ||||||
chr11:369999 | C | T | 6 | a0001c0003t0002g0024 a0001c0003t0002g0025 a0001c0003t0002g0026 others(3): Show |
6 | HG01074.hp2 HG01346.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.151+45C>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 369999 | |||||||
chr11:369999 | CG | C | 11 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0170 others(8): Show |
11 | HG00323.hp1 HG00438.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.151+51delG | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 369999 | ||||||
chr11:370003 | G | C | 2 | a0002c0002t0001g0178 a0002c0009t0001g0177 |
2 | HG00408.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.151+49G>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 370003 | |||||||
chr11:370003 | G | GGGCGCGG others(11): Show |
3 | a0001c0001t0001g0138 a0002c0002t0001g0137 a0019c0018t0001g0139 |
3 | HG03490.hp1 HG03492.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.151+76_151+93dupGG others(16): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 370003 | ||||||
chr11:370003 | G | GGGCGCGG others(29): Show |
4 | a0002c0002t0001g0140 a0002c0002t0001g0141 a0002c0002t0001g0142 others(1): Show |
4 | HG00140.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.151+58_151+93dupGG others(34): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 370003 | ||||||
chr11:370003 | G | GGGCGCGG others(20): Show |
18 | a0002c0002t0001g0145 a0002c0002t0001g0146 a0002c0002t0001g0149 others(15): Show |
18 | HG00099.hp2 HG00544.hp1 HG01978.hp1 others(15): Show |
intron_variant | MODIFIER | c.151+66_151+67insGG others(25): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 370003 | ||||||
chr11:370003 | G | GGGCGCGG others(39): Show |
1 | a0002c0002t0001g0162 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.151+66_151+67insGG others(44): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 370003 | ||||||
chr11:370003 | G | GGGCGCGG others(137): Show |
1 | a0002c0002t0001g0163 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.151+66_151+67insGG others(142): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 370003 | ||||||
chr11:370003 | GGGCGCGG others(11): Show |
G | 9 | a0001c0003t0002g0024 a0001c0003t0002g0025 a0001c0003t0002g0026 others(6): Show |
9 | HG01074.hp2 HG01243.hp2 HG01346.hp2 others(6): Show |
intron_variant | MODIFIER | c.151+76_151+93delGG others(16): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 370003 | ||||||
chr11:370004 | G | C | 1 | a0002c0009t0001g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.151+50G>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 370004 | |||||||
chr11:370004 | GGCGCGGG others(10): Show |
G | 1 | a0001c0003t0002g0164 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.151+52_151+68delCG others(15): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 370004 | ||||||
chr11:370005 | G | T | 12 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0001c0001t0001g0170 others(9): Show |
12 | HG00323.hp1 HG00438.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.151+51G>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 370005 | |||||||
chr11:370012 | G | C | 1 | a0001c0003t0004g0014 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.151+58G>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 370012 | |||||||
chr11:370012 | G | GGGCGCGG others(2): Show |
9 | a0001c0001t0003g0019 a0001c0001t0004g0016 a0001c0003t0003g0018 others(6): Show |
9 | HG00642.hp1 HG01106.hp2 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.151+67_151+75dupCG others(7): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 370012 | ||||||
chr11:370026 | C | CGGGGGGC others(30): Show |
1 | a0002c0002t0006g0076 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.151+93_151+94insGG others(35): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 370026 | ||||||
chr11:370039 | C | G | 5 | a0001c0003t0002g0024 a0001c0003t0002g0025 a0001c0003t0002g0026 others(2): Show |
5 | HG01074.hp2 HG01346.hp2 HG02273.hp2 others(2): Show |
intron_variant | MODIFIER | c.151+85C>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 370039 | |||||||
chr11:370052 | G | GCGGGCGG others(2): Show |
14 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(11): Show |
14 | HG00408.hp2 HG00544.hp2 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.151+98_151+99insCG others(7): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 370052 | |||||||
chr11:370052 | G | T | 2 | a0001c0001t0001g0135 a0001c0003t0001g0136 |
2 | HG03239.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.151+98G>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 370052 | |||||||
chr11:370252 | T | C | 6 | a0001c0003t0002g0024 a0001c0003t0002g0025 a0001c0003t0002g0026 others(3): Show |
6 | HG01074.hp2 HG01346.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.151+298T>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 370252 | |||||||
chr11:370258 | C | A | 1 | a0001c0001t0001g0048 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.151+304C>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 370258 | |||||||
chr11:370303 | C | T | 6 | a0001c0003t0002g0024 a0001c0003t0002g0025 a0001c0003t0002g0026 others(3): Show |
6 | HG01074.hp2 HG01346.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.151+349C>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 370303 | |||||||
chr11:370331 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.151+377C>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 370331 | |||||||
chr11:370426 | G | GT | 2 | a0002c0004t0001g0176 a0003c0006t0001g0133 |
2 | HG01243.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.151+473dupT | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 370426 | ||||||
chr11:370475 | G | C | 1 | a0016c0027t0001g0015 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.151+521G>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 370475 | |||||||
chr11:370653 | A | AGGCGCAG others(34): Show |
1 | a0001c0003t0003g0018 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.151+702_151+742dup others(41): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 370653 | ||||||
chr11:370682 | T | G | 12 | a0001c0001t0004g0016 a0001c0003t0004g0017 a0001c0003t0004g0050 others(9): Show |
12 | HG01891.hp1 HG02559.hp1 HG02683.hp2 others(9): Show |
intron_variant | MODIFIER | c.151+728T>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 370682 | |||||||
chr11:370694 | T | C | 12 | a0001c0001t0004g0016 a0001c0003t0004g0017 a0001c0003t0004g0050 others(9): Show |
12 | HG01891.hp1 HG02559.hp1 HG02683.hp2 others(9): Show |
intron_variant | MODIFIER | c.151+740T>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 370694 | |||||||
chr11:370698 | G | GCAGAATG others(4): Show |
1 | a0004c0044t0001g0032 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.151+746_151+756dup others(11): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 370698 | ||||||
chr11:370704 | T | C | 19 | a0001c0001t0003g0019 a0001c0001t0004g0016 a0001c0003t0003g0018 others(16): Show |
19 | HG00642.hp1 HG01106.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.151+750T>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 370704 | |||||||
chr11:370709 | C | A | 19 | a0001c0001t0003g0019 a0001c0001t0004g0016 a0001c0003t0003g0018 others(16): Show |
19 | HG00642.hp1 HG01106.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.151+755C>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 370709 | |||||||
chr11:370831 | T | C | 92 | a0001c0001t0003g0019 a0001c0001t0004g0016 a0001c0003t0002g0024 others(89): Show |
93 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.151+877T>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 370831 | |||||||
chr11:370876 | A | G | 6 | a0001c0003t0002g0024 a0001c0003t0002g0025 a0001c0003t0002g0026 others(3): Show |
6 | HG01074.hp2 HG01346.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.151+922A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 370876 | |||||||
chr11:370884 | G | A | 1 | a0002c0002t0001g0054 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.151+930G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 370884 | |||||||
chr11:371047 | A | G | 66 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0010 others(63): Show |
67 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.152-1062A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 371047 | |||||||
chr11:371059 | C | T | 9 | a0004c0014t0002g0029 a0004c0014t0002g0051 a0004c0042t0001g0031 others(6): Show |
9 | HG01243.hp2 HG02559.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.152-1050C>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 371059 | |||||||
chr11:371114 | GAGGGGGC others(8): Show |
G | 1 | a0002c0002t0001g0055 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.152-990_152-976del others(15): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 371114 | ||||||
chr11:371251 | G | A | 20 | a0001c0001t0003g0019 a0001c0001t0004g0016 a0001c0003t0003g0018 others(17): Show |
20 | HG00642.hp1 HG01106.hp2 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.152-858G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 371251 | |||||||
chr11:371265 | C | A | 6 | a0001c0003t0002g0024 a0001c0003t0002g0025 a0001c0003t0002g0026 others(3): Show |
6 | HG01074.hp2 HG01346.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-844C>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 371265 | |||||||
chr11:371275 | G | A | 1 | a0007c0011t0001g0158 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.152-834G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 371275 | |||||||
chr11:371325 | C | G | 6 | a0001c0003t0002g0024 a0001c0003t0002g0025 a0001c0003t0002g0026 others(3): Show |
6 | HG01074.hp2 HG01346.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-784C>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 371325 | |||||||
chr11:371412 | A | G | 1 | a0002c0002t0001g0161 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.152-697A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 371412 | |||||||
chr11:371494 | C | T | 6 | a0001c0003t0002g0024 a0001c0003t0002g0025 a0001c0003t0002g0026 others(3): Show |
6 | HG01074.hp2 HG01346.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-615C>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 371494 | |||||||
chr11:371514 | T | C | 6 | a0001c0003t0002g0024 a0001c0003t0002g0025 a0001c0003t0002g0026 others(3): Show |
6 | HG01074.hp2 HG01346.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.152-595T>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 371514 | |||||||
chr11:371617 | C | CTCAAATC others(5): Show |
1 | a0009c0012t0003g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.152-491_152-480dup others(12): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 371617 | ||||||
chr11:371706 | C | T | 2 | a0001c0003t0004g0017 a0001c0003t0004g0050 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.152-403C>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 371706 | |||||||
chr11:371882 | CTGGGCTG others(12): Show |
C | 1 | a0002c0002t0001g0160 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.152-222_152-204del others(19): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr11 | 371882 | ||||||
chr11:371924 | T | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0087 a0001c0001t0001g0088 others(97): Show |
102 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.152-185T>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 371924 | |||||||
chr11:371961 | A | T | 78 | a0001c0026t0002g0049 a0002c0002t0001g0008 a0002c0002t0001g0009 others(75): Show |
79 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.152-148A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 371961 | |||||||
chr11:372081 | C | A | 1 | a0001c0026t0002g0049 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.152-28C>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 372081 | |||||||
chr11:372095 | T | C | 9 | a0001c0001t0001g0002 a0001c0001t0001g0087 a0001c0003t0002g0024 others(6): Show |
10 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.152-14T>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 1/19 | chr11 | 372095 | |||||||
chr11:372225 | C | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0087 a0001c0003t0002g0024 others(6): Show |
10 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.255+13C>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 2/19 | chr11 | 372225 | |||||||
chr11:372437 | G | A | 2 | a0004c0014t0002g0051 a0004c0043t0001g0028 |
2 | HG03195.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.255+225G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 2/19 | chr11 | 372437 | |||||||
chr11:372456 | C | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0087 a0001c0003t0002g0024 others(6): Show |
10 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.256-206C>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 2/19 | chr11 | 372456 | |||||||
chr11:372457 | A | G | 97 | a0001c0001t0001g0002 a0001c0001t0001g0087 a0001c0001t0003g0019 others(94): Show |
99 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.256-205A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 2/19 | chr11 | 372457 | |||||||
chr11:372542 | C | CGGGCATT others(20): Show |
1 | a0001c0003t0001g0091 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.256-119_256-93dupG others(26): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 2/19 | INFO_REALIGN_3_PRIME | chr11 | 372542 | ||||||
chr11:372589 | A | C | 2 | a0002c0004t0002g0084 a0002c0004t0002g0085 |
2 | HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.256-73A>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 2/19 | chr11 | 372589 | |||||||
chr11:372767 | G | A | 1 | a0001c0001t0001g0099 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.348+13G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 3/19 | chr11 | 372767 | |||||||
chr11:372784 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0092 a0001c0001t0001g0093 others(1): Show |
5 | HG00735.hp2 HG01081.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.348+30G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 3/19 | chr11 | 372784 | |||||||
chr11:372794 | G | A | 2 | a0018c0029t0004g0053 a0025c0028t0001g0052 |
2 | HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.348+40G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 3/19 | chr11 | 372794 | |||||||
chr11:372805 | C | CG | 31 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(28): Show |
31 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.349-40dupG | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr11 | 372805 | ||||||
chr11:372806 | G | C | 2 | a0001c0003t0004g0017 a0001c0003t0004g0050 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.349-46G>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 3/19 | chr11 | 372806 | |||||||
chr11:372962 | T | TG | 6 | a0001c0001t0001g0095 a0001c0003t0001g0129 a0002c0002t0001g0145 others(3): Show |
6 | HG00735.hp1 HG01255.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.444+21dupG | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr11 | 372962 | ||||||
chr11:373137 | C | T | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0173 |
3 | HG02965.hp1 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.535+21C>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 5/19 | chr11 | 373137 | |||||||
chr11:373287 | G | GCAAGGTA others(8): Show |
1 | a0026c0025t0003g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.634_636+12dupAAGGT others(10): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr11 | 373287 | ||||||
chr11:373310 | T | TGGTGTCG others(5): Show |
1 | a0011c0022t0001g0126 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.636+22_636+33dupTG others(10): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr11 | 373310 | ||||||
chr11:373317 | G | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0087 a0001c0003t0002g0024 others(6): Show |
10 | HG00639.hp1 HG00639.hp2 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.636+26G>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 6/19 | chr11 | 373317 | |||||||
chr11:373396 | G | T | 1 | a0013c0020t0001g0046 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.637-53G>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 6/19 | chr11 | 373396 | |||||||
chr11:373404 | G | A | 81 | a0001c0001t0001g0088 a0001c0001t0003g0019 a0001c0003t0001g0097 others(78): Show |
82 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.637-45G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 6/19 | chr11 | 373404 | |||||||
chr11:373408 | AC | A | 82 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(79): Show |
86 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.637-30delC | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr11 | 373408 | ||||||
chr11:373409 | C | A | 1 | a0006c0007t0001g0041 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.637-40C>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 6/19 | chr11 | 373409 | |||||||
chr11:373413 | C | G | 1 | a0002c0008t0001g0144 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.637-36C>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 6/19 | chr11 | 373413 | |||||||
chr11:373416 | C | G | 1 | a0001c0001t0001g0048 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.637-33C>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 6/19 | chr11 | 373416 | |||||||
chr11:373419 | C | CCCCGCCA | 22 | a0001c0001t0003g0019 a0002c0002t0001g0055 a0002c0002t0001g0061 others(19): Show |
22 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(19): Show |
intron_variant | MODIFIER | c.637-30_637-29insCC others(5): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 6/19 | chr11 | 373419 | |||||||
chr11:373419 | C | CCCGCCA | 45 | a0001c0003t0001g0097 a0001c0003t0003g0018 a0001c0003t0004g0014 others(42): Show |
46 | HG00099.hp2 HG00140.hp1 HG00733.hp1 others(43): Show |
intron_variant | MODIFIER | c.637-30_637-29insCC others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 6/19 | chr11 | 373419 | |||||||
chr11:373427 | C | T | 79 | a0001c0001t0001g0088 a0001c0001t0003g0019 a0001c0003t0001g0097 others(76): Show |
80 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.637-22C>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 6/19 | chr11 | 373427 | |||||||
chr11:373437 | A | G | 1 | a0001c0003t0001g0129 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.637-12A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 6/19 | chr11 | 373437 | |||||||
chr11:373542 | G | A | 2 | a0018c0029t0004g0053 a0025c0028t0001g0052 |
2 | HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.704+26G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 7/19 | chr11 | 373542 | |||||||
chr11:373616 | GAGCACCC others(9): Show |
G | 1 | a0003c0006t0001g0077 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.704+104_705-115del others(16): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 7/19 | INFO_REALIGN_3_PRIME | chr11 | 373616 | ||||||
chr11:373661 | G | A | 3 | a0016c0027t0001g0015 a0018c0029t0004g0053 a0025c0028t0001g0052 |
3 | HG03130.hp1 HG03486.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.705-89G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 7/19 | chr11 | 373661 | |||||||
chr11:373664 | G | A | 2 | a0002c0004t0001g0001 a0004c0043t0001g0028 |
3 | HG02258.hp1 HG02258.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.705-86G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 7/19 | chr11 | 373664 | |||||||
chr11:373740 | G | A | 2 | a0002c0004t0002g0085 a0004c0014t0002g0051 |
2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.705-10G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 7/19 | chr11 | 373740 | |||||||
chr11:373905 | C | A | 5 | a0002c0004t0001g0056 a0002c0004t0001g0176 a0002c0004t0002g0084 others(2): Show |
5 | HG01243.hp1 HG03486.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.783+77C>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 373905 | |||||||
chr11:373943 | T | C | 1 | a0016c0027t0001g0015 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.783+115T>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 373943 | |||||||
chr11:373984 | G | A | 2 | a0002c0004t0001g0056 a0002c0004t0001g0176 |
2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.783+156G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 373984 | |||||||
chr11:374024 | CT | C | 2 | a0002c0002t0001g0061 a0002c0002t0001g0157 |
2 | HG01978.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.783+198delT | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374024 | ||||||
chr11:374055 | T | C | 1 | a0014c0030t0004g0011 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.783+227T>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374055 | |||||||
chr11:374142 | C | A | 1 | a0001c0001t0001g0042 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.783+314C>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374142 | |||||||
chr11:374220 | GTCCTGAG others(15): Show |
G | 1 | a0013c0020t0001g0046 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.783+394_783+415del others(22): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374220 | ||||||
chr11:374262 | C | A | 1 | a0002c0008t0001g0081 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.783+434C>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374262 | |||||||
chr11:374288 | TG | T | 5 | a0001c0001t0001g0043 a0002c0002t0001g0140 a0002c0004t0002g0085 others(2): Show |
5 | HG00738.hp1 HG01070.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.783+465delG | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374288 | ||||||
chr11:374297 | G | A | 1 | a0013c0020t0001g0046 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.783+469G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374297 | |||||||
chr11:374298 | A | T | 1 | a0013c0020t0001g0046 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.783+470A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374298 | |||||||
chr11:374358 | A | G | 1 | a0011c0022t0001g0126 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.783+530A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374358 | |||||||
chr11:374370 | G | T | 1 | a0002c0004t0002g0085 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.783+542G>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374370 | |||||||
chr11:374404 | G | T | 1 | a0013c0020t0001g0046 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.783+576G>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374404 | |||||||
chr11:374405 | G | GT | 2 | a0002c0002t0001g0162 a0006c0007t0001g0041 |
2 | HG01255.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.783+577_783+578ins others(1): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374405 | |||||||
chr11:374409 | T | G | 2 | a0002c0002t0001g0162 a0006c0007t0001g0041 |
2 | HG01255.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.783+581T>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374409 | |||||||
chr11:374409 | T | TG | 9 | a0001c0001t0001g0094 a0001c0003t0004g0050 a0002c0002t0001g0075 others(6): Show |
9 | HG00735.hp2 HG01361.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.783+587dupG | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374409 | ||||||
chr11:374409 | T | TGGGGGGC others(8): Show |
1 | a0002c0002t0001g0160 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.783+594_783+595ins others(15): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374409 | ||||||
chr11:374579 | T | TG | 8 | a0001c0001t0001g0138 a0001c0003t0001g0091 a0001c0003t0004g0017 others(5): Show |
8 | HG01255.hp2 HG01993.hp2 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.783+756dupG | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374579 | ||||||
chr11:374648 | T | G | 1 | a0019c0018t0001g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.784-813T>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374648 | |||||||
chr11:374650 | G | T | 1 | a0019c0018t0001g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.784-811G>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374650 | |||||||
chr11:374669 | G | A | 3 | a0001c0001t0001g0004 a0001c0001t0002g0130 a0003c0036t0001g0079 |
4 | HG00733.hp2 HG01081.hp2 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.784-792G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374669 | |||||||
chr11:374673 | C | CG | 9 | a0001c0003t0001g0129 a0002c0002t0001g0055 a0002c0002t0001g0060 others(6): Show |
9 | HG01255.hp2 HG02559.hp1 HG03486.hp2 others(6): Show |
intron_variant | MODIFIER | c.784-781dupG | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374673 | ||||||
chr11:374678 | G | T | 1 | a0001c0003t0004g0014 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.784-783G>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374678 | |||||||
chr11:374684 | C | CAGGAGGG others(140): Show |
1 | a0021c0019t0001g0033 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.784-774_784-773ins others(147): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374684 | ||||||
chr11:374684 | C | CAGGGAGG others(156): Show |
1 | a0002c0004t0002g0084 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.784-766_784-765ins others(163): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374684 | ||||||
chr11:374684 | C | CAGGGAGG others(188): Show |
1 | a0002c0004t0002g0085 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.784-766_784-765ins others(195): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374684 | ||||||
chr11:374684 | C | CAGGGAGG others(643): Show |
1 | a0001c0003t0004g0014 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.784-766_784-765ins others(650): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374684 | ||||||
chr11:374684 | CAGGG | C | 22 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0043 others(19): Show |
22 | HG00438.hp2 HG00642.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.784-764_784-761del others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374684 | ||||||
chr11:374684 | CAGGGAGG others(12): Show |
C | 1 | a0002c0002t0001g0151 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.784-764_784-746del others(19): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374684 | ||||||
chr11:374684 | CAGGGAGG others(374): Show |
C | 1 | a0001c0001t0001g0100 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.784-765_784-385del | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374684 | ||||||
chr11:374688 | G | A | 1 | a0021c0019t0001g0033 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.784-773G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374688 | |||||||
chr11:374688 | G | GAGGGAGG others(4): Show |
9 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0167 others(6): Show |
10 | HG02258.hp1 HG02258.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.784-766_784-765ins others(11): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374688 | ||||||
chr11:374688 | G | GAGGGAGG others(190): Show |
1 | a0004c0014t0002g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.784-766_784-765ins others(197): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374688 | ||||||
chr11:374688 | G | GAGGGAGG others(34): Show |
3 | a0001c0001t0001g0044 a0003c0039t0001g0058 a0008c0013t0001g0057 |
3 | HG00408.hp2 HG01433.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.784-766_784-765ins others(41): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374688 | ||||||
chr11:374688 | G | GAGGGAGG others(307): Show |
1 | a0005c0010t0001g0174 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.784-766_784-765ins others(314): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374688 | ||||||
chr11:374688 | G | GAGGGAGG others(49): Show |
1 | a0001c0003t0001g0129 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.784-766_784-765ins others(56): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374688 | ||||||
chr11:374688 | G | GAGGGAGG others(79): Show |
1 | a0002c0009t0001g0168 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.784-766_784-765ins others(86): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374688 | ||||||
chr11:374688 | G | GAGGGAGG others(349): Show |
1 | a0001c0003t0002g0027 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.784-766_784-765ins others(356): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374688 | ||||||
chr11:374688 | G | GAGGGAGG others(304): Show |
1 | a0005c0010t0001g0037 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.784-766_784-765ins others(311): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374688 | ||||||
chr11:374688 | G | GAGGGAGG others(214): Show |
1 | a0001c0001t0001g0039 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.784-766_784-765ins others(221): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374688 | ||||||
chr11:374688 | G | GAGGGAGG others(229): Show |
1 | a0001c0001t0001g0042 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.784-766_784-765ins others(236): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374688 | ||||||
chr11:374688 | G | GAGGGAGG others(113): Show |
1 | a0001c0001t0001g0101 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.784-766_784-765ins others(120): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374688 | ||||||
chr11:374688 | G | GAGGGAGG others(64): Show |
1 | a0001c0001t0001g0102 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.784-766_784-765ins others(71): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374688 | ||||||
chr11:374688 | G | GAGGGAGG others(19): Show |
1 | a0009c0012t0001g0103 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.784-766_784-765ins others(26): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374688 | ||||||
chr11:374688 | G | GAGGGAGG others(656): Show |
1 | a0025c0028t0001g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.784-766_784-765ins others(663): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374688 | ||||||
chr11:374688 | G | GAGGGGAG others(165): Show |
1 | a0006c0007t0001g0041 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.784-769_784-768ins others(172): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374688 | ||||||
chr11:374688 | G | GGAGGGAG others(186): Show |
1 | a0013c0020t0001g0046 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.784-773_784-772ins others(193): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374688 | |||||||
chr11:374689 | A | AGGGAGGA others(210): Show |
1 | a0010c0017t0001g0086 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.784-766_784-765ins others(217): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374689 | ||||||
chr11:374690 | G | GGGAGGAG others(3): Show |
1 | a0002c0004t0001g0176 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.784-766_784-765ins others(10): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374690 | ||||||
chr11:374700 | G | A | 45 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(42): Show |
45 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.784-761G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374700 | |||||||
chr11:374700 | G | GA | 2 | a0003c0039t0001g0058 a0008c0013t0001g0057 |
2 | HG01433.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.784-761_784-760ins others(1): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374700 | |||||||
chr11:374700 | G | GGAGGGAG others(365): Show |
1 | a0011c0022t0001g0126 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.784-760_784-759ins others(372): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374700 | ||||||
chr11:374700 | G | GGGAAGGG others(23): Show |
27 | a0001c0003t0001g0136 a0002c0002t0001g0008 a0002c0002t0001g0009 others(24): Show |
27 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(24): Show |
intron_variant | MODIFIER | c.784-747_784-746ins others(30): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374700 | ||||||
chr11:374700 | G | GGGAAGGG others(211): Show |
1 | a0002c0002t0001g0137 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.784-747_784-746ins others(218): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374700 | ||||||
chr11:374700 | G | GGGAAGGG others(443): Show |
1 | a0002c0008t0001g0144 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.784-747_784-746ins others(450): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374700 | ||||||
chr11:374700 | G | GGGAAGGG others(24): Show |
1 | a0002c0002t0001g0157 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.784-747_784-746ins others(31): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374700 | ||||||
chr11:374700 | G | T | 2 | a0001c0003t0001g0129 a0001c0003t0002g0027 |
2 | HG03831.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.784-761G>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374700 | |||||||
chr11:374701 | G | A | 1 | a0004c0014t0002g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.784-760G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374701 | |||||||
chr11:374703 | A | G | 1 | a0004c0014t0002g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.784-758A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374703 | |||||||
chr11:374707 | G | A | 2 | a0004c0014t0002g0029 a0009c0012t0003g0023 |
2 | HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.784-754G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374707 | |||||||
chr11:374708 | A | G | 1 | a0009c0012t0003g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.784-753A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374708 | |||||||
chr11:374712 | A | AGGAGGAA others(4): Show |
1 | a0005c0010t0001g0174 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.784-747_784-746ins others(11): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374712 | ||||||
chr11:374715 | G | A | 90 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(87): Show |
91 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.784-746G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374715 | |||||||
chr11:374715 | G | GGGAAGGG others(259): Show |
1 | a0002c0002t0001g0061 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.784-736_784-735ins others(266): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374715 | ||||||
chr11:374715 | G | GGGAAGGG others(117): Show |
2 | a0001c0005t0002g0116 a0001c0005t0002g0117 |
2 | HG01952.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.784-672_784-671ins others(124): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374715 | ||||||
chr11:374715 | G | GGGAAGGG others(316): Show |
1 | a0001c0001t0001g0118 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.784-672_784-671ins others(323): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374715 | ||||||
chr11:374715 | G | GGGAAGGG others(470): Show |
1 | a0001c0001t0001g0119 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.784-672_784-671ins others(477): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374715 | ||||||
chr11:374715 | G | GGGAAGGG others(117): Show |
1 | a0001c0001t0001g0120 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.784-672_784-671ins others(124): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374715 | ||||||
chr11:374715 | G | GGGAAGGG others(166): Show |
1 | a0001c0001t0001g0121 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.784-687_784-686ins others(173): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374715 | ||||||
chr11:374715 | G | GGGAAGGG others(349): Show |
1 | a0001c0001t0001g0095 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.784-724_784-723ins others(356): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374715 | ||||||
chr11:374715 | G | T | 4 | a0001c0001t0001g0044 a0002c0009t0001g0168 a0010c0017t0001g0086 others(1): Show |
4 | HG00408.hp2 HG00639.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-746G>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374715 | |||||||
chr11:374718 | A | AAGGGAGG others(42): Show |
2 | a0001c0003t0001g0097 a0024c0021t0001g0096 |
2 | HG02080.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.784-717_784-716ins others(49): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374718 | ||||||
chr11:374727 | A | AGGAGGAA others(9): Show |
1 | a0001c0003t0001g0106 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.784-732_784-717dup others(16): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374727 | ||||||
chr11:374730 | A | AGGAAGGG others(360): Show |
1 | a0017c0031t0004g0012 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.784-642_784-641ins others(367): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374730 | ||||||
chr11:374730 | A | AGGAAGGG others(522): Show |
1 | a0002c0002t0001g0074 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.784-657_784-656ins others(529): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374730 | ||||||
chr11:374730 | A | AGGAAGGG others(339): Show |
1 | a0007c0011t0001g0068 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.784-702_784-701ins others(346): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374730 | ||||||
chr11:374730 | A | G | 1 | a0002c0004t0001g0001 | 2 | HG02258.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.784-731A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374730 | |||||||
chr11:374733 | A | AAGGGAGG others(420): Show |
1 | a0002c0002t0001g0145 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.784-687_784-686ins others(427): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374733 | ||||||
chr11:374733 | A | AAGGGAGG others(8): Show |
1 | a0006c0007t0001g0175 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.784-714_784-713ins others(15): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374733 | ||||||
chr11:374733 | A | AAGGGAGG others(31): Show |
1 | a0001c0001t0001g0124 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.784-717_784-716ins others(38): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374733 | ||||||
chr11:374745 | A | AGGAAGGG others(233): Show |
1 | a0001c0001t0001g0099 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.784-612_784-611ins others(240): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374745 | ||||||
chr11:374745 | A | AGGAAGGG others(72): Show |
1 | a0001c0005t0002g0108 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.784-672_784-671ins others(79): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374745 | ||||||
chr11:374745 | A | AGGAAGGG others(375): Show |
1 | a0002c0002t0001g0066 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.784-702_784-701ins others(382): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374745 | ||||||
chr11:374745 | A | AGGAAGGG others(8): Show |
1 | a0022c0015t0001g0040 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.784-702_784-701ins others(15): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374745 | ||||||
chr11:374745 | A | G | 16 | a0001c0001t0001g0105 a0001c0001t0001g0134 a0001c0001t0001g0135 others(13): Show |
16 | HG00733.hp1 HG01975.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.784-716A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374745 | |||||||
chr11:374745 | A | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0038 |
2 | NA19002.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.784-716A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374745 | |||||||
chr11:374748 | A | AAGGGAGG others(12): Show |
1 | a0002c0002t0001g0146 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.784-705_784-687dup others(19): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374748 | ||||||
chr11:374748 | A | AAGGGAGG others(182): Show |
1 | a0001c0001t0001g0035 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.784-612_784-611ins others(189): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374748 | ||||||
chr11:374748 | A | AAGGGAGG others(240): Show |
1 | a0002c0002t0003g0153 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.784-687_784-686ins others(247): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374748 | ||||||
chr11:374748 | A | AAGGGAGG others(195): Show |
1 | a0002c0002t0001g0073 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.784-687_784-686ins others(202): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374748 | ||||||
chr11:374748 | A | AAGGGAGG others(564): Show |
1 | a0002c0002t0001g0062 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.784-702_784-701ins others(571): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374748 | ||||||
chr11:374752 | G | A | 1 | a0019c0018t0001g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.784-709G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374752 | |||||||
chr11:374757 | A | AGGAGGAA others(5): Show |
1 | a0004c0043t0001g0028 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.784-697_784-686dup others(12): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374757 | ||||||
chr11:374760 | A | AGGAAGGG others(687): Show |
1 | a0001c0024t0003g0022 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.784-657_784-656ins others(694): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374760 | ||||||
chr11:374760 | A | AGGAAGGG others(23): Show |
1 | a0002c0008t0001g0081 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.784-687_784-686ins others(30): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374760 | ||||||
chr11:374760 | A | G | 4 | a0002c0002t0001g0069 a0002c0002t0001g0075 a0002c0004t0001g0001 others(1): Show |
5 | HG02258.hp1 HG02258.hp2 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-701A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374760 | |||||||
chr11:374760 | A | T | 5 | a0001c0001t0001g0123 a0001c0001t0003g0019 a0001c0003t0002g0027 others(2): Show |
5 | HG02040.hp2 HG03453.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-701A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374760 | |||||||
chr11:374761 | G | T | 1 | a0001c0003t0004g0050 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.784-700G>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374761 | |||||||
chr11:374763 | A | AAGGG | 14 | a0001c0001t0001g0048 a0001c0001t0001g0094 a0001c0003t0001g0136 others(11): Show |
14 | HG00099.hp2 HG00140.hp1 HG00735.hp2 others(11): Show |
intron_variant | MODIFIER | c.784-690_784-687dup others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374763 | ||||||
chr11:374763 | A | AAGGGAGG others(31): Show |
1 | a0001c0001t0001g0135 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.784-672_784-671ins others(38): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374763 | ||||||
chr11:374763 | A | AAGGGAGG others(749): Show |
1 | a0002c0002t0001g0008 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.784-687_784-686ins others(756): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374763 | ||||||
chr11:374763 | A | AAGGGAGG others(692): Show |
1 | a0002c0002t0001g0009 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.784-687_784-686ins others(699): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374763 | ||||||
chr11:374763 | A | AAGGGAGG others(550): Show |
1 | a0002c0002t0001g0178 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.784-687_784-686ins others(557): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374763 | ||||||
chr11:374763 | A | AAGGGAGG others(180): Show |
2 | a0002c0002t0001g0067 a0002c0002t0001g0080 |
2 | HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.784-687_784-686ins others(187): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374763 | ||||||
chr11:374763 | A | G | 2 | a0002c0002t0001g0010 a0004c0042t0001g0031 |
2 | HG01993.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.784-698A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374763 | |||||||
chr11:374767 | GAGGGAGG others(34): Show |
G | 1 | a0006c0007t0001g0122 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.784-686_784-646del others(41): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374767 | ||||||
chr11:374772 | A | AGGGAGGA others(137): Show |
1 | a0002c0035t0001g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.784-687_784-686ins others(144): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374772 | ||||||
chr11:374772 | A | AGGGAGGA others(165): Show |
1 | a0002c0002t0001g0072 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.784-687_784-686ins others(172): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374772 | ||||||
chr11:374774 | G | GGAGGAGG others(31): Show |
1 | a0002c0002t0006g0076 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.784-687_784-686ins others(38): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374774 | |||||||
chr11:374774 | G | GGAGGAGG others(20): Show |
1 | a0002c0002t0001g0055 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.784-687_784-686ins others(27): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374774 | |||||||
chr11:374775 | A | AGGAAGGG others(28): Show |
1 | a0016c0027t0001g0015 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.784-672_784-671ins others(35): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374775 | ||||||
chr11:374775 | A | AGGAAGGG others(42): Show |
2 | a0001c0005t0002g0107 a0001c0005t0002g0131 |
2 | HG00323.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.784-672_784-671ins others(49): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374775 | ||||||
chr11:374775 | A | G | 2 | a0001c0003t0001g0097 a0024c0021t0001g0096 |
2 | HG02080.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.784-686A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374775 | |||||||
chr11:374775 | A | T | 4 | a0001c0001t0001g0128 a0001c0001t0001g0167 a0003c0006t0001g0077 others(1): Show |
4 | HG00639.hp2 HG03098.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.784-686A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374775 | |||||||
chr11:374778 | A | AAGGG | 12 | a0001c0001t0001g0093 a0001c0001t0001g0112 a0001c0001t0001g0124 others(9): Show |
12 | HG00140.hp2 HG01074.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.784-675_784-672dup others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374778 | ||||||
chr11:374778 | A | AAGGGAGG others(31): Show |
1 | a0001c0003t0001g0091 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.784-657_784-656ins others(38): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374778 | ||||||
chr11:374778 | A | AAGGGAGG others(686): Show |
1 | a0001c0001t0001g0123 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.784-657_784-656ins others(693): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374778 | ||||||
chr11:374778 | A | AAGGGAGG others(27): Show |
1 | a0001c0001t0001g0044 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.784-705_784-672dup others(34): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374778 | ||||||
chr11:374778 | A | AAGGGAGG others(316): Show |
1 | a0001c0001t0001g0170 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.784-672_784-671ins others(323): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374778 | ||||||
chr11:374778 | A | AAGGGAGG others(47): Show |
1 | a0001c0001t0001g0098 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.784-672_784-671ins others(54): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374778 | ||||||
chr11:374778 | A | AAGGGAGG others(151): Show |
1 | a0009c0012t0003g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.784-672_784-671ins others(158): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374778 | ||||||
chr11:374778 | A | AAGGGAGG others(278): Show |
1 | a0004c0014t0002g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.784-672_784-671ins others(285): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374778 | ||||||
chr11:374778 | A | G | 3 | a0002c0002t0001g0055 a0002c0002t0006g0076 a0003c0006t0001g0078 |
3 | HG01361.hp2 HG03453.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.784-683A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374778 | |||||||
chr11:374779 | A | AGGGAGGG others(535): Show |
1 | a0001c0003t0004g0017 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.784-646_784-645ins others(542): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374779 | ||||||
chr11:374779 | A | AGTGGAGG others(375): Show |
1 | a0001c0003t0004g0050 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.784-681_784-680ins others(382): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374779 | ||||||
chr11:374787 | A | AGGGAGGA others(59): Show |
1 | a0003c0006t0001g0133 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.784-672_784-671ins others(66): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374787 | ||||||
chr11:374789 | G | A | 1 | a0019c0018t0001g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.784-672G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374789 | |||||||
chr11:374789 | G | GGAGGAGG others(31): Show |
1 | a0003c0006t0001g0154 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.784-672_784-671ins others(38): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374789 | |||||||
chr11:374789 | G | GGGGAAGG others(42): Show |
1 | a0002c0037t0001g0156 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.784-672_784-671ins others(49): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374789 | |||||||
chr11:374790 | A | AGGAAGGG others(8): Show |
1 | a0003c0036t0001g0079 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.784-657_784-656ins others(15): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374790 | ||||||
chr11:374790 | A | T | 8 | a0001c0001t0001g0092 a0001c0001t0001g0127 a0001c0001t0001g0173 others(5): Show |
8 | HG01081.hp1 HG02965.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.784-671A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374790 | |||||||
chr11:374793 | A | AAGGG | 13 | a0001c0001t0001g0048 a0001c0001t0001g0138 a0001c0001t0004g0016 others(10): Show |
13 | HG01255.hp1 HG01346.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.784-660_784-657dup others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374793 | ||||||
chr11:374793 | A | AAGGGAGG others(16): Show |
2 | a0001c0001t0001g0134 a0002c0033t0001g0070 |
2 | HG02040.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.784-657_784-656ins others(23): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374793 | ||||||
chr11:374793 | A | AAGGGAGG others(46): Show |
1 | a0012c0040t0001g0007 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.784-657_784-656ins others(53): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374793 | ||||||
chr11:374793 | A | AAGGGAGG others(73): Show |
1 | a0003c0006t0001g0065 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.784-657_784-656ins others(80): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374793 | ||||||
chr11:374793 | A | AAGGGAGG others(35): Show |
1 | a0002c0002t0001g0060 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.784-657_784-656ins others(42): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374793 | ||||||
chr11:374793 | A | AAGGGAGG others(125): Show |
1 | a0001c0001t0001g0135 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.784-657_784-656ins others(132): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374793 | ||||||
chr11:374793 | A | G | 4 | a0001c0003t0003g0018 a0002c0037t0001g0156 a0003c0006t0001g0154 others(1): Show |
4 | HG01106.hp2 HG02148.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-668A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374793 | |||||||
chr11:374797 | G | A | 1 | a0002c0004t0001g0056 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.784-664G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374797 | |||||||
chr11:374798 | A | T | 1 | a0002c0004t0001g0056 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.784-663A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374798 | |||||||
chr11:374802 | A | AGGAGGAA others(104): Show |
1 | a0002c0002t0001g0162 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.784-642_784-641ins others(111): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374802 | ||||||
chr11:374802 | A | AGGAGGAA others(55): Show |
1 | a0003c0006t0001g0078 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.784-642_784-641ins others(62): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374802 | ||||||
chr11:374804 | G | GGAGGAGG others(1): Show |
5 | a0001c0001t0001g0105 a0001c0026t0002g0049 a0002c0004t0001g0176 others(2): Show |
5 | HG01243.hp1 HG02132.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-657_784-656ins others(8): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374804 | |||||||
chr11:374804 | G | GGAGGAGG others(31): Show |
4 | a0002c0002t0001g0064 a0002c0002t0001g0082 a0002c0002t0001g0159 others(1): Show |
4 | HG00733.hp1 HG04199.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-657_784-656ins others(38): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374804 | |||||||
chr11:374804 | G | GGAGGAGG others(35): Show |
2 | a0002c0002t0001g0054 a0002c0002t0001g0083 |
2 | NA18747.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.784-657_784-656ins others(42): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374804 | |||||||
chr11:374804 | G | GGAGGAGG others(114): Show |
1 | a0002c0008t0001g0148 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.784-657_784-656ins others(121): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374804 | |||||||
chr11:374805 | A | T | 17 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(14): Show |
21 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.784-656A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374805 | |||||||
chr11:374808 | A | AAGGG | 17 | a0001c0001t0001g0094 a0001c0001t0005g0171 a0001c0001t0005g0172 others(14): Show |
17 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(14): Show |
intron_variant | MODIFIER | c.784-645_784-642dup others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374808 | ||||||
chr11:374808 | A | AAGGGAGG others(759): Show |
1 | a0002c0004t0001g0001 | 2 | HG02258.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.784-641_784-640ins others(766): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374808 | ||||||
chr11:374808 | A | AAGGGAGG others(1343): Show |
1 | a0001c0003t0001g0106 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.784-627_784-626ins others(1350): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374808 | ||||||
chr11:374808 | A | AAGGGAGG others(26): Show |
1 | a0002c0002t0001g0160 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.784-642_784-641ins others(33): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374808 | ||||||
chr11:374808 | A | AAGGGAGG others(77): Show |
1 | a0003c0006t0001g0077 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.784-642_784-641ins others(84): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374808 | ||||||
chr11:374808 | A | AAGGGAGG others(237): Show |
1 | a0001c0003t0001g0091 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.784-642_784-641ins others(244): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374808 | ||||||
chr11:374808 | A | G | 13 | a0001c0001t0001g0105 a0001c0026t0002g0049 a0002c0002t0001g0054 others(10): Show |
13 | HG00733.hp1 HG01243.hp1 HG02132.hp2 others(10): Show |
intron_variant | MODIFIER | c.784-653A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374808 | |||||||
chr11:374811 | G | A | 1 | a0002c0004t0001g0056 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.784-650G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374811 | |||||||
chr11:374817 | A | AGGAAGGG others(21): Show |
1 | a0004c0042t0001g0031 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.784-641_784-640ins others(28): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374817 | ||||||
chr11:374817 | A | AGGAGGAA others(55): Show |
1 | a0002c0002t0001g0151 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.784-627_784-626ins others(62): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374817 | ||||||
chr11:374820 | A | AGGAAGGG others(8): Show |
1 | a0002c0002t0001g0063 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.784-627_784-626ins others(15): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374820 | ||||||
chr11:374820 | A | G | 2 | a0002c0002t0001g0069 a0002c0002t0001g0075 |
2 | NA19012.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.784-641A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374820 | |||||||
chr11:374820 | A | T | 6 | a0001c0001t0001g0048 a0001c0001t0001g0113 a0001c0001t0001g0114 others(3): Show |
6 | HG01069.hp2 HG02040.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.784-641A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374820 | |||||||
chr11:374823 | A | AAGGG | 6 | a0001c0001t0001g0093 a0001c0001t0004g0016 a0001c0003t0001g0097 others(3): Show |
6 | HG01258.hp1 HG01891.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.784-630_784-627dup others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374823 | ||||||
chr11:374823 | A | AAGGGAGG others(70): Show |
1 | a0002c0002t0001g0054 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.784-626_784-625ins others(77): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374823 | ||||||
chr11:374823 | A | AAGGGAGG others(71): Show |
1 | a0001c0001t0001g0043 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.784-612_784-611ins others(78): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374823 | ||||||
chr11:374823 | A | AAGGGAGG others(183): Show |
1 | a0009c0012t0001g0103 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.784-627_784-626ins others(190): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374823 | ||||||
chr11:374823 | A | G | 2 | a0001c0003t0001g0091 a0003c0006t0001g0133 |
2 | HG02080.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.784-638A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374823 | |||||||
chr11:374823 | AAGGGAGG others(12): Show |
A | 2 | a0001c0001t0001g0005 a0001c0001t0001g0087 |
3 | HG00099.hp1 HG00639.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.784-554_784-536del others(19): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374823 | ||||||
chr11:374832 | A | AGGAGGAA others(39): Show |
1 | a0020c0032t0001g0147 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.784-612_784-611ins others(46): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374832 | ||||||
chr11:374834 | G | GGGGAAGG others(1433): Show |
1 | a0004c0043t0001g0028 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.784-627_784-626ins others(1440): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374834 | |||||||
chr11:374835 | A | G | 15 | a0001c0001t0001g0094 a0001c0001t0001g0105 a0001c0001t0001g0134 others(12): Show |
15 | HG00735.hp2 HG01255.hp2 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.784-626A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374835 | |||||||
chr11:374835 | A | T | 5 | a0001c0001t0001g0112 a0001c0003t0002g0047 a0002c0002t0001g0161 others(2): Show |
5 | HG01943.hp1 HG03927.hp2 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-626A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374835 | |||||||
chr11:374836 | G | A | 14 | a0001c0001t0001g0105 a0001c0001t0001g0134 a0001c0001t0001g0138 others(11): Show |
14 | HG01255.hp2 HG02040.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.784-625G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374836 | |||||||
chr11:374838 | A | AAGGGAGG others(8): Show |
1 | a0004c0042t0001g0031 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.784-619_784-605dup others(15): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374838 | ||||||
chr11:374838 | A | G | 14 | a0001c0001t0001g0105 a0001c0001t0001g0134 a0001c0001t0001g0138 others(11): Show |
14 | HG01255.hp2 HG02040.hp2 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.784-623A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374838 | |||||||
chr11:374838 | AAGGG | A | 6 | a0001c0026t0002g0049 a0002c0002t0001g0010 a0002c0002t0001g0064 others(3): Show |
6 | HG00733.hp1 HG01993.hp2 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.784-611_784-608del others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374838 | ||||||
chr11:374839 | A | G | 2 | a0001c0001t0001g0105 a0018c0029t0004g0053 |
2 | HG03486.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.784-622A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374839 | |||||||
chr11:374840 | G | GGGAGGGA others(53): Show |
1 | a0003c0006t0001g0077 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.784-612_784-611ins others(60): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374840 | ||||||
chr11:374842 | G | A | 13 | a0001c0001t0001g0105 a0001c0001t0001g0134 a0001c0001t0001g0138 others(10): Show |
13 | HG01106.hp2 HG02040.hp2 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.784-619G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374842 | |||||||
chr11:374842 | G | GAGGGAGG others(4): Show |
15 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0045 others(12): Show |
16 | HG00140.hp2 HG00323.hp2 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.784-612_784-611ins others(11): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374842 | ||||||
chr11:374842 | G | GAGGGAGG others(19): Show |
1 | a0001c0001t0001g0042 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.784-612_784-611ins others(26): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374842 | ||||||
chr11:374842 | G | GAGGGAGG others(49): Show |
1 | a0001c0001t0001g0165 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.784-612_784-611ins others(56): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374842 | ||||||
chr11:374842 | G | GAGGGAGG others(64): Show |
1 | a0001c0001t0001g0128 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.784-612_784-611ins others(71): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374842 | ||||||
chr11:374842 | G | GAGGGAGG others(139): Show |
1 | a0001c0001t0001g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.784-612_784-611ins others(146): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374842 | ||||||
chr11:374842 | G | GAGGGAGG others(1048): Show |
1 | a0001c0016t0001g0104 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.784-612_784-611ins others(1055): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374842 | ||||||
chr11:374842 | G | GAGGGAGG others(679): Show |
1 | a0001c0003t0002g0164 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.784-612_784-611ins others(686): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374842 | ||||||
chr11:374842 | G | GAGGGAGG others(214): Show |
1 | a0001c0003t0002g0025 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.784-612_784-611ins others(221): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374842 | ||||||
chr11:374842 | G | GAGGGAGG others(65): Show |
1 | a0022c0015t0001g0040 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.784-612_784-611ins others(72): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374842 | ||||||
chr11:374842 | G | GAGGGAGG others(147): Show |
1 | a0004c0044t0001g0032 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.784-612_784-611ins others(154): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374842 | ||||||
chr11:374842 | G | GAGGGAGG others(49): Show |
1 | a0001c0001t0004g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.784-612_784-611ins others(56): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374842 | ||||||
chr11:374842 | G | GAGGGAGG others(124): Show |
1 | a0002c0009t0001g0168 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.784-612_784-611ins others(131): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374842 | ||||||
chr11:374842 | G | GAGGGAGG others(80): Show |
1 | a0002c0002t0001g0157 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.784-612_784-611ins others(87): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374842 | ||||||
chr11:374842 | G | GAGGGAGG others(98): Show |
1 | a0007c0011t0001g0158 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.784-612_784-611ins others(105): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374842 | ||||||
chr11:374842 | G | GAGGGAGG others(191): Show |
1 | a0002c0002t0001g0137 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.784-612_784-611ins others(198): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374842 | ||||||
chr11:374842 | G | GAGGGAGG others(342): Show |
1 | a0001c0001t0001g0093 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.784-611_784-610ins others(349): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374842 | ||||||
chr11:374842 | G | GAGGGAGG others(79): Show |
1 | a0002c0009t0001g0166 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.784-612_784-611ins others(86): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374842 | ||||||
chr11:374842 | G | GAGGGAGG others(229): Show |
1 | a0001c0003t0002g0047 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.784-612_784-611ins others(236): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374842 | ||||||
chr11:374842 | G | GAGGGAGG others(259): Show |
1 | a0001c0003t0002g0026 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.784-612_784-611ins others(266): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374842 | ||||||
chr11:374843 | A | AGGGAGGA others(166): Show |
1 | a0001c0001t0001g0173 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.784-612_784-611ins others(173): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374843 | ||||||
chr11:374846 | G | GAGGAGGA | 10 | a0001c0001t0001g0101 a0001c0001t0001g0113 a0001c0001t0001g0127 others(7): Show |
10 | HG00438.hp2 HG02040.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.784-612_784-611ins others(7): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374846 | ||||||
chr11:374846 | G | GAGGAGGA others(120): Show |
1 | a0002c0008t0001g0081 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.784-612_784-611ins others(127): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374846 | ||||||
chr11:374846 | G | GAGGAGGA others(19): Show |
8 | a0001c0003t0001g0136 a0002c0002t0001g0140 a0002c0002t0001g0141 others(5): Show |
8 | HG00099.hp2 HG00140.hp1 HG01070.hp2 others(5): Show |
intron_variant | MODIFIER | c.784-612_784-611ins others(26): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374846 | ||||||
chr11:374848 | G | GGA | 3 | a0002c0037t0001g0156 a0008c0013t0001g0059 a0021c0019t0001g0033 |
3 | HG02630.hp1 HG03239.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.784-612_784-611ins others(2): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374848 | ||||||
chr11:374850 | G | A | 1 | a0003c0036t0001g0079 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.784-611G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374850 | |||||||
chr11:374851 | A | AAG | 2 | a0002c0037t0001g0156 a0008c0013t0001g0059 |
2 | HG02630.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.784-610_784-609ins others(2): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374851 | |||||||
chr11:374851 | A | AG | 13 | a0001c0001t0001g0173 a0001c0003t0001g0136 a0002c0002t0001g0140 others(10): Show |
13 | HG00099.hp2 HG00140.hp1 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.784-608dupG | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374851 | ||||||
chr11:374851 | A | AGGAGGAA others(5): Show |
2 | a0002c0002t0006g0076 a0003c0006t0001g0154 |
2 | HG01361.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.784-604_784-593dup others(12): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374851 | ||||||
chr11:374851 | A | AGGAGGAA others(54): Show |
1 | a0002c0002t0001g0066 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.784-593_784-592ins others(61): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374851 | ||||||
chr11:374851 | A | AGGAGGGG others(62): Show |
1 | a0018c0029t0004g0053 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.784-605_784-604ins others(69): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374851 | ||||||
chr11:374851 | A | G | 2 | a0001c0001t0001g0094 a0003c0036t0001g0079 |
2 | HG00735.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.784-610A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374851 | |||||||
chr11:374853 | G | A | 2 | a0001c0001t0001g0094 a0003c0036t0001g0079 |
2 | HG00735.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.784-608G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374853 | |||||||
chr11:374854 | A | G | 12 | a0001c0001t0001g0101 a0001c0001t0001g0113 a0001c0001t0001g0127 others(9): Show |
12 | HG00438.hp2 HG02040.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.784-607A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374854 | |||||||
chr11:374854 | A | T | 2 | a0001c0003t0002g0027 a0010c0017t0001g0086 |
2 | HG00639.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.784-607A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374854 | |||||||
chr11:374855 | G | A | 12 | a0001c0001t0001g0101 a0001c0001t0001g0113 a0001c0001t0001g0127 others(9): Show |
12 | HG00438.hp2 HG02040.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.784-606G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374855 | |||||||
chr11:374855 | G | T | 1 | a0009c0012t0001g0103 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.784-606G>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374855 | |||||||
chr11:374857 | A | AAGGGAGG others(66): Show |
1 | a0002c0009t0001g0177 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.784-593_784-592ins others(73): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374857 | ||||||
chr11:374857 | A | AGGGAGGG others(3): Show |
1 | a0001c0003t0004g0017 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.784-604_784-603ins others(10): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374857 | |||||||
chr11:374857 | A | G | 19 | a0001c0001t0001g0094 a0001c0001t0001g0101 a0001c0001t0001g0113 others(16): Show |
19 | HG00438.hp2 HG00735.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.784-604A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374857 | |||||||
chr11:374857 | AAGGG | A | 2 | a0002c0002t0001g0061 a0005c0010t0001g0174 |
2 | HG00438.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.784-592_784-589del others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374857 | ||||||
chr11:374858 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.784-603A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374858 | |||||||
chr11:374859 | G | GGGAGGGA others(479): Show |
1 | a0012c0040t0001g0007 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.784-593_784-592ins others(486): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374859 | ||||||
chr11:374861 | G | A | 16 | a0001c0001t0001g0092 a0001c0001t0001g0101 a0001c0001t0001g0113 others(13): Show |
16 | HG00438.hp2 HG01081.hp1 HG02040.hp1 others(13): Show |
intron_variant | MODIFIER | c.784-600G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374861 | |||||||
chr11:374861 | G | GAGGAGAG others(105): Show |
1 | a0021c0019t0001g0033 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.784-597_784-596ins others(112): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374861 | ||||||
chr11:374861 | G | GAGGAGGA | 3 | a0001c0001t0001g0094 a0002c0037t0001g0156 a0008c0013t0001g0059 |
3 | HG00735.hp2 HG02630.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.784-597_784-596ins others(7): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374861 | ||||||
chr11:374861 | G | GAGGGAGG others(47): Show |
1 | a0002c0002t0001g0149 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.784-593_784-592ins others(54): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374861 | ||||||
chr11:374861 | G | GAGGGAGG others(35): Show |
1 | a0002c0002t0001g0146 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.784-593_784-592ins others(42): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374861 | ||||||
chr11:374861 | G | GAGGGAGG others(77): Show |
1 | a0019c0018t0001g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.784-593_784-592ins others(84): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374861 | ||||||
chr11:374861 | G | GAGGGAGG others(4): Show |
20 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0048 others(17): Show |
20 | HG00323.hp1 HG00323.hp2 HG00544.hp2 others(17): Show |
intron_variant | MODIFIER | c.784-593_784-592ins others(11): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374861 | ||||||
chr11:374861 | G | GAGGGAGG others(68): Show |
1 | a0002c0004t0001g0056 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.784-593_784-592ins others(75): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374861 | ||||||
chr11:374861 | G | GAGGGAGG others(34): Show |
2 | a0001c0001t0001g0036 a0001c0001t0001g0135 |
2 | NA18747.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.784-593_784-592ins others(41): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374861 | ||||||
chr11:374861 | G | GAGGGAGG others(109): Show |
1 | a0002c0002t0001g0063 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.784-593_784-592ins others(116): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374861 | ||||||
chr11:374861 | G | GAGGGAGG others(184): Show |
1 | a0001c0001t0001g0118 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.784-593_784-592ins others(191): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374861 | ||||||
chr11:374861 | G | GAGGGAGG others(349): Show |
1 | a0001c0001t0001g0120 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.784-593_784-592ins others(356): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374861 | ||||||
chr11:374861 | G | GAGGGAGG others(109): Show |
1 | a0017c0031t0004g0012 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.784-593_784-592ins others(116): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374861 | ||||||
chr11:374861 | G | GAGGGAGG others(109): Show |
1 | a0001c0003t0002g0024 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.784-593_784-592ins others(116): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374861 | ||||||
chr11:374861 | G | GAGGGAGG others(214): Show |
2 | a0001c0005t0002g0108 a0001c0005t0002g0117 |
2 | HG01934.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.784-593_784-592ins others(221): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374861 | ||||||
chr11:374861 | G | GAGGGAGG others(229): Show |
1 | a0001c0005t0002g0116 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.784-593_784-592ins others(236): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374861 | ||||||
chr11:374861 | G | GAGGGAGG others(319): Show |
1 | a0001c0001t0001g0095 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.784-593_784-592ins others(326): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374861 | ||||||
chr11:374861 | G | GAGGGAGG others(94): Show |
1 | a0002c0002t0001g0161 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.784-593_784-592ins others(101): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374861 | ||||||
chr11:374861 | G | GAGGGAGG others(472): Show |
1 | a0014c0030t0004g0011 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.784-593_784-592ins others(479): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374861 | ||||||
chr11:374861 | G | GAGGGAGG others(124): Show |
1 | a0001c0001t0001g0121 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.784-593_784-592ins others(131): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374861 | ||||||
chr11:374861 | G | GAGGGAGG others(8): Show |
2 | a0001c0001t0001g0102 a0001c0003t0001g0129 |
2 | HG02015.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.784-588_784-574dup others(15): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374861 | ||||||
chr11:374861 | G | GAGGGAGG others(4): Show |
2 | a0001c0001t0001g0004 a0001c0001t0002g0130 |
3 | HG00733.hp2 HG01081.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.784-593_784-592ins others(11): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374861 | ||||||
chr11:374863 | G | GGGAGGGA others(286): Show |
1 | a0009c0012t0003g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.784-586_784-585ins others(293): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374863 | ||||||
chr11:374865 | G | GAGGAGGA | 4 | a0001c0001t0001g0045 a0001c0001t0001g0098 a0001c0003t0001g0106 others(1): Show |
4 | HG03688.hp1 NA18947.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.784-593_784-592ins others(7): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374865 | ||||||
chr11:374865 | G | GAGGAGGA others(18): Show |
1 | a0008c0013t0001g0057 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.784-593_784-592ins others(25): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374865 | ||||||
chr11:374865 | G | GAGGAGGA others(262): Show |
1 | a0003c0039t0001g0058 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.784-593_784-592ins others(269): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374865 | ||||||
chr11:374868 | GGAGGAGG others(73): Show |
G | 1 | a0006c0007t0001g0122 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.784-592_784-513del others(80): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374868 | |||||||
chr11:374869 | G | A | 3 | a0001c0001t0001g0128 a0001c0003t0002g0025 a0001c0026t0002g0049 |
3 | HG01074.hp2 HG02683.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.784-592G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374869 | |||||||
chr11:374870 | A | AGGAGGAA others(5): Show |
1 | a0009c0012t0001g0103 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.784-585_784-574dup others(12): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374870 | ||||||
chr11:374870 | A | G | 4 | a0001c0001t0001g0128 a0001c0003t0002g0025 a0001c0026t0002g0049 others(1): Show |
4 | HG01074.hp2 HG01255.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-591A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374870 | |||||||
chr11:374872 | G | A | 4 | a0001c0001t0001g0128 a0001c0003t0002g0025 a0001c0026t0002g0049 others(1): Show |
4 | HG01074.hp2 HG01255.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-589G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374872 | |||||||
chr11:374873 | A | AG | 3 | a0001c0003t0004g0017 a0001c0003t0004g0050 a0005c0010t0001g0109 |
3 | HG01361.hp1 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.784-586dupG | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374873 | ||||||
chr11:374873 | A | G | 5 | a0001c0001t0001g0045 a0001c0001t0001g0098 a0001c0003t0001g0106 others(2): Show |
5 | HG03688.hp1 HG04115.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.784-588A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374873 | |||||||
chr11:374873 | A | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0138 a0001c0003t0002g0164 |
3 | HG01081.hp1 HG02300.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.784-588A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374873 | |||||||
chr11:374874 | G | A | 5 | a0001c0001t0001g0045 a0001c0001t0001g0098 a0001c0003t0001g0106 others(2): Show |
5 | HG03688.hp1 HG04115.hp1 NA18947.hp1 others(2): Show |
intron_variant | MODIFIER | c.784-587G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374874 | |||||||
chr11:374876 | A | G | 20 | a0001c0001t0001g0045 a0001c0001t0001g0098 a0001c0001t0001g0128 others(17): Show |
20 | HG00408.hp1 HG01074.hp2 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.784-585A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374876 | |||||||
chr11:374876 | AAGGG | A | 2 | a0001c0001t0001g0112 a0001c0001t0004g0016 |
2 | HG01891.hp1 HG01943.hp1 |
intron_variant | MODIFIER | c.784-573_784-570del others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374876 | ||||||
chr11:374880 | G | A | 4 | a0001c0001t0001g0045 a0001c0001t0001g0098 a0001c0003t0001g0106 others(1): Show |
4 | HG03688.hp1 NA18947.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.784-581G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374880 | |||||||
chr11:374880 | G | GAGGGAGG others(1): Show |
14 | a0001c0001t0001g0134 a0001c0003t0001g0136 a0002c0002t0001g0060 others(11): Show |
14 | HG00099.hp2 HG00140.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.784-574_784-573ins others(8): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(616): Show |
1 | a0002c0038t0003g0020 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.784-574_784-573ins others(623): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(483): Show |
1 | a0002c0002t0001g0082 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.784-574_784-573ins others(490): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(469): Show |
1 | a0002c0002t0001g0064 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.784-574_784-573ins others(476): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(401): Show |
1 | a0002c0002t0001g0055 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.784-574_784-573ins others(408): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(484): Show |
2 | a0002c0002t0001g0159 a0002c0002t0001g0163 |
2 | NA19057.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.784-574_784-573ins others(491): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(170): Show |
1 | a0001c0001t0005g0172 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.784-574_784-573ins others(177): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(48): Show |
1 | a0002c0002t0001g0010 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.784-574_784-573ins others(55): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(4): Show |
14 | a0001c0001t0001g0004 a0001c0001t0001g0038 a0001c0001t0001g0048 others(11): Show |
15 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.784-574_784-573ins others(11): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(581): Show |
1 | a0025c0028t0001g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.784-574_784-573ins others(588): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(34): Show |
3 | a0001c0001t0001g0167 a0002c0009t0001g0166 a0002c0009t0001g0168 |
3 | HG02976.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.784-574_784-573ins others(41): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(251): Show |
1 | a0001c0003t0001g0091 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.784-574_784-573ins others(258): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(538): Show |
1 | a0002c0002t0001g0054 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.784-574_784-573ins others(545): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(514): Show |
1 | a0002c0002t0001g0069 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.784-574_784-573ins others(521): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(514): Show |
1 | a0002c0002t0001g0075 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.784-574_784-573ins others(521): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(166): Show |
1 | a0002c0008t0001g0144 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.784-574_784-573ins others(173): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(109): Show |
1 | a0001c0003t0002g0164 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.784-574_784-573ins others(116): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(301): Show |
1 | a0002c0002t0001g0072 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.784-574_784-573ins others(308): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(395): Show |
1 | a0002c0002t0001g0067 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.784-574_784-573ins others(402): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(81): Show |
1 | a0002c0002t0001g0160 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.784-574_784-573ins others(88): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(626): Show |
1 | a0002c0002t0001g0008 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.784-574_784-573ins others(633): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(668): Show |
1 | a0002c0002t0001g0009 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.784-574_784-573ins others(675): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(543): Show |
1 | a0026c0025t0003g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.784-574_784-573ins others(550): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(87): Show |
1 | a0002c0002t0001g0074 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.784-574_784-573ins others(94): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(87): Show |
1 | a0002c0002t0001g0178 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.784-574_784-573ins others(94): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(109): Show |
1 | a0001c0001t0001g0093 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.784-574_784-573ins others(116): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(301): Show |
1 | a0002c0035t0001g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.784-574_784-573ins others(308): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(248): Show |
2 | a0002c0002t0001g0073 a0002c0002t0001g0080 |
2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.784-574_784-573ins others(255): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(271): Show |
1 | a0002c0002t0003g0153 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.784-574_784-573ins others(278): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(8): Show |
1 | a0007c0011t0001g0068 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.784-569_784-555dup others(15): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(457): Show |
1 | a0002c0002t0001g0083 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.784-555_784-554ins others(464): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(552): Show |
1 | a0002c0033t0001g0070 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.784-555_784-554ins others(559): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(117): Show |
1 | a0001c0001t0001g0111 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.784-521_784-520ins others(124): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(4): Show |
1 | a0001c0003t0002g0027 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.784-574_784-573ins others(11): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGAGG others(53): Show |
1 | a0006c0007t0001g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.784-574_784-573ins others(60): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGGGGA others(469): Show |
1 | a0006c0007t0001g0175 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.784-577_784-576ins others(476): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374880 | G | GAGGTGGA | 2 | a0001c0001t0001g0128 a0001c0003t0002g0025 |
2 | HG01074.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.784-578_784-577ins others(7): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374880 | ||||||
chr11:374882 | G | GGGAGGGA others(8): Show |
1 | a0018c0029t0004g0053 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.784-565_784-564ins others(15): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374882 | ||||||
chr11:374884 | G | A | 1 | a0001c0026t0002g0049 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.784-577G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374884 | |||||||
chr11:374884 | G | GAGAAGGA others(54): Show |
1 | a0001c0001t0001g0123 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.784-575_784-574ins others(61): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374884 | ||||||
chr11:374884 | G | GAGGAGGA | 9 | a0001c0001t0001g0036 a0001c0001t0001g0127 a0001c0001t0001g0165 others(6): Show |
9 | HG00639.hp2 HG00642.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.784-574_784-573ins others(7): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374884 | ||||||
chr11:374884 | G | GAGGAGGA others(15): Show |
1 | a0004c0014t0002g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.784-574_784-573ins others(22): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374884 | ||||||
chr11:374884 | G | GAGGTGGA | 2 | a0001c0003t0002g0026 a0001c0003t0002g0047 |
2 | HG02273.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.784-574_784-573ins others(7): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374884 | ||||||
chr11:374885 | A | C | 1 | a0005c0010t0001g0109 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.784-576A>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374885 | |||||||
chr11:374887 | GGAGGAGG others(1): Show |
G | 3 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0005c0023t0001g0125 |
3 | HG00735.hp2 HG01081.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.784-573_784-566del others(8): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374887 | |||||||
chr11:374888 | G | A | 6 | a0001c0001t0001g0105 a0001c0001t0001g0114 a0001c0001t0001g0173 others(3): Show |
6 | HG01069.hp2 HG01346.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.784-573G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374888 | |||||||
chr11:374889 | A | G | 5 | a0001c0001t0001g0105 a0001c0001t0001g0114 a0001c0001t0001g0173 others(2): Show |
5 | HG01069.hp2 HG01346.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-572A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374889 | |||||||
chr11:374891 | G | A | 5 | a0001c0001t0001g0105 a0001c0001t0001g0114 a0001c0001t0001g0173 others(2): Show |
5 | HG01069.hp2 HG01346.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-570G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374891 | |||||||
chr11:374892 | A | AAGGGAGG others(536): Show |
1 | a0002c0002t0001g0137 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.784-569_784-568ins others(543): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374892 | |||||||
chr11:374892 | A | G | 13 | a0001c0001t0001g0036 a0001c0001t0001g0127 a0001c0001t0001g0165 others(10): Show |
13 | HG00639.hp2 HG00642.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.784-569A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374892 | |||||||
chr11:374892 | A | T | 1 | a0001c0003t0002g0164 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.784-569A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374892 | |||||||
chr11:374893 | G | A | 13 | a0001c0001t0001g0036 a0001c0001t0001g0127 a0001c0001t0001g0165 others(10): Show |
13 | HG00639.hp2 HG00642.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.784-568G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374893 | |||||||
chr11:374895 | A | G | 24 | a0001c0001t0001g0036 a0001c0001t0001g0105 a0001c0001t0001g0114 others(21): Show |
24 | HG00438.hp1 HG00639.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.784-566A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374895 | |||||||
chr11:374895 | AAGGG | A | 6 | a0001c0001t0001g0034 a0001c0001t0001g0095 a0001c0003t0004g0014 others(3): Show |
6 | HG00438.hp2 HG00735.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.784-554_784-551del others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374895 | ||||||
chr11:374896 | A | G | 1 | a0002c0002t0001g0137 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.784-565A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374896 | |||||||
chr11:374897 | G | GGGAGGGA others(64): Show |
1 | a0021c0019t0001g0033 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.784-555_784-554ins others(71): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374897 | ||||||
chr11:374899 | G | A | 18 | a0001c0001t0001g0036 a0001c0001t0001g0092 a0001c0001t0001g0094 others(15): Show |
18 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(15): Show |
intron_variant | MODIFIER | c.784-562G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374899 | |||||||
chr11:374899 | G | GAGGAGGA | 2 | a0001c0001t0005g0171 a0005c0010t0001g0174 |
2 | HG00438.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.784-559_784-558ins others(7): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374899 | ||||||
chr11:374899 | G | GAGGGAGG others(4): Show |
13 | a0001c0001t0001g0038 a0001c0001t0001g0048 a0001c0001t0001g0099 others(10): Show |
13 | HG00323.hp2 HG00544.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.784-555_784-554ins others(11): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374899 | ||||||
chr11:374899 | G | GAGGGAGG others(19): Show |
1 | a0004c0042t0001g0031 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.784-555_784-554ins others(26): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374899 | ||||||
chr11:374899 | G | GAGGGAGG others(94): Show |
1 | a0001c0005t0002g0131 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.784-555_784-554ins others(101): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374899 | ||||||
chr11:374899 | G | GAGGGAGG others(225): Show |
1 | a0002c0004t0002g0085 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.784-550_784-549ins others(232): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374899 | ||||||
chr11:374899 | G | GAGGGAGG others(8): Show |
1 | a0002c0004t0001g0001 | 2 | HG02258.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.784-535_784-521dup others(15): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374899 | ||||||
chr11:374899 | G | GAGGGAGG others(215): Show |
1 | a0004c0044t0001g0032 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.784-554_784-553ins others(222): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374899 | ||||||
chr11:374899 | G | GAGGTGGA | 6 | a0001c0001t0001g0105 a0001c0001t0001g0114 a0001c0001t0001g0173 others(3): Show |
6 | HG01069.hp2 HG01346.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.784-559_784-558ins others(7): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374899 | ||||||
chr11:374904 | A | AGGAGGAA others(591): Show |
1 | a0001c0003t0003g0018 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.784-555_784-554ins others(598): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374904 | ||||||
chr11:374905 | G | A | 1 | a0005c0010t0001g0109 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.784-556G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374905 | |||||||
chr11:374907 | G | A | 2 | a0001c0001t0001g0003 a0020c0032t0001g0147 |
2 | HG01433.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.784-554G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374907 | |||||||
chr11:374908 | A | G | 2 | a0001c0001t0001g0003 a0020c0032t0001g0147 |
2 | HG01433.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.784-553A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374908 | |||||||
chr11:374910 | G | A | 2 | a0001c0001t0001g0003 a0020c0032t0001g0147 |
2 | HG01433.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.784-551G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374910 | |||||||
chr11:374910 | G | GA | 2 | a0002c0004t0002g0084 a0004c0014t0002g0051 |
2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.784-550dupA | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374910 | ||||||
chr11:374911 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.784-550A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374911 | |||||||
chr11:374911 | A | T | 5 | a0001c0001t0001g0094 a0001c0003t0002g0025 a0001c0003t0002g0164 others(2): Show |
5 | HG00735.hp2 HG01074.hp2 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-550A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374911 | |||||||
chr11:374914 | A | AAGGG | 5 | a0001c0001t0001g0004 a0001c0001t0001g0042 a0001c0001t0001g0102 others(2): Show |
6 | HG00733.hp2 HG01081.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.784-539_784-536dup others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374914 | ||||||
chr11:374914 | A | G | 21 | a0001c0001t0001g0003 a0001c0001t0001g0134 a0001c0003t0001g0136 others(18): Show |
21 | HG00099.hp2 HG00140.hp1 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.784-547A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374914 | |||||||
chr11:374915 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.784-546A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374915 | |||||||
chr11:374918 | G | GAGGGAGG others(158): Show |
2 | a0002c0004t0002g0084 a0004c0014t0002g0051 |
2 | HG03486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.784-502_784-501ins others(165): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374918 | ||||||
chr11:374923 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.784-538A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374923 | |||||||
chr11:374926 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.784-535A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374926 | |||||||
chr11:374926 | A | T | 3 | a0001c0003t0002g0024 a0001c0003t0002g0027 a0010c0017t0001g0086 |
3 | HG00639.hp2 HG01346.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.784-535A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374926 | |||||||
chr11:374929 | A | G | 1 | a0020c0032t0001g0147 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.784-532A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374929 | |||||||
chr11:374929 | AAGGG | A | 9 | a0001c0001t0001g0045 a0001c0001t0001g0098 a0001c0005t0002g0108 others(6): Show |
9 | HG00642.hp1 HG01934.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.784-520_784-517del others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374929 | ||||||
chr11:374930 | A | AGGGAGGG others(66): Show |
1 | a0001c0001t0001g0127 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.784-521_784-520ins others(73): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374930 | ||||||
chr11:374930 | A | G | 1 | a0009c0012t0003g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.784-531A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374930 | |||||||
chr11:374933 | G | A | 3 | a0001c0001t0001g0044 a0002c0004t0001g0056 a0009c0012t0003g0023 |
3 | HG00408.hp2 HG03041.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.784-528G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374933 | |||||||
chr11:374933 | G | GAGGGAGG others(4): Show |
11 | a0001c0001t0001g0038 a0001c0001t0001g0048 a0001c0001t0001g0093 others(8): Show |
11 | HG01069.hp2 HG01070.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.784-521_784-520ins others(11): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374933 | ||||||
chr11:374933 | G | GAGGGAGG others(34): Show |
1 | a0013c0020t0001g0046 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.784-521_784-520ins others(41): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374933 | ||||||
chr11:374933 | G | GAGGGAGG others(49): Show |
2 | a0001c0001t0001g0035 a0001c0001t0005g0171 |
2 | HG02559.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.784-521_784-520ins others(56): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374933 | ||||||
chr11:374933 | G | GAGGGAGG others(64): Show |
2 | a0001c0001t0001g0043 a0002c0037t0001g0156 |
2 | HG03239.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.784-521_784-520ins others(71): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374933 | ||||||
chr11:374933 | G | GAGGGAGG others(109): Show |
1 | a0001c0001t0005g0169 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.784-521_784-520ins others(116): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374933 | ||||||
chr11:374933 | G | GAGGGAGG others(551): Show |
1 | a0001c0001t0001g0042 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.784-521_784-520ins others(558): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374933 | ||||||
chr11:374933 | G | GAGGGAGG others(339): Show |
1 | a0002c0002t0001g0149 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.784-521_784-520ins others(346): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374933 | ||||||
chr11:374933 | G | GAGGGAGG others(79): Show |
1 | a0019c0018t0001g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.784-521_784-520ins others(86): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374933 | ||||||
chr11:374933 | G | GAGGGAGG others(181): Show |
1 | a0006c0007t0001g0041 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.784-521_784-520ins others(188): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374933 | ||||||
chr11:374933 | G | GAGGGAGG others(185): Show |
1 | a0001c0001t0001g0039 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.784-521_784-520ins others(192): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374933 | ||||||
chr11:374933 | G | GAGGGAGG others(107): Show |
1 | a0001c0003t0004g0017 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.784-521_784-520ins others(114): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374933 | ||||||
chr11:374933 | G | GAGGGAGG others(49): Show |
1 | a0001c0001t0003g0019 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.784-521_784-520ins others(56): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374933 | ||||||
chr11:374933 | G | GAGGGAGG others(202): Show |
1 | a0001c0001t0001g0120 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.784-521_784-520ins others(209): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374933 | ||||||
chr11:374933 | G | GAGGGAGG others(206): Show |
1 | a0007c0011t0001g0158 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.784-521_784-520ins others(213): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374933 | ||||||
chr11:374933 | G | GAGGGAGG others(113): Show |
1 | a0001c0001t0001g0118 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.784-521_784-520ins others(120): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374933 | ||||||
chr11:374933 | G | GAGGGAGG others(109): Show |
1 | a0015c0041t0001g0030 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.784-521_784-520ins others(116): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374933 | ||||||
chr11:374933 | G | GAGGGAGG others(319): Show |
1 | a0001c0001t0001g0121 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.784-521_784-520ins others(326): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374933 | ||||||
chr11:374933 | G | GAGGGAGG others(230): Show |
1 | a0001c0001t0001g0112 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.784-521_784-520ins others(237): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374933 | ||||||
chr11:374933 | G | GAGGGAGG others(8): Show |
1 | a0001c0001t0001g0099 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.784-516_784-502dup others(15): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374933 | ||||||
chr11:374933 | G | GAGGGAGG others(51): Show |
1 | a0008c0013t0001g0059 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.784-502_784-501ins others(58): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374933 | ||||||
chr11:374933 | G | GAGGGAGG others(199): Show |
1 | a0001c0001t0001g0170 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.784-514_784-513ins others(206): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374933 | ||||||
chr11:374933 | G | GAGGGAGG others(184): Show |
1 | a0006c0007t0001g0175 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.784-514_784-513ins others(191): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374933 | ||||||
chr11:374933 | G | GAGGGGAG others(5): Show |
1 | a0022c0015t0001g0040 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.784-524_784-523ins others(12): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374933 | ||||||
chr11:374933 | G | GGGGAGGG others(120): Show |
1 | a0005c0010t0001g0174 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.784-528_784-527ins others(127): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374933 | |||||||
chr11:374934 | A | G | 1 | a0009c0012t0003g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.784-527A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374934 | |||||||
chr11:374935 | G | GGGAGGAG others(105): Show |
1 | a0001c0003t0004g0050 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.784-521_784-520ins others(112): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374935 | ||||||
chr11:374937 | G | A | 1 | a0011c0022t0001g0126 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.784-524G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374937 | |||||||
chr11:374937 | G | GAGGAGGA | 2 | a0001c0003t0002g0024 a0001c0003t0002g0164 |
2 | HG01346.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.784-521_784-520ins others(7): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374937 | ||||||
chr11:374937 | G | GAGGTGGA | 2 | a0001c0001t0001g0094 a0001c0003t0002g0025 |
2 | HG00735.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.784-521_784-520ins others(7): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374937 | ||||||
chr11:374940 | GGAGGAGG others(69): Show |
G | 1 | a0001c0026t0002g0049 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.784-520_784-445del others(76): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374940 | |||||||
chr11:374941 | G | T | 1 | a0002c0002t0001g0161 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.784-520G>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374941 | |||||||
chr11:374942 | A | G | 1 | a0002c0002t0001g0161 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.784-519A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374942 | |||||||
chr11:374944 | G | A | 1 | a0002c0002t0001g0161 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.784-517G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374944 | |||||||
chr11:374945 | A | G | 5 | a0001c0001t0001g0094 a0001c0003t0002g0024 a0001c0003t0002g0025 others(2): Show |
5 | HG00735.hp2 HG00738.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-516A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374945 | |||||||
chr11:374945 | A | T | 4 | a0001c0003t0002g0026 a0001c0003t0002g0027 a0001c0003t0002g0047 others(1): Show |
4 | HG00639.hp2 HG02273.hp2 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-516A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374945 | |||||||
chr11:374946 | G | A | 5 | a0001c0001t0001g0094 a0001c0003t0002g0024 a0001c0003t0002g0025 others(2): Show |
5 | HG00735.hp2 HG00738.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.784-515G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374946 | |||||||
chr11:374948 | A | AAGGGAGG others(8): Show |
1 | a0003c0006t0001g0133 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.784-509_784-495dup others(15): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374948 | ||||||
chr11:374948 | A | G | 28 | a0001c0001t0001g0094 a0001c0001t0001g0134 a0001c0001t0001g0167 others(25): Show |
28 | HG00099.hp2 HG00140.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.784-513A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374948 | |||||||
chr11:374948 | AAGGG | A | 7 | a0001c0001t0001g0034 a0001c0003t0001g0091 a0002c0002t0001g0055 others(4): Show |
7 | HG02080.hp1 HG03834.hp2 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.784-501_784-498del others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374948 | ||||||
chr11:374949 | A | G | 1 | a0001c0003t0004g0017 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.784-512A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374949 | |||||||
chr11:374949 | A | T | 1 | a0006c0007t0001g0122 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.784-512A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374949 | |||||||
chr11:374952 | G | A | 8 | a0001c0001t0001g0094 a0001c0003t0002g0024 a0001c0003t0002g0025 others(5): Show |
8 | HG00735.hp2 HG00738.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.784-509G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374952 | |||||||
chr11:374952 | G | GAGGAGGA | 2 | a0002c0009t0001g0166 a0002c0009t0001g0168 |
2 | HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.784-506_784-505ins others(7): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374952 | ||||||
chr11:374952 | G | GAGGAGGA others(225): Show |
1 | a0001c0001t0001g0167 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.784-506_784-505ins others(232): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374952 | ||||||
chr11:374952 | G | GAGGGAGA others(4): Show |
1 | a0009c0012t0003g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.784-503_784-502ins others(11): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374952 | ||||||
chr11:374952 | G | GAGGGAGG others(423): Show |
1 | a0002c0002t0001g0157 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.784-502_784-501ins others(430): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374952 | ||||||
chr11:374952 | G | GAGGGAGG others(317): Show |
1 | a0002c0004t0001g0176 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.784-502_784-501ins others(324): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374952 | ||||||
chr11:374952 | G | GAGGGAGG others(4): Show |
23 | a0001c0001t0001g0036 a0001c0001t0001g0044 a0001c0001t0001g0048 others(20): Show |
23 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.784-502_784-501ins others(11): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374952 | ||||||
chr11:374952 | G | GAGGGAGG others(19): Show |
2 | a0006c0007t0001g0132 a0007c0011t0001g0068 |
2 | HG03098.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.784-502_784-501ins others(26): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374952 | ||||||
chr11:374952 | G | GAGGGAGG others(49): Show |
1 | a0001c0001t0005g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.784-502_784-501ins others(56): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374952 | ||||||
chr11:374952 | G | GAGGGAGG others(79): Show |
1 | a0002c0035t0001g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.784-502_784-501ins others(86): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374952 | ||||||
chr11:374952 | G | GAGGGAGG others(672): Show |
1 | a0001c0001t0001g0165 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.784-502_784-501ins others(679): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374952 | ||||||
chr11:374952 | G | GAGGGAGG others(512): Show |
1 | a0002c0002t0001g0141 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.784-502_784-501ins others(519): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374952 | ||||||
chr11:374952 | G | GAGGGAGG others(79): Show |
1 | a0001c0003t0002g0026 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.784-502_784-501ins others(86): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374952 | ||||||
chr11:374952 | G | GAGGGAGG others(38): Show |
1 | a0002c0002t0001g0178 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.784-502_784-501ins others(45): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374952 | ||||||
chr11:374952 | G | GAGGGAGG others(49): Show |
1 | a0001c0001t0004g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.784-502_784-501ins others(56): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374952 | ||||||
chr11:374952 | G | GAGGGAGG others(57): Show |
1 | a0002c0002t0001g0146 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.784-502_784-501ins others(64): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374952 | ||||||
chr11:374952 | G | GAGGGAGG others(49): Show |
1 | a0001c0001t0001g0095 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.784-502_784-501ins others(56): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374952 | ||||||
chr11:374952 | G | GAGGGAGG others(454): Show |
2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.784-502_784-501ins others(461): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374952 | ||||||
chr11:374952 | G | GAGGGAGG others(263): Show |
1 | a0001c0016t0001g0104 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.784-502_784-501ins others(270): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374952 | ||||||
chr11:374952 | G | GAGGGAGG others(23): Show |
1 | a0001c0003t0001g0136 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.784-482_784-453dup others(30): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374952 | ||||||
chr11:374952 | G | GAGGGAGG others(409): Show |
1 | a0003c0006t0001g0078 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.784-495_784-494ins others(416): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374952 | ||||||
chr11:374952 | G | GAGGGAGG others(4): Show |
1 | a0001c0001t0001g0114 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.784-502_784-501ins others(11): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374952 | ||||||
chr11:374952 | G | GGAGGGAG others(5): Show |
1 | a0022c0015t0001g0040 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.784-509_784-508ins others(12): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374952 | |||||||
chr11:374952 | G | GGGAGGGA others(1650): Show |
1 | a0002c0002t0001g0061 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.784-509_784-508ins others(1657): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374952 | |||||||
chr11:374953 | A | AGGGAGGA others(1642): Show |
1 | a0002c0002t0001g0145 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.784-502_784-501ins others(1649): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374953 | ||||||
chr11:374954 | G | GGAGGAGG others(31): Show |
1 | a0025c0028t0001g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.784-506_784-505ins others(38): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374954 | ||||||
chr11:374958 | G | GGAGGAAG others(3): Show |
1 | a0019c0018t0001g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.784-502_784-501ins others(10): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374958 | ||||||
chr11:374960 | G | A | 5 | a0002c0002t0001g0149 a0002c0004t0001g0001 a0003c0039t0001g0058 others(2): Show |
6 | HG01433.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.784-501G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374960 | |||||||
chr11:374961 | A | G | 5 | a0002c0002t0001g0149 a0002c0004t0001g0001 a0003c0039t0001g0058 others(2): Show |
6 | HG01433.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.784-500A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374961 | |||||||
chr11:374963 | G | A | 5 | a0002c0002t0001g0149 a0002c0004t0001g0001 a0003c0039t0001g0058 others(2): Show |
6 | HG01433.hp1 HG02109.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.784-498G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374963 | |||||||
chr11:374964 | A | T | 2 | a0001c0001t0001g0127 a0006c0007t0001g0132 |
2 | HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.784-497A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374964 | |||||||
chr11:374967 | A | AAGGG | 11 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0092 others(8): Show |
11 | HG00140.hp2 HG01081.hp1 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.784-486_784-483dup others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374967 | ||||||
chr11:374967 | A | AAGGGAGG others(547): Show |
1 | a0001c0003t0001g0129 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.784-453_784-452ins others(554): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374967 | ||||||
chr11:374967 | A | AAGGGAGG others(392): Show |
1 | a0003c0006t0001g0154 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.784-453_784-452ins others(399): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374967 | ||||||
chr11:374967 | A | AAGGGAGG others(377): Show |
2 | a0002c0002t0001g0142 a0002c0002t0001g0155 |
2 | HG00140.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.784-453_784-452ins others(384): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374967 | ||||||
chr11:374967 | A | AAGGGAGG others(362): Show |
1 | a0002c0002t0001g0152 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.784-453_784-452ins others(369): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374967 | ||||||
chr11:374967 | A | AAGGGAGG others(317): Show |
1 | a0007c0011t0001g0150 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.784-453_784-452ins others(324): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374967 | ||||||
chr11:374967 | A | G | 8 | a0002c0002t0001g0149 a0002c0002t0001g0162 a0002c0004t0001g0001 others(5): Show |
9 | HG01255.hp2 HG01433.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.784-494A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374967 | |||||||
chr11:374974 | GGAGGAGG others(129): Show |
G | 1 | a0005c0010t0001g0109 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.784-486_784-351del | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374974 | |||||||
chr11:374979 | A | G | 4 | a0001c0005t0002g0108 a0001c0005t0002g0116 a0001c0005t0002g0117 others(1): Show |
4 | HG01934.hp2 HG01952.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.784-482A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374979 | |||||||
chr11:374979 | A | T | 3 | a0001c0001t0001g0128 a0001c0003t0002g0024 a0016c0027t0001g0015 |
3 | HG01346.hp2 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.784-482A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374979 | |||||||
chr11:374982 | A | AAGGG | 4 | a0001c0001t0001g0004 a0001c0001t0002g0130 a0002c0002t0001g0009 others(1): Show |
5 | HG00733.hp2 HG01081.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.784-471_784-468dup others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374982 | ||||||
chr11:374982 | A | G | 3 | a0001c0001t0001g0113 a0001c0003t0004g0050 a0002c0002t0001g0137 |
3 | HG02040.hp1 NA18522.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.784-479A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374982 | |||||||
chr11:374990 | G | A | 1 | a0002c0002t0001g0067 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.784-471G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374990 | |||||||
chr11:374994 | A | G | 7 | a0001c0001t0001g0092 a0001c0001t0001g0105 a0001c0005t0002g0108 others(4): Show |
7 | HG01081.hp1 HG01934.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.784-467A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374994 | |||||||
chr11:374994 | A | T | 1 | a0016c0027t0001g0015 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.784-467A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374994 | |||||||
chr11:374995 | G | A | 4 | a0001c0001t0001g0092 a0001c0001t0001g0105 a0002c0002t0001g0151 others(1): Show |
4 | HG01081.hp1 HG02132.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-466G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374995 | |||||||
chr11:374997 | A | AAGGGAGG others(57): Show |
2 | a0001c0001t0001g0134 a0002c0002t0001g0060 |
2 | HG02074.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.784-453_784-452ins others(64): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374997 | ||||||
chr11:374997 | A | G | 4 | a0001c0001t0001g0092 a0001c0001t0001g0105 a0002c0002t0001g0151 others(1): Show |
4 | HG01081.hp1 HG02132.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-464A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374997 | |||||||
chr11:374997 | AAGGG | A | 2 | a0001c0001t0001g0113 a0001c0001t0005g0169 |
2 | HG02040.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.784-452_784-449del others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 374997 | ||||||
chr11:374998 | A | T | 1 | a0009c0012t0003g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.784-463A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 374998 | |||||||
chr11:375001 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0105 |
2 | HG01081.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.784-460G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375001 | |||||||
chr11:375001 | G | GAGGGAGG others(4): Show |
18 | a0001c0001t0001g0036 a0001c0001t0001g0045 a0001c0001t0001g0119 others(15): Show |
18 | HG00140.hp2 HG00642.hp2 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.784-453_784-452ins others(11): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(19): Show |
1 | a0002c0002t0001g0067 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.784-453_784-452ins others(26): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(34): Show |
4 | a0001c0003t0001g0106 a0002c0002t0001g0159 a0002c0002t0001g0163 others(1): Show |
4 | HG03688.hp1 NA18970.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-453_784-452ins others(41): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(103): Show |
1 | a0002c0004t0002g0085 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.784-453_784-452ins others(110): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(49): Show |
1 | a0002c0002t0001g0064 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.784-453_784-452ins others(56): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(64): Show |
1 | a0002c0002t0001g0083 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.784-453_784-452ins others(71): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(79): Show |
2 | a0002c0033t0001g0070 a0012c0040t0001g0007 |
2 | HG01975.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.784-453_784-452ins others(86): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(109): Show |
1 | a0001c0001t0001g0123 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.784-453_784-452ins others(116): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(98): Show |
2 | a0002c0002t0001g0073 a0002c0002t0001g0080 |
2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.784-453_784-452ins others(105): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(431): Show |
1 | a0002c0002t0001g0054 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.784-453_784-452ins others(438): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(98): Show |
1 | a0002c0002t0001g0074 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.784-453_784-452ins others(105): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(256): Show |
1 | a0001c0001t0001g0135 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.784-453_784-452ins others(263): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(353): Show |
2 | a0014c0030t0004g0011 a0017c0031t0004g0012 |
2 | HG02723.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.784-453_784-452ins others(360): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(354): Show |
1 | a0001c0001t0001g0102 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.784-453_784-452ins others(361): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(79): Show |
1 | a0023c0034t0001g0090 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.784-453_784-452ins others(86): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(245): Show |
1 | a0001c0001t0001g0095 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.784-453_784-452ins others(252): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(606): Show |
1 | a0002c0002t0006g0076 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.784-453_784-452ins others(613): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(64): Show |
1 | a0002c0008t0001g0089 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.784-453_784-452ins others(71): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(1231): Show |
1 | a0001c0001t0001g0138 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.784-453_784-452ins others(1238): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(248): Show |
1 | a0010c0017t0001g0086 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.784-453_784-452ins others(255): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(696): Show |
2 | a0002c0002t0001g0140 a0002c0002t0001g0143 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.784-453_784-452ins others(703): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(1497): Show |
1 | a0001c0003t0002g0024 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.784-453_784-452ins others(1504): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(57): Show |
1 | a0001c0005t0002g0131 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.784-453_784-452ins others(64): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(323): Show |
1 | a0001c0003t0002g0027 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.784-453_784-452ins others(330): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(139): Show |
1 | a0001c0003t0002g0025 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.784-453_784-452ins others(146): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(2080): Show |
1 | a0004c0043t0001g0028 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.784-453_784-452ins others(2087): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(4): Show |
1 | a0001c0001t0001g0112 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.784-453_784-452ins others(11): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(19): Show |
1 | a0004c0042t0001g0031 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.784-453_784-452ins others(26): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GAGGGAGG others(113): Show |
1 | a0001c0003t0002g0047 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.784-453_784-452ins others(120): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375001 | G | GGAGGGAG others(72): Show |
1 | a0022c0015t0001g0040 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.784-460_784-459ins others(79): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375001 | |||||||
chr11:375001 | GAGGGAGG others(117): Show |
G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0110 |
4 | HG00099.hp1 HG03492.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-433_784-310del | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375001 | ||||||
chr11:375005 | G | GAGGAGGA | 10 | a0001c0001t0001g0034 a0001c0001t0001g0173 a0001c0001t0003g0019 others(7): Show |
10 | HG00544.hp2 HG02300.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.784-453_784-452ins others(7): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375005 | ||||||
chr11:375005 | G | GAGGAGGA others(515): Show |
1 | a0001c0001t0001g0048 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.784-453_784-452ins others(522): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375005 | ||||||
chr11:375005 | G | GAGGTGGA | 2 | a0001c0001t0001g0127 a0016c0027t0001g0015 |
2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.784-453_784-452ins others(7): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375005 | ||||||
chr11:375008 | G | GTGGAAGG others(55): Show |
1 | a0002c0002t0001g0162 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.784-453_784-452ins others(62): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375008 | |||||||
chr11:375008 | GGAGGAGG others(1): Show |
G | 3 | a0001c0001t0001g0094 a0001c0001t0001g0098 a0006c0007t0001g0122 |
3 | HG00735.hp2 HG03669.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.784-452_784-445del others(8): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375008 | |||||||
chr11:375009 | G | A | 2 | a0001c0001t0001g0128 a0003c0006t0001g0133 |
2 | HG03579.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.784-452G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375009 | |||||||
chr11:375010 | A | AGGAGGAA others(5): Show |
2 | a0003c0039t0001g0058 a0008c0013t0001g0057 |
2 | HG01433.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.784-445_784-434dup others(12): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375010 | ||||||
chr11:375010 | A | G | 4 | a0001c0001t0001g0128 a0002c0002t0001g0162 a0003c0006t0001g0133 others(1): Show |
4 | HG01255.hp2 HG03579.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.784-451A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375010 | |||||||
chr11:375012 | G | A | 2 | a0001c0001t0001g0128 a0003c0006t0001g0133 |
2 | HG03579.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.784-449G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375012 | |||||||
chr11:375013 | A | G | 12 | a0001c0001t0001g0034 a0001c0001t0001g0048 a0001c0001t0001g0127 others(9): Show |
12 | HG00544.hp2 HG02300.hp2 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.784-448A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375013 | |||||||
chr11:375013 | A | T | 4 | a0001c0003t0002g0026 a0001c0003t0002g0047 a0001c0003t0004g0014 others(1): Show |
4 | HG00639.hp2 HG02273.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-448A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375013 | |||||||
chr11:375014 | G | A | 12 | a0001c0001t0001g0034 a0001c0001t0001g0048 a0001c0001t0001g0127 others(9): Show |
12 | HG00544.hp2 HG02300.hp2 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.784-447G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375014 | |||||||
chr11:375016 | A | AAGGAGGG others(768): Show |
1 | a0001c0003t0004g0017 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.784-442_784-441ins others(775): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375016 | ||||||
chr11:375016 | A | G | 15 | a0001c0001t0001g0034 a0001c0001t0001g0048 a0001c0001t0001g0127 others(12): Show |
15 | HG00544.hp2 HG02300.hp2 HG02965.hp1 others(12): Show |
intron_variant | MODIFIER | c.784-445A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375016 | |||||||
chr11:375016 | AAGGG | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0002g0130 others(5): Show |
9 | HG00733.hp2 HG01081.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.784-433_784-430del others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375016 | ||||||
chr11:375020 | G | A | 17 | a0001c0001t0001g0034 a0001c0001t0001g0048 a0001c0001t0001g0094 others(14): Show |
17 | HG00544.hp2 HG00735.hp2 HG02300.hp2 others(14): Show |
intron_variant | MODIFIER | c.784-441G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375020 | |||||||
chr11:375020 | G | GAGGGAGG others(248): Show |
1 | a0007c0011t0001g0158 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.784-434_784-433ins others(255): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(4): Show |
33 | a0001c0001t0001g0036 a0001c0001t0001g0042 a0001c0001t0001g0045 others(30): Show |
33 | HG00408.hp1 HG00438.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.784-434_784-433ins others(11): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(80): Show |
1 | a0002c0002t0001g0061 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.784-434_784-433ins others(87): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(19): Show |
5 | a0001c0001t0001g0099 a0001c0001t0001g0118 a0001c0001t0004g0016 others(2): Show |
5 | HG01891.hp1 HG01952.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.784-434_784-433ins others(26): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(34): Show |
2 | a0002c0002t0001g0062 a0003c0006t0001g0078 |
2 | HG03453.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.784-434_784-433ins others(41): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(49): Show |
1 | a0001c0001t0001g0038 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.784-434_784-433ins others(56): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(109): Show |
1 | a0001c0003t0001g0097 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.784-434_784-433ins others(116): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(188): Show |
1 | a0002c0002t0001g0009 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.784-434_784-433ins others(195): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(158): Show |
1 | a0002c0002t0001g0008 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.784-434_784-433ins others(165): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(143): Show |
1 | a0002c0002t0001g0072 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.784-434_784-433ins others(150): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(248): Show |
1 | a0001c0001t0001g0035 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.784-434_784-433ins others(255): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(128): Show |
1 | a0002c0038t0003g0020 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.784-434_784-433ins others(135): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(64): Show |
1 | a0021c0019t0001g0033 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.784-434_784-433ins others(71): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(308): Show |
1 | a0001c0003t0002g0026 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.784-434_784-433ins others(315): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(237): Show |
1 | a0002c0002t0001g0055 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.784-434_784-433ins others(244): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(289): Show |
1 | a0002c0004t0001g0001 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.784-434_784-433ins others(296): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(272): Show |
1 | a0002c0004t0001g0001 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.784-434_784-433ins others(279): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(64): Show |
1 | a0002c0008t0001g0144 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.784-434_784-433ins others(71): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(81): Show |
1 | a0013c0020t0001g0046 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.784-434_784-433ins others(88): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(267): Show |
1 | a0001c0001t0001g0044 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.784-434_784-433ins others(274): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(181): Show |
1 | a0002c0002t0001g0063 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.784-434_784-433ins others(188): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(894): Show |
1 | a0001c0001t0001g0101 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.784-434_784-433ins others(901): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(179): Show |
1 | a0001c0016t0001g0104 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.784-434_784-433ins others(186): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(49): Show |
1 | a0002c0035t0001g0071 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.784-434_784-433ins others(56): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(1198): Show |
1 | a0005c0010t0001g0174 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.784-434_784-433ins others(1205): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(482): Show |
1 | a0001c0001t0001g0170 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.784-434_784-433ins others(489): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(365): Show |
1 | a0002c0002t0003g0153 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.784-434_784-433ins others(372): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(23): Show |
1 | a0001c0005t0002g0108 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.784-434_784-433ins others(30): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(112): Show |
1 | a0002c0002t0001g0157 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.784-434_784-433ins others(119): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(53): Show |
1 | a0006c0007t0001g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.784-434_784-433ins others(60): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(192): Show |
2 | a0002c0002t0001g0069 a0002c0002t0001g0075 |
2 | NA19012.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.784-434_784-433ins others(199): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(53): Show |
1 | a0001c0003t0001g0091 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.784-434_784-433ins others(60): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(64): Show |
1 | a0002c0009t0001g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.784-434_784-433ins others(71): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(1830): Show |
1 | a0002c0002t0001g0010 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.784-434_784-433ins others(1837): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(19): Show |
1 | a0001c0001t0001g0093 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.784-434_784-433ins others(26): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(364): Show |
1 | a0001c0001t0001g0121 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.784-434_784-433ins others(371): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(83): Show |
1 | a0001c0005t0002g0107 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.784-433_784-432ins others(90): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGGAGG others(4): Show |
4 | a0001c0001t0001g0102 a0002c0002t0001g0054 a0014c0030t0004g0011 others(1): Show |
4 | HG02015.hp1 HG02723.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-434_784-433ins others(11): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | G | GAGGTGGA | 2 | a0001c0001t0001g0128 a0003c0006t0001g0133 |
2 | HG03579.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.784-438_784-437ins others(7): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375020 | GAGGGAGG others(8): Show |
G | 1 | a0005c0023t0001g0125 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.784-429_784-415del others(15): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375020 | ||||||
chr11:375022 | G | GGGAGGAG others(3): Show |
1 | a0001c0001t0001g0095 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.784-434_784-433ins others(10): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375022 | ||||||
chr11:375028 | G | A | 6 | a0001c0001t0001g0119 a0001c0001t0005g0169 a0001c0005t0002g0116 others(3): Show |
6 | HG01952.hp1 HG01975.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.784-433G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375028 | |||||||
chr11:375029 | A | G | 5 | a0001c0001t0001g0119 a0001c0001t0005g0169 a0001c0005t0002g0116 others(2): Show |
5 | HG01952.hp1 HG01975.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.784-432A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375029 | |||||||
chr11:375031 | G | A | 5 | a0001c0001t0001g0119 a0001c0001t0005g0169 a0001c0005t0002g0116 others(2): Show |
5 | HG01952.hp1 HG01975.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.784-430G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375031 | |||||||
chr11:375032 | T | A | 110 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0035 others(107): Show |
111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.784-429T>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375032 | |||||||
chr11:375032 | T | G | 1 | a0002c0002t0001g0067 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.784-429T>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375032 | |||||||
chr11:375032 | T | TGGAAGGG others(8): Show |
2 | a0001c0001t0001g0036 a0001c0001t0001g0038 |
2 | NA19002.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.784-414_784-400dup others(15): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375032 | ||||||
chr11:375032 | T | TGGAAGGG others(23): Show |
1 | a0001c0001t0001g0173 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.784-400_784-399ins others(30): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375032 | ||||||
chr11:375032 | T | TGGAAGGG others(83): Show |
1 | a0001c0001t0004g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.784-400_784-399ins others(90): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375032 | ||||||
chr11:375035 | A | AAGGG | 8 | a0001c0001t0001g0092 a0001c0001t0001g0105 a0001c0001t0001g0135 others(5): Show |
8 | HG01081.hp1 HG02132.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.784-418_784-415dup others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375035 | ||||||
chr11:375035 | A | AAGGGAGG others(224): Show |
1 | a0002c0004t0001g0176 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.784-400_784-399ins others(231): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375035 | ||||||
chr11:375035 | A | AAGGGAGG others(57): Show |
1 | a0026c0025t0003g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.784-412_784-411ins others(64): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375035 | ||||||
chr11:375035 | A | AAGGGAGG others(16): Show |
1 | a0001c0001t0001g0114 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.784-415_784-414ins others(23): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375035 | ||||||
chr11:375035 | A | G | 8 | a0001c0001t0001g0119 a0001c0001t0005g0169 a0001c0003t0001g0136 others(5): Show |
8 | HG01952.hp1 HG02109.hp1 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.784-426A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375035 | |||||||
chr11:375035 | A | GAGGGAGG others(23): Show |
1 | a0001c0005t0002g0117 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.784-427_784-426ins others(30): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375035 | |||||||
chr11:375037 | G | A | 1 | a0004c0044t0001g0032 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.784-424G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375037 | |||||||
chr11:375038 | G | A | 1 | a0002c0004t0001g0056 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.784-423G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375038 | |||||||
chr11:375039 | GAGGGAGG others(49): Show |
G | 1 | a0001c0001t0001g0113 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.784-414_784-359del others(56): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375039 | ||||||
chr11:375047 | A | G | 1 | a0001c0005t0002g0131 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.784-414A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375047 | |||||||
chr11:375047 | A | T | 5 | a0001c0001t0001g0094 a0002c0008t0001g0144 a0004c0044t0001g0032 others(2): Show |
5 | HG00735.hp2 HG01243.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.784-414A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375047 | |||||||
chr11:375050 | A | AAGGG | 6 | a0001c0001t0005g0171 a0001c0003t0001g0097 a0002c0002t0001g0140 others(3): Show |
6 | HG01070.hp2 HG01071.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.784-403_784-400dup others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375050 | ||||||
chr11:375050 | A | AAGGGAGG others(1451): Show |
1 | a0018c0029t0004g0053 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.784-400_784-399ins others(1458): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375050 | ||||||
chr11:375050 | A | G | 3 | a0002c0002t0001g0066 a0002c0002t0001g0160 a0003c0006t0001g0077 |
3 | NA18947.hp2 NA18963.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.784-411A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375050 | |||||||
chr11:375061 | G | A | 1 | a0016c0027t0001g0015 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.784-400G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375061 | |||||||
chr11:375062 | T | A | 110 | a0001c0001t0001g0003 a0001c0001t0001g0034 a0001c0001t0001g0035 others(107): Show |
110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.784-399T>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375062 | |||||||
chr11:375062 | T | AGGAAGGG others(23): Show |
1 | a0002c0002t0001g0067 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.784-400_784-399ins others(30): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375062 | |||||||
chr11:375062 | T | G | 1 | a0001c0005t0002g0131 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.784-399T>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375062 | |||||||
chr11:375062 | T | TGGAAGGG others(8): Show |
1 | a0022c0015t0001g0040 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.784-384_784-370dup others(15): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375062 | ||||||
chr11:375062 | T | TGGAAGGG others(38): Show |
1 | a0001c0001t0001g0111 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.784-370_784-369ins others(45): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375062 | ||||||
chr11:375062 | T | TGGAAGGG others(533): Show |
1 | a0001c0001t0003g0019 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.784-370_784-369ins others(540): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375062 | ||||||
chr11:375062 | T | TGGAAGGG others(68): Show |
1 | a0002c0004t0001g0001 | 2 | HG02258.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.784-385_784-384ins others(75): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375062 | ||||||
chr11:375065 | A | AAGGG | 3 | a0001c0001t0001g0120 a0001c0001t0001g0165 a0004c0014t0002g0029 |
3 | HG00642.hp2 HG02074.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.784-388_784-385dup others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375065 | ||||||
chr11:375065 | A | AAGGGAGG others(122): Show |
1 | a0001c0001t0005g0172 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.784-385_784-384ins others(129): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375065 | ||||||
chr11:375065 | A | AAGGGAGG others(16): Show |
1 | a0026c0025t0003g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.784-385_784-384ins others(23): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375065 | ||||||
chr11:375065 | A | AGGGGAGG others(7): Show |
1 | a0009c0012t0003g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.784-396_784-395ins others(14): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375065 | |||||||
chr11:375065 | A | G | 1 | a0003c0006t0001g0077 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.784-396A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375065 | |||||||
chr11:375069 | GAGGGAGG others(49): Show |
G | 1 | a0001c0001t0001g0003 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.784-384_784-329del others(56): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375069 | ||||||
chr11:375071 | G | GGGAGGAG others(683): Show |
1 | a0001c0003t0004g0050 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.784-373_784-372ins others(690): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375071 | ||||||
chr11:375076 | G | GTGGAAGG others(106): Show |
1 | a0002c0033t0001g0070 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.784-385_784-384ins others(113): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375076 | |||||||
chr11:375077 | A | AGGAAGGG others(1051): Show |
1 | a0001c0003t0003g0018 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.784-370_784-369ins others(1058): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375077 | ||||||
chr11:375077 | A | T | 8 | a0001c0001t0001g0048 a0001c0003t0001g0136 a0001c0003t0002g0024 others(5): Show |
9 | HG01346.hp2 HG02258.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.784-384A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375077 | |||||||
chr11:375080 | A | AAGGG | 5 | a0001c0001t0001g0105 a0002c0002t0001g0145 a0002c0002t0001g0161 others(2): Show |
5 | HG02132.hp1 HG02132.hp2 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.784-373_784-370dup others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375080 | ||||||
chr11:375080 | A | AAGGGAGG others(12): Show |
3 | a0002c0002t0001g0064 a0002c0002t0001g0159 a0002c0002t0001g0163 |
3 | HG04199.hp1 NA19057.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.784-370_784-369ins others(19): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375080 | ||||||
chr11:375080 | A | G | 3 | a0001c0001t0001g0114 a0002c0033t0001g0070 a0005c0010t0001g0037 |
3 | HG00544.hp2 HG01069.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.784-381A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375080 | |||||||
chr11:375084 | GAGGGAGG others(34): Show |
G | 2 | a0001c0001t0001g0092 a0005c0023t0001g0125 |
2 | HG01081.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.784-369_784-329del others(41): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375084 | ||||||
chr11:375085 | A | AGGGAGGA others(9): Show |
1 | a0004c0014t0002g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.784-370_784-369ins others(16): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375085 | ||||||
chr11:375092 | T | A | 104 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(101): Show |
105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.784-369T>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375092 | |||||||
chr11:375092 | T | TGGAAGGG others(8): Show |
2 | a0001c0001t0001g0119 a0001c0005t0002g0116 |
2 | HG01952.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.784-309_784-295dup others(15): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375092 | ||||||
chr11:375092 | T | TGGAAGGG others(353): Show |
1 | a0010c0017t0001g0086 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.784-340_784-339ins others(360): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375092 | ||||||
chr11:375092 | T | TGGAAGGG others(116): Show |
1 | a0001c0001t0001g0123 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.784-340_784-339ins others(123): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375092 | ||||||
chr11:375095 | A | AAGGG | 2 | a0001c0001t0001g0099 a0018c0029t0004g0053 |
2 | HG03486.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.784-358_784-355dup others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375095 | ||||||
chr11:375095 | A | AAGGGAGG others(151): Show |
1 | a0002c0009t0001g0168 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.784-295_784-294ins others(158): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375095 | ||||||
chr11:375095 | A | AAGGGAGG others(121): Show |
1 | a0001c0024t0003g0022 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.784-340_784-339ins others(128): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375095 | ||||||
chr11:375095 | A | AAGGGAGG others(392): Show |
2 | a0003c0039t0001g0058 a0008c0013t0001g0057 |
2 | HG01433.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.784-355_784-354ins others(399): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375095 | ||||||
chr11:375095 | A | AGGGAGGG others(41): Show |
1 | a0001c0003t0001g0106 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.784-366_784-365ins others(48): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375095 | |||||||
chr11:375098 | G | A | 1 | a0004c0014t0002g0029 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.784-363G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375098 | |||||||
chr11:375100 | A | T | 1 | a0001c0003t0004g0050 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.784-361A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375100 | |||||||
chr11:375107 | A | AGGAAGGG others(381): Show |
1 | a0004c0042t0001g0031 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.784-325_784-324ins others(388): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375107 | ||||||
chr11:375107 | A | AGGAAGGG others(27): Show |
1 | a0007c0011t0001g0068 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.784-325_784-324ins others(34): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375107 | ||||||
chr11:375107 | A | AGGAAGGG others(23): Show |
1 | a0015c0041t0001g0030 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.784-325_784-324ins others(30): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375107 | ||||||
chr11:375107 | A | AGGAAGGG others(8): Show |
1 | a0001c0003t0001g0129 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.784-340_784-339ins others(15): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375107 | ||||||
chr11:375107 | A | AGGAAGGG others(38): Show |
1 | a0001c0003t0004g0050 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.784-340_784-339ins others(45): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375107 | ||||||
chr11:375107 | A | T | 8 | a0001c0001t0001g0048 a0001c0001t0001g0170 a0001c0003t0002g0025 others(5): Show |
9 | HG00323.hp1 HG01074.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.784-354A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375107 | |||||||
chr11:375110 | A | AAGGG | 6 | a0001c0001t0001g0094 a0001c0005t0002g0131 a0002c0002t0003g0153 others(3): Show |
6 | HG00735.hp2 HG01070.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.784-343_784-340dup others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375110 | ||||||
chr11:375110 | A | AAGGGAGG others(706): Show |
1 | a0002c0004t0002g0084 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.784-344_784-343ins others(713): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375110 | ||||||
chr11:375110 | A | AAGGGAGG others(463): Show |
1 | a0004c0014t0002g0051 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.784-344_784-343ins others(470): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375110 | ||||||
chr11:375110 | A | AAGGGAGG others(228): Show |
1 | a0002c0002t0001g0061 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.784-339_784-338ins others(235): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375110 | ||||||
chr11:375110 | A | AAGGGAGG others(489): Show |
1 | a0001c0001t0001g0124 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.784-295_784-294ins others(496): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375110 | ||||||
chr11:375110 | A | AAGGGAGG others(136): Show |
1 | a0002c0009t0001g0166 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.784-295_784-294ins others(143): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375110 | ||||||
chr11:375110 | A | AAGGGAGG others(121): Show |
1 | a0002c0002t0001g0082 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.784-325_784-324ins others(128): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375110 | ||||||
chr11:375110 | A | AGGGAGGG others(154): Show |
1 | a0009c0012t0003g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.784-351_784-350ins others(161): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375110 | |||||||
chr11:375110 | A | G | 1 | a0026c0025t0003g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.784-351A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375110 | |||||||
chr11:375112 | G | GGAGGGAG others(102): Show |
1 | a0025c0028t0001g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.784-348_784-347ins others(109): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375112 | ||||||
chr11:375112 | G | GGGAGGGA others(3): Show |
1 | a0001c0001t0001g0101 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.784-345_784-336dup others(10): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375112 | ||||||
chr11:375115 | A | AGGGAGGA others(10): Show |
1 | a0001c0003t0004g0017 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.784-332_784-331ins others(17): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375115 | ||||||
chr11:375120 | G | GGAGGAAG others(25): Show |
1 | a0009c0012t0003g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.784-313_784-312ins others(32): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375120 | ||||||
chr11:375121 | G | GGAGGAAG others(97): Show |
1 | a0002c0002t0001g0157 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.784-340_784-339ins others(104): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375121 | |||||||
chr11:375121 | G | GGAGGAGG others(31): Show |
1 | a0002c0002t0001g0062 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.784-340_784-339ins others(38): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375121 | |||||||
chr11:375121 | G | GTGGAAGG others(121): Show |
1 | a0002c0002t0001g0083 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.784-340_784-339ins others(128): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375121 | |||||||
chr11:375121 | G | GTGGAAGG others(106): Show |
1 | a0002c0002t0001g0178 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.784-340_784-339ins others(113): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375121 | |||||||
chr11:375122 | A | AGGAAGGG others(23): Show |
1 | a0002c0009t0001g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.784-310_784-309ins others(30): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375122 | ||||||
chr11:375122 | A | AGGAAGGG others(166): Show |
1 | a0001c0003t0004g0014 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.784-325_784-324ins others(173): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375122 | ||||||
chr11:375122 | A | T | 8 | a0001c0001t0001g0138 a0001c0001t0005g0172 a0002c0002t0001g0054 others(5): Show |
8 | HG00438.hp2 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.784-339A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375122 | |||||||
chr11:375125 | A | AAGGG | 11 | a0001c0001t0001g0105 a0001c0001t0001g0114 a0002c0002t0001g0064 others(8): Show |
11 | HG00544.hp2 HG01069.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.784-328_784-325dup others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375125 | ||||||
chr11:375125 | A | AAGGGAGG others(694): Show |
1 | a0002c0002t0001g0060 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.784-295_784-294ins others(701): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375125 | ||||||
chr11:375125 | A | AAGGGAGG others(132): Show |
1 | a0001c0001t0001g0045 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.784-295_784-294ins others(139): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375125 | ||||||
chr11:375125 | A | AAGGGAGG others(117): Show |
1 | a0001c0001t0001g0034 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.784-295_784-294ins others(124): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375125 | ||||||
chr11:375125 | A | AAGGGAGG others(527): Show |
1 | a0002c0002t0001g0066 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.784-295_784-294ins others(534): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375125 | ||||||
chr11:375125 | A | AAGGGAGG others(482): Show |
1 | a0002c0002t0001g0146 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.784-295_784-294ins others(489): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375125 | ||||||
chr11:375125 | A | AAGGGAGG others(181): Show |
1 | a0007c0011t0001g0150 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.784-295_784-294ins others(188): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375125 | ||||||
chr11:375125 | A | AAGGGAGG others(475): Show |
1 | a0001c0003t0001g0136 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.784-295_784-294ins others(482): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375125 | ||||||
chr11:375125 | A | AAGGGAGG others(61): Show |
1 | a0002c0037t0001g0156 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.784-310_784-309ins others(68): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375125 | ||||||
chr11:375125 | A | AAGGGAGG others(455): Show |
1 | a0007c0011t0001g0158 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.784-310_784-309ins others(462): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375125 | ||||||
chr11:375125 | A | AAGGGAGG others(237): Show |
1 | a0001c0003t0001g0091 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.784-310_784-309ins others(244): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375125 | ||||||
chr11:375125 | A | AAGGGAGG others(159): Show |
1 | a0002c0002t0001g0152 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.784-310_784-309ins others(166): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375125 | ||||||
chr11:375125 | A | AAGGGAGG others(31): Show |
1 | a0001c0001t0001g0134 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.784-325_784-324ins others(38): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375125 | ||||||
chr11:375125 | A | AAGGGAGG others(46): Show |
4 | a0002c0002t0001g0055 a0002c0002t0001g0069 a0002c0002t0001g0075 others(1): Show |
4 | HG04115.hp2 NA18970.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-325_784-324ins others(53): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375125 | ||||||
chr11:375125 | A | AAGGGAGG others(197): Show |
1 | a0002c0002t0001g0151 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.784-325_784-324ins others(204): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375125 | ||||||
chr11:375125 | A | AAGGGAGG others(505): Show |
1 | a0020c0032t0001g0147 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.784-325_784-324ins others(512): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375125 | ||||||
chr11:375125 | A | G | 4 | a0002c0002t0001g0062 a0002c0002t0001g0083 a0002c0002t0001g0157 others(1): Show |
4 | HG00408.hp1 HG01978.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.784-336A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375125 | |||||||
chr11:375130 | A | AGGGAGGA others(589): Show |
1 | a0003c0006t0001g0133 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.784-310_784-309ins others(596): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375130 | ||||||
chr11:375131 | G | T | 1 | a0013c0020t0001g0046 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.784-330G>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375131 | |||||||
chr11:375136 | G | GGAGGAGG others(282): Show |
1 | a0009c0012t0001g0103 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.784-325_784-324ins others(289): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375136 | |||||||
chr11:375137 | A | AGGAAGGG others(391): Show |
1 | a0002c0038t0003g0020 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.784-295_784-294ins others(398): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375137 | ||||||
chr11:375137 | A | AGGAAGGG others(38): Show |
2 | a0001c0001t0001g0093 a0001c0003t0002g0027 |
2 | HG01258.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.784-310_784-309ins others(45): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375137 | ||||||
chr11:375137 | A | AGGAAGGG others(2217): Show |
1 | a0001c0003t0002g0047 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.784-310_784-309ins others(2224): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375137 | ||||||
chr11:375137 | A | T | 8 | a0001c0001t0001g0048 a0001c0001t0001g0170 a0002c0002t0001g0140 others(5): Show |
9 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.784-324A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375137 | |||||||
chr11:375140 | A | AAGGG | 5 | a0001c0001t0001g0099 a0001c0003t0001g0106 a0002c0004t0001g0056 others(2): Show |
5 | HG01433.hp1 HG03225.hp2 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.784-313_784-310dup others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375140 | ||||||
chr11:375140 | A | AAGGGAGG others(907): Show |
1 | a0023c0034t0001g0090 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.784-295_784-294ins others(914): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375140 | ||||||
chr11:375140 | A | AAGGGAGG others(857): Show |
1 | a0001c0001t0001g0042 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.784-295_784-294ins others(864): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375140 | ||||||
chr11:375140 | A | AAGGGAGG others(50): Show |
1 | a0002c0002t0001g0073 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.784-295_784-294ins others(57): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375140 | ||||||
chr11:375140 | A | AAGGGAGG others(846): Show |
1 | a0002c0008t0001g0089 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.784-306_784-305ins others(853): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375140 | ||||||
chr11:375140 | A | AAGGGAGG others(46): Show |
1 | a0002c0002t0001g0074 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.784-310_784-309ins others(53): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375140 | ||||||
chr11:375140 | A | AAGGGAGG others(1612): Show |
1 | a0008c0013t0001g0059 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.784-310_784-309ins others(1619): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375140 | ||||||
chr11:375140 | A | AAGGGAGG others(69): Show |
1 | a0002c0002t0001g0080 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.784-310_784-309ins others(76): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375140 | ||||||
chr11:375140 | A | AAGGGAGG others(65): Show |
1 | a0003c0006t0001g0078 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.784-310_784-309ins others(72): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375140 | ||||||
chr11:375140 | A | AAGGGAGG others(258): Show |
1 | a0012c0040t0001g0007 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.784-310_784-309ins others(265): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375140 | ||||||
chr11:375140 | A | AAGGGAGG others(65): Show |
2 | a0002c0002t0001g0008 a0002c0002t0001g0009 |
2 | HG01258.hp2 HG01934.hp1 |
intron_variant | MODIFIER | c.784-310_784-309ins others(72): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375140 | ||||||
chr11:375140 | A | AAGGGAGG others(69): Show |
1 | a0002c0002t0001g0010 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.784-310_784-309ins others(76): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375140 | ||||||
chr11:375140 | A | AAGGGAGG others(136): Show |
1 | a0003c0006t0001g0154 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.784-310_784-309ins others(143): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375140 | ||||||
chr11:375140 | A | AGGAAGGG others(518): Show |
1 | a0006c0007t0001g0175 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.784-321_784-320ins others(525): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375140 | |||||||
chr11:375140 | A | G | 1 | a0009c0012t0001g0103 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.784-321A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375140 | |||||||
chr11:375145 | A | G | 1 | a0005c0010t0001g0109 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.784-316A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375145 | |||||||
chr11:375146 | G | A | 1 | a0005c0010t0001g0109 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.784-315G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375146 | |||||||
chr11:375146 | G | GGAGGTGG others(6): Show |
1 | a0001c0003t0003g0018 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.784-314_784-313ins others(13): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375146 | ||||||
chr11:375151 | G | GGAGGAGG others(31): Show |
2 | a0002c0002t0001g0072 a0002c0035t0001g0071 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.784-310_784-309ins others(38): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375151 | |||||||
chr11:375152 | A | T | 7 | a0001c0003t0001g0097 a0001c0003t0004g0050 a0002c0002t0001g0067 others(4): Show |
7 | HG02080.hp2 HG02723.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.784-309A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375152 | |||||||
chr11:375152 | AGGAAGGG others(8): Show |
A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0098 a0001c0001t0002g0130 others(3): Show |
7 | HG00733.hp2 HG01081.hp2 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.784-294_784-280del others(15): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375152 | ||||||
chr11:375155 | A | AAGGG | 2 | a0002c0002t0003g0153 a0002c0002t0006g0076 |
2 | HG01361.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.784-298_784-295dup others(4): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375155 | ||||||
chr11:375155 | A | AAGGGAGG others(196): Show |
1 | a0002c0002t0001g0142 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.784-295_784-294ins others(203): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375155 | ||||||
chr11:375155 | A | AAGGGAGG others(46): Show |
2 | a0002c0002t0001g0063 a0003c0006t0001g0065 |
2 | HG03831.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.784-295_784-294ins others(53): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375155 | ||||||
chr11:375155 | A | G | 2 | a0002c0002t0001g0072 a0002c0035t0001g0071 |
2 | HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.784-306A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375155 | |||||||
chr11:375157 | G | GGGAGGGA others(7): Show |
1 | a0001c0003t0003g0018 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.784-301_784-288dup others(14): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375157 | ||||||
chr11:375160 | A | AGGGAGGA others(1538): Show |
1 | a0011c0022t0001g0126 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.784-295_784-294ins others(1545): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375160 | ||||||
chr11:375161 | G | GGAGGAGG others(112): Show |
1 | a0001c0001t0001g0043 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.784-299_784-298ins others(119): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375161 | ||||||
chr11:375164 | A | T | 1 | a0003c0006t0001g0133 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.784-297A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375164 | |||||||
chr11:375167 | T | A | 138 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0034 others(135): Show |
140 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(137): Show |
intron_variant | MODIFIER | c.784-294T>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375167 | |||||||
chr11:375167 | T | TGGAAGGG others(8): Show |
1 | a0018c0029t0004g0053 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.784-259_784-245dup others(15): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375167 | ||||||
chr11:375167 | T | TGGAAGGG others(23): Show |
4 | a0001c0003t0001g0097 a0001c0003t0004g0014 a0002c0002t0001g0140 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG02080.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-274_784-245dup others(30): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375167 | ||||||
chr11:375167 | T | TGGAAGGG others(38): Show |
2 | a0001c0005t0002g0131 a0001c0016t0001g0104 |
2 | HG01070.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.784-289_784-245dup others(45): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375167 | ||||||
chr11:375167 | T | TGGAAGGG others(870): Show |
1 | a0002c0009t0001g0177 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.784-245_784-244ins others(877): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375167 | ||||||
chr11:375167 | T | TGGAAGGG others(53): Show |
1 | a0001c0001t0005g0169 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.784-265_784-264ins others(60): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375167 | ||||||
chr11:375167 | T | TGGAAGGG others(68): Show |
1 | a0001c0001t0005g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.784-265_784-264ins others(75): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375167 | ||||||
chr11:375167 | T | TGGAAGGG others(497): Show |
1 | a0002c0002t0001g0155 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.784-265_784-264ins others(504): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375167 | ||||||
chr11:375167 | T | TGGAAGGG others(166): Show |
2 | a0002c0002t0001g0141 a0002c0002t0001g0149 |
2 | HG01358.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.784-265_784-264ins others(173): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375167 | ||||||
chr11:375167 | T | TGGAAGGG others(822): Show |
1 | a0001c0003t0002g0025 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.784-280_784-279ins others(829): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375167 | ||||||
chr11:375167 | T | TGGAAGGG others(23): Show |
1 | a0016c0027t0001g0015 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.784-280_784-279ins others(30): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375167 | ||||||
chr11:375167 | T | TGGAAGGG others(21): Show |
1 | a0005c0010t0001g0174 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.784-280_784-279ins others(28): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375167 | ||||||
chr11:375167 | T | TGGAGGGA others(1057): Show |
1 | a0019c0018t0001g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.784-291_784-290ins others(1064): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375167 | ||||||
chr11:375170 | A | AAGGGAGG others(8): Show |
1 | a0025c0028t0001g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.784-277_784-276ins others(15): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375170 | ||||||
chr11:375170 | A | AAGGGAGG others(523): Show |
1 | a0002c0002t0001g0162 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.784-280_784-279ins others(530): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375170 | ||||||
chr11:375170 | A | C | 1 | a0001c0003t0001g0091 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.784-291A>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375170 | |||||||
chr11:375176 | G | GGGAGGAG others(2134): Show |
1 | a0001c0003t0002g0026 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.784-265_784-264ins others(2141): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375176 | ||||||
chr11:375182 | A | AGGAAGGG others(1103): Show |
1 | a0003c0006t0001g0077 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.784-245_784-244ins others(1110): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375182 | ||||||
chr11:375182 | A | AGGAAGGG others(379): Show |
1 | a0002c0002t0001g0160 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.784-265_784-264ins others(386): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375182 | ||||||
chr11:375182 | A | T | 1 | a0007c0011t0001g0068 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.784-279A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375182 | |||||||
chr11:375187 | G | GGGAGGGA others(22): Show |
1 | a0001c0003t0002g0026 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.784-273_784-245dup others(29): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375187 | ||||||
chr11:375191 | G | GGGAGGAG others(22): Show |
1 | a0001c0001t0001g0043 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.784-245_784-244ins others(29): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375191 | ||||||
chr11:375193 | G | A | 1 | a0005c0010t0001g0109 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.784-268G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375193 | |||||||
chr11:375194 | A | G | 1 | a0005c0010t0001g0109 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.784-267A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375194 | |||||||
chr11:375197 | A | AGGAGGAA others(664): Show |
1 | a0002c0004t0002g0085 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.784-261_784-260ins others(671): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375197 | ||||||
chr11:375203 | G | GGAGGGAG others(23): Show |
1 | a0002c0004t0001g0056 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.784-245_784-244ins others(30): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375203 | ||||||
chr11:375209 | A | AGGAGGAA others(8): Show |
1 | a0011c0022t0001g0126 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.784-245_784-244ins others(15): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375209 | ||||||
chr11:375209 | A | AGGGAGAG others(900): Show |
1 | a0004c0044t0001g0032 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.784-250_784-249ins others(907): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375209 | ||||||
chr11:375209 | A | T | 1 | a0003c0006t0001g0077 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.784-252A>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375209 | |||||||
chr11:375215 | A | AAGGGAGG others(81): Show |
1 | a0006c0007t0001g0132 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.784-245_784-244ins others(88): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | INFO_REALIGN_3_PRIME | chr11 | 375215 | ||||||
chr11:375215 | A | AGGGAGGG others(19): Show |
1 | a0003c0006t0001g0077 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.784-246_784-245ins others(26): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375215 | |||||||
chr11:375230 | A | C | 1 | a0001c0003t0002g0026 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.784-231A>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375230 | |||||||
chr11:375348 | A | C | 1 | a0005c0010t0001g0174 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.784-113A>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 8/19 | chr11 | 375348 | |||||||
chr11:375535 | C | A | 1 | a0001c0001t0001g0101 | 1 | HG03669.hp1 | splice_region_variant&intron_variant | LOW | c.850+8C>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 9/19 | chr11 | 375535 | |||||||
chr11:375544 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.850+17C>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 9/19 | chr11 | 375544 | |||||||
chr11:375554 | G | A | 1 | a0001c0026t0002g0049 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.850+27G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 9/19 | chr11 | 375554 | |||||||
chr11:375569 | G | C | 1 | a0001c0001t0003g0019 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.850+42G>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 9/19 | chr11 | 375569 | |||||||
chr11:375617 | C | T | 4 | a0001c0001t0001g0034 a0001c0001t0001g0042 a0001c0001t0001g0043 others(1): Show |
4 | NA18952.hp2 NA19002.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.851-22C>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 9/19 | chr11 | 375617 | |||||||
chr11:375780 | G | A | 1 | a0004c0044t0001g0032 | 1 | HG01243.hp2 | splice_region_variant&intron_variant | LOW | c.985+7G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 10/19 | chr11 | 375780 | |||||||
chr11:375791 | C | CG | 11 | a0001c0001t0001g0134 a0001c0005t0002g0108 a0001c0024t0003g0022 others(8): Show |
11 | HG00438.hp1 HG00642.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.985+23dupG | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr11 | 375791 | ||||||
chr11:375797 | C | G | 1 | a0003c0006t0001g0077 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.985+24C>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 10/19 | chr11 | 375797 | |||||||
chr11:375804 | G | A | 8 | a0001c0001t0001g0111 a0001c0003t0002g0024 a0001c0003t0002g0025 others(5): Show |
8 | HG00639.hp2 HG01074.hp1 HG01074.hp2 others(5): Show |
intron_variant | MODIFIER | c.985+31G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 10/19 | chr11 | 375804 | |||||||
chr11:376057 | G | GC | 9 | a0001c0003t0004g0017 a0002c0002t0001g0010 a0002c0008t0001g0144 others(6): Show |
9 | HG00544.hp1 HG00544.hp2 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.1096-10dupC | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 11/19 | INFO_REALIGN_3_PRIME | chr11 | 376057 | ||||||
chr11:376064 | C | A | 3 | a0001c0003t0001g0091 a0001c0003t0001g0097 a0024c0021t0001g0096 |
3 | HG02080.hp1 HG02080.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.1096-10C>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 11/19 | chr11 | 376064 | |||||||
chr11:376070 | C | G | 1 | a0002c0002t0001g0160 | 1 | NA18963.hp2 | splice_region_variant&intron_variant | LOW | c.1096-4C>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 11/19 | chr11 | 376070 | |||||||
chr11:376176 | T | TG | 3 | a0002c0004t0002g0085 a0020c0032t0001g0147 a0021c0019t0001g0033 |
3 | HG03490.hp2 HG03516.hp1 NA18963.hp1 |
splice_region_variant&intron_variant | LOW | c.1196+5dupG | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr11 | 376176 | ||||||
chr11:376245 | C | T | 2 | a0001c0024t0003g0022 a0002c0038t0003g0020 |
2 | HG00642.hp1 NA19240.hp2 |
splice_region_variant&intron_variant | LOW | c.1197-6C>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 12/19 | chr11 | 376245 | |||||||
chr11:376393 | G | A | 1 | a0002c0002t0001g0067 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1298-28G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 13/19 | chr11 | 376393 | |||||||
chr11:377341 | C | T | 2 | a0007c0011t0001g0150 a0020c0032t0001g0147 |
2 | HG03490.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.2204+14C>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/19 | chr11 | 377341 | |||||||
chr11:377369 | C | CG | 4 | a0001c0003t0003g0018 a0001c0005t0002g0108 a0005c0010t0001g0174 others(1): Show |
4 | HG00438.hp1 HG01106.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.2204+46dupG | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr11 | 377369 | ||||||
chr11:377437 | T | C | 6 | a0001c0003t0002g0024 a0001c0003t0002g0025 a0001c0003t0002g0026 others(3): Show |
6 | HG01074.hp2 HG01346.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.2204+110T>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/19 | chr11 | 377437 | |||||||
chr11:377519 | C | T | 66 | a0001c0003t0001g0091 a0001c0003t0001g0097 a0001c0003t0001g0106 others(63): Show |
66 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.2204+192C>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/19 | chr11 | 377519 | |||||||
chr11:377581 | CTTGCACC others(31): Show |
C | 1 | a0001c0001t0001g0170 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2204+255_2204+292d others(40): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/19 | chr11 | 377581 | |||||||
chr11:377712 | C | A | 92 | a0001c0003t0001g0091 a0001c0003t0001g0097 a0001c0003t0001g0106 others(89): Show |
93 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.2204+385C>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/19 | chr11 | 377712 | |||||||
chr11:377773 | C | T | 9 | a0001c0003t0004g0017 a0001c0003t0004g0050 a0003c0039t0001g0058 others(6): Show |
9 | HG01433.hp1 HG02109.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.2204+446C>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/19 | chr11 | 377773 | |||||||
chr11:377785 | G | A | 1 | a0025c0028t0001g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2204+458G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/19 | chr11 | 377785 | |||||||
chr11:377795 | G | A | 86 | a0001c0003t0001g0091 a0001c0003t0001g0097 a0001c0003t0001g0106 others(83): Show |
87 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.2204+468G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/19 | chr11 | 377795 | |||||||
chr11:377904 | G | A | 1 | a0005c0010t0001g0174 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2204+577G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/19 | chr11 | 377904 | |||||||
chr11:377906 | G | A | 1 | a0005c0010t0001g0174 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2204+579G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/19 | chr11 | 377906 | |||||||
chr11:378093 | G | A | 3 | a0001c0001t0001g0173 a0002c0002t0001g0061 a0002c0008t0001g0081 |
3 | HG01346.hp1 HG02965.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.2204+766G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/19 | chr11 | 378093 | |||||||
chr11:378188 | T | C | 92 | a0001c0003t0001g0091 a0001c0003t0001g0097 a0001c0003t0001g0106 others(89): Show |
93 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.2204+861T>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/19 | chr11 | 378188 | |||||||
chr11:378363 | C | T | 6 | a0001c0003t0002g0024 a0001c0003t0002g0025 a0001c0003t0002g0026 others(3): Show |
6 | HG01074.hp2 HG01346.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.2204+1036C>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/19 | chr11 | 378363 | |||||||
chr11:378405 | T | C | 86 | a0001c0003t0001g0091 a0001c0003t0001g0097 a0001c0003t0001g0106 others(83): Show |
87 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.2205-1013T>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/19 | chr11 | 378405 | |||||||
chr11:378411 | G | A | 2 | a0001c0003t0004g0014 a0018c0029t0004g0053 |
2 | HG02630.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2205-1007G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/19 | chr11 | 378411 | |||||||
chr11:378658 | G | A | 6 | a0001c0001t0001g0165 a0001c0001t0001g0167 a0002c0009t0001g0013 others(3): Show |
6 | HG00639.hp2 HG00642.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.2205-760G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/19 | chr11 | 378658 | |||||||
chr11:378773 | G | A | 2 | a0002c0002t0001g0069 a0002c0002t0001g0075 |
2 | NA19012.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.2205-645G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/19 | chr11 | 378773 | |||||||
chr11:378846 | G | T | 1 | a0001c0001t0005g0169 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2205-572G>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/19 | chr11 | 378846 | |||||||
chr11:378847 | A | G | 92 | a0001c0003t0001g0091 a0001c0003t0001g0097 a0001c0003t0001g0106 others(89): Show |
93 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.2205-571A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/19 | chr11 | 378847 | |||||||
chr11:378919 | C | G | 1 | a0002c0004t0001g0056 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2205-499C>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/19 | chr11 | 378919 | |||||||
chr11:379042 | T | C | 3 | a0001c0001t0005g0169 a0001c0001t0005g0171 a0001c0001t0005g0172 |
3 | HG02559.hp2 HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2205-376T>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/19 | chr11 | 379042 | |||||||
chr11:379061 | A | G | 1 | a0006c0007t0001g0122 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2205-357A>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/19 | chr11 | 379061 | |||||||
chr11:379097 | T | C | 76 | a0001c0003t0001g0091 a0001c0003t0001g0097 a0001c0003t0001g0106 others(73): Show |
77 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.2205-321T>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/19 | chr11 | 379097 | |||||||
chr11:379107 | A | AG | 5 | a0001c0001t0001g0118 a0001c0001t0001g0165 a0001c0003t0001g0129 others(2): Show |
5 | HG00438.hp2 HG00642.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.2205-306dupG | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr11 | 379107 | ||||||
chr11:379841 | G | GCC | 12 | a0001c0003t0002g0024 a0001c0003t0002g0025 a0001c0003t0002g0027 others(9): Show |
12 | HG01074.hp2 HG01346.hp2 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.2489-18_2489-17dup others(2): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 15/19 | INFO_REALIGN_3_PRIME | chr11 | 379841 | ||||||
chr11:379848 | C | G | 1 | a0005c0010t0001g0174 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2489-18C>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 15/19 | chr11 | 379848 | |||||||
chr11:380078 | G | A | 1 | a0002c0002t0001g0073 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2643-52G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 16/19 | chr11 | 380078 | |||||||
chr11:380211 | G | C | 1 | a0022c0015t0001g0040 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.2715+9G>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 17/19 | chr11 | 380211 | |||||||
chr11:380242 | G | A | 6 | a0001c0003t0002g0024 a0001c0003t0002g0025 a0001c0003t0002g0026 others(3): Show |
6 | HG01074.hp2 HG01346.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.2715+40G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 17/19 | chr11 | 380242 | |||||||
chr11:380244 | G | T | 1 | a0019c0018t0001g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2715+42G>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 17/19 | chr11 | 380244 | |||||||
chr11:380245 | C | G | 1 | a0019c0018t0001g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2715+43C>G | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 17/19 | chr11 | 380245 | |||||||
chr11:380248 | G | C | 1 | a0019c0018t0001g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2716-44G>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 17/19 | chr11 | 380248 | |||||||
chr11:380461 | T | TC | 6 | a0001c0003t0002g0024 a0001c0003t0002g0025 a0001c0003t0002g0026 others(3): Show |
6 | HG01074.hp2 HG01346.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.2869+19dupC | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr11 | 380461 | ||||||
chr11:380623 | G | T | 1 | a0004c0044t0001g0032 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2869+178G>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 18/19 | chr11 | 380623 | |||||||
chr11:380649 | G | C | 1 | a0014c0030t0004g0011 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2870-176G>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 18/19 | chr11 | 380649 | |||||||
chr11:380724 | C | A | 2 | a0001c0003t0004g0017 a0001c0003t0004g0050 |
2 | HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2870-101C>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 18/19 | chr11 | 380724 | |||||||
chr11:380744 | G | A | 16 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(13): Show |
16 | HG00408.hp2 HG00544.hp2 HG01943.hp2 others(13): Show |
intron_variant | MODIFIER | c.2870-81G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 18/19 | chr11 | 380744 | |||||||
chr11:380774 | A | AC | 86 | a0001c0003t0001g0091 a0001c0003t0001g0097 a0001c0003t0001g0106 others(83): Show |
87 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.2870-49dupC | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 18/19 | INFO_REALIGN_3_PRIME | chr11 | 380774 | ||||||
chr11:380774 | A | C | 1 | a0001c0003t0004g0014 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2870-51A>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 18/19 | chr11 | 380774 | |||||||
chr11:381041 | C | T | 1 | a0025c0028t0001g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2996+90C>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 19/19 | chr11 | 381041 | |||||||
chr11:381072 | C | T | 6 | a0001c0003t0002g0024 a0001c0003t0002g0025 a0001c0003t0002g0026 others(3): Show |
6 | HG01074.hp2 HG01346.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.2996+121C>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 19/19 | chr11 | 381072 | |||||||
chr11:381073 | G | C | 6 | a0001c0003t0002g0024 a0001c0003t0002g0025 a0001c0003t0002g0026 others(3): Show |
6 | HG01074.hp2 HG01346.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.2996+122G>C | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 19/19 | chr11 | 381073 | |||||||
chr11:381147 | G | A | 6 | a0001c0003t0002g0024 a0001c0003t0002g0025 a0001c0003t0002g0026 others(3): Show |
6 | HG01074.hp2 HG01346.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.2996+196G>A | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 19/19 | chr11 | 381147 | |||||||
chr11:381288 | ACTGACCA others(89): Show |
A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0111 |
2 | HG00738.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.2997-319_2997-224d others(98): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr11 | 381288 | ||||||
chr11:381288 | ACTGACCA others(217): Show |
A | 6 | a0001c0003t0002g0024 a0001c0003t0002g0025 a0001c0003t0002g0026 others(3): Show |
6 | HG01074.hp2 HG01346.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.2997-319_2997-96de others(1): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr11 | 381288 | ||||||
chr11:381306 | C | T | 1 | a0002c0002t0001g0073 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2996+355C>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 19/19 | chr11 | 381306 | |||||||
chr11:381318 | G | GTCCTGAC others(313): Show |
1 | a0001c0001t0001g0170 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2997-46_2997-45ins others(320): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr11 | 381318 | ||||||
chr11:381318 | GTCCTGAC others(57): Show |
G | 1 | a0025c0028t0001g0052 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2997-109_2997-46de others(65): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr11 | 381318 | ||||||
chr11:381318 | GTCCTGAC others(121): Show |
G | 21 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(18): Show |
21 | HG00408.hp2 HG00544.hp2 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.2997-173_2997-46de others(1): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr11 | 381318 | ||||||
chr11:381318 | GTCCTGAC others(185): Show |
G | 84 | a0001c0003t0001g0091 a0001c0003t0001g0097 a0001c0003t0001g0106 others(81): Show |
85 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.2997-237_2997-46de others(1): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr11 | 381318 | ||||||
chr11:381336 | CCCCCGGC others(184): Show |
C | 1 | a0020c0032t0001g0147 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2997-328_2997-138d others(2): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr11 | 381336 | ||||||
chr11:381350 | GTCCTGAC others(153): Show |
G | 1 | a0002c0002t0001g0151 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2997-287_2997-128d others(2): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr11 | 381350 | ||||||
chr11:381382 | TTCCTGAC others(89): Show |
T | 1 | a0001c0001t0001g0005 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2997-255_2997-160d others(98): Show |
B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr11 | 381382 | ||||||
chr11:381400 | C | T | 1 | a0001c0016t0001g0104 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2997-269C>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 19/19 | chr11 | 381400 | |||||||
chr11:381560 | C | T | 87 | a0001c0003t0001g0091 a0001c0003t0001g0097 a0001c0003t0001g0106 others(84): Show |
88 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.2997-109C>T | B4GALNT4 | ENSG00000182272.12 | transcript | ENST00000329962.11 | protein_coding | 19/19 | chr11 | 381560 |