Item | Value |
---|---|
geneid | 124872 |
ensemblid | ENSG00000167080.9 |
hgncid | 24136 |
symbol | B4GALNT2 |
name | beta-1,4-N-acetyl-galactosaminyltransferase 2 |
refseq_nuc | NM_001159387.2 |
refseq_prot | NP_001152859.1 |
ensembl_nuc | ENST00000393354.7 |
ensembl_prot | ENSP00000377022.3 |
mane_status | MANE Select |
chr | chr17 |
start | 49132769 |
end | 49176840 |
strand | + |
ver | v1.2 |
region | chr17:49132769-49176840 |
region5000 | chr17:49127769-49181840 |
regionname0 | B4GALNT2_chr17_49132769_49176840 |
regionname5000 | B4GALNT2_chr17_49127769_49181840 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 506 | 324 | 64 | 64 | 149 | 9 | 36 | 113 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | MTSGG others(501): Show |
chr17 | 49127769 | 49181840 |
a0002 | 0/0 | 506 | 37 | 16 | 8 | 5 | 2 | 6 | 3 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | MTSGG others(501): Show |
chr17 | 49127769 | 49181840 |
a0003 | 0/0 | 433 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | MTSGG others(428): Show |
chr17 | 49127769 | 49181840 |
a0004 | 0/0 | 506 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | MTSGG others(501): Show |
chr17 | 49127769 | 49181840 |
a0005 | 0/0 | 506 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | MTSGG others(501): Show |
chr17 | 49127769 | 49181840 |
a0006 | 0/0 | 506 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | MTSGG others(501): Show |
chr17 | 49127769 | 49181840 |
a0007 | 0/0 | 506 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | MTSGG others(501): Show |
chr17 | 49127769 | 49181840 |
a0008 | 0/0 | 506 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | MTSGG others(501): Show |
chr17 | 49127769 | 49181840 |
a0009 | 0/0 | 506 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | MTSGG others(501): Show |
chr17 | 49127769 | 49181840 |
a0010 | 0/0 | 506 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | MTSGG others(501): Show |
chr17 | 49127769 | 49181840 |
a0011 | 0/0 | 506 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | MTSGG others(501): Show |
chr17 | 49127769 | 49181840 |
a0012 | 0/0 | 506 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | MTSGG others(501): Show |
chr17 | 49127769 | 49181840 |
a0013 | 0/0 | 506 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | MTSGG others(501): Show |
chr17 | 49127769 | 49181840 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1518 | 314 | 57 | 62 | 149 | 9 | 36 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | ATGAC others(1513): Show |
chr17 | 49127769 | 49181840 | ||
a0001c0004 | 0/0 | 1518 | 5 | 5 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | ATGAC others(1513): Show |
chr17 | 49127769 | 49181840 | ||
a0001c0005 | 0/0 | 1518 | 3 | 1 | 2 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | ATGAC others(1513): Show |
chr17 | 49127769 | 49181840 | ||
a0001c0011 | 1/0 | 1518 | 2 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | ATGAC others(1513): Show |
chr17 | 49127769 | 49181840 | ||
a0002c0002 | 0/0 | 1518 | 32 | 13 | 6 | 5 | 2 | 6 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | ATGAC others(1513): Show |
chr17 | 49127769 | 49181840 | ||
a0002c0006 | 0/0 | 1518 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | ATGAC others(1513): Show |
chr17 | 49127769 | 49181840 | ||
a0002c0007 | 0/0 | 1518 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | ATGAC others(1513): Show |
chr17 | 49127769 | 49181840 | ||
a0003c0003 | 0/0 | 1518 | 5 | 5 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | ATGAC others(1513): Show |
chr17 | 49127769 | 49181840 | ||
a0004c0012 | 0/0 | 1518 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | ATGAC others(1513): Show |
chr17 | 49127769 | 49181840 | ||
a0005c0008 | 0/0 | 1518 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | ATGAC others(1513): Show |
chr17 | 49127769 | 49181840 | ||
a0006c0010 | 0/0 | 1518 | 2 | 0 | 0 | 0 | 1 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | ATGAC others(1513): Show |
chr17 | 49127769 | 49181840 | ||
a0007c0009 | 0/0 | 1518 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | ATGAC others(1513): Show |
chr17 | 49127769 | 49181840 | ||
a0008c0018 | 0/0 | 1518 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | ATGAC others(1513): Show |
chr17 | 49127769 | 49181840 | ||
a0009c0017 | 0/0 | 1518 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | ATGAC others(1513): Show |
chr17 | 49127769 | 49181840 | ||
a0010c0015 | 0/0 | 1518 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | ATGAC others(1513): Show |
chr17 | 49127769 | 49181840 | ||
a0011c0013 | 0/0 | 1518 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | ATGAC others(1513): Show |
chr17 | 49127769 | 49181840 | ||
a0012c0016 | 0/0 | 1518 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | ATGAC others(1513): Show |
chr17 | 49127769 | 49181840 | ||
a0013c0014 | 0/0 | 1518 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | ATGAC others(1513): Show |
chr17 | 49127769 | 49181840 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 8657 | 121 | 8 | 20 | 79 | 4 | 9 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0002 | 0/0 | 8647 | 97 | 22 | 22 | 34 | 2 | 17 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8642): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0003 | 0/0 | 8657 | 34 | 3 | 10 | 17 | 1 | 3 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0006 | 0/0 | 8657 | 8 | 0 | 3 | 0 | 2 | 3 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0007 | 0/0 | 8647 | 4 | 0 | 0 | 3 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8642): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0008 | 0/0 | 8657 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0010 | 0/0 | 8665 | 5 | 5 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8660): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0012 | 0/0 | 8657 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0013 | 0/0 | 8657 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0015 | 0/0 | 8647 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8642): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0016 | 0/0 | 8647 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8642): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0017 | 0/0 | 8657 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0018 | 0/0 | 8675 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8670): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0019 | 0/0 | 8657 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0020 | 0/0 | 8657 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0022 | 0/0 | 8647 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8642): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0023 | 0/0 | 8647 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8642): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0024 | 0/0 | 8647 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8642): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0025 | 0/0 | 8647 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8642): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0026 | 0/0 | 8647 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8642): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0027 | 0/0 | 8647 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8642): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0028 | 0/0 | 8657 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0030 | 0/0 | 8647 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8642): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0031 | 0/0 | 8647 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8642): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0032 | 0/0 | 8647 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8642): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0033 | 0/0 | 8647 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8642): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0034 | 0/0 | 8657 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0036 | 0/0 | 8647 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8642): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0037 | 0/0 | 8647 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8642): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0038 | 0/0 | 8657 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0039 | 0/0 | 8657 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0040 | 0/0 | 8657 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0041 | 0/0 | 8657 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0043 | 0/0 | 8657 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0044 | 0/0 | 8657 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0045 | 0/0 | 8657 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0046 | 0/0 | 8657 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0047 | 0/0 | 8657 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0048 | 0/0 | 8657 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0051 | 0/0 | 8657 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0052 | 0/0 | 8657 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0056 | 0/0 | 8634 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8629): Show |
chr17 | 49127769 | 49181840 |
a0001c0001t0057 | 0/0 | 8665 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8660): Show |
chr17 | 49127769 | 49181840 |
a0001c0004t0008 | 0/0 | 8657 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0004t0020 | 0/0 | 8657 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0004t0049 | 0/0 | 8657 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0004t0050 | 0/0 | 8657 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0005t0008 | 0/0 | 8657 | 3 | 1 | 2 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0011t0013 | 1/0 | 8657 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0001c0011t0042 | 0/0 | 8657 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0002c0002t0004 | 0/0 | 8678 | 19 | 1 | 5 | 5 | 2 | 6 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8673): Show |
chr17 | 49127769 | 49181840 |
a0002c0002t0005 | 0/0 | 8678 | 9 | 8 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8673): Show |
chr17 | 49127769 | 49181840 |
a0002c0002t0011 | 0/0 | 8674 | 3 | 3 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8669): Show |
chr17 | 49127769 | 49181840 |
a0002c0002t0054 | 0/0 | 8678 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8673): Show |
chr17 | 49127769 | 49181840 |
a0002c0006t0021 | 0/0 | 8676 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8671): Show |
chr17 | 49127769 | 49181840 |
a0002c0006t0055 | 0/0 | 8676 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8671): Show |
chr17 | 49127769 | 49181840 |
a0002c0007t0004 | 0/0 | 8678 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8673): Show |
chr17 | 49127769 | 49181840 |
a0003c0003t0009 | 0/0 | 8657 | 5 | 5 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0004c0012t0007 | 0/0 | 8647 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8642): Show |
chr17 | 49127769 | 49181840 |
a0005c0008t0014 | 0/0 | 8674 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8669): Show |
chr17 | 49127769 | 49181840 |
a0006c0010t0003 | 0/0 | 8657 | 2 | 0 | 0 | 0 | 1 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0007c0009t0002 | 0/0 | 8647 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8642): Show |
chr17 | 49127769 | 49181840 |
a0008c0018t0029 | 0/0 | 8647 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8642): Show |
chr17 | 49127769 | 49181840 |
a0009c0017t0035 | 0/0 | 8657 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0010c0015t0053 | 0/0 | 8674 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8669): Show |
chr17 | 49127769 | 49181840 |
a0011c0013t0001 | 0/0 | 8657 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0012c0016t0003 | 0/0 | 8657 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8652): Show |
chr17 | 49127769 | 49181840 |
a0013c0014t0002 | 0/0 | 8647 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | AGTCT others(8642): Show |
chr17 | 49127769 | 49181840 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0323 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0003g0001 | 0/0 | 8 | 1 | 2 | 5 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0003g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0003g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0006g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0006g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0006g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0006g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0006g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0006g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0006g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0006g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0007g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0007g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0007g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0007g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0008g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0010g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0010g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0010g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0010g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0012g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0012g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0012g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0013g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0013g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0015g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0015g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0016g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0016g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0017g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0017g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0018g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0018g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0019g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0020g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0022g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0023g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0024g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0025g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0026g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0027g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0028g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0030g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0031g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0032g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0033g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0034g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0036g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0037g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0038g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0039g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0040g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0041g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0043g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0044g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0045g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0046g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0047g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0048g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0051g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0052g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0056g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0001t0057g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0004t0008g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0004t0008g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0004t0020g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0004t0049g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0004t0050g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0005t0008g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0005t0008g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0011t0013g0029 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0001c0011t0042g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0004g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0004g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0004g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0004g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0004g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0004g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0004g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0004g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0004g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0004g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0004g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0004g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0005g0005 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0005g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0005g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0005g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0011g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0011g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0011g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0002t0054g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0006t0021g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0006t0021g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0006t0055g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0002c0007t0004g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0003c0003t0009g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0003c0003t0009g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0003c0003t0009g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0003c0003t0009g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0003c0003t0009g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0004c0012t0007g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0004c0012t0007g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0005c0008t0014g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0005c0008t0014g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0006c0010t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0006c0010t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0007c0009t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0007c0009t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0008c0018t0029g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0009c0017t0035g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0010c0015t0053g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0011c0013t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0012c0016t0003g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
a0013c0014t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0257 | EUR | GBR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | GBR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00323 | hp1 | a0002 | c0002 | t0004 | g0184 | EUR | FIN | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0172 | EUR | FIN | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | CHS | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | CHS | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00438 | hp1 | a0002 | c0002 | t0004 | g0100 | EAS | CHS | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00544 | hp1 | a0001 | c0001 | t0038 | g0266 | EAS | CHS | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00544 | hp2 | a0001 | c0001 | t0043 | g0331 | EAS | CHS | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | CHS | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | CHS | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | CHS | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | CHS | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0173 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00735 | hp1 | a0001 | c0001 | t0006 | g0200 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00735 | hp2 | a0001 | c0001 | t0041 | g0187 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0168 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0277 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG00741 | hp2 | a0002 | c0002 | t0004 | g0247 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01069 | hp2 | a0001 | c0005 | t0008 | g0011 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01070 | hp1 | a0001 | c0001 | t0031 | g0224 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01070 | hp2 | a0002 | c0007 | t0004 | g0017 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01071 | hp1 | a0001 | c0005 | t0008 | g0011 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01071 | hp2 | a0002 | c0007 | t0004 | g0017 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01074 | hp1 | a0002 | c0002 | t0004 | g0204 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0228 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01081 | hp2 | a0002 | c0002 | t0004 | g0039 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01106 | hp1 | a0002 | c0002 | t0005 | g0005 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01106 | hp2 | a0002 | c0002 | t0004 | g0178 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0010 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01168 | hp2 | a0001 | c0001 | t0030 | g0232 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01175 | hp2 | a0001 | c0001 | t0048 | g0175 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0322 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01243 | hp2 | a0001 | c0001 | t0051 | g0348 | AMR | PUR | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0303 | AMR | CLM | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | CLM | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | CLM | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01261 | hp1 | a0001 | c0001 | t0052 | g0196 | AMR | CLM | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0283 | AMR | CLM | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | CLM | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | CLM | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01358 | hp1 | a0001 | c0001 | t0006 | g0332 | AMR | CLM | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | CLM | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0167 | AMR | CLM | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01433 | hp2 | a0001 | c0001 | t0006 | g0197 | AMR | CLM | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0188 | EUR | IBS | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01515 | hp2 | a0001 | c0001 | t0006 | g0145 | EUR | IBS | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | IBS | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01516 | hp2 | a0001 | c0001 | t0006 | g0098 | EUR | IBS | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01884 | hp1 | a0001 | c0001 | t0012 | g0156 | AFR | ACB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01884 | hp2 | a0003 | c0003 | t0009 | g0260 | AFR | ACB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0215 | AFR | ACB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01891 | hp2 | a0008 | c0018 | t0029 | g0203 | AFR | ACB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01928 | hp1 | a0002 | c0002 | t0004 | g0128 | AMR | PEL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0304 | AMR | PEL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0164 | AMR | PEL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0122 | AMR | PEL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0226 | AMR | PEL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0344 | AMR | PEL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0171 | AMR | PEL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0174 | AMR | PEL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0142 | AMR | PEL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02015 | hp2 | a0002 | c0002 | t0004 | g0306 | EAS | KHV | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02055 | hp1 | a0001 | c0001 | t0026 | g0121 | AFR | ACB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02071 | hp2 | a0004 | c0012 | t0007 | g0337 | EAS | KHV | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | KHV | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02080 | hp2 | a0001 | c0001 | t0033 | g0309 | EAS | KHV | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02083 | hp2 | a0001 | c0001 | t0007 | g0325 | EAS | KHV | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0185 | EAS | KHV | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | KHV | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02135 | hp2 | a0004 | c0012 | t0007 | g0336 | EAS | KHV | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02145 | hp1 | a0001 | c0001 | t0036 | g0275 | AFR | ACB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | ACB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | CDX | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0280 | EAS | CDX | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02257 | hp1 | a0002 | c0002 | t0004 | g0216 | AFR | ACB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0345 | AFR | ACB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02258 | hp2 | a0001 | c0004 | t0050 | g0116 | AFR | ACB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PEL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02280 | hp1 | a0001 | c0001 | t0010 | g0013 | AFR | ACB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02280 | hp2 | a0009 | c0017 | t0035 | g0262 | AFR | ACB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | PEL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0110 | AMR | PEL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02451 | hp1 | a0005 | c0008 | t0014 | g0221 | AFR | ACB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02451 | hp2 | a0001 | c0001 | t0057 | g0161 | AFR | ACB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | KHV | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0246 | EAS | KHV | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02572 | hp1 | a0002 | c0002 | t0011 | g0154 | AFR | GWD | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0302 | AFR | GWD | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02602 | hp1 | a0001 | c0001 | t0006 | g0151 | SAS | PJL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02602 | hp2 | a0001 | c0001 | t0025 | g0195 | SAS | PJL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02615 | hp1 | a0002 | c0002 | t0005 | g0248 | AFR | GWD | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02615 | hp2 | a0001 | c0001 | t0012 | g0152 | AFR | GWD | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02630 | hp1 | a0001 | c0004 | t0008 | g0264 | AFR | GWD | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0261 | AFR | GWD | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02683 | hp1 | a0001 | c0001 | t0037 | g0225 | SAS | PJL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0333 | SAS | PJL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0292 | SAS | PJL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02717 | hp1 | a0001 | c0001 | t0023 | g0276 | AFR | GWD | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02717 | hp2 | a0001 | c0004 | t0008 | g0263 | AFR | GWD | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0227 | AFR | GWD | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02723 | hp2 | a0001 | c0001 | t0010 | g0230 | AFR | GWD | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02735 | hp1 | a0002 | c0002 | t0004 | g0194 | SAS | PJL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0279 | SAS | PJL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02738 | hp1 | a0002 | c0002 | t0004 | g0220 | SAS | PJL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0327 | SAS | PJL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02809 | hp1 | a0001 | c0001 | t0044 | g0160 | AFR | GWD | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02818 | hp2 | a0003 | c0003 | t0009 | g0210 | AFR | GWD | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02886 | hp1 | a0001 | c0001 | t0020 | g0273 | AFR | GWD | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0180 | AFR | GWD | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02895 | hp1 | a0003 | c0003 | t0009 | g0240 | AFR | GWD | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02895 | hp2 | a0002 | c0002 | t0005 | g0158 | AFR | GWD | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0207 | AFR | GWD | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02897 | hp2 | a0003 | c0003 | t0009 | g0239 | AFR | GWD | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02965 | hp1 | a0002 | c0002 | t0005 | g0005 | AFR | ESN | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | ESN | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02976 | hp1 | a0005 | c0008 | t0014 | g0222 | AFR | ESN | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02976 | hp2 | a0010 | c0015 | t0053 | g0237 | AFR | ESN | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03017 | hp1 | a0002 | c0002 | t0004 | g0219 | SAS | PJL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0252 | SAS | PJL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0241 | AFR | GWD | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03098 | hp2 | a0002 | c0002 | t0054 | g0101 | AFR | MSL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03130 | hp1 | a0001 | c0001 | t0013 | g0155 | AFR | ESN | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | ESN | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03139 | hp1 | a0001 | c0004 | t0049 | g0346 | AFR | ESN | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03139 | hp2 | a0002 | c0002 | t0005 | g0351 | AFR | ESN | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03195 | hp1 | a0002 | c0002 | t0005 | g0211 | AFR | ESN | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03195 | hp2 | a0001 | c0001 | t0010 | g0289 | AFR | ESN | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03209 | hp1 | a0001 | c0001 | t0019 | g0015 | AFR | MSL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03225 | hp1 | a0002 | c0002 | t0011 | g0153 | AFR | MSL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03225 | hp2 | a0001 | c0001 | t0056 | g0288 | AFR | MSL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03453 | hp1 | a0001 | c0001 | t0012 | g0132 | AFR | MSL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | MSL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03486 | hp1 | a0001 | c0001 | t0019 | g0015 | AFR | MSL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03486 | hp2 | a0002 | c0002 | t0005 | g0005 | AFR | MSL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03490 | hp1 | a0002 | c0002 | t0004 | g0335 | SAS | PJL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0165 | SAS | PJL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03516 | hp1 | a0001 | c0011 | t0042 | g0131 | AFR | ESN | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03516 | hp2 | a0001 | c0001 | t0013 | g0350 | AFR | ESN | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03540 | hp1 | a0001 | c0001 | t0039 | g0078 | AFR | GWD | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03540 | hp2 | a0001 | c0001 | t0008 | g0254 | AFR | GWD | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0259 | AFR | MSL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | MSL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03654 | hp2 | a0002 | c0002 | t0004 | g0299 | SAS | PJL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03669 | hp1 | a0006 | c0010 | t0003 | g0084 | SAS | PJL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0278 | SAS | PJL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03688 | hp1 | a0001 | c0001 | t0024 | g0018 | SAS | STU | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0324 | SAS | STU | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03704 | hp2 | a0001 | c0001 | t0007 | g0293 | SAS | PJL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0328 | SAS | PJL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0199 | SAS | PJL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | BEB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | BEB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03834 | hp2 | a0001 | c0001 | t0006 | g0179 | SAS | BEB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | BEB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | BEB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0135 | SAS | BEB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0143 | SAS | BEB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | STU | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0326 | SAS | STU | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0093 | SAS | BEB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0334 | SAS | BEB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG04199 | hp1 | a0011 | c0013 | t0001 | g0295 | SAS | STU | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0130 | SAS | STU | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | STU | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG04204 | hp2 | a0002 | c0002 | t0004 | g0038 | SAS | STU | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0148 | SAS | STU | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG04228 | hp2 | a0001 | c0001 | t0006 | g0137 | SAS | STU | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18522 | hp1 | a0001 | c0005 | t0008 | g0082 | AFR | YRI | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0255 | AFR | YRI | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18612 | hp1 | a0001 | c0001 | t0015 | g0321 | EAS | CHB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0096 | EAS | CHB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | CHB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18906 | hp1 | a0001 | c0001 | t0032 | g0129 | AFR | YRI | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18906 | hp2 | a0007 | c0009 | t0002 | g0234 | AFR | YRI | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18942 | hp2 | a0001 | c0001 | t0017 | g0106 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18946 | hp1 | a0001 | c0001 | t0016 | g0251 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18948 | hp1 | a0001 | c0001 | t0022 | g0019 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0342 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18954 | hp1 | a0002 | c0002 | t0004 | g0312 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18962 | hp2 | a0001 | c0001 | t0015 | g0146 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18969 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0060 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18990 | hp2 | a0002 | c0002 | t0004 | g0305 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18992 | hp1 | a0001 | c0001 | t0045 | g0107 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18997 | hp2 | a0001 | c0001 | t0016 | g0085 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19009 | hp2 | a0001 | c0001 | t0018 | g0282 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19010 | hp1 | a0001 | c0001 | t0027 | g0062 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0236 | AFR | LWK | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0249 | AFR | LWK | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19043 | hp1 | a0001 | c0001 | t0010 | g0243 | AFR | LWK | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | LWK | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19054 | hp1 | a0001 | c0001 | t0046 | g0091 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19062 | hp1 | a0001 | c0001 | t0007 | g0136 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19066 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19068 | hp1 | a0001 | c0001 | t0017 | g0105 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19074 | hp2 | a0001 | c0001 | t0018 | g0284 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19084 | hp1 | a0001 | c0001 | t0007 | g0317 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19084 | hp2 | a0012 | c0016 | t0003 | g0343 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19088 | hp1 | a0013 | c0014 | t0002 | g0330 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19089 | hp1 | a0002 | c0002 | t0004 | g0307 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19240 | hp1 | a0001 | c0001 | t0034 | g0349 | AFR | YRI | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA19240 | hp2 | a0002 | c0006 | t0021 | g0099 | AFR | YRI | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0285 | AFR | ASW | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0201 | AFR | ASW | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0231 | EUR | TSI | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0205 | EUR | TSI | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA20805 | hp1 | a0006 | c0010 | t0003 | g0229 | EUR | TSI | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA20805 | hp2 | a0002 | c0002 | t0004 | g0163 | EUR | TSI | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01123 | hp1 | a0001 | c0001 | t0028 | g0140 | AMR | CLM | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02109 | hp1 | a0002 | c0006 | t0055 | g0272 | AFR | ACB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02109 | hp2 | a0001 | c0004 | t0020 | g0253 | AFR | ACB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02486 | hp1 | a0002 | c0002 | t0011 | g0274 | AFR | ACB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02486 | hp2 | a0002 | c0002 | t0005 | g0265 | AFR | ACB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0256 | AFR | ACB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03471 | hp1 | a0002 | c0002 | t0005 | g0115 | AFR | MSL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG03471 | hp2 | a0001 | c0001 | t0047 | g0086 | AFR | MSL | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | USA | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
HG06807 | hp2 | a0001 | c0001 | t0010 | g0013 | AFR | USA | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18955 | hp1 | a0001 | c0001 | t0040 | g0049 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA20300 | hp1 | a0002 | c0006 | t0021 | g0036 | AFR | USA | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | USA | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA21309 | hp1 | a0003 | c0003 | t0009 | g0347 | AFR | LWK | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
NA21309 | hp2 | a0007 | c0009 | t0002 | g0133 | AFR | LWK | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0323 | REF | REF | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
homoSapiens | grch38p0 | a0001 | c0011 | t0013 | g0029 | REF | REF | B4GALNT2_chr17_49127769_49181840 | B4GALNT2 | chr17 | 49127769 | 49181840 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:49141375 | C | T | 1 | a0008 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.143C>T | p.Ala48Val | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 2/11 | 167/8657 | 143/1521 | 48/506 | chr17 | 49141375 | |||
chr17:49142166 | A | G | 1 | a0009 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.347A>G | p.Gln116Arg | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/11 | 371/8657 | 347/1521 | 116/506 | chr17 | 49142166 | |||
chr17:49152814 | G | A | 1 | a0011 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.368G>A | p.Arg123His | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/11 | 392/8657 | 368/1521 | 123/506 | chr17 | 49152814 | |||
chr17:49164127 | C | T | 1 | a0012 | 1 | NA19084.hp2 | missense_variant | MODERATE | c.806C>T | p.Thr269Ile | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 8/11 | 830/8657 | 806/1521 | 269/506 | chr17 | 49164127 | |||
chr17:49164165 | A | G | 1 | a0004 | 2 | HG02071.hp2 HG02135.hp2 |
missense_variant | MODERATE | c.844A>G | p.Ser282Gly | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 8/11 | 868/8657 | 844/1521 | 282/506 | chr17 | 49164165 | |||
chr17:49164263 | G | A | 1 | a0005 | 2 | HG02451.hp1 HG02976.hp1 |
missense_variant | MODERATE | c.942G>A | p.Met314Ile | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 8/11 | 966/8657 | 942/1521 | 314/506 | chr17 | 49164263 | |||
chr17:49166246 | C | G | 1 | a0010 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.1087C>G | p.Leu363Val | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 9/11 | 1111/8657 | 1087/1521 | 363/506 | chr17 | 49166246 | |||
chr17:49168801 | T | C | 3 | a0002 a0005 a0010 |
40 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(37): Show |
missense_variant | MODERATE | c.1216T>C | p.Cys406Arg | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 10/11 | 1240/8657 | 1216/1521 | 406/506 | chr17 | 49168801 | |||
chr17:49168877 | G | A | 1 | a0007 | 2 | NA18906.hp2 NA21309.hp2 |
missense_variant | MODERATE | c.1292G>A | p.Arg431His | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 10/11 | 1316/8657 | 1292/1521 | 431/506 | chr17 | 49168877 | |||
chr17:49168885 | C | T | 1 | a0003 | 5 | HG01884.hp2 HG02818.hp2 HG02895.hp1 others(2): Show |
stop_gained | HIGH | c.1300C>T | p.Arg434* | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 10/11 | 1324/8657 | 1300/1521 | 434/506 | chr17 | 49168885 | |||
chr17:49169594 | C | T | 1 | a0006 | 2 | HG03669.hp1 NA20805.hp1 |
missense_variant | MODERATE | c.1387C>T | p.Arg463Trp | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 1411/8657 | 1387/1521 | 463/506 | chr17 | 49169594 | |||
chr17:49169652 | G | A | 1 | a0013 | 1 | NA19088.hp1 | missense_variant | MODERATE | c.1445G>A | p.Arg482Gln | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 1469/8657 | 1445/1521 | 482/506 | chr17 | 49169652 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:49132804 | C | A | 1 | a0002c0007 | 2 | HG01070.hp2 HG01071.hp2 |
splice_region_variant&synonymous_variant | LOW | c.12C>A | p.Gly4Gly | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/11 | 36/8657 | 12/1521 | 4/506 | chr17 | 49132804 | |||
chr17:49152842 | C | T | 1 | a0001c0004 | 5 | HG02109.hp2 HG02258.hp2 HG02630.hp1 others(2): Show |
synonymous_variant | LOW | c.396C>T | p.Asn132Asn | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/11 | 420/8657 | 396/1521 | 132/506 | chr17 | 49152842 | |||
chr17:49159189 | G | A | 1 | a0001c0005 | 3 | HG01069.hp2 HG01071.hp1 NA18522.hp1 |
synonymous_variant | LOW | c.651G>A | p.Thr217Thr | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 6/11 | 675/8657 | 651/1521 | 217/506 | chr17 | 49159189 | |||
chr17:49164242 | T | C | 17 | a0001c0001 a0001c0004 a0001c0005 others(14): Show |
377 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(374): Show |
synonymous_variant | LOW | c.921T>C | p.Asn307Asn | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 8/11 | 945/8657 | 921/1521 | 307/506 | chr17 | 49164242 | |||
chr17:49169617 | A | G | 4 | a0002c0002 a0002c0007 a0005c0008 others(1): Show |
37 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(34): Show |
synonymous_variant | LOW | c.1410A>G | p.Glu470Glu | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 1434/8657 | 1410/1521 | 470/506 | chr17 | 49169617 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:49169895 | C | T | 10 | a0001c0001t0010 a0001c0001t0056 a0001c0001t0057 others(7): Show |
42 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*167C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 167 | chr17 | 49169895 | ||||||
chr17:49170031 | T | C | 7 | a0002c0002t0004 a0002c0002t0005 a0002c0002t0011 others(4): Show |
37 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*303T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 303 | chr17 | 49170031 | ||||||
chr17:49170124 | C | T | 1 | a0001c0001t0052 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*396C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 396 | chr17 | 49170124 | ||||||
chr17:49170144 | T | C | 35 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(32): Show |
173 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*416T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 416 | chr17 | 49170144 | ||||||
chr17:49170149 | T | C | 1 | a0001c0001t0022 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*421T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 421 | chr17 | 49170149 | ||||||
chr17:49170166 | G | A | 1 | a0010c0015t0053 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*438G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 438 | chr17 | 49170166 | ||||||
chr17:49170318 | C | T | 7 | a0002c0002t0004 a0002c0002t0005 a0002c0002t0011 others(4): Show |
37 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*590C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 590 | chr17 | 49170318 | ||||||
chr17:49170328 | A | C | 3 | a0001c0001t0010 a0001c0001t0056 a0001c0001t0057 |
7 | HG02280.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*600A>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 600 | chr17 | 49170328 | ||||||
chr17:49170394 | C | A | 1 | a0001c0001t0017 | 2 | NA18942.hp2 NA19068.hp1 |
3_prime_UTR_variant | MODIFIER | c.*666C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 666 | chr17 | 49170394 | ||||||
chr17:49170433 | C | T | 7 | a0002c0002t0004 a0002c0002t0005 a0002c0002t0011 others(4): Show |
37 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*705C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 705 | chr17 | 49170433 | ||||||
chr17:49170562 | CT | C | 7 | a0002c0002t0004 a0002c0002t0005 a0002c0002t0011 others(4): Show |
37 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*835delT | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 835 | chr17 | 49170562 | ||||||
chr17:49170565 | A | C | 7 | a0002c0002t0004 a0002c0002t0005 a0002c0002t0011 others(4): Show |
37 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*837A>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 837 | chr17 | 49170565 | ||||||
chr17:49170596 | C | T | 1 | a0001c0001t0057 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*868C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 868 | chr17 | 49170596 | ||||||
chr17:49170864 | G | GGAAACAA others(11): Show |
1 | a0001c0001t0018 | 2 | NA19009.hp2 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1154_*1171dupCGAA others(14): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 1172 | INFO_REALIGN_3_PRIME | chr17 | 49170864 | |||||
chr17:49170946 | G | T | 1 | a0001c0001t0037 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1218G>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 1218 | chr17 | 49170946 | ||||||
chr17:49170960 | T | G | 1 | a0001c0001t0023 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1232T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 1232 | chr17 | 49170960 | ||||||
chr17:49170984 | G | A | 1 | a0001c0001t0038 | 1 | HG00544.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1256G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 1256 | chr17 | 49170984 | ||||||
chr17:49170997 | G | C | 2 | a0001c0001t0010 a0001c0001t0056 |
6 | HG02280.hp1 HG02723.hp2 HG03195.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1269G>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 1269 | chr17 | 49170997 | ||||||
chr17:49171029 | A | G | 12 | a0001c0001t0010 a0001c0001t0056 a0001c0001t0057 others(9): Show |
47 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1301A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 1301 | chr17 | 49171029 | ||||||
chr17:49171045 | C | T | 1 | a0001c0001t0051 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1317C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 1317 | chr17 | 49171045 | ||||||
chr17:49171049 | T | G | 10 | a0001c0001t0010 a0001c0001t0056 a0001c0001t0057 others(7): Show |
44 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1321T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 1321 | chr17 | 49171049 | ||||||
chr17:49171052 | G | A | 2 | a0001c0001t0012 a0001c0001t0039 |
4 | HG01884.hp1 HG02615.hp2 HG03453.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1324G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 1324 | chr17 | 49171052 | ||||||
chr17:49171121 | T | C | 2 | a0002c0006t0021 a0002c0006t0055 |
3 | HG02109.hp1 NA19240.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1393T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 1393 | chr17 | 49171121 | ||||||
chr17:49171130 | A | C | 5 | a0001c0001t0008 a0001c0004t0008 a0001c0004t0049 others(2): Show |
8 | HG01069.hp2 HG01071.hp1 HG02258.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1402A>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 1402 | chr17 | 49171130 | ||||||
chr17:49171131 | G | C | 5 | a0001c0001t0008 a0001c0004t0008 a0001c0004t0049 others(2): Show |
8 | HG01069.hp2 HG01071.hp1 HG02258.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1403G>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 1403 | chr17 | 49171131 | ||||||
chr17:49171138 | G | A | 7 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0018 others(4): Show |
44 | HG00597.hp2 HG00609.hp2 HG00621.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*1410G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 1410 | chr17 | 49171138 | ||||||
chr17:49171235 | C | T | 2 | a0002c0006t0021 a0002c0006t0055 |
3 | HG02109.hp1 NA19240.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1507C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 1507 | chr17 | 49171235 | ||||||
chr17:49171322 | A | C | 1 | a0001c0001t0039 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1594A>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 1594 | chr17 | 49171322 | ||||||
chr17:49171328 | A | G | 1 | a0001c0001t0048 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1600A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 1600 | chr17 | 49171328 | ||||||
chr17:49171421 | G | C | 1 | a0001c0001t0024 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1693G>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 1693 | chr17 | 49171421 | ||||||
chr17:49171569 | T | C | 3 | a0001c0001t0010 a0001c0001t0056 a0001c0001t0057 |
7 | HG02280.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1841T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 1841 | chr17 | 49171569 | ||||||
chr17:49171585 | A | G | 1 | a0002c0006t0021 | 2 | NA19240.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1857A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 1857 | chr17 | 49171585 | ||||||
chr17:49171597 | C | T | 6 | a0002c0002t0004 a0002c0002t0005 a0002c0002t0011 others(3): Show |
35 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*1869C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 1869 | chr17 | 49171597 | ||||||
chr17:49171686 | GT | G | 7 | a0002c0002t0004 a0002c0002t0005 a0002c0002t0011 others(4): Show |
37 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1959delT | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 1959 | chr17 | 49171686 | ||||||
chr17:49171768 | T | C | 36 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(33): Show |
174 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*2040T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 2040 | chr17 | 49171768 | ||||||
chr17:49171770 | C | T | 1 | a0001c0001t0040 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2042C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 2042 | chr17 | 49171770 | ||||||
chr17:49171781 | C | T | 3 | a0001c0001t0010 a0001c0001t0056 a0001c0001t0057 |
7 | HG02280.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2053C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 2053 | chr17 | 49171781 | ||||||
chr17:49171849 | C | CAAAT | 4 | a0002c0002t0004 a0002c0002t0005 a0002c0002t0054 others(1): Show |
31 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2123_*2126dupAATA | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 2127 | INFO_REALIGN_3_PRIME | chr17 | 49171849 | |||||
chr17:49171883 | A | G | 1 | a0001c0001t0047 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2155A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 2155 | chr17 | 49171883 | ||||||
chr17:49171906 | G | A | 1 | a0001c0001t0025 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2178G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 2178 | chr17 | 49171906 | ||||||
chr17:49171959 | C | T | 4 | a0002c0002t0004 a0002c0002t0005 a0002c0002t0054 others(1): Show |
31 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*2231C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 2231 | chr17 | 49171959 | ||||||
chr17:49172137 | A | G | 1 | a0001c0001t0036 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2409A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 2409 | chr17 | 49172137 | ||||||
chr17:49172180 | G | A | 2 | a0002c0006t0021 a0002c0006t0055 |
3 | HG02109.hp1 NA19240.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2452G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 2452 | chr17 | 49172180 | ||||||
chr17:49172198 | TGGGGTCC others(35): Show |
T | 1 | a0001c0001t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2473_*2514delGGTC others(38): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 2473 | INFO_REALIGN_3_PRIME | chr17 | 49172198 | |||||
chr17:49172238 | A | G | 9 | a0001c0001t0010 a0001c0001t0057 a0002c0002t0004 others(6): Show |
43 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*2510A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 2510 | chr17 | 49172238 | ||||||
chr17:49172290 | C | T | 10 | a0001c0001t0010 a0001c0001t0056 a0001c0001t0057 others(7): Show |
44 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*2562C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 2562 | chr17 | 49172290 | ||||||
chr17:49172328 | T | C | 2 | a0001c0001t0023 a0001c0001t0026 |
2 | HG02055.hp1 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2600T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 2600 | chr17 | 49172328 | ||||||
chr17:49172357 | A | G | 1 | a0009c0017t0035 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2629A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 2629 | chr17 | 49172357 | ||||||
chr17:49172401 | G | A | 7 | a0002c0002t0004 a0002c0002t0005 a0002c0002t0011 others(4): Show |
37 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2673G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 2673 | chr17 | 49172401 | ||||||
chr17:49172408 | T | G | 36 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(33): Show |
174 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*2680T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 2680 | chr17 | 49172408 | ||||||
chr17:49172452 | G | T | 1 | a0001c0001t0034 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2724G>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 2724 | chr17 | 49172452 | ||||||
chr17:49172555 | G | A | 1 | a0001c0001t0027 | 1 | NA19010.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2827G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 2827 | chr17 | 49172555 | ||||||
chr17:49172700 | C | T | 65 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(62): Show |
375 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(372): Show |
3_prime_UTR_variant | MODIFIER | c.*2972C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 2972 | chr17 | 49172700 | ||||||
chr17:49173018 | C | T | 1 | a0001c0004t0050 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3290C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 3290 | chr17 | 49173018 | ||||||
chr17:49173082 | C | A | 4 | a0002c0002t0004 a0002c0002t0005 a0002c0002t0054 others(1): Show |
31 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*3354C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 3354 | chr17 | 49173082 | ||||||
chr17:49173114 | C | T | 3 | a0001c0001t0010 a0001c0001t0056 a0001c0001t0057 |
7 | HG02280.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3386C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 3386 | chr17 | 49173114 | ||||||
chr17:49173203 | T | C | 1 | a0010c0015t0053 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3475T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 3475 | chr17 | 49173203 | ||||||
chr17:49173215 | A | G | 1 | a0001c0001t0033 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3487A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 3487 | chr17 | 49173215 | ||||||
chr17:49173226 | G | A | 1 | a0001c0001t0043 | 1 | HG00544.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3498G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 3498 | chr17 | 49173226 | ||||||
chr17:49173501 | T | C | 3 | a0001c0001t0010 a0001c0001t0056 a0001c0001t0057 |
7 | HG02280.hp1 HG02451.hp2 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3773T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 3773 | chr17 | 49173501 | ||||||
chr17:49173523 | C | A | 1 | a0001c0001t0044 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3795C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 3795 | chr17 | 49173523 | ||||||
chr17:49173587 | G | A | 1 | a0001c0001t0045 | 1 | NA18992.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3859G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 3859 | chr17 | 49173587 | ||||||
chr17:49173632 | A | G | 34 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(31): Show |
172 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*3904A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 3904 | chr17 | 49173632 | ||||||
chr17:49173809 | C | T | 5 | a0001c0001t0007 a0001c0001t0024 a0001c0001t0033 others(2): Show |
9 | HG02071.hp2 HG02080.hp2 HG02083.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4081C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 4081 | chr17 | 49173809 | ||||||
chr17:49173863 | TGAGCTTT others(3): Show |
T | 20 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0015 others(17): Show |
123 | HG00323.hp2 HG00408.hp2 HG00639.hp1 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*4138_*4147delGCTT others(6): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 4138 | INFO_REALIGN_3_PRIME | chr17 | 49173863 | |||||
chr17:49173906 | C | T | 1 | a0001c0001t0034 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4178C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 4178 | chr17 | 49173906 | ||||||
chr17:49173910 | T | G | 1 | a0001c0001t0019 | 2 | HG03209.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4182T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 4182 | chr17 | 49173910 | ||||||
chr17:49173926 | C | T | 3 | a0001c0001t0006 a0001c0001t0028 a0001c0001t0052 |
10 | HG00735.hp1 HG01123.hp1 HG01261.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*4198C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 4198 | chr17 | 49173926 | ||||||
chr17:49173964 | A | AATAGGTT others(4): Show |
12 | a0001c0001t0010 a0001c0001t0056 a0001c0001t0057 others(9): Show |
47 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*4238_*4239insAGGT others(7): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 4239 | INFO_REALIGN_3_PRIME | chr17 | 49173964 | |||||
chr17:49174088 | G | A | 1 | a0001c0011t0042 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4360G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 4360 | chr17 | 49174088 | ||||||
chr17:49174122 | G | A | 2 | a0001c0001t0023 a0001c0001t0026 |
2 | HG02055.hp1 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4394G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 4394 | chr17 | 49174122 | ||||||
chr17:49174320 | A | G | 1 | a0002c0002t0054 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4592A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 4592 | chr17 | 49174320 | ||||||
chr17:49174621 | A | C | 1 | a0001c0004t0049 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4893A>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 4893 | chr17 | 49174621 | ||||||
chr17:49174628 | A | G | 1 | a0001c0001t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4900A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 4900 | chr17 | 49174628 | ||||||
chr17:49174632 | G | A | 1 | a0001c0001t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4904G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 4904 | chr17 | 49174632 | ||||||
chr17:49174655 | T | A | 1 | a0001c0001t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4927T>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 4927 | chr17 | 49174655 | ||||||
chr17:49174656 | T | C | 1 | a0001c0001t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4928T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 4928 | chr17 | 49174656 | ||||||
chr17:49174657 | T | A | 1 | a0001c0001t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4929T>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 4929 | chr17 | 49174657 | ||||||
chr17:49174660 | CTAATTGT others(4): Show |
C | 2 | a0001c0001t0010 a0001c0001t0057 |
6 | HG02280.hp1 HG02451.hp2 HG02723.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4936_*4946delTTGT others(7): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 4936 | INFO_REALIGN_3_PRIME | chr17 | 49174660 | |||||
chr17:49174661 | T | C | 1 | a0001c0001t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4933T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 4933 | chr17 | 49174661 | ||||||
chr17:49174662 | A | T | 1 | a0001c0001t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4934A>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 4934 | chr17 | 49174662 | ||||||
chr17:49174665 | T | C | 1 | a0001c0001t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4937T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 4937 | chr17 | 49174665 | ||||||
chr17:49174670 | A | C | 1 | a0001c0001t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4942A>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 4942 | chr17 | 49174670 | ||||||
chr17:49174671 | G | T | 1 | a0001c0001t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4943G>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 4943 | chr17 | 49174671 | ||||||
chr17:49174686 | G | T | 19 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0015 others(16): Show |
122 | HG00323.hp2 HG00408.hp2 HG00639.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*4958G>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 4958 | chr17 | 49174686 | ||||||
chr17:49174728 | A | T | 1 | a0001c0001t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5000A>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 5000 | chr17 | 49174728 | ||||||
chr17:49174732 | T | A | 1 | a0001c0001t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5004T>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 5004 | chr17 | 49174732 | ||||||
chr17:49174738 | A | T | 1 | a0001c0001t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5010A>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 5010 | chr17 | 49174738 | ||||||
chr17:49174742 | G | C | 1 | a0001c0001t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5014G>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 5014 | chr17 | 49174742 | ||||||
chr17:49174746 | A | T | 1 | a0001c0001t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5018A>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 5018 | chr17 | 49174746 | ||||||
chr17:49174749 | A | T | 1 | a0001c0001t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5021A>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 5021 | chr17 | 49174749 | ||||||
chr17:49174752 | T | G | 1 | a0001c0001t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5024T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 5024 | chr17 | 49174752 | ||||||
chr17:49174758 | G | C | 1 | a0001c0001t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5030G>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 5030 | chr17 | 49174758 | ||||||
chr17:49174759 | T | A | 1 | a0001c0001t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5031T>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 5031 | chr17 | 49174759 | ||||||
chr17:49174762 | A | T | 1 | a0001c0001t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5034A>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 5034 | chr17 | 49174762 | ||||||
chr17:49174774 | C | A | 1 | a0001c0001t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5046C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 5046 | chr17 | 49174774 | ||||||
chr17:49174781 | A | T | 1 | a0001c0001t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5053A>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 5053 | chr17 | 49174781 | ||||||
chr17:49174787 | G | T | 1 | a0001c0001t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5059G>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 5059 | chr17 | 49174787 | ||||||
chr17:49174790 | A | C | 1 | a0001c0001t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5062A>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 5062 | chr17 | 49174790 | ||||||
chr17:49174794 | A | T | 1 | a0001c0001t0056 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5066A>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 5066 | chr17 | 49174794 | ||||||
chr17:49174889 | C | T | 1 | a0003c0003t0009 | 5 | HG01884.hp2 HG02818.hp2 HG02895.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*5161C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 5161 | chr17 | 49174889 | ||||||
chr17:49174964 | A | G | 4 | a0002c0002t0004 a0002c0002t0005 a0002c0002t0054 others(1): Show |
31 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*5236A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 5236 | chr17 | 49174964 | ||||||
chr17:49175001 | T | C | 1 | a0002c0006t0021 | 2 | NA19240.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5273T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 5273 | chr17 | 49175001 | ||||||
chr17:49175030 | C | T | 7 | a0002c0002t0004 a0002c0002t0005 a0002c0002t0011 others(4): Show |
37 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*5302C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 5302 | chr17 | 49175030 | ||||||
chr17:49175032 | T | G | 35 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0010 others(32): Show |
173 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*5304T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 5304 | chr17 | 49175032 | ||||||
chr17:49175042 | C | A | 1 | a0002c0006t0021 | 2 | NA19240.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5314C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 5314 | chr17 | 49175042 | ||||||
chr17:49175049 | C | T | 14 | a0001c0001t0010 a0001c0001t0034 a0001c0001t0056 others(11): Show |
49 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*5321C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 5321 | chr17 | 49175049 | ||||||
chr17:49175340 | C | T | 1 | a0001c0001t0032 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5612C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 5612 | chr17 | 49175340 | ||||||
chr17:49175516 | C | A | 2 | a0001c0001t0010 a0001c0001t0056 |
6 | HG02280.hp1 HG02723.hp2 HG03195.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*5788C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 5788 | chr17 | 49175516 | ||||||
chr17:49175625 | G | T | 1 | a0001c0001t0016 | 2 | NA18946.hp1 NA18997.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5897G>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 5897 | chr17 | 49175625 | ||||||
chr17:49175677 | C | T | 1 | a0001c0001t0015 | 2 | NA18612.hp1 NA18962.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5949C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 5949 | chr17 | 49175677 | ||||||
chr17:49175728 | G | A | 2 | a0001c0001t0020 a0001c0004t0020 |
2 | HG02109.hp2 HG02886.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6000G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 6000 | chr17 | 49175728 | ||||||
chr17:49175839 | G | A | 1 | a0002c0006t0021 | 2 | NA19240.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6111G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 6111 | chr17 | 49175839 | ||||||
chr17:49176027 | C | T | 1 | a0001c0001t0031 | 1 | HG01070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6299C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 6299 | chr17 | 49176027 | ||||||
chr17:49176152 | C | A | 19 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0015 others(16): Show |
122 | HG00323.hp2 HG00408.hp2 HG00639.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*6424C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 6424 | chr17 | 49176152 | ||||||
chr17:49176188 | C | T | 4 | a0002c0002t0004 a0002c0002t0005 a0002c0002t0054 others(1): Show |
31 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*6460C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 6460 | chr17 | 49176188 | ||||||
chr17:49176321 | G | A | 1 | a0010c0015t0053 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6593G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 6593 | chr17 | 49176321 | ||||||
chr17:49176323 | A | G | 10 | a0001c0001t0010 a0001c0001t0056 a0001c0001t0057 others(7): Show |
44 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(41): Show |
3_prime_UTR_variant | MODIFIER | c.*6595A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 6595 | chr17 | 49176323 | ||||||
chr17:49176347 | C | T | 1 | a0008c0018t0029 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6619C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 6619 | chr17 | 49176347 | ||||||
chr17:49176405 | A | G | 7 | a0002c0002t0004 a0002c0002t0005 a0002c0002t0011 others(4): Show |
37 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*6677A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 6677 | chr17 | 49176405 | ||||||
chr17:49176457 | T | C | 7 | a0002c0002t0004 a0002c0002t0005 a0002c0002t0011 others(4): Show |
37 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*6729T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 6729 | chr17 | 49176457 | ||||||
chr17:49176473 | C | CAGCAGGA others(1): Show |
12 | a0001c0001t0010 a0001c0001t0056 a0001c0001t0057 others(9): Show |
47 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*6745_*6746insAGCA others(4): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 6746 | chr17 | 49176473 | ||||||
chr17:49176490 | A | G | 1 | a0001c0001t0036 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6762A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 6762 | chr17 | 49176490 | ||||||
chr17:49176494 | C | T | 2 | a0001c0001t0046 a0010c0015t0053 |
2 | HG02976.hp2 NA19054.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6766C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 6766 | chr17 | 49176494 | ||||||
chr17:49176658 | T | A | 2 | a0002c0002t0005 a0002c0002t0054 |
10 | HG01106.hp1 HG02486.hp2 HG02615.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*6930T>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 6930 | chr17 | 49176658 | ||||||
chr17:49176836 | C | A | 1 | a0001c0001t0030 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7108C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 11/11 | 7108 | chr17 | 49176836 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:49132880 | C | T | 1 | a0002c0002t0005g0351 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.14+74C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49132880 | |||||||
chr17:49133039 | G | A | 1 | a0001c0001t0024g0018 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.14+233G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49133039 | |||||||
chr17:49133067 | A | G | 229 | a0001c0001t0001g0014 a0001c0001t0001g0134 a0001c0001t0001g0138 others(226): Show |
246 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.14+261A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49133067 | |||||||
chr17:49133107 | G | A | 19 | a0001c0001t0001g0134 a0001c0001t0001g0138 a0001c0001t0001g0141 others(16): Show |
19 | HG00741.hp1 HG01069.hp1 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.14+301G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49133107 | |||||||
chr17:49133144 | C | A | 125 | a0001c0001t0001g0014 a0001c0001t0001g0177 a0001c0001t0001g0181 others(122): Show |
133 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.14+338C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49133144 | |||||||
chr17:49133509 | TTTTG | T | 4 | a0001c0001t0012g0152 a0001c0001t0013g0155 a0002c0002t0011g0153 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.14+709_14+712delTT others(2): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 49133509 | ||||||
chr17:49133537 | A | G | 154 | a0001c0001t0001g0014 a0001c0001t0001g0123 a0001c0001t0001g0124 others(151): Show |
167 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.14+731A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49133537 | |||||||
chr17:49133580 | A | G | 3 | a0001c0001t0002g0267 a0001c0001t0002g0268 a0001c0001t0002g0269 |
3 | NA18997.hp1 NA19058.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.14+774A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49133580 | |||||||
chr17:49133655 | G | A | 1 | a0002c0006t0055g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.14+849G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49133655 | |||||||
chr17:49133661 | C | T | 4 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(1): Show |
4 | HG02258.hp2 HG02896.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.14+855C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49133661 | |||||||
chr17:49133746 | C | G | 11 | a0001c0001t0001g0235 a0001c0001t0002g0236 a0001c0001t0012g0132 others(8): Show |
12 | HG01243.hp2 HG02109.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.14+940C>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49133746 | |||||||
chr17:49133841 | A | G | 2 | a0002c0002t0005g0115 a0003c0003t0009g0347 |
2 | HG03471.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.14+1035A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49133841 | |||||||
chr17:49133858 | G | A | 2 | a0001c0011t0042g0131 a0002c0006t0055g0272 |
2 | HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.14+1052G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49133858 | |||||||
chr17:49133860 | C | T | 1 | a0001c0001t0001g0114 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.14+1054C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49133860 | |||||||
chr17:49133913 | AAAAC | A | 9 | a0001c0001t0012g0132 a0001c0001t0012g0152 a0001c0001t0013g0155 others(6): Show |
10 | HG01243.hp2 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.14+1123_14+1126del others(4): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 49133913 | ||||||
chr17:49133930 | AAAACAAA others(1): Show |
A | 14 | a0001c0001t0001g0235 a0001c0001t0002g0010 a0001c0001t0002g0157 others(11): Show |
16 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.14+1140_14+1147del others(8): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 49133930 | ||||||
chr17:49133945 | ACAAAC | A | 5 | a0001c0001t0001g0238 a0001c0001t0012g0156 a0001c0001t0034g0349 others(2): Show |
5 | HG01358.hp2 HG01884.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.14+1140_14+1144del others(5): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49133945 | |||||||
chr17:49133956 | G | A | 1 | a0001c0001t0002g0016 | 2 | NA18947.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.14+1150G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49133956 | |||||||
chr17:49134006 | G | A | 14 | a0001c0001t0001g0235 a0001c0001t0002g0010 a0001c0001t0002g0120 others(11): Show |
16 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.14+1200G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49134006 | |||||||
chr17:49134069 | C | T | 2 | a0001c0001t0001g0113 a0001c0001t0038g0266 |
2 | HG00423.hp2 HG00544.hp1 |
intron_variant | MODIFIER | c.14+1263C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49134069 | |||||||
chr17:49134082 | A | T | 33 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 others(30): Show |
35 | HG01069.hp2 HG01071.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.14+1276A>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49134082 | |||||||
chr17:49134119 | G | A | 24 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(21): Show |
33 | HG00423.hp1 HG00597.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.14+1313G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49134119 | |||||||
chr17:49134146 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.14+1340A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49134146 | |||||||
chr17:49134153 | A | G | 74 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0090 others(71): Show |
75 | HG00099.hp1 HG00438.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.14+1347A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49134153 | |||||||
chr17:49134198 | A | G | 196 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(193): Show |
207 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(204): Show |
intron_variant | MODIFIER | c.14+1392A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49134198 | |||||||
chr17:49134296 | C | G | 234 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0021 others(231): Show |
253 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(250): Show |
intron_variant | MODIFIER | c.14+1490C>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49134296 | |||||||
chr17:49134409 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.14+1603A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49134409 | |||||||
chr17:49134411 | T | G | 133 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0022 others(130): Show |
143 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.14+1605T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49134411 | |||||||
chr17:49134429 | C | T | 1 | a0001c0001t0001g0339 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.14+1623C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49134429 | |||||||
chr17:49134529 | C | T | 1 | a0001c0001t0002g0174 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.14+1723C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49134529 | |||||||
chr17:49134532 | A | G | 198 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0021 others(195): Show |
217 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(214): Show |
intron_variant | MODIFIER | c.14+1726A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49134532 | |||||||
chr17:49134735 | A | C | 1 | a0001c0001t0001g0192 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.14+1929A>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49134735 | |||||||
chr17:49134772 | G | A | 4 | a0001c0001t0051g0348 a0002c0006t0021g0036 a0002c0006t0021g0099 others(1): Show |
4 | HG01243.hp2 HG02280.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.14+1966G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49134772 | |||||||
chr17:49134843 | A | G | 8 | a0001c0001t0002g0108 a0001c0001t0002g0120 a0001c0001t0026g0121 others(5): Show |
8 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.14+2037A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49134843 | |||||||
chr17:49134878 | A | G | 9 | a0001c0001t0001g0177 a0001c0001t0002g0010 a0001c0001t0002g0165 others(6): Show |
11 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.14+2072A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49134878 | |||||||
chr17:49135026 | T | A | 1 | a0001c0001t0013g0350 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.14+2220T>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49135026 | |||||||
chr17:49135078 | A | G | 1 | a0001c0001t0002g0226 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.14+2272A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49135078 | |||||||
chr17:49135143 | A | AT | 56 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(53): Show |
57 | HG00323.hp1 HG00408.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.14+2341dupT | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 49135143 | ||||||
chr17:49135214 | T | C | 1 | a0001c0001t0051g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.14+2408T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49135214 | |||||||
chr17:49135363 | C | A | 1 | a0001c0001t0051g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.14+2557C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49135363 | |||||||
chr17:49135385 | C | T | 2 | a0001c0001t0015g0146 a0001c0001t0015g0321 |
2 | NA18612.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.14+2579C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49135385 | |||||||
chr17:49135402 | C | G | 1 | a0001c0001t0001g0297 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.14+2596C>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49135402 | |||||||
chr17:49135434 | A | G | 1 | a0001c0001t0051g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.14+2628A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49135434 | |||||||
chr17:49135500 | C | T | 2 | a0001c0001t0051g0348 a0001c0001t0057g0161 |
2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.14+2694C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49135500 | |||||||
chr17:49135501 | A | G | 2 | a0001c0001t0051g0348 a0001c0001t0057g0161 |
2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.14+2695A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49135501 | |||||||
chr17:49135537 | C | T | 2 | a0001c0001t0002g0025 a0001c0001t0046g0091 |
2 | NA19054.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.14+2731C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49135537 | |||||||
chr17:49135551 | C | T | 1 | a0001c0001t0057g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.14+2745C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49135551 | |||||||
chr17:49135553 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0189 |
2 | NA18951.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.14+2747C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49135553 | |||||||
chr17:49135594 | T | C | 2 | a0001c0001t0051g0348 a0001c0001t0057g0161 |
2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.14+2788T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49135594 | |||||||
chr17:49135603 | C | T | 1 | a0001c0001t0002g0193 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.14+2797C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49135603 | |||||||
chr17:49135680 | C | T | 1 | a0001c0001t0051g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.14+2874C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49135680 | |||||||
chr17:49135713 | C | T | 1 | a0001c0001t0057g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.14+2907C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49135713 | |||||||
chr17:49135786 | C | G | 6 | a0001c0001t0013g0155 a0001c0001t0013g0350 a0001c0001t0044g0160 others(3): Show |
6 | HG01243.hp2 HG02109.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.14+2980C>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49135786 | |||||||
chr17:49135794 | T | C | 1 | a0002c0006t0055g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.14+2988T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49135794 | |||||||
chr17:49135806 | G | A | 7 | a0001c0001t0012g0152 a0001c0001t0039g0078 a0001c0004t0008g0263 others(4): Show |
7 | HG02109.hp2 HG02258.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.14+3000G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49135806 | |||||||
chr17:49135846 | G | A | 1 | a0001c0001t0051g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.14+3040G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49135846 | |||||||
chr17:49135880 | G | A | 1 | a0001c0001t0003g0020 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.14+3074G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49135880 | |||||||
chr17:49135891 | G | A | 1 | a0001c0001t0057g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.14+3085G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49135891 | |||||||
chr17:49136050 | T | C | 1 | a0001c0001t0001g0034 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.14+3244T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49136050 | |||||||
chr17:49136062 | A | G | 2 | a0001c0001t0051g0348 a0001c0001t0057g0161 |
2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.14+3256A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49136062 | |||||||
chr17:49136082 | C | A | 1 | a0001c0001t0057g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.14+3276C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49136082 | |||||||
chr17:49136082 | C | CA | 168 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(165): Show |
181 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.14+3291dupA | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 49136082 | ||||||
chr17:49136318 | A | G | 1 | a0001c0001t0057g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.14+3512A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49136318 | |||||||
chr17:49136404 | G | A | 3 | a0002c0006t0021g0036 a0002c0006t0021g0099 a0009c0017t0035g0262 |
3 | HG02280.hp2 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.14+3598G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49136404 | |||||||
chr17:49136456 | A | G | 1 | a0001c0001t0006g0200 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.14+3650A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49136456 | |||||||
chr17:49136518 | G | GTTTA | 13 | a0001c0001t0001g0076 a0001c0001t0001g0087 a0001c0001t0001g0212 others(10): Show |
13 | HG00408.hp1 HG00438.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.14+3752_14+3755dup others(4): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 49136518 | ||||||
chr17:49136518 | GTTTA | G | 19 | a0001c0001t0001g0190 a0001c0001t0001g0192 a0001c0001t0001g0311 others(16): Show |
20 | HG00323.hp1 HG00639.hp1 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.14+3752_14+3755del others(4): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 49136518 | ||||||
chr17:49136518 | GTTTATTT others(1): Show |
G | 16 | a0001c0001t0002g0010 a0001c0001t0002g0165 a0001c0001t0002g0166 others(13): Show |
18 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.14+3748_14+3755del others(8): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 49136518 | ||||||
chr17:49136518 | GTTTATTT others(5): Show |
G | 57 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0024 others(54): Show |
68 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.14+3744_14+3755del others(12): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 49136518 | ||||||
chr17:49136518 | GTTTATTT others(9): Show |
G | 1 | a0001c0001t0051g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.14+3740_14+3755del others(16): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 49136518 | ||||||
chr17:49136522 | A | G | 1 | a0001c0001t0032g0129 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.14+3716A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49136522 | |||||||
chr17:49136647 | A | C | 1 | a0001c0001t0002g0199 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.14+3841A>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49136647 | |||||||
chr17:49136660 | T | C | 1 | a0001c0001t0057g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.14+3854T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49136660 | |||||||
chr17:49136795 | T | C | 1 | a0001c0001t0057g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.14+3989T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49136795 | |||||||
chr17:49136796 | C | T | 1 | a0001c0001t0045g0107 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.14+3990C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49136796 | |||||||
chr17:49136816 | G | C | 27 | a0001c0001t0001g0037 a0001c0001t0001g0144 a0001c0001t0001g0198 others(24): Show |
27 | HG00735.hp1 HG00738.hp1 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.14+4010G>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49136816 | |||||||
chr17:49136826 | C | T | 1 | a0001c0001t0051g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.14+4020C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49136826 | |||||||
chr17:49136827 | G | A | 1 | a0001c0001t0003g0327 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.14+4021G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49136827 | |||||||
chr17:49137017 | G | A | 1 | a0001c0001t0057g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.14+4211G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49137017 | |||||||
chr17:49137018 | G | A | 1 | a0001c0001t0057g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.14+4212G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49137018 | |||||||
chr17:49137064 | C | CT | 22 | a0001c0001t0002g0010 a0001c0001t0002g0165 a0001c0001t0002g0166 others(19): Show |
24 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(21): Show |
intron_variant | MODIFIER | c.15-4173dupT | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 49137064 | ||||||
chr17:49137186 | T | C | 1 | a0001c0001t0057g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.15-4061T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49137186 | |||||||
chr17:49137353 | G | A | 1 | a0001c0001t0057g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.15-3894G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49137353 | |||||||
chr17:49137406 | C | T | 1 | a0001c0001t0002g0095 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.15-3841C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49137406 | |||||||
chr17:49137450 | C | T | 1 | a0001c0001t0051g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.15-3797C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49137450 | |||||||
chr17:49137462 | G | C | 1 | a0001c0001t0001g0041 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.15-3785G>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49137462 | |||||||
chr17:49137549 | C | T | 1 | a0001c0001t0051g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.15-3698C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49137549 | |||||||
chr17:49137587 | A | G | 1 | a0001c0001t0057g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.15-3660A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49137587 | |||||||
chr17:49137592 | C | A | 2 | a0001c0001t0051g0348 a0001c0001t0057g0161 |
2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.15-3655C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49137592 | |||||||
chr17:49137668 | A | G | 2 | a0001c0001t0012g0152 a0001c0001t0039g0078 |
2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.15-3579A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49137668 | |||||||
chr17:49137812 | A | C | 2 | a0001c0001t0002g0165 a0001c0001t0002g0166 |
2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.15-3435A>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49137812 | |||||||
chr17:49138009 | G | A | 1 | a0008c0018t0029g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.15-3238G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49138009 | |||||||
chr17:49138059 | A | G | 2 | a0001c0001t0002g0172 a0001c0001t0028g0140 |
2 | HG00323.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.15-3188A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49138059 | |||||||
chr17:49138131 | C | T | 47 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0030 others(44): Show |
56 | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.15-3116C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49138131 | |||||||
chr17:49138159 | T | G | 5 | a0001c0004t0008g0263 a0001c0004t0008g0264 a0001c0004t0020g0253 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.15-3088T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49138159 | |||||||
chr17:49138280 | A | C | 1 | a0001c0001t0002g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.15-2967A>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49138280 | |||||||
chr17:49138431 | A | G | 1 | a0007c0009t0002g0234 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.15-2816A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49138431 | |||||||
chr17:49138618 | G | A | 2 | a0001c0001t0002g0031 a0001c0001t0002g0246 |
2 | HG02257.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.15-2629G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49138618 | |||||||
chr17:49138670 | T | G | 2 | a0001c0001t0051g0348 a0001c0001t0057g0161 |
2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.15-2577T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49138670 | |||||||
chr17:49138706 | G | A | 5 | a0001c0004t0008g0263 a0001c0004t0008g0264 a0001c0004t0020g0253 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.15-2541G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49138706 | |||||||
chr17:49138743 | G | C | 1 | a0001c0001t0051g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.15-2504G>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49138743 | |||||||
chr17:49138772 | G | C | 1 | a0001c0001t0051g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.15-2475G>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49138772 | |||||||
chr17:49138819 | G | A | 1 | a0001c0001t0051g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.15-2428G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49138819 | |||||||
chr17:49138832 | G | C | 5 | a0001c0004t0008g0263 a0001c0004t0008g0264 a0001c0004t0020g0253 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.15-2415G>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49138832 | |||||||
chr17:49138842 | A | G | 5 | a0001c0004t0008g0263 a0001c0004t0008g0264 a0001c0004t0020g0253 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.15-2405A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49138842 | |||||||
chr17:49138926 | C | T | 1 | a0001c0001t0002g0208 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.15-2321C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49138926 | |||||||
chr17:49138985 | G | A | 77 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(74): Show |
86 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.15-2262G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49138985 | |||||||
chr17:49139127 | C | T | 66 | a0001c0001t0001g0021 a0001c0001t0001g0037 a0001c0001t0001g0198 others(63): Show |
70 | HG00438.hp1 HG00735.hp1 HG00741.hp2 others(67): Show |
intron_variant | MODIFIER | c.15-2120C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49139127 | |||||||
chr17:49139152 | C | T | 1 | a0007c0009t0002g0133 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.15-2095C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49139152 | |||||||
chr17:49139157 | C | T | 4 | a0001c0001t0002g0201 a0001c0001t0002g0202 a0001c0001t0002g0206 others(1): Show |
4 | HG02145.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.15-2090C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49139157 | |||||||
chr17:49139158 | G | A | 1 | a0001c0001t0001g0059 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.15-2089G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49139158 | |||||||
chr17:49139245 | G | GT | 35 | a0001c0001t0001g0041 a0001c0001t0001g0053 a0001c0001t0001g0054 others(32): Show |
37 | HG00099.hp2 HG01069.hp2 HG01071.hp1 others(34): Show |
intron_variant | MODIFIER | c.15-1992dupT | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 49139245 | ||||||
chr17:49139280 | C | T | 13 | a0001c0001t0001g0037 a0001c0001t0001g0198 a0001c0001t0001g0217 others(10): Show |
13 | HG00735.hp1 HG01167.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.15-1967C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49139280 | |||||||
chr17:49139317 | T | C | 5 | a0001c0004t0008g0263 a0001c0004t0008g0264 a0001c0004t0020g0253 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.15-1930T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49139317 | |||||||
chr17:49139395 | T | C | 2 | a0001c0001t0051g0348 a0001c0001t0057g0161 |
2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.15-1852T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49139395 | |||||||
chr17:49139469 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.15-1778G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49139469 | |||||||
chr17:49139475 | C | T | 1 | a0001c0001t0057g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.15-1772C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49139475 | |||||||
chr17:49139531 | T | C | 5 | a0001c0004t0008g0263 a0001c0004t0008g0264 a0001c0004t0020g0253 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.15-1716T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49139531 | |||||||
chr17:49139642 | C | G | 158 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(155): Show |
172 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.15-1605C>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49139642 | |||||||
chr17:49139650 | A | C | 1 | a0001c0001t0051g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.15-1597A>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49139650 | |||||||
chr17:49139729 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.15-1518C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49139729 | |||||||
chr17:49139844 | C | G | 31 | a0001c0001t0001g0021 a0001c0001t0001g0328 a0001c0001t0002g0168 others(28): Show |
33 | HG00438.hp1 HG00738.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.15-1403C>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49139844 | |||||||
chr17:49139844 | C | T | 1 | a0001c0001t0057g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.15-1403C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49139844 | |||||||
chr17:49140049 | A | T | 2 | a0001c0001t0051g0348 a0001c0001t0057g0161 |
2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.15-1198A>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49140049 | |||||||
chr17:49140050 | T | C | 2 | a0001c0001t0051g0348 a0001c0001t0057g0161 |
2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.15-1197T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49140050 | |||||||
chr17:49140052 | ATATAATA others(5): Show |
A | 2 | a0001c0001t0051g0348 a0001c0001t0057g0161 |
2 | HG01243.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.15-1187_15-1176del others(12): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 49140052 | ||||||
chr17:49140162 | G | A | 1 | a0001c0001t0057g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.15-1085G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49140162 | |||||||
chr17:49140186 | C | T | 1 | a0001c0001t0051g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.15-1061C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49140186 | |||||||
chr17:49140249 | C | T | 5 | a0001c0004t0008g0263 a0001c0004t0008g0264 a0001c0004t0020g0253 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.15-998C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49140249 | |||||||
chr17:49140250 | G | A | 2 | a0001c0001t0003g0278 a0001c0001t0003g0279 |
2 | HG02735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.15-997G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49140250 | |||||||
chr17:49140275 | T | C | 1 | a0001c0001t0057g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.15-972T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49140275 | |||||||
chr17:49140276 | A | G | 20 | a0001c0001t0002g0010 a0001c0001t0002g0165 a0001c0001t0002g0166 others(17): Show |
22 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.15-971A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49140276 | |||||||
chr17:49140544 | T | C | 52 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(49): Show |
53 | HG00323.hp1 HG00639.hp1 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.15-703T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49140544 | |||||||
chr17:49140637 | A | AT | 16 | a0001c0001t0002g0010 a0001c0001t0002g0165 a0001c0001t0002g0166 others(13): Show |
18 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.15-608dupT | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 49140637 | ||||||
chr17:49140681 | T | C | 1 | a0002c0002t0004g0194 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.15-566T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49140681 | |||||||
chr17:49140682 | T | C | 9 | a0001c0001t0002g0010 a0001c0001t0002g0165 a0001c0001t0002g0166 others(6): Show |
11 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.15-565T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49140682 | |||||||
chr17:49140725 | C | CT | 249 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0021 others(246): Show |
266 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(263): Show |
intron_variant | MODIFIER | c.15-507dupT | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 49140725 | ||||||
chr17:49140725 | C | CTT | 85 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(82): Show |
94 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.15-508_15-507dupTT | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 49140725 | ||||||
chr17:49140725 | C | CTTT | 12 | a0001c0001t0002g0010 a0001c0001t0002g0165 a0001c0001t0002g0166 others(9): Show |
14 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.15-509_15-507dupTT others(1): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 49140725 | ||||||
chr17:49140777 | G | T | 1 | a0001c0001t0057g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.15-470G>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49140777 | |||||||
chr17:49140867 | C | A | 1 | a0001c0001t0013g0155 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.15-380C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49140867 | |||||||
chr17:49140951 | G | T | 1 | a0001c0001t0057g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.15-296G>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49140951 | |||||||
chr17:49140977 | A | G | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(75): Show |
87 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.15-270A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49140977 | |||||||
chr17:49141023 | CT | C | 5 | a0001c0001t0031g0224 a0001c0001t0051g0348 a0002c0002t0004g0184 others(2): Show |
6 | HG00323.hp1 HG01070.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.15-213delT | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr17 | 49141023 | ||||||
chr17:49141033 | T | G | 1 | a0003c0003t0009g0347 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.15-214T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49141033 | |||||||
chr17:49141077 | C | T | 1 | a0001c0001t0018g0284 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.15-170C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 1/10 | chr17 | 49141077 | |||||||
chr17:49141508 | A | G | 1 | a0001c0001t0051g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.215+61A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 2/10 | chr17 | 49141508 | |||||||
chr17:49141537 | A | C | 79 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(76): Show |
88 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.215+90A>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 2/10 | chr17 | 49141537 | |||||||
chr17:49141597 | G | A | 53 | a0001c0001t0001g0021 a0001c0001t0001g0328 a0001c0001t0002g0010 others(50): Show |
57 | HG00438.hp1 HG00741.hp2 HG01069.hp2 others(54): Show |
intron_variant | MODIFIER | c.215+150G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 2/10 | chr17 | 49141597 | |||||||
chr17:49141612 | C | T | 14 | a0001c0001t0002g0010 a0001c0001t0002g0165 a0001c0001t0002g0166 others(11): Show |
16 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.215+165C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 2/10 | chr17 | 49141612 | |||||||
chr17:49141637 | A | C | 25 | a0001c0001t0001g0021 a0001c0001t0001g0328 a0001c0001t0006g0179 others(22): Show |
27 | HG00438.hp1 HG00741.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.215+190A>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 2/10 | chr17 | 49141637 | |||||||
chr17:49141663 | G | C | 1 | a0001c0001t0003g0096 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.215+216G>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 2/10 | chr17 | 49141663 | |||||||
chr17:49142180 | G | A | 127 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(124): Show |
140 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(137): Show |
splice_region_variant&intron_variant | LOW | c.353+8G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49142180 | |||||||
chr17:49142250 | A | C | 1 | a0001c0001t0006g0179 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.353+78A>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49142250 | |||||||
chr17:49142263 | G | A | 1 | a0001c0001t0012g0156 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.353+91G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49142263 | |||||||
chr17:49142305 | T | C | 4 | a0001c0001t0013g0155 a0001c0001t0013g0350 a0001c0001t0044g0160 others(1): Show |
4 | HG02109.hp1 HG02809.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.353+133T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49142305 | |||||||
chr17:49142460 | T | C | 1 | a0001c0001t0001g0245 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.353+288T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49142460 | |||||||
chr17:49142502 | C | A | 2 | a0004c0012t0007g0336 a0004c0012t0007g0337 |
2 | HG02071.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.353+330C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49142502 | |||||||
chr17:49142527 | C | CA | 106 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(103): Show |
117 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.353+359dupA | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49142527 | ||||||
chr17:49142553 | A | G | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(75): Show |
87 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.353+381A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49142553 | |||||||
chr17:49142700 | GCAAAAA | G | 101 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(98): Show |
112 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.353+553_353+558del others(6): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49142700 | ||||||
chr17:49142780 | T | G | 4 | a0001c0001t0002g0012 a0001c0001t0002g0227 a0001c0001t0002g0259 others(1): Show |
5 | HG02559.hp2 HG02630.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.353+608T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49142780 | |||||||
chr17:49142846 | T | C | 5 | a0001c0004t0008g0263 a0001c0004t0008g0264 a0001c0004t0020g0253 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.353+674T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49142846 | |||||||
chr17:49142907 | C | G | 18 | a0001c0001t0002g0010 a0001c0001t0002g0165 a0001c0001t0002g0166 others(15): Show |
20 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.353+735C>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49142907 | |||||||
chr17:49142912 | G | T | 1 | a0001c0001t0047g0086 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.353+740G>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49142912 | |||||||
chr17:49142925 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.353+753A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49142925 | |||||||
chr17:49142987 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.353+815G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49142987 | |||||||
chr17:49143024 | G | A | 5 | a0001c0004t0008g0263 a0001c0004t0008g0264 a0001c0004t0020g0253 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.353+852G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49143024 | |||||||
chr17:49143046 | C | T | 1 | a0001c0001t0002g0043 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.353+874C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49143046 | |||||||
chr17:49143220 | A | G | 217 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(214): Show |
232 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(229): Show |
intron_variant | MODIFIER | c.353+1048A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49143220 | |||||||
chr17:49143301 | C | CAAAAAAA others(2): Show |
170 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(167): Show |
184 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.353+1135_353+1143d others(11): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49143301 | ||||||
chr17:49143364 | C | T | 279 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(276): Show |
305 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.353+1192C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49143364 | |||||||
chr17:49143635 | G | A | 1 | a0003c0003t0009g0347 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.353+1463G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49143635 | |||||||
chr17:49143710 | T | C | 1 | a0008c0018t0029g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.353+1538T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49143710 | |||||||
chr17:49143839 | C | CTCT | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(129): Show |
145 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.353+1672_353+1674d others(5): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49143839 | ||||||
chr17:49143934 | G | A | 1 | a0008c0018t0029g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.353+1762G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49143934 | |||||||
chr17:49143949 | G | A | 1 | a0008c0018t0029g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.353+1777G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49143949 | |||||||
chr17:49144199 | C | G | 3 | a0002c0006t0021g0036 a0002c0006t0021g0099 a0009c0017t0035g0262 |
3 | HG02280.hp2 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.353+2027C>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49144199 | |||||||
chr17:49144263 | T | C | 1 | a0001c0001t0002g0031 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.353+2091T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49144263 | |||||||
chr17:49144281 | A | G | 15 | a0001c0001t0002g0010 a0001c0001t0002g0165 a0001c0001t0002g0166 others(12): Show |
17 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.353+2109A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49144281 | |||||||
chr17:49144386 | C | G | 1 | a0001c0001t0001g0123 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.353+2214C>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49144386 | |||||||
chr17:49144407 | C | T | 1 | a0001c0001t0032g0129 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.353+2235C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49144407 | |||||||
chr17:49144438 | T | C | 1 | a0003c0003t0009g0347 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.353+2266T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49144438 | |||||||
chr17:49144910 | A | G | 2 | a0001c0001t0001g0112 a0001c0001t0002g0236 |
2 | HG01516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.353+2738A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49144910 | |||||||
chr17:49144970 | A | G | 134 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(131): Show |
147 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.353+2798A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49144970 | |||||||
chr17:49145014 | G | A | 2 | a0001c0001t0044g0160 a0002c0006t0055g0272 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.353+2842G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49145014 | |||||||
chr17:49145075 | A | G | 1 | a0001c0001t0051g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.353+2903A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49145075 | |||||||
chr17:49145290 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.353+3118C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49145290 | |||||||
chr17:49145301 | G | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(104): Show |
118 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.353+3129G>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49145301 | |||||||
chr17:49145920 | T | C | 107 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(104): Show |
118 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.353+3748T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49145920 | |||||||
chr17:49145995 | G | A | 1 | a0008c0018t0029g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.353+3823G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49145995 | |||||||
chr17:49146013 | T | G | 1 | a0001c0001t0001g0022 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.353+3841T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49146013 | |||||||
chr17:49146070 | C | T | 1 | a0001c0001t0047g0086 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.353+3898C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49146070 | |||||||
chr17:49146121 | C | G | 1 | a0001c0001t0001g0223 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.353+3949C>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49146121 | |||||||
chr17:49146158 | C | T | 1 | a0001c0001t0057g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.353+3986C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49146158 | |||||||
chr17:49146224 | C | T | 10 | a0001c0001t0044g0160 a0001c0001t0051g0348 a0001c0004t0008g0263 others(7): Show |
10 | HG01243.hp2 HG01891.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.353+4052C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49146224 | |||||||
chr17:49146364 | G | A | 2 | a0001c0001t0013g0155 a0001c0001t0013g0350 |
2 | HG03130.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.353+4192G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49146364 | |||||||
chr17:49146373 | C | T | 5 | a0001c0001t0001g0258 a0001c0001t0002g0109 a0001c0001t0002g0164 others(2): Show |
5 | HG01346.hp2 HG01934.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.353+4201C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49146373 | |||||||
chr17:49146459 | C | T | 8 | a0001c0001t0051g0348 a0001c0004t0008g0263 a0001c0004t0008g0264 others(5): Show |
8 | HG01243.hp2 HG01891.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.353+4287C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49146459 | |||||||
chr17:49146577 | C | T | 2 | a0001c0001t0044g0160 a0002c0006t0055g0272 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.353+4405C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49146577 | |||||||
chr17:49146589 | G | A | 1 | a0001c0001t0051g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.353+4417G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49146589 | |||||||
chr17:49146645 | A | G | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(85): Show |
97 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.353+4473A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49146645 | |||||||
chr17:49146721 | G | A | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(85): Show |
97 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.353+4549G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49146721 | |||||||
chr17:49146782 | T | C | 3 | a0001c0001t0002g0010 a0001c0005t0008g0011 a0001c0005t0008g0082 |
5 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.353+4610T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49146782 | |||||||
chr17:49146839 | T | C | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(85): Show |
97 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.353+4667T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49146839 | |||||||
chr17:49146842 | G | T | 1 | a0001c0001t0034g0349 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.353+4670G>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49146842 | |||||||
chr17:49146891 | T | C | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(85): Show |
97 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.353+4719T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49146891 | |||||||
chr17:49146987 | G | A | 13 | a0001c0001t0001g0021 a0001c0001t0001g0328 a0002c0002t0004g0038 others(10): Show |
13 | HG00438.hp1 HG00741.hp2 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.353+4815G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49146987 | |||||||
chr17:49146995 | T | C | 2 | a0001c0001t0003g0006 a0001c0001t0003g0280 |
3 | HG00597.hp2 HG00609.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.353+4823T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49146995 | |||||||
chr17:49147083 | C | T | 1 | a0002c0002t0004g0128 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.353+4911C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49147083 | |||||||
chr17:49147225 | T | C | 1 | a0008c0018t0029g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.353+5053T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49147225 | |||||||
chr17:49147272 | A | G | 1 | a0003c0003t0009g0347 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.353+5100A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49147272 | |||||||
chr17:49147374 | C | CTTTT | 6 | a0001c0001t0044g0160 a0001c0004t0008g0263 a0001c0004t0008g0264 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.353+5205_353+5206i others(6): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49147374 | ||||||
chr17:49147376 | TTC | T | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(73): Show |
85 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.353+5206_353+5207d others(4): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49147376 | ||||||
chr17:49147378 | C | CT | 8 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0057g0161 others(5): Show |
8 | HG00423.hp1 HG00438.hp1 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.353+5220dupT | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49147378 | ||||||
chr17:49147378 | C | T | 10 | a0001c0001t0044g0160 a0001c0001t0051g0348 a0001c0004t0008g0263 others(7): Show |
10 | HG01243.hp2 HG01891.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.353+5206C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49147378 | |||||||
chr17:49147415 | C | T | 2 | a0001c0001t0001g0198 a0001c0001t0002g0322 |
2 | HG01167.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.353+5243C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49147415 | |||||||
chr17:49147584 | C | T | 1 | a0001c0001t0051g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.354-5216C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49147584 | |||||||
chr17:49147599 | C | T | 6 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0002g0170 others(3): Show |
6 | HG00738.hp1 HG01433.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.354-5201C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49147599 | |||||||
chr17:49147601 | C | T | 6 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0002g0170 others(3): Show |
6 | HG00738.hp1 HG01433.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.354-5199C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49147601 | |||||||
chr17:49147819 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.354-4981T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49147819 | |||||||
chr17:49147839 | T | TTA | 25 | a0001c0001t0001g0021 a0001c0001t0001g0328 a0001c0001t0006g0179 others(22): Show |
27 | HG00438.hp1 HG00741.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.354-4951_354-4950d others(4): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49147839 | ||||||
chr17:49147849 | A | ATATG | 3 | a0001c0001t0001g0045 a0001c0001t0001g0053 a0001c0001t0046g0091 |
3 | NA18977.hp2 NA18993.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.354-4950_354-4949i others(6): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49147849 | ||||||
chr17:49147849 | A | ATG | 81 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(78): Show |
90 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.354-4935_354-4934d others(4): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49147849 | ||||||
chr17:49147849 | A | G | 1 | a0008c0018t0029g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.354-4951A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49147849 | |||||||
chr17:49147867 | A | G | 114 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(111): Show |
125 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.354-4933A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49147867 | |||||||
chr17:49147952 | GT | G | 17 | a0001c0001t0001g0021 a0001c0001t0001g0328 a0001c0001t0002g0012 others(14): Show |
18 | HG00438.hp1 HG00741.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.354-4841delT | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49147952 | ||||||
chr17:49147966 | T | TTA | 16 | a0001c0001t0002g0010 a0001c0001t0002g0109 a0001c0001t0002g0162 others(13): Show |
18 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.354-4816_354-4815d others(4): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49147966 | ||||||
chr17:49147966 | T | TTATATAT others(3): Show |
2 | a0002c0006t0021g0099 a0009c0017t0035g0262 |
2 | HG02280.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.354-4824_354-4815d others(12): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49147966 | ||||||
chr17:49147966 | TTATA | T | 113 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(110): Show |
124 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.354-4818_354-4815d others(6): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49147966 | ||||||
chr17:49148125 | C | A | 3 | a0001c0001t0002g0031 a0001c0001t0002g0073 a0001c0001t0002g0246 |
3 | HG02257.hp2 HG02523.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.354-4675C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49148125 | |||||||
chr17:49148300 | G | A | 1 | a0001c0001t0057g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.354-4500G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49148300 | |||||||
chr17:49148310 | T | A | 1 | a0001c0001t0001g0070 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.354-4490T>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49148310 | |||||||
chr17:49148311 | A | T | 1 | a0001c0001t0001g0070 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.354-4489A>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49148311 | |||||||
chr17:49148365 | A | G | 113 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(110): Show |
124 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.354-4435A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49148365 | |||||||
chr17:49148565 | A | G | 1 | a0001c0001t0057g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.354-4235A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49148565 | |||||||
chr17:49148728 | A | G | 1 | a0001c0001t0003g0080 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.354-4072A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49148728 | |||||||
chr17:49148818 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.354-3982G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49148818 | |||||||
chr17:49148819 | A | G | 1 | a0001c0001t0001g0070 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.354-3981A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49148819 | |||||||
chr17:49148884 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.354-3916C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49148884 | |||||||
chr17:49148965 | A | T | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(85): Show |
97 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.354-3835A>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49148965 | |||||||
chr17:49148972 | T | C | 171 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(168): Show |
185 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.354-3828T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49148972 | |||||||
chr17:49148985 | G | A | 1 | a0002c0002t0004g0335 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.354-3815G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49148985 | |||||||
chr17:49148999 | T | G | 1 | a0003c0003t0009g0347 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.354-3801T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49148999 | |||||||
chr17:49149004 | C | A | 1 | a0001c0001t0002g0326 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.354-3796C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49149004 | |||||||
chr17:49149041 | C | T | 2 | a0001c0001t0002g0201 a0001c0001t0002g0202 |
2 | HG02145.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.354-3759C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49149041 | |||||||
chr17:49149054 | C | CA | 8 | a0001c0001t0001g0052 a0001c0001t0001g0318 a0001c0001t0002g0130 others(5): Show |
8 | HG01255.hp1 HG01891.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.354-3731dupA | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49149054 | ||||||
chr17:49149054 | C | CAA | 76 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(73): Show |
85 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.354-3732_354-3731d others(4): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49149054 | ||||||
chr17:49149115 | G | A | 3 | a0001c0001t0023g0276 a0003c0003t0009g0239 a0003c0003t0009g0240 |
3 | HG02717.hp1 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.354-3685G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49149115 | |||||||
chr17:49149191 | TC | T | 15 | a0001c0001t0002g0010 a0001c0001t0002g0165 a0001c0001t0002g0166 others(12): Show |
17 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.354-3606delC | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49149191 | ||||||
chr17:49149289 | G | T | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(129): Show |
145 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.354-3511G>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49149289 | |||||||
chr17:49149372 | G | A | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(75): Show |
87 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.354-3428G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49149372 | |||||||
chr17:49149541 | G | A | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(85): Show |
97 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.354-3259G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49149541 | |||||||
chr17:49149913 | C | A | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(85): Show |
97 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.354-2887C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49149913 | |||||||
chr17:49149935 | A | G | 1 | a0001c0001t0002g0093 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.354-2865A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49149935 | |||||||
chr17:49149954 | T | A | 1 | a0008c0018t0029g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.354-2846T>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49149954 | |||||||
chr17:49149991 | A | G | 113 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(110): Show |
124 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.354-2809A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49149991 | |||||||
chr17:49150068 | TC | T | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(75): Show |
87 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.354-2731delC | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150068 | |||||||
chr17:49150068 | TCG | T | 10 | a0001c0001t0044g0160 a0001c0001t0051g0348 a0001c0004t0008g0263 others(7): Show |
10 | HG01243.hp2 HG01891.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.354-2731_354-2730d others(4): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150068 | |||||||
chr17:49150069 | CG | C | 15 | a0001c0001t0001g0242 a0001c0001t0001g0308 a0001c0001t0002g0016 others(12): Show |
16 | HG02071.hp2 HG02080.hp2 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.354-2723delG | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49150069 | ||||||
chr17:49150102 | C | T | 1 | a0001c0001t0051g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.354-2698C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150102 | |||||||
chr17:49150104 | C | G | 1 | a0001c0001t0002g0109 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.354-2696C>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150104 | |||||||
chr17:49150104 | C | T | 1 | a0001c0001t0007g0293 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.354-2696C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150104 | |||||||
chr17:49150109 | A | G | 113 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(110): Show |
124 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.354-2691A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150109 | |||||||
chr17:49150122 | C | G | 7 | a0001c0001t0001g0111 a0001c0001t0002g0025 a0001c0001t0002g0051 others(4): Show |
7 | NA18941.hp1 NA18952.hp2 NA19011.hp1 others(4): Show |
intron_variant | MODIFIER | c.354-2678C>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150122 | |||||||
chr17:49150145 | T | G | 1 | a0001c0001t0003g0281 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.354-2655T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150145 | |||||||
chr17:49150163 | T | C | 8 | a0001c0001t0002g0042 a0001c0001t0002g0267 a0001c0001t0002g0268 others(5): Show |
8 | HG03654.hp2 NA18948.hp2 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.354-2637T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150163 | |||||||
chr17:49150165 | T | TGCCTAGC others(42): Show |
1 | a0001c0004t0050g0116 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.354-2634_354-2633i others(51): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49150165 | ||||||
chr17:49150166 | G | GCCCAGCC others(91): Show |
8 | a0001c0001t0001g0046 a0001c0001t0001g0054 a0001c0001t0001g0055 others(5): Show |
8 | HG00099.hp2 HG01361.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.354-2634_354-2633i others(100): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150166 | |||||||
chr17:49150167 | T | C | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(85): Show |
97 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.354-2633T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150167 | |||||||
chr17:49150167 | T | TCCGGCCA others(42): Show |
3 | a0001c0001t0002g0074 a0001c0001t0002g0148 a0002c0002t0004g0194 |
3 | HG02735.hp1 HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.354-2565_354-2517d others(51): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49150167 | ||||||
chr17:49150167 | TCCGGCCA others(42): Show |
T | 30 | a0001c0001t0001g0021 a0001c0001t0001g0070 a0001c0001t0001g0328 others(27): Show |
32 | HG00438.hp1 HG00741.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.354-2565_354-2517d others(51): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49150167 | ||||||
chr17:49150170 | G | A | 79 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(76): Show |
88 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.354-2630G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150170 | |||||||
chr17:49150202 | GGGTCAGC others(9): Show |
G | 1 | a0001c0001t0057g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.354-2595_354-2580d others(18): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49150202 | ||||||
chr17:49150215 | G | A | 1 | a0001c0004t0050g0116 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.354-2585G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150215 | |||||||
chr17:49150215 | G | GCCCGGCC others(42): Show |
67 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(64): Show |
76 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.354-2550_354-2549i others(51): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49150215 | ||||||
chr17:49150235 | C | T | 1 | a0002c0002t0004g0305 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.354-2565C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150235 | |||||||
chr17:49150236 | G | A | 1 | a0001c0001t0002g0290 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.354-2564G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150236 | |||||||
chr17:49150247 | GGGGGGGT others(41): Show |
G | 1 | a0002c0002t0004g0305 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.354-2546_354-2499d others(50): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49150247 | ||||||
chr17:49150251 | G | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0320 |
2 | HG00639.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.354-2549G>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150251 | |||||||
chr17:49150257 | GCCCCCCG others(44): Show |
G | 2 | a0001c0001t0001g0083 a0001c0001t0001g0103 |
2 | HG00639.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.354-2536_354-2486d others(53): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49150257 | ||||||
chr17:49150264 | G | A | 9 | a0001c0001t0001g0320 a0001c0001t0044g0160 a0001c0001t0051g0348 others(6): Show |
9 | HG01243.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.354-2536G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150264 | |||||||
chr17:49150284 | T | C | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(75): Show |
87 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.354-2516T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150284 | |||||||
chr17:49150294 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.354-2506G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150294 | |||||||
chr17:49150294 | G | T | 1 | a0002c0002t0004g0307 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.354-2506G>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150294 | |||||||
chr17:49150295 | T | G | 1 | a0002c0002t0004g0307 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.354-2505T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150295 | |||||||
chr17:49150295 | TG | T | 70 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(67): Show |
79 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.354-2497delG | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49150295 | ||||||
chr17:49150296 | G | GGGGGGGT others(41): Show |
7 | a0001c0001t0044g0160 a0001c0001t0051g0348 a0001c0004t0008g0263 others(4): Show |
7 | HG01243.hp2 HG02109.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.354-2498_354-2497i others(50): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49150296 | ||||||
chr17:49150307 | GC | G | 347 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(344): Show |
375 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(372): Show |
intron_variant | MODIFIER | c.354-2485delC | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49150307 | ||||||
chr17:49150308 | C | CCCCCCGC others(41): Show |
1 | a0001c0001t0001g0320 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.354-2487_354-2486i others(50): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49150308 | ||||||
chr17:49150311 | C | T | 12 | a0001c0001t0001g0037 a0001c0001t0001g0198 a0001c0001t0001g0217 others(9): Show |
12 | HG00735.hp1 HG01167.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.354-2489C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150311 | |||||||
chr17:49150319 | T | G | 17 | a0001c0001t0002g0010 a0001c0001t0002g0165 a0001c0001t0002g0166 others(14): Show |
19 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.354-2481T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150319 | |||||||
chr17:49150397 | T | C | 2 | a0001c0001t0044g0160 a0002c0006t0055g0272 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.354-2403T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150397 | |||||||
chr17:49150423 | A | G | 1 | a0001c0001t0002g0241 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.354-2377A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150423 | |||||||
chr17:49150444 | G | T | 1 | a0001c0001t0001g0037 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.354-2356G>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150444 | |||||||
chr17:49150476 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.354-2324A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150476 | |||||||
chr17:49150523 | C | T | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(85): Show |
97 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.354-2277C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150523 | |||||||
chr17:49150568 | T | C | 88 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(85): Show |
97 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.354-2232T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150568 | |||||||
chr17:49150573 | T | C | 1 | a0001c0001t0002g0031 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.354-2227T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150573 | |||||||
chr17:49150587 | C | A | 15 | a0001c0001t0002g0010 a0001c0001t0002g0165 a0001c0001t0002g0166 others(12): Show |
17 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.354-2213C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150587 | |||||||
chr17:49150617 | C | T | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(75): Show |
87 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.354-2183C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150617 | |||||||
chr17:49150670 | A | G | 41 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0035 others(38): Show |
45 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.354-2130A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150670 | |||||||
chr17:49150719 | C | A | 3 | a0001c0001t0002g0002 a0001c0001t0002g0026 a0001c0001t0002g0340 |
6 | NA18943.hp1 NA18960.hp1 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.354-2081C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150719 | |||||||
chr17:49150720 | G | A | 1 | a0003c0003t0009g0347 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.354-2080G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150720 | |||||||
chr17:49150732 | G | C | 1 | a0001c0001t0057g0161 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.354-2068G>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150732 | |||||||
chr17:49150786 | G | C | 1 | a0002c0002t0011g0274 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.354-2014G>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150786 | |||||||
chr17:49150793 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.354-2007C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150793 | |||||||
chr17:49150844 | C | T | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(129): Show |
145 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.354-1956C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150844 | |||||||
chr17:49150875 | A | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(129): Show |
145 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.354-1925A>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150875 | |||||||
chr17:49150895 | C | T | 1 | a0001c0001t0001g0339 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.354-1905C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150895 | |||||||
chr17:49150920 | T | A | 9 | a0001c0001t0044g0160 a0001c0001t0051g0348 a0001c0004t0008g0263 others(6): Show |
9 | HG01243.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.354-1880T>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150920 | |||||||
chr17:49150991 | A | C | 1 | a0001c0001t0002g0183 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.354-1809A>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49150991 | |||||||
chr17:49151477 | G | A | 3 | a0001c0001t0012g0152 a0001c0001t0012g0156 a0001c0001t0039g0078 |
3 | HG01884.hp1 HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.354-1323G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49151477 | |||||||
chr17:49151675 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.354-1125G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49151675 | |||||||
chr17:49151686 | C | A | 13 | a0001c0001t0001g0037 a0001c0001t0001g0198 a0001c0001t0001g0217 others(10): Show |
13 | HG00735.hp1 HG01167.hp1 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.354-1114C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49151686 | |||||||
chr17:49151738 | C | CT | 6 | a0001c0001t0001g0014 a0001c0001t0001g0117 a0001c0001t0001g0118 others(3): Show |
7 | HG02818.hp1 HG02896.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.354-1061dupT | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49151738 | ||||||
chr17:49151738 | C | T | 1 | a0001c0001t0019g0015 | 2 | HG03209.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.354-1062C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49151738 | |||||||
chr17:49151744 | C | CA | 7 | a0001c0001t0001g0092 a0001c0001t0001g0214 a0001c0001t0001g0250 others(4): Show |
7 | HG00408.hp2 HG01175.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.354-1040dupA | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49151744 | ||||||
chr17:49151744 | CA | C | 20 | a0001c0001t0002g0010 a0001c0001t0002g0165 a0001c0001t0002g0166 others(17): Show |
22 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.354-1040delA | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr17 | 49151744 | ||||||
chr17:49151745 | A | C | 113 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(110): Show |
124 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.354-1055A>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49151745 | |||||||
chr17:49151763 | G | A | 11 | a0001c0001t0001g0111 a0001c0001t0002g0002 a0001c0001t0002g0025 others(8): Show |
14 | HG02129.hp2 NA18941.hp1 NA18943.hp1 others(11): Show |
intron_variant | MODIFIER | c.354-1037G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49151763 | |||||||
chr17:49152034 | G | A | 1 | a0001c0001t0002g0180 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.354-766G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49152034 | |||||||
chr17:49152051 | T | G | 1 | a0001c0001t0006g0197 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.354-749T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49152051 | |||||||
chr17:49152076 | A | T | 12 | a0001c0001t0001g0218 a0001c0001t0001g0313 a0001c0001t0002g0176 others(9): Show |
13 | HG02258.hp1 HG02280.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.354-724A>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49152076 | |||||||
chr17:49152092 | G | C | 9 | a0001c0001t0002g0010 a0001c0001t0002g0165 a0001c0001t0002g0166 others(6): Show |
11 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(8): Show |
intron_variant | MODIFIER | c.354-708G>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49152092 | |||||||
chr17:49152326 | C | T | 1 | a0001c0001t0002g0143 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.354-474C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49152326 | |||||||
chr17:49152332 | T | A | 27 | a0001c0001t0001g0021 a0001c0001t0001g0328 a0001c0001t0006g0179 others(24): Show |
29 | HG00438.hp1 HG00741.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.354-468T>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49152332 | |||||||
chr17:49152517 | T | C | 1 | a0001c0001t0003g0167 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.354-283T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49152517 | |||||||
chr17:49152536 | C | T | 1 | a0001c0001t0002g0208 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.354-264C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49152536 | |||||||
chr17:49152634 | C | G | 7 | a0001c0001t0001g0014 a0001c0001t0001g0117 a0001c0001t0001g0118 others(4): Show |
9 | HG02818.hp1 HG02896.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.354-166C>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 3/10 | chr17 | 49152634 | |||||||
chr17:49152998 | T | G | 55 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0034 others(52): Show |
58 | HG00408.hp2 HG00438.hp2 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.460+92T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49152998 | |||||||
chr17:49153044 | A | G | 2 | a0001c0001t0044g0160 a0002c0006t0055g0272 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.460+138A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49153044 | |||||||
chr17:49153148 | C | T | 3 | a0002c0006t0021g0036 a0002c0006t0021g0099 a0009c0017t0035g0262 |
3 | HG02280.hp2 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.460+242C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49153148 | |||||||
chr17:49153149 | G | A | 1 | a0001c0001t0001g0217 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.460+243G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49153149 | |||||||
chr17:49153271 | T | A | 128 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0009 others(125): Show |
135 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.460+365T>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49153271 | |||||||
chr17:49153280 | C | T | 1 | a0001c0011t0042g0131 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.460+374C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49153280 | |||||||
chr17:49153338 | C | T | 11 | a0001c0001t0001g0079 a0001c0001t0001g0087 a0001c0001t0001g0088 others(8): Show |
11 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(8): Show |
intron_variant | MODIFIER | c.460+432C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49153338 | |||||||
chr17:49153347 | C | T | 39 | a0001c0001t0001g0021 a0001c0001t0001g0328 a0001c0001t0002g0176 others(36): Show |
42 | HG00438.hp1 HG00741.hp2 HG01069.hp2 others(39): Show |
intron_variant | MODIFIER | c.460+441C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49153347 | |||||||
chr17:49153375 | A | G | 3 | a0001c0005t0008g0011 a0001c0005t0008g0082 a0001c0011t0042g0131 |
4 | HG01069.hp2 HG01071.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.460+469A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49153375 | |||||||
chr17:49153463 | T | C | 24 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(21): Show |
26 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.460+557T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49153463 | |||||||
chr17:49153507 | A | AT | 124 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0059 others(121): Show |
134 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.460+615dupT | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 49153507 | ||||||
chr17:49153507 | A | T | 1 | a0002c0002t0004g0204 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.460+601A>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49153507 | |||||||
chr17:49153576 | G | A | 1 | a0002c0002t0004g0335 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.460+670G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49153576 | |||||||
chr17:49153652 | A | G | 1 | a0001c0011t0042g0131 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.460+746A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49153652 | |||||||
chr17:49153780 | C | T | 1 | a0001c0011t0042g0131 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.460+874C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49153780 | |||||||
chr17:49153799 | C | T | 113 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0030 others(110): Show |
123 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.460+893C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49153799 | |||||||
chr17:49153951 | T | C | 1 | a0001c0011t0042g0131 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.460+1045T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49153951 | |||||||
chr17:49153972 | T | A | 1 | a0001c0001t0001g0117 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.460+1066T>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49153972 | |||||||
chr17:49154010 | C | CT | 10 | a0001c0001t0001g0037 a0001c0001t0001g0123 a0001c0001t0001g0134 others(7): Show |
10 | HG01243.hp2 HG02056.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.460+1116dupT | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 49154010 | ||||||
chr17:49154017 | T | C | 1 | a0001c0001t0002g0033 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.460+1111T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49154017 | |||||||
chr17:49154021 | T | G | 1 | a0001c0001t0001g0147 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.460+1115T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49154021 | |||||||
chr17:49154022 | T | G | 36 | a0001c0001t0001g0003 a0001c0001t0001g0035 a0001c0001t0001g0045 others(33): Show |
40 | HG00099.hp1 HG00099.hp2 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.460+1116T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49154022 | |||||||
chr17:49154023 | G | T | 144 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0024 others(141): Show |
156 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(153): Show |
intron_variant | MODIFIER | c.460+1117G>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49154023 | |||||||
chr17:49154028 | C | T | 1 | a0002c0002t0005g0211 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.460+1122C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49154028 | |||||||
chr17:49154037 | G | GCT | 117 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0030 others(114): Show |
127 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.460+1132_460+1133d others(4): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 49154037 | ||||||
chr17:49154220 | C | T | 1 | a0013c0014t0002g0330 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.460+1314C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49154220 | |||||||
chr17:49154298 | G | T | 1 | a0001c0001t0002g0016 | 2 | NA18947.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.460+1392G>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49154298 | |||||||
chr17:49154696 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.460+1790A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49154696 | |||||||
chr17:49154734 | G | C | 1 | a0001c0001t0001g0244 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.460+1828G>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49154734 | |||||||
chr17:49154851 | G | T | 1 | a0001c0001t0022g0019 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.461-1715G>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49154851 | |||||||
chr17:49155070 | G | A | 119 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0030 others(116): Show |
129 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.461-1496G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49155070 | |||||||
chr17:49155079 | C | A | 1 | a0003c0003t0009g0347 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.461-1487C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49155079 | |||||||
chr17:49155125 | A | G | 23 | a0001c0001t0001g0021 a0001c0001t0001g0328 a0001c0001t0006g0179 others(20): Show |
25 | HG00438.hp1 HG00741.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.461-1441A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49155125 | |||||||
chr17:49155200 | C | G | 2 | a0001c0001t0001g0218 a0001c0001t0008g0254 |
2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.461-1366C>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49155200 | |||||||
chr17:49155202 | T | G | 119 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0030 others(116): Show |
129 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.461-1364T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49155202 | |||||||
chr17:49155218 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.461-1348A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49155218 | |||||||
chr17:49155228 | G | A | 1 | a0001c0001t0044g0160 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.461-1338G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49155228 | |||||||
chr17:49155230 | G | A | 1 | a0001c0001t0002g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.461-1336G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49155230 | |||||||
chr17:49155255 | A | G | 23 | a0001c0001t0001g0021 a0001c0001t0001g0328 a0001c0001t0006g0179 others(20): Show |
25 | HG00438.hp1 HG00741.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.461-1311A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49155255 | |||||||
chr17:49155297 | C | CA | 40 | a0001c0001t0001g0022 a0001c0001t0001g0037 a0001c0001t0001g0044 others(37): Show |
40 | HG00423.hp2 HG00438.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.461-1246dupA | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 49155297 | ||||||
chr17:49155297 | C | CAA | 7 | a0001c0001t0002g0301 a0001c0001t0003g0327 a0001c0001t0025g0195 others(4): Show |
7 | HG02109.hp2 HG02135.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.461-1247_461-1246d others(4): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 49155297 | ||||||
chr17:49155297 | CA | C | 30 | a0001c0001t0001g0021 a0001c0001t0001g0040 a0001c0001t0001g0070 others(27): Show |
32 | HG00438.hp1 HG00741.hp2 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.461-1246delA | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 49155297 | ||||||
chr17:49155297 | CAA | C | 101 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0030 others(98): Show |
111 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.461-1247_461-1246d others(4): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 49155297 | ||||||
chr17:49155312 | A | G | 1 | a0001c0001t0001g0223 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.461-1254A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49155312 | |||||||
chr17:49155477 | C | A | 2 | a0001c0001t0044g0160 a0002c0006t0055g0272 |
2 | HG02109.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.461-1089C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49155477 | |||||||
chr17:49155601 | C | CA | 5 | a0001c0004t0008g0263 a0001c0004t0008g0264 a0001c0004t0020g0253 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.461-956dupA | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr17 | 49155601 | ||||||
chr17:49155808 | C | T | 5 | a0001c0004t0008g0263 a0001c0004t0008g0264 a0001c0004t0020g0253 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.461-758C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49155808 | |||||||
chr17:49155897 | T | G | 6 | a0001c0001t0002g0255 a0001c0001t0018g0284 a0001c0011t0042g0131 others(3): Show |
7 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.461-669T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49155897 | |||||||
chr17:49156084 | A | C | 1 | a0001c0001t0006g0332 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.461-482A>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49156084 | |||||||
chr17:49156132 | C | T | 1 | a0001c0001t0040g0049 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.461-434C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49156132 | |||||||
chr17:49156214 | C | T | 23 | a0001c0001t0001g0021 a0001c0001t0001g0328 a0001c0001t0006g0179 others(20): Show |
25 | HG00438.hp1 HG00741.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.461-352C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49156214 | |||||||
chr17:49156289 | G | A | 117 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0030 others(114): Show |
127 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.461-277G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49156289 | |||||||
chr17:49156424 | G | A | 1 | a0001c0011t0042g0131 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.461-142G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49156424 | |||||||
chr17:49156458 | T | C | 5 | a0001c0004t0008g0263 a0001c0004t0008g0264 a0001c0004t0020g0253 others(2): Show |
5 | HG02109.hp2 HG02258.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.461-108T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49156458 | |||||||
chr17:49156562 | C | A | 1 | a0001c0001t0032g0129 | 1 | NA18906.hp1 | splice_region_variant&intron_variant | LOW | c.461-4C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 4/10 | chr17 | 49156562 | |||||||
chr17:49156683 | C | T | 2 | a0001c0001t0003g0278 a0001c0001t0003g0279 |
2 | HG02735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.498+80C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49156683 | |||||||
chr17:49156755 | T | G | 146 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0024 others(143): Show |
158 | HG00323.hp1 HG00423.hp1 HG00438.hp1 others(155): Show |
intron_variant | MODIFIER | c.498+152T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49156755 | |||||||
chr17:49156860 | G | A | 12 | a0001c0001t0001g0111 a0001c0001t0002g0002 a0001c0001t0002g0025 others(9): Show |
15 | NA18939.hp2 NA18941.hp1 NA18943.hp1 others(12): Show |
intron_variant | MODIFIER | c.498+257G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49156860 | |||||||
chr17:49156997 | A | T | 1 | a0008c0018t0029g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.498+394A>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49156997 | |||||||
chr17:49157220 | C | G | 111 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0030 others(108): Show |
121 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.498+617C>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49157220 | |||||||
chr17:49157221 | C | T | 5 | a0001c0001t0001g0258 a0001c0001t0002g0109 a0001c0001t0002g0164 others(2): Show |
5 | HG01346.hp2 HG01934.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.498+618C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49157221 | |||||||
chr17:49157245 | T | A | 1 | a0001c0001t0002g0170 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.498+642T>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49157245 | |||||||
chr17:49157314 | C | A | 1 | a0001c0001t0002g0043 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.498+711C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49157314 | |||||||
chr17:49157326 | A | AT | 33 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0028 others(30): Show |
35 | HG00408.hp1 HG00423.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.498+735dupT | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 49157326 | ||||||
chr17:49157326 | AT | A | 23 | a0001c0001t0001g0021 a0001c0001t0001g0328 a0001c0001t0006g0179 others(20): Show |
25 | HG00438.hp1 HG00741.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.498+735delT | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 49157326 | ||||||
chr17:49157355 | CTGT | C | 108 | a0001c0001t0001g0008 a0001c0001t0001g0030 a0001c0001t0001g0059 others(105): Show |
118 | HG00323.hp1 HG00544.hp1 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.498+753_498+755del others(3): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49157355 | |||||||
chr17:49157363 | TAG | T | 108 | a0001c0001t0001g0008 a0001c0001t0001g0030 a0001c0001t0001g0059 others(105): Show |
118 | HG00323.hp1 HG00544.hp1 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.498+761_498+762del others(2): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49157363 | |||||||
chr17:49157368 | T | C | 108 | a0001c0001t0001g0008 a0001c0001t0001g0030 a0001c0001t0001g0059 others(105): Show |
118 | HG00323.hp1 HG00544.hp1 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.498+765T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49157368 | |||||||
chr17:49157369 | GGAGTGCA others(18): Show |
G | 108 | a0001c0001t0001g0008 a0001c0001t0001g0030 a0001c0001t0001g0059 others(105): Show |
118 | HG00323.hp1 HG00544.hp1 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.498+767_498+791del others(25): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49157369 | |||||||
chr17:49157396 | C | G | 108 | a0001c0001t0001g0008 a0001c0001t0001g0030 a0001c0001t0001g0059 others(105): Show |
118 | HG00323.hp1 HG00544.hp1 HG00597.hp1 others(115): Show |
intron_variant | MODIFIER | c.498+793C>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49157396 | |||||||
chr17:49157562 | T | G | 1 | a0001c0001t0001g0218 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.498+959T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49157562 | |||||||
chr17:49157691 | C | T | 3 | a0001c0001t0001g0218 a0001c0001t0013g0155 a0001c0001t0013g0350 |
3 | HG03130.hp1 HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.498+1088C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49157691 | |||||||
chr17:49157711 | C | G | 2 | a0001c0001t0002g0180 a0001c0001t0002g0290 |
2 | HG00408.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.498+1108C>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49157711 | |||||||
chr17:49157801 | C | T | 1 | a0009c0017t0035g0262 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.498+1198C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49157801 | |||||||
chr17:49157809 | G | C | 1 | a0009c0017t0035g0262 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.498+1206G>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49157809 | |||||||
chr17:49157959 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.499-1078A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49157959 | |||||||
chr17:49158259 | A | T | 347 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(344): Show |
375 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(372): Show |
intron_variant | MODIFIER | c.499-778A>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49158259 | |||||||
chr17:49158451 | C | A | 1 | a0001c0001t0051g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.499-586C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49158451 | |||||||
chr17:49158463 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.499-574G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49158463 | |||||||
chr17:49158575 | T | C | 1 | a0008c0018t0029g0203 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.499-462T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49158575 | |||||||
chr17:49158622 | G | A | 1 | a0001c0001t0002g0199 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.499-415G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49158622 | |||||||
chr17:49158636 | C | CA | 209 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(206): Show |
225 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.499-380dupA | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 49158636 | ||||||
chr17:49158636 | C | CAA | 25 | a0001c0001t0001g0009 a0001c0001t0001g0044 a0001c0001t0001g0088 others(22): Show |
26 | HG00735.hp1 HG00738.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.499-381_499-380dup others(2): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 49158636 | ||||||
chr17:49158636 | CA | C | 28 | a0001c0001t0001g0021 a0001c0001t0001g0328 a0001c0001t0002g0207 others(25): Show |
31 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.499-380delA | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr17 | 49158636 | ||||||
chr17:49158782 | G | A | 1 | a0001c0001t0002g0139 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.499-255G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49158782 | |||||||
chr17:49158848 | A | G | 1 | a0002c0006t0055g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.499-189A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49158848 | |||||||
chr17:49158924 | C | G | 2 | a0001c0001t0003g0278 a0001c0001t0003g0279 |
2 | HG02735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.499-113C>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49158924 | |||||||
chr17:49158943 | C | T | 1 | a0001c0001t0003g0285 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.499-94C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49158943 | |||||||
chr17:49158975 | T | C | 1 | a0002c0006t0055g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.499-62T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 5/10 | chr17 | 49158975 | |||||||
chr17:49159289 | C | T | 4 | a0002c0002t0004g0184 a0002c0002t0004g0220 a0002c0002t0004g0299 others(1): Show |
5 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.679+72C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 6/10 | chr17 | 49159289 | |||||||
chr17:49159332 | T | G | 1 | a0002c0006t0055g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.679+115T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 6/10 | chr17 | 49159332 | |||||||
chr17:49159334 | G | GTTTGT | 213 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(210): Show |
231 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(228): Show |
intron_variant | MODIFIER | c.679+136_679+140dup others(5): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 49159334 | ||||||
chr17:49159334 | GTTTGT | G | 6 | a0001c0001t0008g0254 a0001c0004t0008g0263 a0001c0004t0008g0264 others(3): Show |
6 | HG02109.hp2 HG02258.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.679+136_679+140del others(5): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr17 | 49159334 | ||||||
chr17:49159365 | G | A | 1 | a0002c0006t0021g0036 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.679+148G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 6/10 | chr17 | 49159365 | |||||||
chr17:49159372 | C | T | 5 | a0002c0002t0011g0153 a0002c0002t0011g0154 a0002c0002t0011g0274 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.679+155C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 6/10 | chr17 | 49159372 | |||||||
chr17:49159430 | C | A | 1 | a0001c0001t0002g0135 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.679+213C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 6/10 | chr17 | 49159430 | |||||||
chr17:49159482 | C | T | 1 | a0002c0006t0055g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.679+265C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 6/10 | chr17 | 49159482 | |||||||
chr17:49159598 | C | T | 348 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(345): Show |
376 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(373): Show |
intron_variant | MODIFIER | c.679+381C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 6/10 | chr17 | 49159598 | |||||||
chr17:49159910 | G | A | 1 | a0001c0001t0002g0326 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.680-645G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 6/10 | chr17 | 49159910 | |||||||
chr17:49160112 | G | A | 10 | a0001c0001t0002g0142 a0001c0001t0002g0182 a0001c0001t0002g0208 others(7): Show |
10 | HG00735.hp2 HG01074.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.680-443G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 6/10 | chr17 | 49160112 | |||||||
chr17:49160429 | A | C | 3 | a0001c0001t0002g0176 a0001c0001t0002g0255 a0001c0001t0002g0345 |
3 | HG02258.hp1 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.680-126A>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 6/10 | chr17 | 49160429 | |||||||
chr17:49160460 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.680-95A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 6/10 | chr17 | 49160460 | |||||||
chr17:49160498 | A | G | 1 | a0001c0001t0002g0162 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.680-57A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 6/10 | chr17 | 49160498 | |||||||
chr17:49160666 | C | T | 348 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(345): Show |
376 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(373): Show |
intron_variant | MODIFIER | c.766+25C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49160666 | |||||||
chr17:49160723 | G | A | 1 | a0001c0001t0007g0325 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.766+82G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49160723 | |||||||
chr17:49160861 | G | A | 2 | a0008c0018t0029g0203 a0009c0017t0035g0262 |
2 | HG01891.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.766+220G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49160861 | |||||||
chr17:49160884 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.766+243A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49160884 | |||||||
chr17:49161076 | A | G | 268 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(265): Show |
289 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.766+435A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49161076 | |||||||
chr17:49161161 | G | A | 1 | a0001c0001t0002g0095 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.766+520G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49161161 | |||||||
chr17:49161193 | T | G | 348 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(345): Show |
376 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(373): Show |
intron_variant | MODIFIER | c.766+552T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49161193 | |||||||
chr17:49161275 | G | GA | 339 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(336): Show |
366 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(363): Show |
intron_variant | MODIFIER | c.766+647dupA | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 49161275 | ||||||
chr17:49161296 | A | G | 348 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(345): Show |
376 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(373): Show |
intron_variant | MODIFIER | c.766+655A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49161296 | |||||||
chr17:49161354 | A | G | 1 | a0001c0001t0002g0159 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.766+713A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49161354 | |||||||
chr17:49161539 | G | A | 1 | a0001c0001t0002g0236 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.766+898G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49161539 | |||||||
chr17:49161681 | G | GA | 345 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(342): Show |
373 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(370): Show |
intron_variant | MODIFIER | c.766+1048dupA | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 49161681 | ||||||
chr17:49161919 | A | G | 3 | a0001c0001t0034g0349 a0001c0001t0057g0161 a0010c0015t0053g0237 |
3 | HG02451.hp2 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.766+1278A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49161919 | |||||||
chr17:49161961 | T | A | 1 | a0001c0001t0003g0020 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.766+1320T>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49161961 | |||||||
chr17:49162011 | G | A | 226 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(223): Show |
244 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.766+1370G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49162011 | |||||||
chr17:49162018 | T | TG | 6 | a0001c0001t0002g0168 a0001c0001t0002g0169 a0001c0001t0002g0170 others(3): Show |
6 | HG00738.hp1 HG01433.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.766+1378dupG | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 49162018 | ||||||
chr17:49162024 | G | T | 1 | a0001c0001t0039g0078 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.766+1383G>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49162024 | |||||||
chr17:49162051 | G | A | 1 | a0001c0001t0051g0348 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.766+1410G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49162051 | |||||||
chr17:49162081 | G | A | 1 | a0001c0001t0048g0175 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.766+1440G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49162081 | |||||||
chr17:49162101 | C | T | 39 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0034 others(36): Show |
39 | HG00423.hp1 HG00438.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.766+1460C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49162101 | |||||||
chr17:49162132 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.766+1491C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49162132 | |||||||
chr17:49162149 | G | A | 272 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(269): Show |
294 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.766+1508G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49162149 | |||||||
chr17:49162156 | C | A | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(270): Show |
295 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.766+1515C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49162156 | |||||||
chr17:49162285 | C | T | 272 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(269): Show |
294 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(291): Show |
intron_variant | MODIFIER | c.766+1644C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49162285 | |||||||
chr17:49162408 | G | A | 10 | a0001c0001t0051g0348 a0002c0002t0011g0153 a0002c0002t0011g0154 others(7): Show |
10 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.767-1680G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49162408 | |||||||
chr17:49162674 | C | T | 2 | a0004c0012t0007g0336 a0004c0012t0007g0337 |
2 | HG02071.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.767-1414C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49162674 | |||||||
chr17:49162679 | T | G | 3 | a0001c0001t0034g0349 a0001c0001t0057g0161 a0010c0015t0053g0237 |
3 | HG02451.hp2 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.767-1409T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49162679 | |||||||
chr17:49162795 | C | T | 82 | a0001c0001t0001g0022 a0001c0001t0001g0214 a0001c0001t0001g0291 others(79): Show |
89 | HG00323.hp2 HG00408.hp2 HG00673.hp2 others(86): Show |
intron_variant | MODIFIER | c.767-1293C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49162795 | |||||||
chr17:49162827 | C | T | 2 | a0002c0006t0021g0036 a0002c0006t0021g0099 |
2 | NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.767-1261C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49162827 | |||||||
chr17:49162833 | A | G | 2 | a0003c0003t0009g0239 a0003c0003t0009g0240 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.767-1255A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49162833 | |||||||
chr17:49162912 | C | CAA | 30 | a0001c0001t0001g0037 a0001c0001t0001g0087 a0001c0001t0001g0103 others(27): Show |
31 | HG00323.hp1 HG00438.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.767-1154_767-1153d others(4): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 49162912 | ||||||
chr17:49162912 | C | CAAA | 194 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(191): Show |
215 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.767-1155_767-1153d others(5): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 49162912 | ||||||
chr17:49162912 | C | CAAAA | 97 | a0001c0001t0001g0022 a0001c0001t0001g0023 a0001c0001t0001g0024 others(94): Show |
102 | HG00423.hp1 HG00609.hp1 HG00621.hp1 others(99): Show |
intron_variant | MODIFIER | c.767-1156_767-1153d others(6): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 49162912 | ||||||
chr17:49162912 | C | CAAAAA | 22 | a0001c0001t0001g0214 a0001c0001t0002g0025 a0001c0001t0002g0026 others(19): Show |
23 | HG01175.hp1 HG01243.hp1 HG01346.hp1 others(20): Show |
intron_variant | MODIFIER | c.767-1157_767-1153d others(7): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 49162912 | ||||||
chr17:49163131 | G | A | 128 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(125): Show |
145 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.767-957G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49163131 | |||||||
chr17:49163157 | C | T | 1 | a0002c0002t0054g0101 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.767-931C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49163157 | |||||||
chr17:49163331 | T | C | 1 | a0002c0006t0055g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.767-757T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49163331 | |||||||
chr17:49163400 | G | T | 1 | a0001c0001t0022g0019 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.767-688G>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49163400 | |||||||
chr17:49163456 | TC | T | 349 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(346): Show |
377 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(374): Show |
intron_variant | MODIFIER | c.767-630delC | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 49163456 | ||||||
chr17:49163522 | G | A | 273 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(270): Show |
295 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.767-566G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49163522 | |||||||
chr17:49163703 | C | A | 2 | a0002c0006t0021g0036 a0002c0006t0021g0099 |
2 | NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.767-385C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49163703 | |||||||
chr17:49163751 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.767-337C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49163751 | |||||||
chr17:49163756 | C | CA | 63 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0027 others(60): Show |
63 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.767-310dupA | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 49163756 | ||||||
chr17:49163756 | CA | C | 101 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0030 others(98): Show |
111 | HG00099.hp1 HG00544.hp1 HG00597.hp1 others(108): Show |
intron_variant | MODIFIER | c.767-310delA | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 49163756 | ||||||
chr17:49163756 | CAA | C | 75 | a0001c0001t0001g0022 a0001c0001t0001g0214 a0001c0001t0001g0291 others(72): Show |
82 | HG00408.hp2 HG00673.hp2 HG00735.hp2 others(79): Show |
intron_variant | MODIFIER | c.767-311_767-310del others(2): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr17 | 49163756 | ||||||
chr17:49163940 | C | A | 2 | a0002c0006t0021g0036 a0002c0006t0021g0099 |
2 | NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.767-148C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 7/10 | chr17 | 49163940 | |||||||
chr17:49164280 | G | A | 3 | a0001c0001t0006g0098 a0001c0001t0006g0145 a0001c0001t0006g0332 |
3 | HG01358.hp1 HG01515.hp2 HG01516.hp2 |
splice_region_variant&intron_variant | LOW | c.954+5G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 8/10 | chr17 | 49164280 | |||||||
chr17:49164389 | C | T | 2 | a0008c0018t0029g0203 a0009c0017t0035g0262 |
2 | HG01891.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.954+114C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 8/10 | chr17 | 49164389 | |||||||
chr17:49164497 | C | T | 1 | a0001c0001t0002g0148 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.954+222C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 8/10 | chr17 | 49164497 | |||||||
chr17:49164499 | C | A | 1 | a0002c0002t0011g0274 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.954+224C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 8/10 | chr17 | 49164499 | |||||||
chr17:49164500 | AT | A | 120 | a0001c0001t0001g0058 a0001c0001t0001g0190 a0001c0001t0001g0192 others(117): Show |
127 | HG00323.hp2 HG00408.hp2 HG00544.hp2 others(124): Show |
intron_variant | MODIFIER | c.954+244delT | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr17 | 49164500 | ||||||
chr17:49164500 | ATT | A | 215 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(212): Show |
235 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.954+243_954+244del others(2): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr17 | 49164500 | ||||||
chr17:49164500 | ATTT | A | 6 | a0001c0001t0001g0311 a0001c0001t0003g0327 a0001c0001t0006g0137 others(3): Show |
6 | HG01884.hp1 HG02738.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.954+242_954+244del others(3): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr17 | 49164500 | ||||||
chr17:49164540 | C | T | 1 | a0001c0001t0025g0195 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.954+265C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 8/10 | chr17 | 49164540 | |||||||
chr17:49164633 | G | A | 5 | a0001c0001t0010g0013 a0001c0001t0010g0230 a0001c0001t0010g0243 others(2): Show |
6 | HG02280.hp1 HG02723.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.954+358G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 8/10 | chr17 | 49164633 | |||||||
chr17:49164763 | A | G | 7 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(4): Show |
7 | NA18941.hp2 NA18942.hp2 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.954+488A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 8/10 | chr17 | 49164763 | |||||||
chr17:49164856 | C | T | 10 | a0002c0002t0011g0153 a0002c0002t0011g0154 a0002c0002t0011g0274 others(7): Show |
10 | HG01891.hp2 HG02109.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.954+581C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 8/10 | chr17 | 49164856 | |||||||
chr17:49164908 | C | T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0126 a0001c0001t0001g0127 others(1): Show |
5 | HG01099.hp2 HG01928.hp2 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.954+633C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 8/10 | chr17 | 49164908 | |||||||
chr17:49164981 | T | G | 1 | a0001c0001t0001g0314 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.954+706T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 8/10 | chr17 | 49164981 | |||||||
chr17:49165132 | C | T | 5 | a0002c0002t0011g0153 a0002c0002t0011g0154 a0002c0002t0011g0274 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.954+857C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 8/10 | chr17 | 49165132 | |||||||
chr17:49165145 | G | A | 1 | a0001c0001t0013g0350 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.954+870G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 8/10 | chr17 | 49165145 | |||||||
chr17:49165515 | ACTCCCCA others(64): Show |
A | 2 | a0001c0001t0002g0176 a0010c0015t0053g0237 |
2 | HG02976.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.955-584_955-514del others(71): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr17 | 49165515 | ||||||
chr17:49165617 | T | G | 1 | a0001c0001t0001g0217 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.955-497T>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 8/10 | chr17 | 49165617 | |||||||
chr17:49165637 | T | C | 5 | a0001c0001t0010g0013 a0001c0001t0010g0230 a0001c0001t0010g0243 others(2): Show |
6 | HG02280.hp1 HG02723.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.955-477T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 8/10 | chr17 | 49165637 | |||||||
chr17:49166034 | G | T | 1 | a0001c0001t0001g0235 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.955-80G>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 8/10 | chr17 | 49166034 | |||||||
chr17:49166087 | A | C | 10 | a0001c0001t0001g0030 a0001c0001t0001g0059 a0001c0001t0001g0061 others(7): Show |
10 | NA18943.hp2 NA18944.hp1 NA18945.hp2 others(7): Show |
intron_variant | MODIFIER | c.955-27A>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 8/10 | chr17 | 49166087 | |||||||
chr17:49166260 | G | T | 82 | a0001c0001t0001g0076 a0001c0001t0001g0214 a0001c0001t0002g0002 others(79): Show |
88 | HG00323.hp2 HG00408.hp2 HG00738.hp1 others(85): Show |
splice_region_variant&intron_variant | LOW | c.1095+6G>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 9/10 | chr17 | 49166260 | |||||||
chr17:49166322 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1095+68G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 9/10 | chr17 | 49166322 | |||||||
chr17:49166774 | C | T | 1 | a0001c0001t0001g0315 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1095+520C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 9/10 | chr17 | 49166774 | |||||||
chr17:49166898 | G | C | 1 | a0001c0001t0001g0089 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1095+644G>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 9/10 | chr17 | 49166898 | |||||||
chr17:49167050 | C | T | 92 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0016 others(89): Show |
98 | HG00323.hp2 HG00408.hp2 HG00639.hp1 others(95): Show |
intron_variant | MODIFIER | c.1095+796C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 9/10 | chr17 | 49167050 | |||||||
chr17:49167157 | GAGA | G | 137 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(134): Show |
154 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.1095+907_1095+909d others(5): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 49167157 | ||||||
chr17:49167409 | G | A | 7 | a0001c0001t0001g0041 a0001c0001t0001g0103 a0001c0001t0001g0124 others(4): Show |
7 | HG00639.hp2 HG01192.hp1 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.1095+1155G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 9/10 | chr17 | 49167409 | |||||||
chr17:49167414 | G | C | 1 | a0002c0002t0004g0204 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1095+1160G>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 9/10 | chr17 | 49167414 | |||||||
chr17:49167456 | C | CT | 5 | a0002c0002t0011g0153 a0002c0002t0011g0154 a0002c0002t0011g0274 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1095+1205dupT | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 49167456 | ||||||
chr17:49167558 | T | C | 162 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0012 others(159): Show |
173 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(170): Show |
intron_variant | MODIFIER | c.1096-1123T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 9/10 | chr17 | 49167558 | |||||||
chr17:49167559 | G | A | 28 | a0002c0002t0004g0038 a0002c0002t0004g0039 a0002c0002t0004g0100 others(25): Show |
31 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1096-1122G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 9/10 | chr17 | 49167559 | |||||||
chr17:49167608 | C | CT | 110 | a0001c0001t0001g0064 a0001c0001t0001g0123 a0001c0001t0001g0296 others(107): Show |
117 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1096-1054dupT | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 49167608 | ||||||
chr17:49167608 | CT | C | 6 | a0001c0001t0001g0056 a0001c0001t0001g0072 a0001c0001t0001g0189 others(3): Show |
6 | HG00099.hp2 HG01884.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.1096-1054delT | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 49167608 | ||||||
chr17:49167641 | G | A | 5 | a0002c0002t0011g0153 a0002c0002t0011g0154 a0002c0002t0011g0274 others(2): Show |
5 | HG02451.hp1 HG02486.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1096-1040G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 9/10 | chr17 | 49167641 | |||||||
chr17:49167868 | CCAAAGTG others(9): Show |
C | 1 | a0002c0006t0055g0272 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1096-811_1096-796d others(18): Show |
B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr17 | 49167868 | ||||||
chr17:49167895 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1096-786C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 9/10 | chr17 | 49167895 | |||||||
chr17:49167917 | C | T | 1 | a0001c0001t0002g0290 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1096-764C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 9/10 | chr17 | 49167917 | |||||||
chr17:49167928 | A | G | 33 | a0002c0002t0004g0038 a0002c0002t0004g0039 a0002c0002t0004g0100 others(30): Show |
36 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.1096-753A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 9/10 | chr17 | 49167928 | |||||||
chr17:49168164 | T | C | 7 | a0001c0001t0008g0254 a0001c0004t0008g0263 a0001c0004t0008g0264 others(4): Show |
8 | HG01069.hp2 HG01071.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1096-517T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 9/10 | chr17 | 49168164 | |||||||
chr17:49168243 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1096-438G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 9/10 | chr17 | 49168243 | |||||||
chr17:49168414 | C | A | 1 | a0001c0001t0001g0014 | 2 | HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1096-267C>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 9/10 | chr17 | 49168414 | |||||||
chr17:49168444 | T | C | 117 | a0001c0001t0002g0002 a0001c0001t0002g0010 a0001c0001t0002g0012 others(114): Show |
123 | HG00323.hp2 HG00408.hp2 HG00639.hp1 others(120): Show |
intron_variant | MODIFIER | c.1096-237T>C | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 9/10 | chr17 | 49168444 | |||||||
chr17:49168525 | G | A | 33 | a0002c0002t0004g0038 a0002c0002t0004g0039 a0002c0002t0004g0100 others(30): Show |
36 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.1096-156G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 9/10 | chr17 | 49168525 | |||||||
chr17:49168567 | C | T | 39 | a0001c0001t0010g0013 a0001c0001t0010g0230 a0001c0001t0010g0243 others(36): Show |
43 | HG00323.hp1 HG00438.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.1096-114C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 9/10 | chr17 | 49168567 | |||||||
chr17:49168610 | G | A | 2 | a0002c0006t0021g0036 a0002c0006t0021g0099 |
2 | NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1096-71G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 9/10 | chr17 | 49168610 | |||||||
chr17:49168910 | C | T | 2 | a0001c0001t0018g0282 a0001c0001t0018g0284 |
2 | NA19009.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1315+10C>T | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 10/10 | chr17 | 49168910 | |||||||
chr17:49169027 | C | G | 1 | a0001c0001t0002g0205 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1315+127C>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 10/10 | chr17 | 49169027 | |||||||
chr17:49169184 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1315+284A>G | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 10/10 | chr17 | 49169184 | |||||||
chr17:49169485 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1316-38G>A | B4GALNT2 | ENSG00000167080.9 | transcript | ENST00000393354.7 | protein_coding | 10/10 | chr17 | 49169485 |